Peters William P, Rosner Gary L, Vredenburgh James J, Shpall Elizabeth J, Crump Michael, Richardson Paul G, Schuster Michael W, Marks Lawrence B, Cirrincione Constance, Norton Larry, Henderson I C, Schilsky Richard L, Hurd David D
Cancer and Leukemia Group B, 230 W Monroe St, Suite 2050, Chicago, IL 60606, USA.
J Clin Oncol. 2005 Apr 1;23(10):2191-200. doi: 10.1200/JCO.2005.10.202. Epub 2005 Mar 14.
The prognosis for women with primary breast cancer involving multiple axillary nodes remains poor. High-dose chemotherapy with stem-cell support produced promising results in initial clinical trials conducted at single institutions.
Seven hundred eighty-five women aged 22 to 66 years with stage IIA, IIB, or IIIA breast cancer involving 10 or more axillary lymph nodes were randomized after surgery and standard adjuvant chemotherapy to either high-dose cyclophosphamide, cisplatin, and carmustine (HD-CPB) with stem-cell support or intermediate-dose cyclophosphamide, cisplatin, and carmustine (ID-CPB) with G-CSF support but without stem cells. Planned treatment for all patients included locoregional radiation therapy. Hormone-receptor-positive patients were to receive 5 years of tamoxifen. Event-free survival (EFS) was the primary end point.
Median follow-up was 7.3 years. Event-free survival was not significantly different between the two treatment groups (P = .24). The probability of being free of an event at 5 years with HD-CPB was 61% (95% CI, 56% to 65%), and was 58% (95% CI, 53% to 63%) for ID-CPB. Thirty-three patients died of causes attributed to HD-CPB, compared with no therapy-related deaths among women treated with ID-CPB. Overall survival for the two arms was identical at 71% at 5 years (P = .75).
HD-CPB with stem-cell support was not superior to ID-CPB for event-free or overall survival among all randomized women with high-risk primary breast cancer.
原发性乳腺癌累及多个腋窝淋巴结的女性患者预后仍然较差。在单机构进行的初始临床试验中,高剂量化疗联合干细胞支持取得了有前景的结果。
785名年龄在22至66岁之间、患有IIA期、IIB期或IIIA期乳腺癌且累及10个或更多腋窝淋巴结的女性,在手术和标准辅助化疗后,被随机分为接受高剂量环磷酰胺、顺铂和卡莫司汀(HD-CPB)联合干细胞支持治疗组,或接受中剂量环磷酰胺、顺铂和卡莫司汀(ID-CPB)联合G-CSF支持但无干细胞治疗组。所有患者的计划治疗包括局部区域放射治疗。激素受体阳性患者将接受5年的他莫昔芬治疗。无事件生存期(EFS)是主要终点。
中位随访时间为7.3年。两个治疗组之间的无事件生存期无显著差异(P = 0.24)。HD-CPB组5年无事件发生的概率为61%(95%CI,56%至65%),ID-CPB组为58%(95%CI,53%至63%)。33名患者死于HD-CPB相关原因,而ID-CPB治疗的女性中无治疗相关死亡病例。两组的5年总生存率均为71%,无差异(P = 0.75)。
对于所有随机分组的高危原发性乳腺癌女性患者,高剂量化疗联合干细胞支持在无事件生存期或总生存期方面并不优于中剂量化疗联合G-CSF支持。