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喷司他丁治疗难治性慢性淋巴细胞白血病:欧洲癌症研究与治疗组织的一项II期试验

Pentostatin in refractory chronic lymphocytic leukemia: a phase II trial of the European Organization for Research and Treatment of Cancer.

作者信息

Ho A D, Thaler J, Stryckmans P, Coiffier B, Luciani M, Sonneveld P, Lechner K, Rodenhuis S, Peetermans M E, deCataldo F

机构信息

Department of Internal Medicine V, University of Heidelberg, Federal Republic of Germany.

出版信息

J Natl Cancer Inst. 1990 Sep 5;82(17):1416-20. doi: 10.1093/jnci/82.17.1416.

Abstract

Pentostatin was used to treat 26 patients with advanced B-cell chronic lymphocytic leukemia resistant to conventional treatment. Twenty patients had progressive disease on previous regimens and six had had partial remission and then relapsed 3-34 months after previous chemotherapy. Eleven patients had previously been treated with three different regimens. 10 had been treated with two regimens, and five had been treated with one regimen. Pentostatin was administered at a dosage of 4 mg/m2 weekly for 3 weeks, then 4 mg/m2 every other week for 6 weeks and once a month for 6 months. Seven of 26 assessable patients (27%) achieved partial remission and five (19%) achieved clinical improvement. The median duration of partial remission until relapse or death was 210 days. Myelosuppression was minor and transient in responsive patients, indicating some degree of selective effect on lymphocytes. Except for one patient who died of cerebral hemorrhage during the first 6 weeks of treatment, no drug-related deaths were registered. Major toxic effects included nausea in 17 patients (mainly grade 1), infections in 15, and liver enzyme elevations in five. Thus, pentostatin is active, even in patients with advanced B-cell chronic lymphocytic leukemia that is refractory to multiple chemotherapy regimens. Response can be achieved with mild myelosuppression.

摘要

喷司他丁用于治疗26例对传统治疗耐药的晚期B细胞慢性淋巴细胞白血病患者。20例患者在先前治疗方案下病情进展,6例曾获部分缓解,但在先前化疗后3 - 34个月复发。11例患者先前接受过三种不同治疗方案,10例接受过两种治疗方案,5例接受过一种治疗方案。喷司他丁的给药剂量为4mg/m²,每周1次,共3周,然后每2周1次,共6周,之后每月1次,共6个月。26例可评估患者中,7例(27%)获得部分缓解,5例(19%)临床症状改善。部分缓解至复发或死亡的中位持续时间为210天。有反应的患者骨髓抑制轻微且短暂,提示对淋巴细胞有一定程度的选择性作用。除1例患者在治疗的前6周死于脑出血外,未记录到与药物相关的死亡。主要毒性反应包括17例患者出现恶心(主要为1级),15例出现感染,5例出现肝酶升高。因此,喷司他丁即使对多种化疗方案难治的晚期B细胞慢性淋巴细胞白血病患者也有活性。可在轻度骨髓抑制的情况下取得疗效。

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