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2-氯脱氧腺苷疗法治疗华氏巨球蛋白血症。

2-Chlorodeoxyadenosine therapy in Waldenstrom's macroglobulinaemia.

作者信息

Delannoy A, Ferrant A, Martiat P, Bosly A, Zenebergh A, Michaux J L

机构信息

Groupe d'Hématologie de l'Université Catholique de Louvain, Cliniques Universitaires St. Luc, Brussels, Belgium.

出版信息

Nouv Rev Fr Hematol (1978). 1994 Aug;36(4):317-20.

PMID:7971252
Abstract

Despite some encouraging first results, experience with 2-chlorodeoxyadenosine (CdA) in the treatment of Waldenström's macroglobulinaemia (WM) has not as yet been very extensive. The present paper reports a clinical trial of the use of CdA in 18 patients having previously treated (n = 13) or untreated (n = 5) WM. CdA was administered by continuous intravenous infusion at a dose of 4 mg/m2/day for 7 days (5 patients) or as 2-h intravenous infusions at a dose of 5.6 mg/m2/day for 5 days (13 patients). Partial response was obtained in 7 cases. In this small series, no correlation could be found between response to CdA and patient characteristics at inclusion. During the first course of therapy, grade 4 neutropenia (< 0.5 x 10(9)/L) and thrombocytopenia (< 25 x 10(9)/L) developed in respectively 4 and 6 cases. In comparison with earlier reports haematological toxicity was more severe and the overall response rate lower in the present series of patients.

摘要

尽管取得了一些令人鼓舞的初步结果,但2-氯脱氧腺苷(CdA)治疗华氏巨球蛋白血症(WM)的经验尚不十分广泛。本文报告了一项针对18例曾接受治疗(n = 13)或未接受治疗(n = 5)的WM患者使用CdA的临床试验。CdA通过持续静脉输注给药,剂量为4 mg/m²/天,持续7天(5例患者),或通过2小时静脉输注给药,剂量为5.6 mg/m²/天,持续5天(13例患者)。7例患者获得部分缓解。在这个小系列中,未发现对CdA的反应与纳入时的患者特征之间存在相关性。在第一个疗程中,分别有4例和6例患者出现4级中性粒细胞减少(< 0.5×10⁹/L)和血小板减少(< 25×10⁹/L)。与早期报告相比,本系列患者的血液学毒性更严重,总体缓解率更低。

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