Current landscape and future trends in salivary gland oncology research—a bibliometric evaluation
Original Article

Current landscape and future trends in salivary gland oncology research—a bibliometric evaluation

Haoran Ding, Chenzhou Wu, Zhifei Su, Tianyi Wang, Shiyong Zhuang, Chunjie Li, Yi Li

State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Head and Neck Oncology Surgery, West China Hospital of Stomatology, Sichuan University, Chengdu, China

Contributions: (I) Conception and design: Y Li, C Li; (II) Administrative support: Y Li, C Li; (III) Provision of study materials or patients: None; (IV) Collection and assembly of data: H Ding, C Wu, Z Su, T Wang, S Zhuang; (V) Data analysis and interpretation: H Ding, C Wu, Z Su, T Wang, S Zhuang; (VI) Manuscript writing: All authors; (VII) Final approval of manuscript: All authors.

Correspondence to: Yi Li, PhD; Chunjie Li, PhD. State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases & Department of Head and Neck Oncology Surgery, West China Hospital of Stomatology, Number 14, Unit 3, Renmin Nan Road, Chengdu 610041, China. Email: Liyi1012@163.com; lichunjie07@qq.com.

Background: The salivary glands are susceptible to both endogenous and exogenous influences, potentially resulting in the development of oncology. With the wide application of various technologies, research in this area has experienced rapid growth. Therefore, researchers must identify and characterize the current research hot topics to grasp the forefront of developments in the dynamic field of salivary gland oncology. The objective of this study was to thoroughly assess the current status and identify potential future research directions in salivary gland oncology.

Methods: The relevant salivary gland oncology dataset was obtained from the Web of Science Core Collection (WOSCC) database. Subsequently, VoSviewer and CiteSpace were employed for further evaluation.

Results: A total of 9,695 manuscripts were extracted and downloaded from the WOSCC database. Our findings revealed a substantial surge in research volume over the past 12 years. The researchers’ analysis revealed that Abbas Agami showed unparalleled dedication, with over 180 publications, and that RH Spiro had the highest cocitation count, confirming its status as a key figure in the field. The detection of bursts in secretory carcinoma and the integration of artificial intelligence in salivary oncology have attracted increasing interest. Notably, there is a discernible trend towards increased research engagement in the study of salivary gland malignancies.

Conclusions: This study not only evaluated the current research landscape in salivary gland oncology but also anticipates future trends. These insights could contribute to the advancement of knowledge and policymaking in salivary gland oncology.

Keywords: Salivary gland oncology; bibliometric analysis; research hotspots; research trends; sociometric analysis


Submitted Mar 20, 2024. Accepted for publication Jun 11, 2024. Published online Jun 24, 2024.

doi: 10.21037/gs-24-94


Highlight box

Key findings

• This manuscript offers an overview of the current state of research in salivary gland oncology.

• Salivary gland malignancies, target gene therapies, and radiotherapies emerge as hotspots in this field.

• Secretory carcinoma and the integration of artificial intelligence techniques in salivary gland oncology research are potential upcoming research trends in this area.

What is known and what is new?

• The number of studies on salivary gland oncology has significantly increased, benefiting from the wealth of big data available in today’s information-rich environment. This abundance of research data is instrumental in gaining a overview of the current status and projecting future trends in salivary gland oncology.

• Our manuscript integrated VOSviewer and CiteSpace to navigate through the intricate research landscape of salivary gland oncology. By identifying crucial biomarkers and exploring emerging trends, we aim to provide a comprehensive picture of the field's current trajectory and potential future developments.

What is the implication, and what should change now?

• The findings of this study provide valuable insights into the status and future directions of salivary gland oncology research. Clinicians can use this knowledge to enhance diagnostic and treatment strategies for salivary gland malignancies, particularly focusing on areas with heightened research interest such as adenoid cystic carcinoma and secretory carcinoma. Moreover, the emerging trend of integrating artificial intelligence into salivary oncology research presents promising opportunities for developing innovative diagnostic tools and personalized treatment approaches.


Introduction

The salivary glands play a fundamental role in saliva synthesis and secretion and are a key element in maintaining the physiological environment in the oral cavity. The salivary glands are susceptible to a multitude of internal and external factors that can predispose them to tumour formation (1,2). Pathologically, salivary gland tumours (SGTs) are categorized into three primary groups: benign and malignant epithelial tumours and mesenchymal tumours (2). Although the majority of SGTs are benign, malignant SGTs constitute a small proportion of head and neck oncological diseases, approximately 5%. Within this subset, the malignancy rates vary, with those of the parotid gland ranging from 15% to 35%, those of the submandibular gland ranging from 45%, and those of the sublingual glands ranging from 70% to 90%. Furthermore, malignant salivary tumours are predominant in cases involving the minor salivary glands, which are located on the floor of the mouth, the upper palate, the retromolar region, the tongue, and the lips (3). These conditions can lead to severe consequences, including facial paralysis, lung metastasis, and, in extreme cases, death (4,5).

Salivary gland oncology research traces back to the early 1900s when researchers primarily reported medical cases. During this period, fine needle sampling became a notable diagnostic technique (6,7). Simultaneously, researchers were actively involved in establishing surgical considerations and diagnostic standards for SGTs (8). The World Health Organization (WHO) released the initial edition of the histological classification in 1972. This classification divides SGTs into three categories: unclassified tumours, epithelial tumours, and nonepithelial tumours (9). This guideline was in effect for the subsequent two decades. Following further refinement and supplementation, the second edition of the WHO guidelines, published in 1992, incorporated 31 pathologies of SGT (10). In the early 2000s, there was a growing trend in exploring the expression or immunoreactivity of specific biomarkers in malignant SGTs, leading to the reclassification of salivary gland cancer (11). Owing to technological limitations, studies have primarily relied on single pathological or radiological methods, leading to a lack of detailed exploration into the mutual interactions involved in the mechanism of salivary gland cancer.

Through in-depth exploration in salivary gland oncology, the seemingly challenging mission of establishing guidelines for salivary gland oncology in the 1990s became tangible, leading scientists to recognize the genetic alterations associated with SGT. In 2017, the WHO introduced a new edition of the SGT classification system, providing a new perspective on salivary gland classification by emphasizing genetic alterations in SGTs for the first time (12).

The integration of various technologies, such as artificial intelligence, experimental devices, and methods, has driven a significant surge in studies and prompted revisions of the classification of SGTs in recent years (5,13-16). Currently, deep learning methods have recently been employed to differentiate and classify malignant and benign tumours in salivary gland oncology studies (14,17). Nonetheless, single-cell sequencing has been used to trace the tumorigenesis process in salivary gland oncology (18). The integration of these technologies and discoveries has contributed to a surge in the volume of scientific research manuscripts in salivary gland oncology.

In an era of information explosion, it is easy to access big data generated by the vast amount of research. Therefore, there is a need for effective tools to grasp and identify research hotspots and frontiers to comprehensively understand the current state and future research trends in salivary gland oncology.

Bibliometric analysis has become an established scientific specialty and a crucial component of research methodology, providing both qualitative and quantitative insights into scientific publications. VOSviewer is a widely utilized tool for bibliometric analysis and excels in generating knowledge maps through large-scale graphics. This software facilitates the analysis of manuscripts based on keyword occurrences, cocitations, references, authors, etc. It is a valuable tool for comprehending fundamental information in specific research areas. To detect and predict future trends in the area of salivary gland oncology, we used CiteSpace V for our analysis. Developed by Chaomei Chen, CiteSpace is software that can assist in analysing different manuscripts at multiple latitudes, including using keywords to cluster and timelines to analyse research (19-23). In addition, researchers could use this software to explore research trends in certain research fields via burst detection.

To the best of our knowledge, this study represents an inaugural bibliometric evaluation in the field of salivary gland oncology. In this manuscript, we integrated VOSviewer and CiteSpace to unravel the current landscape of research and highlight important biomarkers in salivary gland oncology, all while peering into the horizon to anticipate and depict future trends in this dynamic field.


Methods

Search strategy

The Web of Science Core Collection (WOSCC) database served as the primary source for data collection. The search formula for this study was as follows: “(TS=parotid OR salivary gland OR submandibular gland OR sublingual gland) AND TS= (tumor* OR cancer* OR onco*)”.

The study was limited to manuscripts published in English within the timeframe of 2012–2023. Only original articles were included in our bibliometric analysis. To minimize potential bias due to database updates, the literature search process was conducted within a single day on January 6th, 2024. Since the data for this research were obtained from the WOSCC database, ethical approval was not required for this study.

Statistical analysis

VOSviewer was utilized for co-occurrence analysis, while CiteSpace was applied for cocitation analysis, keyword clustering, and burst detection.

First, we used software to analyse the origin of the research in salivary oncology. Then, to understand the research focus of the scientists in salivary gland oncology, keyword clustering was employed to highlight the themes among the most frequently cocited authors.

Next, for keyword and reference analysis, we integrated VOSviewer and CiteSpace for a more comprehensive analysis. Through keyword clustering among the most cocited authors, we attempted to gain insights into the current research in this area. Next, by categorizing the most cocited references into different clusters by their research keywords, we generated a timeline visualization and depicted the change in each cluster over time.

Finally, burst detection was utilized to identify the keywords and references that experienced citation bursts, offering valuable insights into the upcoming research frontiers in this field. Figure 1 shows the workflow of this study.

Figure 1 The workflow of this study. TS, topic search; WOSCC, Web of Science Core Collection.

Results

Annual distribution of publication output

The data collected from WOSCC were uploaded to CiteSpace for intelligent data cleaning. We found 9,695 original articles concentrating on salivary gland oncology from 2012 to 2023. As illustrated in Figure 2, fewer publications focused on salivary gland oncology from 2012 to 2018, with an aggregate number of approximately 500 manuscripts annually. However, from 2019 to 2023, there was a noticeable increase in publications within the field of salivary gland oncology. This increase in volume indicates that the years from 2021 to 2023 potentially witnessed notable advancements in salivary gland oncological research.

Figure 2 The initial phase of the last 12 years [2012–2018] witnessed limited growth in the quantity of original articles in salivary gland oncology research. However, a significant surge in research output occurred in 2019, continuing to thrive in 2021 and 2022. Nevertheless, there was a decline in the number of manuscripts in 2023.

Contributing countries and journals

To gain a comprehensive understanding of research manuscripts in salivary gland oncology, we then examined the countries and journals that contributed significantly to this field.

As illustrated in Figure 3A, the United States, China, and Japan have emerged as the primary contributors in this domain, collectively accounting for nearly 50% of the total research manuscripts in salivary gland oncology. It is also noteworthy that the United States, England, Canada, and France exhibit relatively higher centrality in their research endeavors, suggesting that they may have made noteworthy discoveries and advancements in the field of salivary gland oncology.

Figure 3 Countries and journals devoted to salivary gland oncology. (A) Top 13 contributing countries: each node represents a country, with node size indicating the quantity of manuscripts. The highlighted outlines signify the centrality of each country, reflecting its significance in the field. Links between nodes depict cooperative relationships. (B) Contributing journals: each node represents a journal, with sizes indicating the quantity of publications in salivary gland oncology. Links denote manuscript citations, and color indicates the year of citation.

According to Figure 3B, spanning from 2012 to 2023, the journals Head and Neck, Oral Surgery Oral Medicine Oral Pathology Oral Radiology, and European Archives of Oto-Rhino-Laryngology have collectively published over 500 manuscripts on salivary gland oncology. These journals are identified as the top three sources contributing to research in this field.

Moreover, we also found that from 2021 to 2023, the number of publications on salivary gland oncology in cancer, Frontiers in Oncology, and Head & Neck Pathology increased, which may also indicate that salivary gland oncology has gained increased attention in these journals. Furthermore, an observed increase in the volume of citations related to salivary gland oncology research is noted in journals such as Cancers, Frontiers in Oncology, and Head & Neck Pathology from 2021 to 2023. This increase suggests that there may be an increasing focus on salivary gland oncology within these journals.

Analysis by researchers

Analysis of active researchers

Among the active researchers, as depicted in Figure 4A, Abbas Agami, Justin A. Bishop and Skalova Alena have emerged as the 3 most productive researchers in salivary gland oncological studies. These researchers have been dedicated to this field and have published more than 180 manuscripts during the last 12 years. Furthermore, our findings indicate that Abbas Agami, also known as the hub node, has relatively high centrality, indicating active collaboration with other researchers in this domain.

Figure 4 Active researchers and research focus of top co-cited researchers. (A) The diagram illustrates the most prolific researchers in salivary gland oncology. Each node represents a scientist, with node sizes denoting the number of publications. The highlighted circle around Abbas Agami emphasizes his significant centrality in this domain. Links between nodes signify collaboration among researchers. (B) Keywords clustering has revealed the hotspots among the most productive authors. (C) Through keyword clustering, we have identified the research focus among the most co-cited authors. Shared keywords have grouped two researchers into the same cluster. (C) 14 clusters, with cluster #0 being the largest, indicating that the top co-cited authors primarily focus on xerostomia in this field.

To reveal the specific research areas of the most productive ones, we utilized keyword clustering in CiteSpace for further evaluation. According to Figure 4B, the research topics in this area can be categorized into 13 clusters. The most substantial clusters included #RET, #Parotid tumor, and #Parotid gland. Moreover, we observed that researchers in this field focused on radiotherapy and proton therapy (clusters #5 and #8) within the domain of salivary gland oncology.

Cocited author analysis

According to the small H parameter, when two authors or publications are cited together, their research focus may be the same. According to the keyword clustering, CiteSpace was then applied to construct a knowledge map of cocited authors. This map aids in a more comprehensive understanding of researchers’ focuses and the commonalities among the most cocited authors in the field of salivary gland oncology.

RH Spiro holds the top position with 699 citations, followed by Raja R. Seethala [643] and Skalova Alena [577]. In Figure 4C, through keyword clustering, nodes representing the most cocited authors are grouped into Cluster #0, Xerostomia, and Cluster #1, Survival. This grouping may suggest potential research foci within the field, shedding light on the shared interests of researchers in salivary gland oncology.

Keyword analysis

Next, to analyse hotspots in salivary gland oncology, VOSviewer and CiteSpace were integrated for keyword analysis, with a focus on generating significant results by excluding redundant and negligible keywords. Using VOSviewer, we produced a network visualization based on keyword occurrences, as shown in Figure 5A. Each node represents an article keyword in this area, and their sizes show the frequency of the keywords mentioned. In Figure 5A, we can see that researchers in this area are concentrating on “adenoid cystic carcinoma”, which is undoubtedly the landmark node in keyword clustering.

Figure 5 Keywords analysis. (A) Most occurrences of article keywords in salivary gland oncology: each node represents an article keyword, and nodes sharing a close relationship are color-coded similarly. Links indicate the co-occurrences of the keywords in the same manuscript. (B) Keyword clustering of the most-cited keywords: our findings emphasize that salivary adenoid carcinoma is a significant hotspot in salivary gland oncology. (C) Top 10 keywords under citation bursts [2012–2023]: burst strength reflects the number of sudden surges of research manuscripts related to each keyword. The bar indicates the time interval between these surges.

CiteSpace was then employed to generate a clustering map for cocited keywords, revealing that the research topics in this area can be categorized into 9 clusters, as shown in Figure 5B. Notably, cluster 0 salivary adenoid cystic carcinoma appears to be common, underscoring its predominant role in salivary gland cancer research.

Additionally, we also noticed a significant number of manuscripts focusing on the salivary gland in relation to other types of cancer, such as thyroid cancer and prostate cancer. Through further exploration, we revealed substantial correlations between treatment methods for these diseases and salivary gland carcinomas (SGCs), which has attracted the attention of researchers in salivary gland oncology.

Furthermore, keywords related to the mechanisms of salivary gland oncology, such as “pathway” and “protein”, were identified in Cluster #0. This cluster encompasses crucial research studies, including one by Praktiknjo et al., who utilized epitope profiling and single-cell transcriptome techniques to investigate tumorigenesis mechanisms in salivary gland squamous cell carcinoma (18). Nonetheless, Weinreb et al. identified the PRKD1 p.Glu710Asp hotspot mutation as a driver of polymorphous low-grade adenocarcinoma (24). Furthermore, Wang et al. applied simvastatin with a miR-21 inhibitor to prevent lung metastasis in salivary adenoid cystic carcinoma, which may suggest a new treatment target for distant metastasis in patients with malignant salivary diseases (25).

In terms of burst detection, as illustrated in Figure 5C, the term “secretory carcinoma” stands out as the keyword with the most significant number of citation bursts. This term can be divided into two distinct phases. In the initial phase, Skalova et al. first reported secretory carcinoma in the salivary glands (26). However, the number of studies on this disease has increased over the past several years. However, burst detection of secretory carcinoma did not occur until 2019. This surge in citations indicates a significant increase in interest or relevance within the field of salivary gland oncology.

Likewise, “machine learning” and “deep learning” have also undergone citation bursts in recent years, which may signify the importance of applying artificial intelligence in diagnosis, treatment and prognosis in salivary gland oncology.

In general, a citation burst signifies a period marked by a sudden increase in citations for a specific keyword, indicating a noteworthy surge in interest or relevance within the field of salivary gland oncology. Consequently, the keywords observed in burst detection not only underscore the current significance of these topics, such as secretory carcinoma and artificial intelligence but also imply a potential focal point for future researchers in salivary gland oncology.

Reference analysis

When composing manuscripts, researchers often cite numerous references related to their research direction. When two references were cited together, they shared the same focus on the topic of research. In our study, 1,175 references were selected from WOSCC, which may provide insights into research hotspots over time and potential future research fronts in this area. Table 1 shows the top 10 references with the highest frequencies of cociting. Among them, a manuscript composed of El-Naggar [2017], which has been cited more than 130 times, has gained the most popularity (12). Researchers have delineated the diagnostic criteria and pathological features in salivary gland oncology. Meanwhile, this study introduced the genetic alterations associated with SGT. Building on the research foundation laid by El-Naggar et al., a manuscript by Seethala et al. [2017] further explored common translocations and gene fusions in SGT, accumulating over 100 citations in studies related to salivary gland oncology (27). In summary, this research introduced an international standard and offered a guide for designing studies and evaluating responses to therapies for salivary oncologists. Moreover, this manuscript has provided a complement to the classification in salivary gland oncology.

Table 1

The top 10 co-cited references in salivary gland oncology

Rank Title Author NOC
1 World Health Organization Classification of Head and Neck Tumours El-Naggar et al. 138
2 Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: Tumors of the Salivary Gland Seethala et al. 118
3 Parotid-sparing intensity modulated versus conventional radiotherapy in head and neck cancer (PARSPORT): a phase 3 multicentre randomised controlled trial Nutting et al. 107
4 Adenoid cystic carcinoma of the head and neck - An update Coca-Pelaz et al. 81
5 Management of Salivary Gland Malignancy: ASCO Guideline Geiger et al. 68
6 Radiotherapy dose-volume effects on salivary gland function Deasy et al. 64
7 Phase II Trial of Trastuzumab and Docetaxel in Patients With Human Epidermal Growth Factor Receptor 2-Positive Salivary Duct Carcinoma Hideki Takahashi et al. 63
8 The Role of Molecular Testing in the Differential Diagnosis of Salivary Gland Carcinomas Skálová et al. 63
9 A prospective phase II study of combined androgen blockade in patients with androgen receptor-positive metastatic or locally advanced unresectable salivary gland carcinoma Fushimi et al. 60
10 Pembrolizumab for the Treatment of Advanced Salivary Gland Carcinoma Findings of the Phase 1b KEYNOTE-028 Study Cohen et al. 59

NOC, number of citations.

According to the keywords of the cocited manuscript, timeline zone view clustering showed that the cocited manuscripts could be categorized into 15 clusters. We list the top 10 clusters in Figure 6A. Each node in the figure represents an original article, and the cocited manuscripts were clustered together when a significant number of articles with shared keywords cited them. Cluster #0, which centers around salivary duct carcinoma, emerged as the largest and most recent cluster, providing valuable insight into future research trends in the domain of SGT.

Figure 6 Reference analysis. (A) Timeline view of the most cited references in salivary gland oncology. Each node represents a manuscript, with keyword clustering dividing the most cocited references into 15 clusters. The traversing link between the nodes depicts the cocitation timeline. The 10 largest clusters are shown in (A). (B) Top 20 references with the strongest citation bursts [2012–2023]: identifies references with the most notable and sudden increases in citations during the specified time frame.

By exploring cluster #0, we traced several noteworthy manuscripts. In a 2018 study, Fushimi et al. conducted a phase II clinical trial involving patients with androgen receptor-positive SGC. Their findings suggest that combined androgen blockade offers comparable efficacy with reduced toxicity compared to conventional chemotherapy (28). Additionally, a study conducted by Arolt in 2020 revealed that elevated expression of lymphocyte activation gene 3 (LAG3) is correlated with reduced event-free survival in adenoid cystic carcinoma patients. This study also highlighted for the first time the potential of LAG3 as a target therapy for SGC (29).

In terms of citation burst detection, as shown in Figure 6B, we discovered that before 2022, there is no unified therapeutic consensus for salivary gland malignancies. To address this gap, Geiger et al. analysed 293 studies related to salivary gland malignancies and proposed guidelines on surgical diagnostic and therapeutic procedures for this disease (30). Notably, this manuscript has recently experienced a citation burst, registering the highest strength of 32.76. Meanwhile, the manuscripts authored by El-Naggar [2017] and Seethala [2017], which have gained significant popularity, are also undergoing a citation burst. This phenomenon may underscore the sustained and increasing interest in these pivotal works within the research community.


Discussion

As the key components involved in synthesizing, modifying and secreting saliva, the salivary glands are crucial for sustaining the physiological environment (31) of the mouth. They contribute significantly to oral health. SGTs are rare among neoplasms in humans, with epithelial-origin salivary tumors being the most common. According to our research, there are currently more than 30,000 manuscripts in the WOSCC, and the earliest ones date back to the 1900s. Researchers have focused primarily on exploring anatomical structures and identifying the pathology of salivary gland diseases. Concurrently, there is a significant body of literature concentrating on surgical considerations in salivary gland oncology. In some salivary gland cancers, several risks have been identified; however, the etiology and pathology of SGTs are poorly understood. Recently, the rapid growth of scientific inquiry in oncological research has been propelled by the application of sequencing technologies and artificial intelligence. The number of manuscripts from 2012 to 2023 alone accounted for more than one-third of the entire database.

The analysis of contributing countries revealed that the United States has been a prominent contributor, publishing 2,588 original articles in the last 12 years, and we have listed the top 10 most cocited manuscripts in the United States in Table 2. Subsequently, in 2017, researchers in the US applied convolutional neural networks in head and neck oncology. By leveraging deep learning methods, they successfully segmented organs at risk of SGT on medical images (32). Moreover, researchers from the United States have significantly contributed to the development of multiple guidelines for treatment modalities and lymph node delineation in salivary gland oncology (30,33,34). This underscores the significant and active contribution of the United States in the field of salivary gland oncology, positioning it as a dominant force in research and advancements in this area.

Table 2

The top 10 popular research in the United States

Rank Title Author NOC
1 Radiotherapy dose-volume effects on salivary gland function Pfister et al. 476
2 Delineation of the neck node levels for head and neck tumors: A 2013 update. DAHANCA, EORTC, HKNPCSG, NCIC CTG, NCRI, RTOG, TROG consensus guidelines Gregoire et al. 445
3 The global incidence of lip, oral cavity, and pharyngeal cancers by subsite in 2012 Shield et al. 438
4 Management of Salivary Gland Malignancy: ASCO Guideline Miettinen et al. 438
5 NCCN Guidelines® Insights Head and Neck Cancers, Version 1.2018 Featured Updates to the NCCN Guidelines Dimitrios Colevas et al. 373
6 The mutational landscape of adenoid cystic carcinoma Ho et al. 334
7 Segmentation of organs-at-risks in head and neck CT images using convolutional neural networks Ibragimov et al. 332
8 Transoral robotic surgery: A multicenter study to assess feasibility, safety, and surgical margins Weinstein et al. 328
9 AnatomyNet: Deep learning for fast and fully automated whole-volume segmentation of head and neck anatomy Zhu et al. 297
10 Oral Complications of Cancer and Cancer Therapy From Cancer Treatment to Survivorship Epstein et al. 295

NOC, number of citations.

In terms of literature resource analysis, the period from 2012 to 2023 revealed that the journal Head and Neck stands out as the largest contributing journal in the field of salivary gland oncology. Following Bradford’s law, we have also identified the following journals as core publications in the field of salivary gland oncology: Head and Neck, Oral Oncology, Laryngoscope, International Journal of Radiation Oncology Biology Physics, Cancer, American Journal of Surgical Pathology, Otolaryngology-Head and Neck Surgery, Journal of Clinical Oncology, Archives of Otolaryngology, and Head & Neck Pathology. Moreover, recent studies in salivary gland oncology have demonstrated an increasing presence in journals such as Cancers, Frontiers in Oncology, and Head & Neck Pathology, indicating a growing interest and acceptance of research in these journals. This trend also suggests that these journals are becoming significant platforms for disseminating and advancing knowledge in the field of salivary gland oncology.

Next, to gain an overall understanding of the research focal points among the most productive and popular researchers, we utilized keyword clustering. Significantly, our findings indicate that the most productive research points revolve around the topics related to the rearranged during transfection (RET) gene fusion, malignant salivary cancer and radiotherapy. On the other hand, when examining the most cocited authors, Cluster #Xerostomia and #Survival were the most common, which may suggest that a significant portion of researchers in salivary gland oncology pay close attention to research related to these topics.

In bibliometric analysis, keyword and reference analyses are efficient tools for revealing current hot topics and research trends in the scientific field. In Figure 5, the most frequent keywords can be categorized into four parts, indicating that the field’s hotspot comprises four well-studied aspects. Each part is centered around a core term: “adenoid cystic carcinoma”, “pleomorphic adenoma”, “radiotherapy”, and “surgery”. Further keyword clustering highlights the ongoing significance of adenoid cystic carcinoma, underscoring its central role in salivary gland oncology research. Moreover, our cocited reference analysis indicates a notable emphasis on salivary duct carcinoma among researchers. However, the frequency of the keyword “salivary duct carcinoma” is relatively low, which may illustrate the growing demand for studies on this disease.

Based on the above findings, in addition to classic salivary gland tumors such as pleomorphic adenoma and adenoid cystic carcinoma, our research and keyword analysis highlighted several current hotspots in salivary gland oncology as follows:

  • RET: SGC represents approximately 5% of head and neck malignancies and is characterized by resistance to cytotoxic chemotherapy and immune checkpoint inhibition therapy. Historically, treatment options were limited to surgery and radiotherapy, leading to poor outcomes due to the diverse clinical behaviors of these cancers. However, there has been a significant shift in the treatment landscape for SGC in recent years (35). Researchers have shown that RET gene fusion is prevalent in SGCs. Specifically, researchers have discovered EVT6-RET gene fusions in salivary duct carcinomas (36). Moreover, RET gene fusions, including TRIM33-RET and NCOA4-RET, have also been reported in other subtypes of salivary gland malignancies (37). The discovery of these gene fusions has advanced our understanding of the oncogenic mechanisms underlying salivary gland tumors and presents a promising treatment target for these cancers.
  • Carbon ion radiotherapy and proton therapy: radical surgery remains the primary treatment modality for SGCs. However, the role of radiotherapy is crucial in the postoperative setting, particularly for managing inoperable malignancies and recurrent tumors (38). Given their proximity to normal organs and resistance to conventional radiotherapies, especially in cases of adenoid cystic carcinoma, SGCs present significant challenges for clinicians. Carbon ion radiotherapy and proton therapy have shown high efficacy and the potential to minimize harmful effects on surrounding organs. Notably, both techniques have demonstrated excellent outcomes in treating adenoid cystic carcinoma. Currently, clinicians are actively working to establish the optimal treatment approach for these tumors by integrating multiple radiotherapies, which may offer improved chances for patients (39,40).
  • Xerostomia: this is the most significant and long-term complication for patients with salivary gland tumors undergoing radiotherapy and is characterized by the loss of salivary gland function. Researchers have shown that intensity-modulated radiotherapy has the greatest potential for preserving salivary gland function. Additionally, techniques such as salivary gland or stem cell transfer may serve as methods for supplementing fluid to the glands (41,42). However, effective strategies are still being sought to preserve salivary gland secretion function postradiotherapy.
  • IgG4-related diseases: IgG4-related diseases are characterized by CD4+ and CD8+ T-cell infiltration, along with elevated serum IgG4 levels, leading to sclerotic and fibrotic changes in affected organs (43). In the salivary gland region, these diseases often manifest as Mikulicz’s disease and Küttner’s tumor, presenting as painless bilateral swelling in the salivary glands. Co-occurrence of IgG4-related diseases with salivary gland malignancies has also been reported (44). However, distinguishing between salivary gland tumors and IgG4-related diseases is challenging due to their similar appearances, leading researchers in salivary gland oncology to focus on improving diagnostic methods. These efforts include biopsies, radiographic exams, DNA sequencing, and blood tests (45,46).
  • Neurotrophic tyrosine receptor kinase (NTRK) and prostate-specific membrane antigen (PSMA): due to the approval of larotrectinib, an effective treatment for NTRK fusion cancers, significant progress has been made in managing cancers such as thyroid cancer, secretory carcinoma of the breast, and salivary glands (47-50). The assessment of NTRK fusion has now become a standard approach for managing these diseases. As a result, numerous manuscripts focusing on topics related to salivary gland oncology and thyroid cancers have emerged.
    We also observed that the keyword “prostate cancer” appeared as the main cluster in the keyword analysis. PSMA, a transmembrane glycoprotein, is known to be overexpressed in prostate cancer. Recently, researchers have reported relatively high expression of this gene in the tumor parenchyma in salivary gland malignancies, particularly in adenoid cystic carcinomas and salivary duct carcinomas (51). Consequently, PSMA radioligand therapy for salivary gland malignancies has garnered increased amounts of attention from researchers (52,53). Studies related to other types of malignancies, including breast cancer, prostate cancer and thyroid cancer, have revealed new treatment options for salivary gland tumors.

Beyond that, burst detection is intended to find related references and keywords under citation bursts, implying a research trend in specific fields.

Interestingly, the keyword ‘stage nasopharyngeal carcinoma’ experienced a citation burst from 2012–2013. Salivary gland nasopharyngeal cancers are rare and have received limited discussion in the literature. During that period, controversies arose regarding the staging and treatment of these diseases because of their diverse clinical manifestations and pathological appearance (54). In 2019, a comprehensive analysis of a large patient cohort with salivary gland nasopharyngeal carcinomas revealed a prognosis similar to that of patients with squamous cell carcinomas, and the prognosis of this disease was determined by various factors, including race, age and histological subtype (55).

Furthermore, we found that the keywords “secretory carcinoma”, “machine learning”, and “deep learning” are associated with citation bursts with the greatest strength. By conducting additional analysis of the manuscripts using CiteSpace and focusing on these keywords, we have summarized the prevalent biomarkers or topics in Tables 3,4. The information related to these keywords is as follows:

  • Secretory carcinoma: this disease was initially described in 2010, with approximately 300 experimental manuscripts related to it in salivary gland oncology. However, burst detection of secretory carcinoma did not occur until 2019. Upon analysing manuscripts published in 2019 with this keyword, a study by Haller et al. had the most citations. This study explored the molecular pathogenesis of salivary gland acinic cell carcinoma, highlighting the influential role of NR4A3 upregulation in cell proliferation within this carcinoma (56). Similarly, in 2019, several studies focused on salivary gland acinic cell carcinoma and gene translocation (57). These outcomes potentially indicate an ongoing upswing in future studies centered around gene translocation in secretory carcinoma.
  • Machine learning and deep learning: given that these are techniques within the domain of artificial intelligence, we added all three keywords—“machine learning”, “deep learning”, and “artificial intelligence”—with the previous search words for salivary oncology in WOSCC and analysed the related manuscripts in CiteSpace. Our investigation revealed that the use of artificial intelligence in salivary gland oncology began in 2013, with a consistent and steady increase in the number of manuscripts in this domain. To date, researchers have utilized artificial intelligence to assimilate data, integrating clinical records with medical images. Artificial intelligence remains the most extensively studied method in the context of diagnosis, classification, and prediction in salivary gland oncology (14,17,58-61). However, despite its prominence, the citation frequency for these keywords in the field is average. This could be attributed to the predominantly single-centered nature of most studies and the significant variability in the format of medical images, resulting in fewer citations across various works.
  • International standards and guidelines: according to burst detection in salivary gland oncology manuscripts, we observed a significant surge in citations for several international standards and guidelines (27,30). Likewise, in our analysis of the most frequently cocited manuscripts, guidelines and standards consistently emerged as top-ranking in terms of citation frequency, especially within the domain of salivary gland malignancies. This trend may be attributed to the lack of a unified consensus on the etiology and pathology of salivary gland cancer. Furthermore, the clinical symptoms and pathological features of SGTs exhibit considerable variation, posing challenges in diagnosis, classification, and treatment procedures in both research and clinical settings. The mission of establishing a unified guideline for SGT has long been a challenge, and it was not until 2017 that the WHO started to include gene alterations in SGT classifications. Thus, the need and challenge for developing more cohesive guidelines in this domain create an opportunity for more in-depth manuscripts focusing on tumor cell behaviors within SGTs, as well as for researchers to contribute meaningfully (27,30).

Table 3

The top 10 co-cited keywords in secretory carcinoma in salivary gland oncology

Rank Keyword NOC
1 Acinic cell carcinoma 73
2 Secretory carcinoma 73
3 Mammary analogue secretory carcinoma 60
4 Analog secretory carcinoma 53
5 Diagnosis 49
6 Adenoid cystic carcinoma 41
7 Fusion 34
8 Translocation 34
9 Mucoepidermoid carcinoma 29
10 Etv6 ntrk3 gene fusion 28

NOC, number of citations.

Table 4

The top 10 co-cited keywords in artificial intelligence in the salivary gland oncology

Rank Keyword NOC
1 Radiotherapy/radiation therapy 35
2 Computed tomography/CT/CT images 32
3 Parotid gland 12
4 Images 12
5 Auto segmentation 12
6 Delineation 11
7 Organs 11
8 Convolutional neural network 9
9 Classification 9
10 Diagnosis 8

NOC, number of citations.

Furthermore, our analysis identified references that experienced a citation burst during the specified years. These references have been categorized into universal guidelines/consensus and related studies, clinical/experimental studies, studies in salivary gland malignancies, and studies focusing on gene biomarkers in salivary gland oncology. Among these categories, we selected the top ten references for each, which are listed in Tables 5-8.

Table 5

The top 10 universal guidelines/consensus and related studies under citation bursts in salivary oncology

Rank References Strength
1 Management of Salivary Gland Malignancy: ASCO Guideline 32.76
2 WHO classification (2019) 26.49
3 Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: Tumors of the Salivary Gland 22.61
4 Head and Neck Cancers, Version 2.2020, NCCN Clinical Practice Guidelines in Oncology 16.8
5 Minor salivary gland tumors of the head and neck—Memorial Sloan Kettering experience: Incidence and outcomes by site and histological type 9.97
6 Multiparametric Magnetic Resonance Imaging for the Diagnosis and Differential Diagnosis of Parotid Gland Tumors 9.28
7 Major and minor salivary gland tumours 9.11
8 Salivary Gland Malignancies 8.93
9 Salivary duct carcinoma: Updates in histology, cytology, molecular biology, and treatment 8.25
10 Who classification of head and neck tumours (2017) 8.1

Table 6

Top 10 clinical/experimental studies under citation bursts in salivary oncology

Rank References Strength
1 Phase II Trial of Trastuzumab and Docetaxel in Patients With Human Epidermal Growth Factor Receptor 2–Positive Salivary Duct Carcinoma 16.01
2 Salivary gland pleomorphic adenoma in the Netherlands: A nationwide observational study of primary tumor incidence, malignant transformation, recurrence, and risk factors for recurrence 13.87
3 Pembrolizumab for the Treatment of Advanced Salivary Gland Carcinoma: Findings of the Phase 1b KEYNOTE-028 Study 11.76
4 Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands 11.42
5 Molecular Profiling of Mammary Analog Secretory Carcinoma Revealed a Subset of Tumors Harboring a Novel ETV6-RET Translocation 11.37
6 A prospective phase II study of combined androgen blockade in patients with androgen receptor-positive metastatic or locally advanced unresectable salivary gland carcinoma 11.13
7 Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours: integrated analysis of three phase 1–2 trials 10.66
8 Phase II Study of Lenvatinib in Patients With Progressive, Recurrent or Metastatic Adenoid Cystic Carcinoma 10.65
9 Efficacy of Larotrectinib in TRK Fusion–Positive Cancers in Adults and Children 10.3
10 Salivary Secretory Carcinoma With a Novel ETV6-MET Fusion
Expanding the Molecular Spectrum of a Recently Described Entity
9.47

Table 7

The top 10 studies with citation bursts in salivary gland malignancies

Rank References Strength
1 Phase II Trial of Trastuzumab and Docetaxel in Patients With Human Epidermal Growth Factor Receptor 2–Positive Salivary Duct Carcinoma 16.01
2 Pembrolizumab for the Treatment of Advanced Salivary Gland Carcinoma Findings of the Phase 1b KEYNOTE-028 Study 11.76
3 Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands 11.42
4 Molecular Profiling of Mammary Analog Secretory Carcinoma Revealed a Subset of Tumors Harboring a Novel ETV6-RET Translocation 11.37
5 A prospective phase II study of combined androgen blockade in patients with androgen receptor-positive metastatic or locally advanced unresectable salivary gland carcinoma 11.13
6 Phase II Study of Lenvatinib in Patients With Progressive, Recurrent or Metastatic Adenoid Cystic Carcinoma 10.65
7 Efficacy of Larotrectinib in TRK Fusion–Positive Cancers in Adults and Children 10.3
8 Microsecretory Adenocarcinoma: A Novel Salivary Gland Tumor Characterized by a Recurrent MEF2C-SS18 Fusion 9.97
9 Nuclear NR4A3 Immunostaining Is a Specific and Sensitive Novel Marker for Acinic Cell Carcinoma of the Salivary Glands 9.97
10 Expanding the Molecular Spectrum of Secretory Carcinoma of Salivary Glands With a Novel VIM-RET Fusion 9.97

There are three manuscripts experiencing citation bursts that have equal strength.

Table 8

The top 10 studies on gene biomarkers with citation bursts in salivary gland oncology

Rank References Strength
1 Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands 11.42
2 Molecular Profiling of Mammary Analog Secretory Carcinoma Revealed a Subset of Tumors Harboring a Novel ETV6-RET Translocation 11.37
3 Entrectinib in patients with advanced or metastatic NTRK fusion-positive solid tumours: integrated analysis of three phase 1–2 trials 10.66
4 Efficacy of Larotrectinib in TRK Fusion–Positive Cancers in Adults and Children 10.3
5 Microsecretory Adenocarcinoma: A Novel Salivary Gland Tumor Characterized by a Recurrent MEF2C-SS18 Fusion 9.97
6 Nuclear NR4A3 Immunostaining Is a Specific and Sensitive Novel Marker for Acinic Cell Carcinoma of the Salivary Glands 9.97
7 Expanding the Molecular Spectrum of Secretory Carcinoma of Salivary Glands With a Novel VIM-RET Fusion 9.97
8 Molecular Profiling of Salivary Gland Intraductal Carcinoma Revealed a Subset of Tumors Harboring NCOA4-RET and Novel TRIM27-RET Fusions 9.73
9 Salivary Secretory Carcinoma With a Novel ETV6-MET Fusion Expanding the Molecular Spectrum of a Recently Described Entity 9.47
10 NCOA4-RET and TRIM27-RET Are Characteristic Gene Fusions in Salivary Intraductal Carcinoma, Including Invasive and Metastatic Tumors: Is “Intraductal” Correct? 9.23

Our study has several limitations. First, we focused on the WOSCC for data collection due to software requirements, thus, not all database were evaluated, which may limit the scope of scientific research analysed. Second, our findings provide only a snapshot of current salivary gland oncology, subject to ongoing updates. Third, despite our primary focus on original articles, the inclusion of some reviews or case report (categorized as articles in the Web of Science) was challenging to filter through the website and the software. Fourth, due to the software’s topic search method, there are some pieces of manuscript related to other types of carcinomas and salivary gland was also included in this research. Lastly, due to the algorithm used in CiteSpace, there may be some misleading display of words in the results. For instance, in Figure 6A, the term “neck cancer” (#1) actually refers to head and neck cancer.

Generally, to understand the current state and explore future research trends in salivary oncology, we used bibliometric methods to evaluate and analyse 9,695 original research articles. To our knowledge, our research represents the first comprehensive bibliometric study focusing specifically on salivary gland oncology. In an era characterized by information explosion, bibliometric analysis offers researchers a new method to grasp the most important and influential studies. By integrating CiteSpace and VOSviewer, we attempted to conduct a series of bibliometric analyses to offer a general view of and research trends in this area.


Conclusions

In an era characterized by information explosion, bibliometric analysis offers researchers a new method to grasp the most important and influential studies. By employing various bibliometric analysis tools, we scrutinized 9,695 original research articles published between 2012 and 2023 in salivary gland oncology, aiming to present a comprehensive view and identify research trends in this domain.

Our research indicates that salivary gland malignancies currently dominate the field of salivary oncology research and will remain the primary research focus in this field. Researchers are actively investigating promising treatment targets for these malignancies, with a particular focus on gene fusion detection. Notably, RET gene fusions have emerged as a key area of interest in salivary gland malignancies. Additionally, studies on various cancers, such as breast cancer, prostate cancer, and thyroid cancer, have revealed new treatment options for salivary gland tumors. For instance, NTRK fusions and PSMA, previously studied in thyroid, breast, and prostate cancers, have recently gained attention in the context of salivary gland malignancies.

While radical surgery remains the primary treatment for SGCs, ongoing efforts are directed towards carbon ion radiotherapy and proton therapy. These modalities have demonstrated increased efficacy and reduced toxicity to nearby organs, showing outstanding treatment outcomes in managing adenoid cystic carcinomas and addressing inoperable or recurrent malignancies (39,40). Consequently, radiotherapy has gained popularity in salivary gland oncology. However, the application of radiotherapies in salivary gland oncology and other malignancies has also raised concerns regarding complications, particularly xerostomia, which remains a significant research focus in the field.

A correct diagnosis is paramount for the prognosis of patients with salivary gland cancer. With diverse clinical and pathological manifestations, the classification and diagnosis of SGTs have posed challenges for researchers in this field. The call for establishing more cohesive guidelines presents researchers with an opportunity to explore deeper into tumor cell behaviors within SGTs, thereby contributing to the advancement of clinical practice and research in this domain.

On the other hand, the application of artificial intelligence has mainly concentrated on the diagnosis and classification of SGCs (62,63). However, the number of studies in this area remains relatively low at this time.

With the progress in artificial intelligence, there is potential to use artificial intelligence algorithms to schedule treatment for patients with salivary gland cancer. These algorithms can identify, classify, and detect gene fusions or alterations, aiding in the development of optimal treatment plans that may include surgery, radiotherapy, and other therapies, either individually or in combination, tailored to each patient’s needs.

In summary, this study represents the first comprehensive bibliometric analysis focused on salivary gland oncology. Our findings provide valuable insights into emerging trends and areas for future investigations in this field. We believe that this study will significantly benefit scientific researchers and clinical oncologists by enhancing their understanding of salivary gland oncology and contributing to the discipline’s further development and policymaking.


Acknowledgments

The author H.D., expresses gratitude to her beloved pet dog, Xi Xi, for the unforgettable and heartwarming companionship he offered.

Funding: This work was supported by the National Natural Science Foundation of China (grant No. 81972546 to Y.L.) and (grant No. 82270994 to C.L).


Footnote

Peer Review File: Available at https://gs.amegroups.com/article/view/10.21037/gs-24-94/prf

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://gs.amegroups.com/article/view/10.21037/gs-24-94/coif). C.L. reports that this work was supported by the National Natural Science Foundation of China (grant No. 82270994). Y.L. reports that this work was supported by the National Natural Science Foundation of China (grant No. 81972546). The other authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.


References

  1. Haghshenas MR, Ghaderi H, Daneste H, et al. Immunological and biological dissection of normal and tumoral salivary glands. Int Rev Immunol 2023;42:139-55. [Crossref] [PubMed]
  2. Żurek M, Fus Ł, Niemczyk K, et al. Salivary gland pathologies: evolution in classification and association with unique genetic alterations. Eur Arch Otorhinolaryngol 2023;280:4739-50. [Crossref] [PubMed]
  3. Alsanie I, Rajab S, Cottom H, et al. Distribution and Frequency of Salivary Gland Tumours: An International Multicenter Study. Head Neck Pathol 2022;16:1043-54. [Crossref] [PubMed]
  4. Zech HB, Betz CS. Special tumor entities in the head and neck region : Nasopharyngeal carcinoma, salivary gland, and thyroid cancer. HNO 2022;70:278-86. [Crossref] [PubMed]
  5. Weaver AN, Lakritz S, Mandair D, et al. A molecular guide to systemic therapy in salivary gland carcinoma. Head Neck 2023;45:1315-26. [Crossref] [PubMed]
  6. Klijanienko J, Lagacé R, Servois V, et al. Fine-needle sampling of primary neuroendocrine carcinomas of salivary glands: cytohistological correlations and clinical analysis. Diagn Cytopathol 2001;24:163-6. [Crossref] [PubMed]
  7. Klijanienko J, Vielh P. Fine-needle sampling of salivary gland lesions. II. Cytology and histology correlation of 71 cases of Warthin's tumor (adenolymphoma). Diagn Cytopathol 1997;16:221-5. [Crossref] [PubMed]
  8. Epker BN, Henny FA. Clinical, histopathologic, and surgical aspects of intraoral minor salivary gland tumors: review of 90 cases. J Oral Surg 1969;27:792-804. [PubMed]
  9. Thackray AC. Histological typing of salivary gland tumours. In: World Health Organization. International histological classification of tumours. Geneva: The Organization; 1972.
  10. Seifert G. Histological typing of salivary gland tumours. In: World Health Organization. International histological classification of tumours. Berlin: Springer-Verlag; 1991.
  11. Barnes L, Eveson JW, Reichart P, et al. World Health Organization classification of tumours. Pathology and genetics of head and neck tumours. 3rd Edition. Lyon: IARC; 2005.
  12. El-Naggar AK, Chan JKC, Grandis JR, et al. editors. WHO Classification of Head and Neck Tumours. Lyon: IARC; 2017.
  13. Weinstein GS, O'Malley BW Jr, Magnuson JS, et al. Transoral robotic surgery: a multicenter study to assess feasibility, safety, and surgical margins. Laryngoscope 2012;122:1701-7. [Crossref] [PubMed]
  14. Zhang G, Zhu L, Huang R, et al. A deep learning model for the differential diagnosis of benign and malignant salivary gland tumors based on ultrasound imaging and clinical data. Quant Imaging Med Surg 2023;13:2989-3000. [Crossref] [PubMed]
  15. Pérez JMT, García-Cosío M, García-Castaño A, et al. Recommendations for the use of biomarkers for head and neck cancer, including salivary gland tumours: A Consensus of the Spanish Society of Medical Oncology and the Spanish Society of Pathology. Rev Esp Patol 2023;56:45-57. [Crossref] [PubMed]
  16. WHO Classification of Tumours Editorial Board (2022) Head and Neck tumours. WHO classification of tumours series. 5th edition. Lyon: IARC. 2022.
  17. Yu Q, Ning Y, Wang A, et al. Deep learning-assisted diagnosis of benign and malignant parotid tumors based on contrast-enhanced CT: a multicenter study. Eur Radiol 2023;33:6054-65. [Crossref] [PubMed]
  18. Praktiknjo SD, Obermayer B, Zhu Q, et al. Tracing tumorigenesis in a solid tumor model at single-cell resolution. Nat Commun 2020;11:991. [Crossref] [PubMed]
  19. Effah NAA, Wang Q, Owusu GMY, et al. Contributions toward sustainable development: a bibliometric analysis of sustainability reporting research. Environ Sci Pollut Res Int 2023;30:104-26. [Crossref] [PubMed]
  20. Chen C, Assoc Comp M, editors. Visualizing and Exploring Scientific Literature with CiteSpace. 3rd ACM SIGIR Conference on Human Information Interaction and Retrieval (CHIIR); 2018 2018 Mar 11-15; New Brunswick, NJ2018.
  21. Ping Q, He J, Chen C. How Many Ways to Use CiteSpace? A Study of User Interactive Events Over 14 Months. J Assoc Inf Sci Technol 2017;68:1234-56. [Crossref]
  22. Chen C, Dubin R, Kim MC. Emerging trends and new developments in regenerative medicine: a scientometric update (2000 - 2014). Expert Opin Biol Ther 2014;14:1295-317. [Crossref] [PubMed]
  23. Chen C, Chen Y, Hou J, et al. CiteSpace II: Detecting and Visualizing Emerging Trends and Transient Patterns in Scientific Literature. Journal of the China Society for Scientific and Technical Information 2009;28:401-21.
  24. Weinreb I, Piscuoglio S, Martelotto LG, et al. Hotspot activating PRKD1 somatic mutations in polymorphous low-grade adenocarcinomas of the salivary glands. Nat Genet 2014;46:1166-9. [Crossref] [PubMed]
  25. Wang C, Li T, Yan F, et al. Effect of simvastatin and microRNA-21 inhibitor on metastasis and progression of human salivary adenoid cystic carcinoma. Biomed Pharmacother 2018;105:1054-61. [Crossref] [PubMed]
  26. Seethala RR, Stenman G. Update from the 4th Edition of the World Health Organization Classification of Head and Neck Tumours: Tumors of the Salivary Gland. Head Neck Pathol 2017;11:55-67.
  27. Fushimi C, Tada Y, Takahashi H, et al. A prospective phase II study of combined androgen blockade in patients with androgen receptor-positive metastatic or locally advanced unresectable salivary gland carcinoma. Ann Oncol 2018;29:979-84. [Crossref] [PubMed]
  28. Arolt C, Meyer M, Ruesseler V, et al. Lymphocyte activation gene 3 (LAG3) protein expression on tumor-infiltrating lymphocytes in aggressive and TP53-mutated salivary gland carcinomas. Cancer Immunol Immunother 2020;69:1363-73. [Crossref] [PubMed]
  29. Skálová A, Vanecek T, Sima R, et al. Mammary analogue secretory carcinoma of salivary glands, containing the ETV6-NTRK3 fusion gene: a hitherto undescribed salivary gland tumor entity. Am J Surg Pathol 2010;34:599-608. [Crossref] [PubMed]
  30. Geiger JL, Ismaila N, Beadle B, et al. Management of Salivary Gland Malignancy: ASCO Guideline. J Clin Oncol 2021;39:1909-41. [Crossref] [PubMed]
  31. Basset CA, Cappello F, Rappa F, et al. Molecular chaperones in tumors of salivary glands. J Mol Histol 2020;51:109-15. [Crossref] [PubMed]
  32. Ibragimov B, Xing L. Segmentation of organs-at-risks in head and neck CT images using convolutional neural networks. Med Phys 2017;44:547-57. [Crossref] [PubMed]
  33. Colevas AD, Yom SS, Pfister DG, et al. NCCN Guidelines Insights: Head and Neck Cancers, Version 1.2018. J Natl Compr Canc Netw 2018;16:479-90. [Crossref] [PubMed]
  34. Epstein JB, Thariat J, Bensadoun RJ, et al. Oral complications of cancer and cancer therapy: from cancer treatment to survivorship. CA Cancer J Clin 2012;62:400-22. [Crossref] [PubMed]
  35. Regua AT, Najjar M, Lo HW. RET signaling pathway and RET inhibitors in human cancer. Front Oncol 2022;12:932353. [Crossref] [PubMed]
  36. Skalova A, Vanecek T, Martinek P, et al. Molecular Profiling of Mammary Analog Secretory Carcinoma Revealed a Subset of Tumors Harboring a Novel ETV6-RET Translocation: Report of 10 Cases. Am J Surg Pathol 2018;42:234-46. [Crossref] [PubMed]
  37. Bishop JA, Nakaguro M, Whaley RD, et al. Oncocytic intraductal carcinoma of salivary glands: a distinct variant with TRIM33-RET fusions and BRAF V600E mutations. Histopathology 2021;79:338-46. [Crossref] [PubMed]
  38. Orlandi E, Iacovelli NA, Bonora M, et al. Salivary Gland. Photon beam and particle radiotherapy: Present and future. Oral Oncol 2016;60:146-56. [Crossref] [PubMed]
  39. Zakeri K, Wang H, Kang JJ, et al. Outcomes and prognostic factors of major salivary gland tumors treated with proton beam radiation therapy. Head Neck 2021;43:1056-62. [Crossref] [PubMed]
  40. Schmid MP, Held T, Lang K, et al. Intensity Modulated Radiotherapy with Carbon Ion Radiotherapy Boost for Acinic Cell Carcinoma of the Salivary Glands. Cancers (Basel) 2021;13:124. [Crossref] [PubMed]
  41. Jensen SB, Vissink A, Limesand KH, et al. Salivary Gland Hypofunction and Xerostomia in Head and Neck Radiation Patients. J Natl Cancer Inst Monogr 2019;2019:lgz016. [Crossref] [PubMed]
  42. Wang X, Eisbruch A. IMRT for head and neck cancer: reducing xerostomia and dysphagia. J Radiat Res 2016;57:i69-75. [Crossref] [PubMed]
  43. Kamiński B, Błochowiak K. Mikulicz's disease and Küttner's tumor as manifestations of IgG4-related diseases: a review of the literature. Reumatologia 2020;58:243-50. [Crossref] [PubMed]
  44. Gill J, Angelo N, Yeong ML, et al. Salivary duct carcinoma arising in IgG4-related autoimmune disease of the parotid gland. Hum Pathol 2009;40:881-6. [Crossref] [PubMed]
  45. Vasilyev VI, Sokol EV, Rodionova EB, et al. IgG4-related salivary gland lesions. Ter Arkh 2015;87:92-102. [Crossref] [PubMed]
  46. Ikeda R, Kurakami K, Ohta N, et al. Malignancies in Patients with IgG4-Related Diseases in Head and Neck Regions. Tohoku J Exp Med 2019;249:285-90. [Crossref] [PubMed]
  47. Solomon JP, Benayed R, Hechtman JF, et al. Identifying patients with NTRK fusion cancer. Ann Oncol 2019;30:viii16-22. [Crossref]
  48. Solomon JP, Linkov I, Rosado A, et al. NTRK fusion detection across multiple assays and 33,997 cases: diagnostic implications and pitfalls. Mod Pathol 2020;33:38-46. [Crossref] [PubMed]
  49. Bebb DG, Banerji S, Blais N, et al. Canadian Consensus for Biomarker Testing and Treatment of TRK Fusion Cancer in Adults. Curr Oncol 2021;28:523-48. [Crossref] [PubMed]
  50. Nguyen MA, Colebatch AJ, Van Beek D, et al. NTRK fusions in solid tumours: what every pathologist needs to know. Pathology 2023;55:596-609. [Crossref] [PubMed]
  51. Wang JH, Kiess AP. PSMA-targeted therapy for non-prostate cancers. Front Oncol 2023;13:1220586. [Crossref] [PubMed]
  52. Wang G, Zhou M, Zang J, et al. A pilot study of (68) Ga-PSMA-617 PET/CT imaging and (177)Lu-EB-PSMA-617 radioligand therapy in patients with adenoid cystic carcinoma. EJNMMI Res 2022;12:52. [Crossref] [PubMed]
  53. van Boxtel W, Lütje S, van Engen-van Grunsven ICH, et al. (68)Ga-PSMA-HBED-CC PET/CT imaging for adenoid cystic carcinoma and salivary duct carcinoma: a phase 2 imaging study. Theranostics 2020;10:2273-83. [Crossref] [PubMed]
  54. Liu TR, Chen FJ, Qian CN, et al. Primary salivary gland type carcinoma of the nasopharynx: therapeutic outcomes and prognostic factors. Head Neck 2010;32:435-44. Erratum in: Head Neck 2011;33:601. [Crossref] [PubMed]
  55. Booth JR, Unsal AA, Tadros S, et al. Salivary Gland Cancers of the Nasopharynx: A Population-Based Analysis of 383 Cases. Otolaryngol Head Neck Surg 2019;161:442-9. [Crossref] [PubMed]
  56. Haller F, Bieg M, Will R, et al. Enhancer hijacking activates oncogenic transcription factor NR4A3 in acinic cell carcinomas of the salivary glands. Nat Commun 2019;10:368. [Crossref] [PubMed]
  57. Xu B, Haroon Al Rasheed MR, Antonescu CR, et al. Pan-Trk immunohistochemistry is a sensitive and specific ancillary tool for diagnosing secretory carcinoma of the salivary gland and detecting ETV6-NTRK3 fusion. Histopathology 2020;76:375-82. [Crossref] [PubMed]
  58. McNutt TR, Jiang W, Lakshminarayanan P, et al. Machine Learning Methods Uncover Radio-Morphologic Dose Patterns in Salivary Glands That Predict Xerostomia in Head and Neck Cancer Patients. International Journal of Radiation Oncology Biology Physics 2018;102:S212. [Crossref]
  59. Liu GS, Shenson JA, Farrell JE, et al. Signal to noise ratio quantifies the contribution of spectral channels to classification of human head and neck tissues ex vivo using deep learning and multispectral imaging. J Biomed Opt 2023;28:016004. [Crossref] [PubMed]
  60. Chang YJ, Huang TY, Liu YJ, et al. Classification of parotid gland tumors by using multimodal MRI and deep learning. NMR Biomed 2021;34:e4408. [Crossref] [PubMed]
  61. Matsuo H, Nishio M, Kanda T, et al. Diagnostic accuracy of deep-learning with anomaly detection for a small amount of imbalanced data: discriminating malignant parotid tumors in MRI. Sci Rep 2020;10:19388. [Crossref] [PubMed]
  62. Mahmood H, Shaban M, Rajpoot N, et al. Artificial Intelligence-based methods in head and neck cancer diagnosis: an overview. Br J Cancer 2021;124:1934-40. [Crossref] [PubMed]
  63. Pertzborn D, Arolt C, Ernst G, et al. Multi-Class Cancer Subtyping in Salivary Gland Carcinomas with MALDI Imaging and Deep Learning. Cancers (Basel) 2022;14:4342. [Crossref] [PubMed]
Cite this article as: Ding H, Wu C, Su Z, Wang T, Zhuang S, Li C, Li Y. Current landscape and future trends in salivary gland oncology research—a bibliometric evaluation. Gland Surg 2024;13(6):969-986. doi: 10.21037/gs-24-94

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