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对 1 周期高剂量阿糖胞苷为基础的诱导化疗难治的急性髓细胞白血病患者的特征和结局。

Characteristics and outcome of patients with acute myeloid leukemia refractory to 1 cycle of high-dose cytarabine-based induction chemotherapy.

机构信息

Department of Leukemia, The University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Blood. 2010 Dec 23;116(26):5818-23; quiz 6153. doi: 10.1182/blood-2010-07-296392. Epub 2010 Oct 5.

Abstract

Pretreatment characteristics and outcome of patients treated with induction regimens containing high-dose ara-C (HiDAC) at M. D. Anderson Cancer Center refractory to 1 cycle of induction were compared with similar patients achieving a complete response (CR). Among 1597 patients treated with HiDAC-based induction from 1995 to 2009, 285 were refractory to 1 cycle. Median age was 59 years (range, 18-85 years). Induction regimens included HiDAC with anthracyclines (n = 181; 64%) or HiDAC with nonanthracycline chemotherapy (n = 104; 36%). Refractory patients were older (median age, 59 vs 56 years; P < .001), more likely with unfavorable cytogenetics (P < .001) and antecedent hematologic disorder (P < .001), and had a higher presentation white blood cell count (P = .04), but not a higher incidence of FLT3 mutations (P = .85), than those achieving CR. Forty-three patients (22%) responded to salvage (35 CR and 8 CR without platelet recovery). With a median follow-up of 72 months (range, 27-118 months) in responders, 11 are alive. Nineteen patients (7%) were alive and in CR for at least 6 months, including 9 who underwent allogeneic stem cell transplantation. On multivariate analysis, severe thrombocytopenia, leukocytosis, increasing marrow blast percentage, unfavorable cytogenetics, and salvage not including allogeneic stem cell transplantation were associated with a worse survival. Alternative strategies are needed for these patients.

摘要

在 M. D. Anderson 癌症中心,我们比较了预处理特征和接受高剂量阿糖胞苷(HiDAC)诱导方案治疗但对 1 个周期诱导无反应的患者与获得完全缓解(CR)的相似患者的结果。在 1995 年至 2009 年期间,共有 1597 例患者接受了基于 HiDAC 的诱导治疗,其中 285 例对 1 个周期无反应。中位年龄为 59 岁(范围,18-85 岁)。诱导方案包括 HiDAC 联合蒽环类药物(n = 181;64%)或 HiDAC 联合非蒽环类化疗(n = 104;36%)。无反应患者年龄更大(中位年龄,59 岁比 56 岁;P <.001),更有可能具有不良细胞遗传学(P <.001)和先前存在的血液系统疾病(P <.001),且白细胞计数更高(P =.04),但 FLT3 突变的发生率没有更高(P =.85)。与获得 CR 的患者相比。43 例患者(22%)对挽救治疗有反应(35 例 CR 和 8 例血小板恢复但无 CR)。在有反应者中,中位随访 72 个月(范围,27-118 个月),有 11 例存活。19 例(7%)存活且至少 6 个月持续 CR,其中 9 例接受了异基因造血干细胞移植。多变量分析显示,严重血小板减少、白细胞增多、骨髓原始细胞比例增加、不良细胞遗传学和不包括异基因造血干细胞移植的挽救治疗与生存不良相关。这些患者需要替代策略。

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