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序贯阿扎胞苷联合来那度胺治疗未经治疗的老年急性髓系白血病。

Sequential azacitidine plus lenalidomide combination for elderly patients with untreated acute myeloid leukemia.

机构信息

Department of Medicine, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Haematologica. 2013 Apr;98(4):591-6. doi: 10.3324/haematol.2012.076414. Epub 2012 Dec 14.

Abstract

There are limited treatment options for older patients with acute myeloid leukemia and prognosis of these patients remains poor, thereby warranting development of novel therapies. We evaluated the efficacy and safety of azacitidine in combination with lenalidomide as front-line therapy for older patients with acute myeloid leukemia. Patients ≥ 60 years of age with untreated acute myeloid leukemia received azacitidine 75 mg/m2 for 7 days followed by escalating doses of lenalidomide daily for 21 days starting on day 8 of each cycle every 6 weeks. Patients received continued therapy until disease progression, unacceptable toxicity, or completion of 12 cycles. Forty-two patients (median age, 74 years) were enrolled with equal distribution according to European LeukemiaNet risk. The overall response rate was 40% (rate of complete remission with or without complete recovery of blood counts = 28%). The median time to complete remission with or without complete recovery of blood counts was 12 weeks, and duration of this status was 28 weeks (range, 4 - >104 weeks). Therapy-related acute myeloid leukemia and a high score on the Hematopoietic Cell Transplantation Comorbidity Index were negative predictors of response. Early death was noted in 17% of patients. Grades ≥ 3 toxicities were uncommon and most adverse events were gastrointestinal, fatigue and myelosuppression. In conclusion, a sequential combination of azacitidine plus lenalidomide has clinical activity in older patients with acute myeloid leukemia, and further studies of this combination are underway.

摘要

对于老年急性髓系白血病患者,治疗选择有限,这些患者的预后仍然较差,因此需要开发新的治疗方法。我们评估了阿扎胞苷联合来那度胺作为老年急性髓系白血病一线治疗的疗效和安全性。年龄≥60 岁、未经治疗的急性髓系白血病患者接受阿扎胞苷 75mg/m2 治疗 7 天,随后在每个周期的第 8 天开始每天递增剂量的来那度胺治疗 21 天,每 6 周一个周期。患者继续接受治疗,直到疾病进展、无法耐受毒性或完成 12 个周期。42 名患者(中位年龄 74 岁)根据欧洲白血病网风险分布均等入组。总体缓解率为 40%(完全缓解伴或不伴血细胞计数完全恢复率=28%)。完全缓解伴或不伴血细胞计数完全恢复的中位时间为 12 周,这种状态的持续时间为 28 周(范围 4->104 周)。治疗相关的急性髓系白血病和造血细胞移植合并症指数高是反应的负预测因素。17%的患者发生早期死亡。≥3 级毒性罕见,大多数不良事件为胃肠道、疲劳和骨髓抑制。总之,阿扎胞苷联合来那度胺序贯治疗在老年急性髓系白血病患者中具有临床活性,正在进行该联合治疗的进一步研究。

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