PMID- 30271212 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20220321 IS - 1179-1322 (Print) IS - 1179-1322 (Electronic) IS - 1179-1322 (Linking) VI - 10 DP - 2018 TI - Efficacy and safety of lenalidomide for the treatment of acute myeloid leukemia: a systematic review and meta-analysis. PG - 3637-3648 LID - 10.2147/CMAR.S168610 [doi] AB - BACKGROUND: Lenalidomide is effective for the treatment of low-risk myelodysplastic syndromes with deletion 5q abnormalities. However, whether lenalidomide leads to a significant improvement in treatment response and overall survival (OS) in cases of acute myeloid leukemia (AML) remains controversial. A systematic review and a meta-analysis were performed to evaluate the efficacy and safety of lenalidomide in the treatment of AML. METHODS: Clinical studies were identified from the Cochrane Central Register of Controlled Trials, PubMed, Embase, and ClinicalTrials.gov. Efficacy outcomes included overall response rate (ORR), complete remission (CR), and OS. Safety was evaluated based on the incidence of grade 3 and 4 treatment-related adverse events (AEs). RESULTS: Eleven studies were included in our meta-analysis; collectively these studies featured 407 AML patients. Pooled estimates for overall ORR and CR were 31% (95% CI: 26%-36%) and 21% (95% CI: 16%-27%), respectively. Thrombocytopenia, anemia, neutropenia, and infection were the most common grade 3 and 4 AEs. CONCLUSION: Lenalidomide may have some clinical activity in AML, but the population that would benefit from lenalidomide and incorporating lenalidomide into combination drug strategies need to be better defined. FAU - Xie, Chun-Hong AU - Xie CH AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Wei, Min AU - Wei M AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Yang, Fei-Yan AU - Yang FY AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Wu, Fu-Zhen AU - Wu FZ AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Chen, Lei AU - Chen L AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Wang, Jian-Kun AU - Wang JK AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Liu, Qin AU - Liu Q AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. FAU - Huang, Jin-Xiong AU - Huang JX AD - Department of Hematology, Affiliated Liuzhou People's Hospital of Guangxi University of Science and Technology (Liuzhou People's Hospital), Liuzhou 545000, Guangxi, China, lzrmyyhjx@126.com. LA - eng PT - Journal Article DEP - 20180918 PL - New Zealand TA - Cancer Manag Res JT - Cancer management and research JID - 101512700 PMC - PMC6152603 OTO - NOTNLM OT - azacitidine OT - cytarabine OT - cytogenetic risk OT - immunomodulatory agent COIS- Disclosure The authors report no conflicts of interest in this work. EDAT- 2018/10/03 06:00 MHDA- 2018/10/03 06:01 PMCR- 2018/09/18 CRDT- 2018/10/02 06:00 PHST- 2018/10/02 06:00 [entrez] PHST- 2018/10/03 06:00 [pubmed] PHST- 2018/10/03 06:01 [medline] PHST- 2018/09/18 00:00 [pmc-release] AID - cmar-10-3637 [pii] AID - 10.2147/CMAR.S168610 [doi] PST - epublish SO - Cancer Manag Res. 2018 Sep 18;10:3637-3648. doi: 10.2147/CMAR.S168610. eCollection 2018.