Department of Medical Oncology, U.O. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, Genova, Italy.
Department of Internal Medicine and Medical Specialties (DiMI), School of Medicine, University of Genova, Genova, Italy.
J Natl Cancer Inst. 2022 Mar 8;114(3):400-408. doi: 10.1093/jnci/djab213.
Although use of gonadotropin-releasing hormone agonist (GnRHa) during chemotherapy is an established strategy to protect ovarian function in premenopausal breast cancer patients, no long-term safety data are available, raising some concerns in women with hormone receptor-positive disease. There are controversial data on its fertility preservation potential.
The Prevention of Menopause Induced by Chemotherapy: a Study in Early Breast Cancer Patients-Gruppo Italiano Mammella 6 (PROMISE-GIM6) trial is a multicenter, randomized, open-label, phase III superiority trial conducted at 16 Italian centers from October 2003 to January 2008. Eligible patients were randomly assigned to (neo)adjuvant chemotherapy alone (control arm) or combined with the GnRHa triptorelin (GnRHa arm). The primary planned endpoint was incidence of chemotherapy-induced premature ovarian insufficiency. Post hoc endpoints were disease-free survival (DFS), overall survival (OS), and post-treatment pregnancies. Hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated.
Of 281 randomly assigned patients, 80.4% had hormone receptor-positive breast cancer. Median follow-up was 12.4 years (interquartile range = 11.3-13.2 years). No differences in 12-year DFS (65.7% [95% CI = 57.0% to 73.1%] in the GnRHa arm vs 69.2% [95% CI = 60.3% to 76.5%] in the control arm; HR = 1.16, 95% CI = 0.76 to 1.77) or in 12-year OS (81.2% [95% CI = 73.6% to 86.8%] in the GnRHa arm vs 81.3% [95% CI = 73.1% to 87.2%] in the control arm; HR = 1.17, 95% CI = 0.67 to 2.03) were observed. In patients with hormone receptor-positive disease, the hazard ratio was 1.02 (95% CI = 0.63 to 1.63) for DFS and 1.12 (95% CI = 0.59 to 2.11) for OS. In the GnRHa and control arms, 9 and 4 patients had a posttreatment pregnancy, respectively (HR = 2.14, 95% CI = 0.66 to 6.92).
Final analysis of the PROMISE-GIM6 trial provides reassuring results on the safety of GnRHa use during chemotherapy as a strategy to preserve ovarian function in premenopausal patients with early breast cancer, including those with hormone receptor-positive disease.
虽然在绝经前乳腺癌患者的化疗中使用促性腺激素释放激素激动剂(GnRHa)是保护卵巢功能的既定策略,但尚无长期安全性数据,这在激素受体阳性疾病患者中引起了一些担忧。关于其生育力保存潜力存在争议数据。
化疗诱导的更年期预防:早期乳腺癌患者研究-意大利乳腺 6 组(PROMISE-GIM6)试验是一项多中心、随机、开放标签、III 期优效性试验,于 2003 年 10 月至 2008 年 1 月在意大利的 16 个中心进行。合格的患者被随机分配接受(新)辅助化疗(对照组)或联合 GnRHa 曲普瑞林(GnRHa 组)。主要计划终点是化疗诱导的卵巢早衰的发生率。事后终点是无病生存期(DFS)、总生存期(OS)和治疗后妊娠。计算了危险比(HR)和 95%置信区间(CI)。
281 名随机分配的患者中,80.4%患有激素受体阳性乳腺癌。中位随访时间为 12.4 年(四分位距=11.3-13.2 年)。12 年 DFS 无差异(GnRHa 组为 65.7%[95%CI=57.0%至 73.1%],对照组为 69.2%[95%CI=60.3%至 76.5%];HR=1.16,95%CI=0.76 至 1.77)或 12 年 OS 无差异(GnRHa 组为 81.2%[95%CI=73.6%至 86.8%],对照组为 81.3%[95%CI=73.1%至 87.2%];HR=1.17,95%CI=0.67 至 2.03)。在激素受体阳性疾病患者中,DFS 的危险比为 1.02(95%CI=0.63 至 1.63),OS 的危险比为 1.12(95%CI=0.59 至 2.11)。GnRHa 组和对照组分别有 9 例和 4 例患者在治疗后怀孕(HR=2.14,95%CI=0.66 至 6.92)。
PROMISE-GIM6 试验的最终分析结果令人放心,即化疗期间使用 GnRHa 作为保护绝经前早期乳腺癌患者卵巢功能的策略是安全的,包括激素受体阳性疾病患者。