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苯丁酸氮芥与泼尼松联合方案对比环磷酰胺、长春新碱与泼尼松联合方案作为慢性淋巴细胞白血病初始治疗的疗效:东部肿瘤协作组一项随机临床试验的长期随访

Comparison of chlorambucil and prednisone versus cyclophosphamide, vincristine, and prednisone as initial treatment for chronic lymphocytic leukemia: long-term follow-up of an Eastern Cooperative Oncology Group randomized clinical trial.

作者信息

Raphael B, Andersen J W, Silber R, Oken M, Moore D, Bennett J, Bonner H, Hahn R, Knospe W H, Mazza J

机构信息

New York University Medical Center, NY 10016.

出版信息

J Clin Oncol. 1991 May;9(5):770-6. doi: 10.1200/JCO.1991.9.5.770.

DOI:10.1200/JCO.1991.9.5.770
PMID:2016618
Abstract

The Eastern Cooperative Oncology Group (ECOG) conducted a study in which patients with advanced chronic lymphocytic leukemia (CLL) were randomized between a regimen consisting of chlorambucil (30 mg/m2 orally day 1) and prednisone (80 mg orally days 1 to 5) (C + P) administered every 2 weeks and a more intensive regimen of cyclosphosphamide (300 mg/m2 orally days 1 to 5), vincristine (1.4 mg/m2 intravenously [IV] day 1), and prednisone (100 mg/m2 orally days 1 to 5) (CVP) given every 3 weeks. Treatment was continued for up to 18 months to maximal response. Of the 122 eligible patients, 60 received C + P, while 62 received CVP. With a median follow-up of 7 years, there were no significant differences in survival (4.8 v 3.9 years, P = .12), complete remission (CR) rate (25% v 23%; P = .83), or duration of response (2.0 v 1.9 years; P = .78) between C + P and CVP. Toxicity was modest despite the prolonged treatment. The long median survival of 4.1 years for stage III and IV patients is superior to that usually reported. This could stem from continuing treatment to maximal response rather than an increase in intensity of therapy. These results are comparable to those reported with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) therapy by other investigators. The data suggest that intermittent C + P administered to maximal response continues to be the standard treatment approach for advanced CLL.

摘要

东部肿瘤协作组(ECOG)开展了一项研究,将晚期慢性淋巴细胞白血病(CLL)患者随机分为两组,一组每2周接受由苯丁酸氮芥(第1天口服30 mg/m²)和泼尼松(第1至5天口服80 mg)组成的方案(C + P),另一组每3周接受更强化的环磷酰胺(第1至5天口服300 mg/m²)、长春新碱(第1天静脉注射[IV]1.4 mg/m²)和泼尼松(第1至5天口服100 mg/m²)的方案(CVP)。治疗持续至最长18个月以达到最大反应。122例符合条件的患者中,60例接受C + P,62例接受CVP。中位随访7年,C + P组和CVP组在生存率(4.8年对3.9年,P = 0.12)、完全缓解(CR)率(25%对23%;P = 0.83)或缓解持续时间(2.0年对1.9年;P = 0.78)方面均无显著差异。尽管治疗时间延长,但毒性较轻。III期和IV期患者4.1年的长中位生存期优于通常报道的生存期。这可能源于持续治疗至最大反应,而非治疗强度的增加。这些结果与其他研究者报道的环磷酰胺、多柔比星、长春新碱和泼尼松(CHOP)疗法的结果相当。数据表明,持续治疗至最大反应的间歇性C + P仍然是晚期CLL的标准治疗方法。

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