Abstract

Background: The hypomethylating agents (HMAs) azacitidine (AZA) and decitabine (DAC) have been widely used in patients with acute myeloid leukemia (AML) and higher-risk myelodysplastic syndrome (HR-MDS). However, few direct clinical trials have been carried out to compare the efficacy and adverse events (AEs) between these two agents. The clinical choice between them is controversial. A systematic review and network meta-analysis (NMA) was performed to compare the efficacy, safety, and survival of DAC and AZA in AML and HR-MDS patients.Methods: We systematically searched MEDLINE, Embase, Web of Science, and Cochrane Library through March 15, 2021. Randomized controlled trials (RCTs) on AML or HR-MDS patients comparing the efficacy and safety between DAC and AZA or comparing one of HMAs to conventional care regimens (CCR) were selected.Results: Eight RCTs (n = 2,184) were identified in the NMA. Four trials compared AZA to CCR, and four compared DAC to CCR. Direct comparisons indicated that, compared to CCR, both AZA and DAC were associated with higher overall response (OR) rate (AZA vs. CCR: relative risk (RR) = 1.48, 95% CI 1.05–2.1; DAC vs. CCR: RR = 2.14, 95% CI 1.21–3.79) and longer overall survival (OS) (AZA vs. CCR: HR = 0.64, 95% CI 0.50–0.82; DAC vs. CCR: HR = 0.84, 95% CI 0.72–0.98), and AZA showed higher rate of complete remission with incomplete blood count recovery (CRi) (HR = 2.52, 95% CI 1.27–5). For the indirect method, DAC showed a higher complete remission (CR) rate than AZA in patients with both AML (RR = 2.28, 95% CI 1.12–4.65) and MDS (RR = 7.57, 95% CI 1.26–45.54). Additionally, DAC significantly increased the risk of 3/4 grade anemia (RR = 1.61, 95% CI: 1.03–2.51), febrile neutropenia (RR = 4.03, 95% CI: 1.41–11.52), and leukopenia (RR = 3.43, 95% CI 1.64–7.16) compared with AZA. No statistical significance was found for the other studied outcomes.Conclusion: Compared to CCR, both AZA and DAC can promote outcomes in patients with AML and HR-MDS. DAC showed higher efficacy especially CR rate than AZA (low-certainty evidence), while AZA experienced lower frequent grade 3/4 cytopenia than patients receiving DAC treatment.

Highlights

  • Acute myeloid leukemia (AML) and higher-risk myelodysplastic syndromes (HR-MDS) are heterogeneous hematologic malignancies with clinical manifestations of anemia, hemorrhage, and infection (Arber, 2019)

  • Direct comparisons indicated that, compared to conventional care regimens (CCR), both AZA and DAC were associated with higher overall response (OR) rate (AZA vs. CCR: relative risk (RR) 1.48, 95% confidence intervals (95% CIs) 1.05–2.1; DAC vs. CCR: RR 2.14, 95% CI 1.21–3.79) and longer overall survival (OS) (AZA vs. CCR: HR 0.64, 95% CI 0.50–0.82; DAC vs. CCR: HR 0.84, 95% CI 0.72–0.98), and AZA showed higher rate of complete remission with incomplete blood count recovery (CRi) (HR 2.52, 95% CI 1.27–5)

  • DAC showed a higher complete remission (CR) rate than AZA in patients with both AML (RR 2.28, 95% CI 1.12–4.65) and MDS (RR 7.57, 95% CI 1.26–45.54)

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Summary

Introduction

Acute myeloid leukemia (AML) and higher-risk myelodysplastic syndromes (HR-MDS) are heterogeneous hematologic malignancies with clinical manifestations of anemia, hemorrhage, and infection (Arber, 2019). The annual incidence rates of AML are higher than 4.2 per 100,000 per year (Shallis et al.,2019). The 2- and 5-year overall survival (OS) rates of elderly AML patients are approximately 10 and 2%, respectively (Menzin et al, 2002; Daly and Paquette, 2019). The hypomethylating agents (HMAs) azacitidine (AZA) and decitabine (DAC) have been widely used in patients with acute myeloid leukemia (AML) and higher-risk myelodysplastic syndrome (HR-MDS). A systematic review and network metaanalysis (NMA) was performed to compare the efficacy, safety, and survival of DAC and AZA in AML and HR-MDS patients

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