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硫唑嘌呤在成人慢性特发性血小板减少性紫癜治疗中作用的再评估:53例报告

Re-evaluation of the role of azathioprine in the treatment of adult chronic idiopathic thrombocytopenic purpura: a report on 53 cases.

作者信息

Quiquandon I, Fenaux P, Caulier M T, Pagniez D, Huart J J, Bauters F

机构信息

Service des Maladies du Sang, C.H.U. Lille, France.

出版信息

Br J Haematol. 1990 Feb;74(2):223-8. doi: 10.1111/j.1365-2141.1990.tb02569.x.

Abstract

We treated 53 adults (mean age 54 years, range 17-89; 37 females and 16 males) with chronic idiopathic thrombocytopenic purpura (ITP) by azathioprine. All patients had received at least one form of therapy (including splenectomy in 40 patients) and had less than 50 x 10(9)/1 platelets. The duration of ITP before azathioprine was started ranged from 6 to 350 months (median 19). All patients initially received 150 mg/d of azathioprine. This was associated with a short initial course of prednisone (0.3-0.5 mg/kg d) in 10 of them, who were refractory to prednisone alone. 34 (64%) patients responded, including 24 (45%) complete remissions (CR), three (6%) partial remissions (PR) and seven (13%) minor responses (MR). Median time to achieve response was 4 months. 17 of the CR persisted after 7-182 months, 10 of them after discontinuation of azathioprine. Seven patients relapsed after 4-26 months, five of them after azathioprine was stopped or its dose was reduced. PR were short and the median duration of MR was 8 months. Overall, 21 patients (40%) had responses lasting 1 year or more and 17 (32%) lasting 2 years or more. Median duration of treatment was 18 months (range 3-84). Five patients died of bleeding while on treatment. No prognostic factors for response to azathioprine were found. Mild leucopenia was seen in seven patients and a moderate (x3) increase in transaminases in two patients. No opportunistic infections were seen and no malignancy has occurred since the onset of azathioprine. We conclude that azathioprine gives a relatively high incidence of durable responses and very limited side effects in chronic ITP, when splenectomy has failed or is contraindicated. This efficacy, in our experience, is superior to that obtained with other therapeutic approaches. As responses may be delayed, a course of azathioprine of 4 months is required before one can infer a failure to respond. In responding patients, however, the optimum duration of treatment remains to be established.

摘要

我们采用硫唑嘌呤治疗了53例慢性特发性血小板减少性紫癜(ITP)成人患者(平均年龄54岁,范围17 - 89岁;女性37例,男性16例)。所有患者均接受过至少一种治疗方式(40例患者接受过脾切除术),且血小板计数低于50×10⁹/L。开始使用硫唑嘌呤前ITP的病程为6至350个月(中位数为19个月)。所有患者最初均接受150mg/d的硫唑嘌呤治疗。其中10例单独使用泼尼松无效的患者,初始阶段联合使用了短疗程的泼尼松(0.3 - 0.5mg/kg·d)。34例(64%)患者有反应,包括24例(45%)完全缓解(CR)、3例(6%)部分缓解(PR)和7例(13%)轻微反应(MR)。达到反应的中位时间为4个月。17例CR患者在7至182个月后仍持续缓解,其中10例在停用硫唑嘌呤后仍持续缓解。7例患者在4至26个月后复发,其中5例在硫唑嘌呤停药或剂量减少后复发。PR持续时间较短,MR的中位持续时间为8个月。总体而言,21例患者(40%)反应持续1年或更长时间,17例(32%)持续2年或更长时间。治疗的中位持续时间为18个月(范围3至84个月)。5例患者在治疗期间死于出血。未发现硫唑嘌呤反应的预后因素。7例患者出现轻度白细胞减少,2例患者转氨酶中度升高(升高3倍)。未观察到机会性感染,自开始使用硫唑嘌呤以来未发生恶性肿瘤。我们得出结论,当脾切除术失败或禁忌时,硫唑嘌呤在慢性ITP中产生持久反应的发生率相对较高,且副作用非常有限。根据我们的经验,这种疗效优于其他治疗方法。由于反应可能延迟,在推断无反应之前需要4个月的硫唑嘌呤疗程。然而,对于有反应的患者,最佳治疗持续时间仍有待确定。

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