Department of Therapeutic Centre of Anemia, Institute of Hematology and Blood Diseases Hospital, Chinese Academy of Medical Science & Peking Union Medical College (CAMS & PUMC), Tianjin, People's Republic of China.
Ann Hematol. 2018 Sep;97(9):1519-1526. doi: 10.1007/s00277-018-3414-6. Epub 2018 Jun 26.
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is most frequently used to treat acute myeloid leukemia (AML). Whether patients should routinely receive consolidation chemotherapy before proceeding to transplant after achieving first complete remission (CR1) has been a subject of debate. We performed a systematic review and meta-analysis of studies examining the impact of post-remission chemotherapy before allo-HSCT in patients with AML in CR1. Six studies including 1659 patients were included in the meta-analysis. The pooled hazard ratio (HR) for overall survival was 0.9 (95% confidence interval [CI] 0.77-1.05, P = 0.182), and the pooled HR for leukemia-free survival was 0.87 (95% CI 0.75-1.0, P = 0.07). No survival advantage was observed for post-remission chemotherapy before reduced-intensity conditioning or myeloablative conditioning (MAC) allo-HSCT for AML in CR1. The pooled relative risk for relapse incidence (RI) was 1.02 (95% CI 0.82-1.28, P = 0.834). Post-remission chemotherapy before allo-HSCT did not significantly affect the RI in patients with AML in CR1. The analyses revealed no significant benefit of post-remission consolidation chemotherapy in patients who received allo-HSCT. We recommend proceeding to allo-HSCT as soon as CR1 is attained.
异基因造血干细胞移植(allo-HSCT)最常用于治疗急性髓系白血病(AML)。在达到首次完全缓解(CR1)后,患者是否应常规在进行移植前接受巩固化疗,这一直是一个有争议的问题。我们对检查 AML 患者在 CR1 后缓解后化疗对 allo-HSCT 影响的研究进行了系统回顾和荟萃分析。荟萃分析纳入了 6 项研究共 1659 名患者。总生存的合并危险比(HR)为 0.9(95%置信区间[CI] 0.77-1.05,P=0.182),无白血病生存的合并 HR 为 0.87(95%CI 0.75-1.0,P=0.07)。在 CR1 的 AML 患者中,缓解后化疗在降低强度预处理或清髓性预处理(MAC)allo-HSCT 前并未带来生存优势。复发发生率(RI)的合并相对风险为 1.02(95%CI 0.82-1.28,P=0.834)。缓解后化疗在 CR1 的 AML 患者中不会显著影响 RI。分析显示,在接受 allo-HSCT 的患者中,缓解后巩固化疗没有明显获益。我们建议一旦达到 CR1 就进行 allo-HSCT。