S. S. Sviluppo Terapie Innovative, Oncologia Medica A, Istituto Nazionale per la Ricerca sul Cancro, L.go R. Benzi 10, 16132 Genova, Italy.
JAMA. 2011 Jul 20;306(3):269-76. doi: 10.1001/jama.2011.991.
Premenopausal patients with breast cancer are at high risk of premature ovarian failure induced by systemic treatments, but no standard strategies for preventing this adverse effect are yet available.
To determine the effect of the temporary ovarian suppression obtained by administering the gonadotropin-releasing hormone analogue triptorelin during chemotherapy on the incidence of early menopause in young patients with breast cancer undergoing adjuvant or neoadjuvant chemotherapy.
DESIGN, SETTING, AND PATIENTS: The PROMISE-GIM6 (Prevention of Menopause Induced by Chemotherapy: A Study in Early Breast Cancer Patients-Gruppo Italiano Mammella 6) study, a parallel, randomized, open-label, phase 3 superiority trial, was conducted at 16 sites in Italy and enrolled 281 patients between October 2003 and January 2008. The patients were premenopausal women with stage I through III breast cancer who were candidates for adjuvant or neoadjuvant chemotherapy. Assuming a 60% rate of early menopause in the group treated with chemotherapy alone, it was estimated that 280 patients had to be enrolled to detect a 20% absolute reduction in early menopause in the group treated with chemotherapy plus triptorelin. The intention-to-treat analysis was performed by including all randomized patients and using imputed values for missing data.
Before beginning chemotherapy, patients were randomly allocated to receive chemotherapy alone or combined with triptorelin. Triptorelin was administered intramuscularly at a dose of 3.75 mg at least 1 week before the start of chemotherapy and then every 4 weeks for the duration of chemotherapy.
Incidence of early menopause (defined as no resumption of menstrual activity and postmenopausal levels of follicle-stimulating hormone and estradiol 1 year after the last cycle of chemotherapy).
The clinical and tumor characteristics of the 133 patients randomized to chemotherapy alone and the 148 patients randomized to chemotherapy plus triptorelin were similar. Twelve months after the last cycle of chemotherapy (last follow-up, August 18, 2009), the rate of early menopause was 25.9% in the chemotherapy-alone group and 8.9% in the chemotherapy plus triptorelin group, an absolute difference of -17% (95% confidence interval, -26% to -7.9%; P < .001). The odds ratio for treatment-related early menopause was 0.28 (95% confidence interval, 0.14 to 0.59; P < .001).
The use of triptorelin-induced temporary ovarian suppression during chemotherapy in premenopausal patients with early-stage breast cancer reduced the occurrence of chemotherapy-induced early menopause.
clinicaltrials.gov Identifier: NCT00311636.
患有乳腺癌的绝经前患者存在因全身治疗而导致卵巢早衰的高危风险,但目前尚无预防这种不良作用的标准策略。
确定在接受化疗期间给予促性腺激素释放激素类似物曲普瑞林进行暂时卵巢抑制对接受辅助或新辅助化疗的年轻乳腺癌患者发生早期绝经的影响。
设计、设置和患者:PROMISE-GIM6(化疗引起的绝经预防:早期乳腺癌患者的研究-意大利乳腺研究组 6)研究是一项在意大利 16 个地点进行的平行、随机、开放标签、3 期优效性试验,共纳入 2003 年 10 月至 2008 年 1 月期间的 281 例患者。这些患者为 I 期至 III 期乳腺癌的绝经前女性,有接受辅助或新辅助化疗的适应证。假设单独接受化疗组有 60%的早期绝经发生率,估计需要纳入 280 例患者,以检测出联合化疗加曲普瑞林治疗组中早期绝经的绝对发生率降低 20%。意向治疗分析包括所有随机分组患者,并对缺失数据进行了插补。
在开始化疗之前,患者被随机分配接受单独化疗或联合曲普瑞林治疗。曲普瑞林以 3.75mg 的剂量肌内注射,至少在化疗开始前 1 周开始,然后每 4 周一次,持续化疗。
早期绝经(定义为化疗结束后 1 年内无月经恢复且卵泡刺激素和雌二醇处于绝经后水平)的发生率。
接受单独化疗的 133 例患者和接受化疗加曲普瑞林的 148 例患者的临床和肿瘤特征相似。化疗结束后 12 个月(最后随访时间为 2009 年 8 月 18 日),单独化疗组的早期绝经发生率为 25.9%,化疗加曲普瑞林组为 8.9%,绝对差异为-17%(95%置信区间,-26%至-7.9%;P<0.001)。与治疗相关的早期绝经的比值比为 0.28(95%置信区间,0.14 至 0.59;P<0.001)。
在早期乳腺癌的绝经前患者中,在化疗期间使用曲普瑞林诱导的暂时卵巢抑制可降低化疗引起的早期绝经的发生。
clinicaltrials.gov 标识符:NCT00311636。