Kim Kidong, Choi Chel Hun, Park Sang-Yoon, Kim Min Kyu, Lee Keun Ho, Lee Eun-Ju, Lim Myong Cheol, Park Young Han, Kyung Min Sun, No Jae Hong, Suh Dong Hoon, Lee Jeong-Won, Ahn Sangjeong, Lee Banghyun
Department of Obstetrics and Gynecology, Seoul National University Bundang Hospital, 82 Gumi-ro, 173 Beon-gil, Bundang-gu, Seongnam-si 13620, Gyeonggi-do, Republic of Korea.
Department of Obstetrics and Gynecology, Samsung Medical Center, Sungkyunkwan University College of Medicine, 81 Irwon- ro, Gangnam-gu, Seoul 06351, Republic of Korea.
Cancers (Basel). 2025 Jul 12;17(14):2320. doi: 10.3390/cancers17142320.
The effects of combining chemotherapy with hormonal therapy based on hormone receptor (HR) expression in epithelial ovarian, fallopian tube, or primary peritoneal (EOC) remain unclear. This study evaluated the efficacy and safety of physician-chosen chemotherapy combined with hormonal therapy in patients with heavily pretreated advanced EOC, stratified by HR expression. This phase II, multicenter, pilot study included patients with heavily pretreated advanced EOC, allocated to estrogen receptor (ER)-dominant or progesterone receptor (PR)-dominant arms. Patients in the ER-dominant arm received tamoxifen plus physician-selected chemotherapy, while those in the PR-dominant arm received megestrol acetate (MA) plus chemotherapy. The primary outcome was the best objective response rate (ORR) for six months, assessed using an optimal two-stage Simon design. Among 33 ER-dominant patients with high-grade serous carcinoma (HGSC), the six-month best ORR was 27.3% (3% complete response, 24.2% partial response). The six-month ORR and clinical benefit rate (CBR) were 18.8% and 37.5%, respectively, with 62.5% experiencing progressive disease (PD). Among three PR-dominant patients (two clear cell carcinoma and one HGSC), the six-month best ORR was 0%. The six-month ORR and CBR were also 0%, and all experienced PD within six months. No unacceptable toxicity related to tamoxifen or MA was encountered. In heavily pretreated advanced HGSC patients with ER-dominant expression, chemotherapy combined with tamoxifen showed encouraging clinical activity with favorable safety. While limited by the study design, these findings suggest a potential role for tailored hormonal therapy combined with chemotherapy based on HR expression in heavily pretreated advanced EOC. Clinical Trial Registration: KCT0004571.
基于激素受体(HR)表达情况,将化疗与激素疗法联合用于上皮性卵巢癌、输卵管癌或原发性腹膜癌(EOC)患者的疗效尚不清楚。本研究评估了在HR表达分层的情况下,由医生选择的化疗联合激素疗法用于预处理严重的晚期EOC患者的疗效和安全性。这项II期多中心试点研究纳入了预处理严重的晚期EOC患者,分为雌激素受体(ER)优势组或孕激素受体(PR)优势组。ER优势组患者接受他莫昔芬加医生选择的化疗,而PR优势组患者接受醋酸甲地孕酮(MA)加化疗。主要结局指标是采用最优两阶段西蒙设计评估的六个月最佳客观缓解率(ORR)。在33例ER优势的高级别浆液性癌(HGSC)患者中,六个月最佳ORR为27.3%(完全缓解率3%,部分缓解率24.2%)。六个月的ORR和临床获益率(CBR)分别为18.8%和37.5%,62.5%的患者疾病进展(PD)。在3例PR优势患者(2例透明细胞癌和1例HGSC)中,六个月最佳ORR为0%。六个月的ORR和CBR也均为0%,且所有患者在六个月内均出现PD。未遇到与他莫昔芬或MA相关的不可接受的毒性。在预处理严重的晚期ER优势表达的HGSC患者中,化疗联合他莫昔芬显示出令人鼓舞的临床活性且安全性良好。尽管受研究设计限制,但这些发现提示在预处理严重的晚期EOC中,基于HR表达的定制化激素疗法联合化疗可能具有潜在作用。临床试验注册号:KCT0004571。