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三种新型方案未能改善复发或难治性急性髓系白血病患者的结局:来自东部肿瘤协作组的报告。

Failure of three novel regimens to improve outcome for patients with relapsed or refractory acute myeloid leukaemia: a report from the Eastern Cooperative Oncology Group.

机构信息

Mayo Clinic, Rochester, MN 55905, USA.

出版信息

Br J Haematol. 2010 Jan;148(2):217-25. doi: 10.1111/j.1365-2141.2009.07917.x. Epub 2009 Oct 5.

Abstract

The treatment of relapsed acute myeloid leukaemia (AML) remains unsatisfactory. We conducted a phase II randomized trial where patients received intermediate-dose cytarabine for 4 d followed by gemtuzumab ozogamicin on day 5 (Arm A), or combined with liposomal daunorubicin for 3 d (Arm B), or cytarabine given for 5 d combined with cyclophosphamide for 3 d and topotecan by continuous infusion for 5 d (Arm C). Eligible patients had primary refractory AML, a first relapse after a remission of <1 year, or a second or greater relapse. The primary objective of this trial was attainment of a conventional complete remission (CR) or a CR without platelet recovery (CRp) in at least 40% of patients. The CR/CRp rates for the 82 eligible patients were 3/26 (12%) in Arm A, 2/29 (7%) in Arm B, and 1/27 (4%) in Arm C. No patients who had relapsed within 6 months of initial CR or who had suffered multiple relapses responded. More than 95% of patients subsequently died of AML. No unexpected toxicities were encountered. We conclude that none of these three regimens were effective enough in the treatment of high-risk relapsed or refractory AML to warrant further study. This trial was registered at http://www.clinicaltrials.gov as #NCT00005962.

摘要

复发急性髓系白血病(AML)的治疗仍不尽如人意。我们进行了一项 II 期随机试验,患者接受 4 天中剂量阿糖胞苷治疗,随后第 5 天接受吉妥珠单抗奥佐米星(Arm A),或联合脂质体多柔比星治疗 3 天(Arm B),或阿糖胞苷治疗 5 天联合环磷酰胺治疗 3 天和拓扑替康持续输注 5 天(Arm C)。符合条件的患者为原发性难治性 AML、缓解时间<1 年的首次复发、或第二次或更大程度的复发。该试验的主要目的是至少 40%的患者达到常规完全缓解(CR)或无血小板恢复的 CR(CRp)。82 例合格患者的 CR/CRp 率分别为 Arm A 组 26 例中的 3 例(12%)、Arm B 组 29 例中的 2 例(7%)和 Arm C 组 27 例中的 1 例(4%)。没有在初始 CR 后 6 个月内复发或多次复发的患者有反应。超过 95%的患者随后死于 AML。未出现意外毒性。我们得出结论,这三种方案在治疗高危复发或难治性 AML 方面均不够有效,不值得进一步研究。该试验在 http://www.clinicaltrials.gov 上注册为 #NCT00005962。

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