University of North Carolina Lineberger Comprehensive Cancer Center, Chapel Hill, NC.
Alliance Statistics and Data Center, Mayo Clinic, Rochester, MN.
J Clin Oncol. 2019 Sep 10;37(26):2338-2348. doi: 10.1200/JCO.19.00647. Epub 2019 Jul 24.
Older women with breast cancer remain under-represented in clinical trials. The Cancer and Leukemia Group B 49907 trial focused on women age 65 years and older. We previously reported the primary analysis after a median follow-up of 2.4 years. Standard adjuvant chemotherapy showed significant improvements in recurrence-free survival (RFS) and overall survival compared with capecitabine. We now update results at a median follow-up of 11.4 years.
Patients age 65 years or older with early breast cancer were randomly assigned to either standard adjuvant chemotherapy (physician's choice of either cyclophosphamide, methotrexate, and fluorouracil or cyclophosphamide and doxorubicin) or capecitabine. An adaptive Bayesian design was used to determine sample size and test noninferiority of capecitabine. The primary end point was RFS.
The design stopped accrual with 633 patients at its first sample size assessment. RFS remains significantly longer for patients treated with standard chemotherapy. At 10 years, in patients treated with standard chemotherapy versus capecitabine, the RFS rates were 56% and 50%, respectively (hazard ratio [HR], 0.80; = .03); breast cancer-specific survival rates were 88% and 82%, respectively (HR, 0.62; = .03); and overall survival rates were 62% and 56%, respectively (HR, 0.84; = .16). With longer follow-up, standard chemotherapy remains superior to capecitabine among hormone receptor-negative patients (HR, 0.66; = .02), but not among hormone receptor-positive patients (HR, 0.89; = .43). Overall, 43.9% of patients have died (13.1% from breast cancer, 16.4% from causes other than breast cancer, and 14.1% from unknown causes). Second nonbreast cancers occurred in 14.1% of patients.
With longer follow-up, RFS remains superior for standard adjuvant chemotherapy versus capecitabine, especially in patients with hormone receptor-negative disease. Competing risks in this older population dilute overall survival benefits.
患有乳腺癌的老年女性在临床试验中代表性仍然不足。癌症和白血病组 B 49907 试验专注于 65 岁及以上的女性。我们之前报道了中位随访 2.4 年后的主要分析结果。与卡培他滨相比,标准辅助化疗显著改善了无复发生存率(RFS)和总生存率。我们现在更新了中位随访 11.4 年后的结果。
65 岁或以上患有早期乳腺癌的患者被随机分配接受标准辅助化疗(医生选择环磷酰胺、甲氨蝶呤和氟尿嘧啶或环磷酰胺和多柔比星)或卡培他滨。采用适应性贝叶斯设计来确定样本量并测试卡培他滨的非劣效性。主要终点是 RFS。
设计在第一次样本量评估时,在 633 名患者时停止入组。接受标准化疗的患者 RFS 明显更长。在 10 年时,接受标准化疗的患者与卡培他滨相比,RFS 率分别为 56%和 50%(风险比[HR],0.80; =.03);乳腺癌特异性生存率分别为 88%和 82%(HR,0.62; =.03);总生存率分别为 62%和 56%(HR,0.84; =.16)。随着随访时间的延长,标准化疗在激素受体阴性患者中仍优于卡培他滨(HR,0.66; =.02),但在激素受体阳性患者中并非如此(HR,0.89; =.43)。总的来说,43.9%的患者死亡(13.1%死于乳腺癌,16.4%死于乳腺癌以外的其他原因,14.1%死于原因不明)。第二位非乳腺癌发生在 14.1%的患者中。
随着随访时间的延长,标准辅助化疗与卡培他滨相比,RFS 仍然更好,尤其是在激素受体阴性疾病患者中。在这个老年人群中,竞争风险会稀释总生存获益。