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一项比较苯丁酸氮芥加泼尼松与环磷酰胺、美法仑和泼尼松治疗B期和C期慢性淋巴细胞白血病的随机试验。

A randomized trial comparing chlorambucil plus prednisone vs cyclophosphamide, melphalan, and prednisone in the treatment of chronic lymphocytic leukemia stages B and C.

作者信息

Montserrat E, Alcalá A, Alonso C, Besalduch J, Moraleda J M, García-Conde J, Gutierrez M, Gomis F, Garijo J, Guzmán M C

机构信息

Postgraduate School of Hematology Farreras Valentí, University of Barcelona, Hospital Clinic, Spain.

出版信息

Nouv Rev Fr Hematol (1978). 1988;30(5-6):429-32.

PMID:3065738
Abstract

Ninety-six previously untreated patients (67 males/29 females; mean age: 63 years; range: 46-84) with CLL in stage B (62 cases) or C (34 cases) were randomized to be treated with either chlorambucil (0.4 mg/kg orally days 5 and 6) plus prednisone (60 mg/m2 orally days 1 to 4) (CL + PDN) every 2 weeks or cyclophosphamide (160 mg/m2 orally days 1 to 4), melphalan (6 mg/m2 orally days 1 to 4), and prednisone (60 mg/m2 orally days 1 to 4) (CMP) every 3 weeks for 10 months. Forty-eight patients were treated with CLR + PDN, and the remaining 48 with CMP. The following types of response were considered: complete response (CR): total disappearance of symptoms and signs related to the disease. Partial response (PR): shift of the disease to a less advanced stage. Stable disease (SD) no change in the stage after treatment. Progressive disease (PD): progression of the disease to a more advanced stage. Thirty-six (75%) responses (27% CR) with CLR + PDN and 26 (54.5%, 12.5% CR) with CMP were observed (p = 0.054). Although more responses were achieved in stage B (69%, 24% CR) than in stage C (54%, 12% CR) this difference did not achieve statistical significance. Survival was statistically not different for those patients treated with LCR + PDN as compared to those receiving CMP.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

96例未经治疗的B期(62例)或C期(34例)慢性淋巴细胞白血病(CLL)患者(67例男性/29例女性;平均年龄:63岁;范围:46 - 84岁)被随机分为两组,一组每2周接受苯丁酸氮芥(第5天和第6天口服0.4mg/kg)加泼尼松(第1至4天口服60mg/m²)(CL + PDN)治疗,另一组每3周接受环磷酰胺(第1至4天口服160mg/m²)、美法仑(第1至4天口服6mg/m²)和泼尼松(第1至4天口服60mg/m²)(CMP)治疗,共治疗10个月。48例患者接受CLR + PDN治疗,其余48例接受CMP治疗。评估以下几种反应类型:完全缓解(CR):与疾病相关的症状和体征完全消失。部分缓解(PR):疾病进展至较早期阶段。疾病稳定(SD):治疗后疾病分期无变化。疾病进展(PD):疾病进展至更晚期阶段。观察到CLR + PDN组有36例(75%)出现反应(27%为CR),CMP组有26例(54.5%,12.5%为CR)(p = 0.054)。虽然B期患者的反应率(69%,24%为CR)高于C期患者(54%,12%为CR),但差异无统计学意义。接受LCR + PDN治疗的患者与接受CMP治疗的患者相比,生存率在统计学上无差异。(摘要截选至250字)

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