TY - JOUR
T1 - Maintenance therapy with hypomethylating agents for patients with acute myeloid leukemia in first remission not eligible for allogeneic hematopoietic cell transplantation
T2 - A systematic review and meta-analysis
AU - Sherban, A.
AU - Raanani, P.
AU - Gurion, R.
AU - Wolach, O.
AU - Gafter-Gvili, A.
N1 - Publisher Copyright:
© 2021
PY - 2022/2
Y1 - 2022/2
N2 - Background: Older patients encompass about 75 % of patients with acute myeloid leukemia (AML). Today therapeutic options to prevent relapse in older patients who managed to achieve complete remission (CR) after intensive chemotherapy are scarce. Recent randomized controlled trials (RCTs) have aimed to reduce the risk of relapse by means of post-CR maintenance therapy. Methods: We performed a systematic review and meta-analysis of RCTs comparing the efficacy and safety of maintenance with hypomethylating agents (HMA) vs. observation, conventional care or placebo in older patients with AML who are not candidates for allogeneic hematopoietic transplantation (allo−HCT). We searched Cochrane Library, PubMed and conference proceedings up to August 2021. Results: Six trials were included. Treatment with hypomethylating agents significantly improved overall survival (HR 0.80, 95 % CI 0.70 to 0.91, I2 = 30 %), and disease control (HR 0.80, 95 % CI 0.70 to 0.91, I2 = 0). A significant decrease was seen in both one year mortality (Risk Ratio [RR] 0.61, 95 % CI 0.48 to 0.77, I2 = 0) and mortality at the end of follow-up (RR 0.77, 95 % CI 0.67 to 0.88, I2 = 0). The rate of relapse at 6 months and at one-two years was lower in the HMA arm vs. control (RR, 0.59; 95 % CI, 0.47−0.72; RR, 0.74, I2 = 0; 95 % CI 0.69 – 0.91, I2 = 41 %, respectively). HMA were associated with a statistically non-significant increase in the risk of serious adverse events (RR 3.44, 95 % CI 0.93–12.74, I2 = 80 %). Conclusions: Our meta-analysis shows that in older patients who are not candidates for allo−HCT, maintenance therapy with HMA improves OS and disease control without a statistically significant increase in adverse events.
AB - Background: Older patients encompass about 75 % of patients with acute myeloid leukemia (AML). Today therapeutic options to prevent relapse in older patients who managed to achieve complete remission (CR) after intensive chemotherapy are scarce. Recent randomized controlled trials (RCTs) have aimed to reduce the risk of relapse by means of post-CR maintenance therapy. Methods: We performed a systematic review and meta-analysis of RCTs comparing the efficacy and safety of maintenance with hypomethylating agents (HMA) vs. observation, conventional care or placebo in older patients with AML who are not candidates for allogeneic hematopoietic transplantation (allo−HCT). We searched Cochrane Library, PubMed and conference proceedings up to August 2021. Results: Six trials were included. Treatment with hypomethylating agents significantly improved overall survival (HR 0.80, 95 % CI 0.70 to 0.91, I2 = 30 %), and disease control (HR 0.80, 95 % CI 0.70 to 0.91, I2 = 0). A significant decrease was seen in both one year mortality (Risk Ratio [RR] 0.61, 95 % CI 0.48 to 0.77, I2 = 0) and mortality at the end of follow-up (RR 0.77, 95 % CI 0.67 to 0.88, I2 = 0). The rate of relapse at 6 months and at one-two years was lower in the HMA arm vs. control (RR, 0.59; 95 % CI, 0.47−0.72; RR, 0.74, I2 = 0; 95 % CI 0.69 – 0.91, I2 = 41 %, respectively). HMA were associated with a statistically non-significant increase in the risk of serious adverse events (RR 3.44, 95 % CI 0.93–12.74, I2 = 80 %). Conclusions: Our meta-analysis shows that in older patients who are not candidates for allo−HCT, maintenance therapy with HMA improves OS and disease control without a statistically significant increase in adverse events.
KW - Acute myeloid leukemia
KW - Hypomethylating
KW - Maintenance
KW - Meta-analysis
UR - http://www.scopus.com/inward/record.url?scp=85123119309&partnerID=8YFLogxK
U2 - 10.1016/j.leukres.2021.106773
DO - 10.1016/j.leukres.2021.106773
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C2 - 35066294
AN - SCOPUS:85123119309
SN - 0145-2126
VL - 113
JO - Leukemia Research
JF - Leukemia Research
M1 - 106773
ER -