Chlorambucil for the treatment of patients with chronic lymphocytic leukemia (CLL) - a systematic review and meta-analysis of randomized trials

被引:15
|
作者
Vidal, Liat [1 ,2 ]
Gurion, Ronit [1 ,2 ]
Ram, Ron [1 ,3 ]
Raanani, Pia [1 ,2 ]
Bairey, Osnat [1 ,2 ]
Robak, Tadeusz [4 ,5 ]
Gafter-Gvili, Anat [1 ,6 ]
Shpilberg, Ofer [1 ,7 ]
机构
[1] Beilinson Med Ctr, Inst Hematol, Rabin Med Ctr, Davidoff Ctr, Petah Tiqwa, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Sourasky Med Ctr, Bone Marrow Transplantat Unit, Tel Aviv, Israel
[4] Med Univ Lodz, Dept Hematol, Lodz, Poland
[5] Copernicus Mem Hosp, Lodz, Poland
[6] Beilinson Med Ctr, Rabin Med Ctr, Dept Med, Petah Tiqwa, Israel
[7] Assuta Med Ctr, Dept Hematol, Tel Aviv, Israel
关键词
Chemotherapy; chlorambucil; chronic lymphocytic leukemia; CLL; SLL; meta-analysis; small lymphocytic lymphoma; systematic review; PREVIOUSLY UNTREATED PATIENTS; HIGH-DOSE CHLORAMBUCIL; PLUS CHLORAMBUCIL; 1ST-LINE THERAPY; OPEN-LABEL; FLUDARABINE; CANCER; CYCLOPHOSPHAMIDE; MULTICENTER; PREDNISONE;
D O I
10.3109/10428194.2016.1154956
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Randomized clinical trials that compared chlorambucil to different regimens, for patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL) do not support an overall survival (OS) benefit. To assess the efficacy and safety of chlorambucil as frontline treatment, we conducted a systematic review and meta-analysis of randomized controlled trials. OS was the primary outcome. Meta-analysis of 18 trials that compared purine analogs, alkylators, alemtuzumab and ibrutinib to chlorambucil demonstrated no OS benefit for therapy without chlorambucil over chlorambucil (pooled HR 0.99, 95% CI 0.91-1.08; 4133 patients). PFS was longer with purine analogs compared with chlorambucil with an increased risk of infection. The risk of secondary malignancies was not increased with chlorambucil. In conclusion, our study showed that chlorambucil is an acceptable chemotherapy backbone for unfit patients with CLL. Purine analogs should be preferred in fit younger patients because of longer PFS. Future trials should focus on unfit patients who are underrepresented in clinical trials.
引用
收藏
页码:2047 / 2057
页数:11
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