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采用高剂量或中剂量阿糖胞苷及安吖啶治疗急变期和加速期慢性粒细胞白血病。

Treatment of chronic myelogenous leukemia in blast crisis and in accelerated phase with high- or intermediate-dose cytosine arabinoside and amsacrine.

作者信息

Bauduer F, Delmer A, Blanc M C, Delmas-Marsalet B, Cadiou M, Rio B, Marie J P, Zittoun R

机构信息

Service d'Hématologie, Hotel-Dieu, Paris, France.

出版信息

Leuk Lymphoma. 1993 Jun;10(3):195-200. doi: 10.3109/10428199309145883.

Abstract

Twenty-two patients (mean age 41 years) in blast crisis or accelerated phase (AP) of chronic myelogenous leukemia (CML) were treated with cytosine arabinoside (Ara-C) 500 mg/m2 [intermediate dose] or 1000 mg/m2 [high dose] twice a day for 6 days and amsacrine (AMSA) 120 mg/m2 for 3 days. Twenty-one cases were of myeloid type and one was a lymphoid BC. The mean duration of aplasia (neutrophils < 0.5 x 10(9)/l) was 21.5 days. Four patients (18%) died of infection during aplasia and minor toxicities were noted for the remainders. Nine patients (41%) achieved a complete remission (CR) and 4 (18%) a partial response. Various additional therapies were proposed after induction treatment including allogeneic bone marrow transplantation (2 patients), Ara-C and AMSA maintenance or other regimens with or without alpha-interferon (9 patients). Median survival for the entire cohort was 20 weeks (wks), significantly superior for complete responders (37 wks) than for others (7 wks) (p = 0.008). In this study, age, sex, initial platelet or basophil counts, interval between diagnosis of CML and blast crisis were not predictive of response. Although inducing a high CR rate and associated with acceptable toxicity, this regimen did not improve the survival of patients with BC or CML, strengthening the need for alternate approaches to be defined.

摘要

22例处于慢性粒细胞白血病(CML)急变期或加速期(AP)的患者(平均年龄41岁)接受了阿糖胞苷(Ara-C)500mg/m²[中等剂量]或1000mg/m²[高剂量],每日2次,共6天的治疗,以及安吖啶(AMSA)120mg/m²,共3天的治疗。21例为髓系类型,1例为淋巴细胞急变期。平均无细胞期(中性粒细胞<0.5×10⁹/L)为21.5天。4例患者(18%)在无细胞期死于感染,其余患者出现轻微毒性反应。9例患者(41%)达到完全缓解(CR),4例(18%)达到部分缓解。诱导治疗后提出了各种额外的治疗方案,包括异基因骨髓移植(2例患者)、Ara-C和AMSA维持治疗或其他含或不含α干扰素的方案(9例患者)。整个队列的中位生存期为20周(wks),完全缓解者(37周)明显优于其他患者(7周)(p = 0.008)。在本研究中,年龄、性别、初始血小板或嗜碱性粒细胞计数、CML诊断至急变期的间隔时间均不能预测反应。尽管该方案诱导的CR率较高且毒性可接受,但并未改善急变期或CML患者的生存率,这强化了定义替代方法的必要性。

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