Kishida Takuma, Enokida Tomohiro, Onaga Ryutaro, Tanaka Nobukazu, Hoshi Yuta, Fujisawa Takao, Kuboki Ryo, Tanaka Hideki, Okano Susumu, Tahara Makoto
Department of Head and Neck Medical Oncology, National Cancer Center East Hospital, 6-5-1 Kashiwanoha, Kashiwa, Chiba, 277-0881, Japan.
Department of Otorhinolaryngology, Head and Neck Surgery, Tokyo Medical University, Shinjuku, Japan.
Int J Clin Oncol. 2025 Jun 24. doi: 10.1007/s10147-025-02785-3.
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.
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.
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.
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).
尽管由促黄体生成素释放激素(LH-RH)激动剂和雄激素受体(AR)抑制剂组成的联合疗法已显示出对复发性和/或转移性唾液腺导管癌(R/M SGC)有良好的临床活性,但关于LH-RH激动剂单药治疗的研究报道较少。
我们对2004年11月至2023年7月在我院接受LH-RH激动剂单药治疗的AR阳性R/M SGC患者进行了回顾性分析。
共纳入19例患者;中位年龄为64岁(范围42 - 82岁),10例为涎腺导管癌(52.6%),3例为未另行特指的腺癌(15.8%)。16例患者(84.2%)将LH-RH激动剂单药治疗作为R/M疾病的一线全身治疗。9例患者(47.4%)实现了靶病灶肿瘤大小缩小,中位肿瘤缩小率为11%(范围1 - 100%),总缓解率和临床获益率(达到完全缓解、部分缓解或疾病稳定持续至少24周的患者比例)分别为15.8%和36.8%。LH-RH激动剂单药治疗的中位疗程为5.1个月(范围0.3 - 63.4),占整个治疗期的35.2%。中位无进展生存期和总生存期分别为3.2个月(95%置信区间(95%CI),1.6 - 6.0)和21.6个月(95%CI 9.9 - 34.4)。未观察到导致治疗中断或停药的严重不良事件。
LH-RH激动剂单药治疗在疗效和安全性之间表现出良好的平衡,可能是一种替代治疗选择,尤其适用于无法耐受联合治疗的患者。 (242字)