Minimal Residual Disease and Survival Outcomes in Patients With Chronic Lymphocytic Leukemia: A Systematic Review and Meta-analysis

被引:25
作者
Molica, Stefano [1 ]
Giannarelli, Diana [2 ]
Montserrat, Emili [3 ]
机构
[1] Azienda Osped Pugliese Ciaccio, Dept Hematol Oncol, Viale Pio X, I-88100 Catanzaro, Italy
[2] Regina Elena Natl Inst Canc Treatment & Res, Biostat Unit, Rome, Italy
[3] Univ Barcelona, Hosp Clin, Barcelona, Spain
关键词
Chemo-immunotherapy; Clinical outcome; Meta-analysis; Minimal residual disease; Prognosis; INDEPENDENT PREDICTOR; PROGRESSION-FREE; OPEN-LABEL; CYCLOPHOSPHAMIDE; FLUDARABINE; RITUXIMAB; PHASE-3; CLL;
D O I
10.1016/j.clml.2019.03.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To assess the magnitude of improvement of progression-free survival or overall survival in patients who achieved undetectable minimal residual disease (MRD) after upfront chemotherapy or chemo-immunotherapy, we conducted a systematic review and meta-analysis. Nine studies (n = 2088) provided data on the impact of MRD on progression-free survival and 6 (n = 1234) on overall survival. Results confirm that undetectable MRD status after treatment with chemotherapy or chemo-immunotherapy in newly diagnosed chronic lymphocytic leukemia is associated with long-term survival. Background: Patients with chronic lymphocytic leukemia (CLL) who achieve undetectable minimal residual disease (U-MRD) (ie, < 10(-4) detectable leukemic cells in peripheral blood or bone marrow) have better outcomes than those with detectable MRD. To assess the magnitude of improvement of progression-free survival (PFS) or overall survival (OS) in patients who achieved U-MRD after upfront chemotherapy (CT) or chemo-immunotherapy (CIT), we conducted a systematic review and meta-analysis. Materials and Methods: The screening process adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Guidelines. The search strategy yielded 365 records, including 22 articles assessed for eligibility. Results: Eleven studies comprising 2457 patients with CLL treated in upfront with CT or CIT were considered suitable for inclusion in the quantitative meta-analysis. Nine studies (n = 2088) provided data on the impact of MRD on PFS and 6 (n = 1234) on OS. MRD was the main endpoint in only 2 of these studies (n = 213). Tests of heterogeneity revealed significant differences among studies for PFS and OS, which highlights differences across studies. U-MRD status was associated with significantly better PFS overall (P <.001) and in patients who achieved conventional complete remission (P = .01). Regarding OS, U-MRD predicted longer OS globally (P <.001) but not in patients having achieved complete remission (P = .82). Conclusions: U-MRD status after treatment with CT or CIT in newly diagnosed CLL is associated with long-term survival. These findings provide quantitative evidence to support the integration of MRD assessment as an end point in clinical trials of CLL. (C) 2019 Published by Elsevier Inc.
引用
收藏
页码:423 / 430
页数:8
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