Azacitidine in Fludarabine-Refractory Chronic Lymphocytic Leukemia: A Phase II Study

被引:11
|
作者
Malik, Asifa [1 ]
Shoulder, Mahran [1 ]
Garcia-Manero, Guillermo [1 ]
Wierda, William [1 ]
Cortes, Jorge [1 ]
Bickel, Susan [1 ]
Keating, Michael J. [1 ]
Estrov, Zeev [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Leukemia, Houston, TX 77030 USA
来源
CLINICAL LYMPHOMA MYELOMA & LEUKEMIA | 2013年 / 13卷 / 03期
基金
美国国家卫生研究院;
关键词
Azacitidine; Chronic lymphocytic leukemia; DNA methylation; RITUXIMAB; CYCLOPHOSPHAMIDE; ALEMTUZUMAB; 5-AZACYTIDINE;
D O I
10.1016/j.clml.2012.11.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Because preclinical data suggested that hypomethylating agents might be effective in chronic lymphocytic leukemia (CLL), we conducted a phase II trial with azacitidine in patients with recurrent fludarabine-refractory CLL. Eight of 9 patients did not respond, and 1 patient experienced reduction of hepatosplenomegaly and a substantial increase in platelet count after 4 cycles of therapy. Further studies of azacitidine in CLL are warranted. Background: Treatment of fludarabine-refractory disease in patients with chronic lymphocytic leukemia (CLL) remains a challenge. Because a recent genome-wide methylation analysis of CLL cells suggested that demethylation therapy might be beneficial in CLL, we conducted a phase II trial with the hyponnethylating agent azacitidine in patients with recurrent fludarabine-refractory CLL. Patients and Methods: Nine patients with recurrent fludarabine-refractory Rai stage IV CLL (median age, 74 years; range, 49-81 years) were enrolled. Azacitidine (75 mg/m(2)) was administered by subcutaneous injection daily for 7 consecutive days every 3 to 8 weeks, and the data were analyzed at a median follow-up of 9 months (range 3-47 months). Results: The trial was prematurely discontinued because of lack of response and slow accrual. The number of cycles administered ranged from 1 to 6. Three patients received 1 cycle, 3 patients received 2 cycles, and the remaining 3 patients received 4, 5, or 6 cycles. Side effects included grade 2 or 3 infectious episodes (resulting from immunosuppression and drug-induced neutropenia), diarrhea, rash, vomiting, anemia, and thrombocytopenia. One patient experienced reduction of hepatosplenomegaly and a substantial increase in platelet count after 4 cycles of therapy. However this response did not qualify as a partial response according to the National Cancer Institute International Workshop on CLL (NCI-IWCLL) criteria. At a median follow-up of 9 months after the start of azacitidine treatment, 3 patients (33%) who went on to receive other treatments were alive. Conclusions: Although no partial or complete responses occurred in these heavily pretreated patients, the encouraging response in 1 of these patients may warrant further studies to investigate the effects of azacitidine in CLL. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:292 / 295
页数:4
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