Bishop J F
Sydney Cancer Centre, Royal Prince Alfred Hospital, Camperdown, N.S.W., Australia.
Acta Haematol. 1998;99(3):133-7. doi: 10.1159/000040827.
Induction therapy of acute myeloid leukaemia (AML) with standard-dose chemotherapy will result in approximately 64% of patients achieving a complete remission (CR). New drugs which are active in induction therapy in randomised clinical trials are etoposide, idarubicin and high dose cytarabine. Intensification of induction treatment with etoposide or high-dose cytarabine does not appear to alter the CR rate but prolongs remission and has some impact on survival. High-dose cytarabine in induction combinations increase relapse-free survival compared to standard approaches. These induction results appear to parallel results obtained with post-remission therapies intensified with high-dose cytarabine. These studies provide clinical evidence that intensified induction with cytarabine in AML influences subsequent outcome but is more toxic, gives more profound myelosuppression post-remission and has benefit confined to younger patients.
采用标准剂量化疗对急性髓系白血病(AML)进行诱导治疗,约64%的患者可实现完全缓解(CR)。在随机临床试验中对诱导治疗有效的新药有依托泊苷、伊达比星和大剂量阿糖胞苷。使用依托泊苷或大剂量阿糖胞苷强化诱导治疗似乎不会改变完全缓解率,但可延长缓解期并对生存率产生一定影响。与标准方法相比,诱导联合方案中使用大剂量阿糖胞苷可提高无复发生存率。这些诱导治疗结果似乎与采用大剂量阿糖胞苷强化缓解后治疗所获得的结果相似。这些研究提供了临床证据,表明AML中使用阿糖胞苷强化诱导治疗会影响后续转归,但毒性更大,缓解后骨髓抑制更严重,且获益仅限于年轻患者。