首页> 外文期刊>Journal of Clinical Oncology >Prospective, randomized comparison of high-dose chemotherapy with stem-cell support versus intermediate-dose chemotherapy after surgery and adjuvant chemotherapy in women with high-risk primary breast cancer: a report of CALGB 9082, SWOG 9114, and NC
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Prospective, randomized comparison of high-dose chemotherapy with stem-cell support versus intermediate-dose chemotherapy after surgery and adjuvant chemotherapy in women with high-risk primary breast cancer: a report of CALGB 9082, SWOG 9114, and NC

机译:高危原发性乳腺癌女性术后高剂量化疗加干细胞支持与中等剂量化疗及辅助化疗后的前瞻性,随机比较:CALGB 9082,SWOG 9114和NC

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PURPOSE: 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. PATIENTS AND METHODS: 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. RESULTS: 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). CONCLUSION: 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.
机译:目的:原发性乳腺癌涉及多个腋窝淋巴结转移的妇女的预后仍然很差。在单个机构进行的初始临床试验中,采用干细胞支持的大剂量化疗产生了可喜的结果。患者和方法:785名年龄在22至66岁,患有IIA,IIB或IIIA期乳腺癌,涉及10个或更多腋窝淋巴结转移的女性在手术和标准辅助化疗后随机分配至大剂量环磷酰胺,顺铂和具有干细胞支持的卡莫司汀(HD-CPB)或具有G-CSF支持但没有干细胞的中剂量环磷酰胺,顺铂和卡莫司汀(ID-CPB)。所有患者的计划治疗包括局部放疗。激素受体阳性患者接受他莫昔芬治疗5年。无事件生存(EFS)是主要终点。结果:中位随访时间为7.3年。两组的无事件生存率无显着差异(P = 0.24)。HD-CPB治疗5年无事件发生的可能性为61%(95%CI,56%至65%), ID-CPB为58%(95%CI,53%至63%)。与HD-CPB相关的原因导致33例患者死亡,而ID-CPB治疗的女性中没有与治疗相关的死亡。两组的总生存率在5年时相同,为71%(P = .75)。结论:在所有高危原发性乳腺癌女性中,具有干细胞支持的HD-CPB在无事件或总体生存方面均不优于ID-CPB。

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