{"title":"rh - rh激动剂单药治疗雄激素受体阳性复发和/或转移性唾液腺癌:一项回顾性研究。","authors":"Takuma Kishida, Tomohiro Enokida, Ryutaro Onaga, Nobukazu Tanaka, Yuta Hoshi, Takao Fujisawa, Ryo Kuboki, Hideki Tanaka, Susumu Okano, Makoto Tahara","doi":"10.1007/s10147-025-02785-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Although combination therapy consisting of a luteinizing hormone-releasing hormone (LH-RH) agonist and an Androgen receptor (AR) inhibitor has demonstrated promising clinical activity for recurrent and/or metastatic SGC (R/M SGC), few studies on LH-RH agonist monotherapy have been reported.</p><p><strong>Methods: </strong>We conducted a retrospective analysis of patients with AR-positive, R/M SGC treated by monotherapy with LH-RH agonists in our institution from November 2004 to July 2023.</p><p><strong>Results: </strong>Nineteen patients were identified; the median age was 64 years (range 42-82), 10 had salivary duct carcinoma (52.6%), and 3 had adenocarcinoma, not otherwise specified (15.8%). LH-RH agonist monotherapy was delivered as first-line systemic therapy for R/M disease in 16 patients (84.2%). Nine patients (47.4%) achieved tumor size reduction in target lesions with a median tumor shrinkage of 11% (range 1-100%), resulting in an overall response rate and clinical benefit rate (rate of patients achieving a complete response, partial response, or stable disease lasting for at least 24 weeks) of 15.8% and 36.8%, respectively. The median duration of treatment with LH-RH agonist monotherapy was 5.1 months (range 0.3-63.4), accounting for 35.2% of the entire treatment period. Median progression-free survival and overall survival was 3.2 months (95% confidence interval (95% CI), 1.6-6.0) and 21.6 months (95% CI 9.9-34.4), respectively. No severe adverse events leading to treatment interruption or discontinuation were seen.</p><p><strong>Conclusion: </strong>LH-RH agonist monotherapy demonstrated a well-balanced profile between efficacy and safety and could be an alternative therapeutic option, especially for subjects not tolerable to combination therapy. (242 words).</p>","PeriodicalId":13869,"journal":{"name":"International Journal of Clinical Oncology","volume":" ","pages":"1562-1571"},"PeriodicalIF":2.8000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"LH-RH agonist monotherapy for androgen receptor-positive recurrent and/or metastatic salivary gland cancer: a retrospective study.\",\"authors\":\"Takuma Kishida, Tomohiro Enokida, Ryutaro Onaga, Nobukazu Tanaka, Yuta Hoshi, Takao Fujisawa, Ryo Kuboki, Hideki Tanaka, Susumu Okano, Makoto Tahara\",\"doi\":\"10.1007/s10147-025-02785-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Although combination therapy consisting of a luteinizing hormone-releasing hormone (LH-RH) agonist and an Androgen receptor (AR) inhibitor has demonstrated promising clinical activity for recurrent and/or metastatic SGC (R/M SGC), few studies on LH-RH agonist monotherapy have been reported.</p><p><strong>Methods: </strong>We conducted a retrospective analysis of patients with AR-positive, R/M SGC treated by monotherapy with LH-RH agonists in our institution from November 2004 to July 2023.</p><p><strong>Results: </strong>Nineteen patients were identified; the median age was 64 years (range 42-82), 10 had salivary duct carcinoma (52.6%), and 3 had adenocarcinoma, not otherwise specified (15.8%). LH-RH agonist monotherapy was delivered as first-line systemic therapy for R/M disease in 16 patients (84.2%). Nine patients (47.4%) achieved tumor size reduction in target lesions with a median tumor shrinkage of 11% (range 1-100%), resulting in an overall response rate and clinical benefit rate (rate of patients achieving a complete response, partial response, or stable disease lasting for at least 24 weeks) of 15.8% and 36.8%, respectively. The median duration of treatment with LH-RH agonist monotherapy was 5.1 months (range 0.3-63.4), accounting for 35.2% of the entire treatment period. Median progression-free survival and overall survival was 3.2 months (95% confidence interval (95% CI), 1.6-6.0) and 21.6 months (95% CI 9.9-34.4), respectively. No severe adverse events leading to treatment interruption or discontinuation were seen.</p><p><strong>Conclusion: </strong>LH-RH agonist monotherapy demonstrated a well-balanced profile between efficacy and safety and could be an alternative therapeutic option, especially for subjects not tolerable to combination therapy. (242 words).</p>\",\"PeriodicalId\":13869,\"journal\":{\"name\":\"International Journal of Clinical Oncology\",\"volume\":\" \",\"pages\":\"1562-1571\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Clinical Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10147-025-02785-3\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/24 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10147-025-02785-3","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/24 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
LH-RH agonist monotherapy for androgen receptor-positive recurrent and/or metastatic salivary gland cancer: a retrospective study.
Background: Although combination therapy consisting of a luteinizing hormone-releasing hormone (LH-RH) agonist and an Androgen receptor (AR) inhibitor has demonstrated promising clinical activity for recurrent and/or metastatic SGC (R/M SGC), few studies on LH-RH agonist monotherapy have been reported.
Methods: We conducted a retrospective analysis of patients with AR-positive, R/M SGC treated by monotherapy with LH-RH agonists in our institution from November 2004 to July 2023.
Results: Nineteen patients were identified; the median age was 64 years (range 42-82), 10 had salivary duct carcinoma (52.6%), and 3 had adenocarcinoma, not otherwise specified (15.8%). LH-RH agonist monotherapy was delivered as first-line systemic therapy for R/M disease in 16 patients (84.2%). Nine patients (47.4%) achieved tumor size reduction in target lesions with a median tumor shrinkage of 11% (range 1-100%), resulting in an overall response rate and clinical benefit rate (rate of patients achieving a complete response, partial response, or stable disease lasting for at least 24 weeks) of 15.8% and 36.8%, respectively. The median duration of treatment with LH-RH agonist monotherapy was 5.1 months (range 0.3-63.4), accounting for 35.2% of the entire treatment period. Median progression-free survival and overall survival was 3.2 months (95% confidence interval (95% CI), 1.6-6.0) and 21.6 months (95% CI 9.9-34.4), respectively. No severe adverse events leading to treatment interruption or discontinuation were seen.
Conclusion: LH-RH agonist monotherapy demonstrated a well-balanced profile between efficacy and safety and could be an alternative therapeutic option, especially for subjects not tolerable to combination therapy. (242 words).
期刊介绍:
The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.