University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
J Clin Oncol. 2012 Jan 20;30(3):291-9. doi: 10.1200/JCO.2011.37.1989. Epub 2011 Dec 19.
In this large cohort of Hodgkin's lymphoma survivors with long follow-up, we estimated the impact of treatment regimens on premature ovarian failure (POF) occurrence and motherhood, including safety of nonalkylating chemotherapy and dose-response relationships for alkylating chemotherapy and age at treatment.
The Life Situation Questionnaire was sent to 1,700 women treated in European Organisation for Research and Treatment of Cancer and Groupe d'Étude des Lymphomes de l'Adulte trials between 1964 and 2004. Women treated between ages 15 and 40 years and currently not using hormonal contraceptives (n = 460) were selected to assess occurrence of POF. Cumulative POF risk was estimated using the life-table method. Predictive factors were assessed by Cox regression analysis.
Median follow-up was 16 years (range, 5 to 45 years). Cumulative risk of POF after alkylating chemotherapy was 60% (95% CI, 41% to 79%) and only 3% (95% CI, 1% to 7%) after nonalkylating chemotherapy (doxorubicin, bleomycin, vinblastine, and dacarbazine; epirubicin, bleomycin, vinblastine, and prednisone). Dose relationship between alkylating chemotherapy and POF occurrence was linear. POF risk increased by 23% per year of age at treatment. In women treated without alkylating chemotherapy at age younger than 32 years and age 32 years or older, cumulative POF risks were 3% (95% CI, 1% to 16%) and 9% (95% CI, 4% to 18%), respectively. If menstruation returned after treatment, cumulative POF risk was independent of age at treatment. Among women who ultimately developed POF, 22% had one or more children after treatment, compared with 41% of women without POF.
Nonalkylating chemotherapy carries little to no excess risk of POF. Dose-response relationships for alkylating chemotherapy and age at treatment are both linear. Timely family planning is important for women at risk of POF.
在这项对霍奇金淋巴瘤幸存者进行的大型队列研究中,我们对不同治疗方案对卵巢早衰(POF)发生和生育的影响进行了评估,包括非烷化剂化疗的安全性以及烷化剂化疗的剂量-反应关系和治疗时的年龄。
1964 年至 2004 年间,欧洲癌症研究与治疗组织和成人淋巴瘤研究组的临床试验中,共向 1700 名女性发放了生活状况调查问卷。我们选择了年龄在 15 至 40 岁之间且目前未使用激素避孕的女性(n=460),以评估 POF 的发生情况。采用寿命表法估计 POF 的累积风险。采用 Cox 回归分析评估预测因素。
中位随访时间为 16 年(范围为 5 至 45 年)。烷化剂化疗后 POF 的累积风险为 60%(95%CI:41%至 79%),而非烷化剂化疗(阿霉素、博来霉素、长春碱和达卡巴嗪;表柔比星、博来霉素、长春碱和泼尼松)后仅为 3%(95%CI:1%至 7%)。烷化剂化疗与 POF 发生之间存在线性剂量关系。治疗时的年龄每增加 1 岁,POF 的风险就增加 23%。在年龄小于 32 岁或 32 岁及以上未接受烷化剂化疗的女性中,累积 POF 风险分别为 3%(95%CI:1%至 16%)和 9%(95%CI:4%至 18%)。如果治疗后月经恢复,则治疗时的年龄与 POF 的累积风险无关。在最终发生 POF 的女性中,22%在治疗后生育了一个或多个孩子,而未发生 POF 的女性中这一比例为 41%。
非烷化剂化疗几乎不会增加 POF 的风险。烷化剂化疗的剂量-反应关系和治疗时的年龄均呈线性。对于有 POF 风险的女性,及时进行生育规划很重要。