Koh L P, Goh Y T, Teoh G, Tan P
Department of Haematology, Singapore General Hospital, 1 Hospital Drive, Singapore 169608.
Ann Acad Med Singap. 2001 Jul;30(4):401-8.
The combination of all-trans retinoic acid (ATRA) with chemotherapy has improved the outcome of acute promyelocytic leukaemia (APL). Effective induction as well as maintenance therapy for APL can be achieved using this combination of anti-leukaemic agents.
Twenty-four consecutive patients with newly-diagnosed APL were treated with ATRA daily together with either daunorubicin or idarubicin. Therapy with ATRA was continued until complete remission (CR) was achieved; thereafter, patients were treated with 2 cycles of an anthracycline-based consolidation chemotherapy (either daunorubicin or idarubicin). Maintenance therapy was achieved using 5 alternating cycles of low-dose methotrexate (MTX) plus 6-mercaptopurine (6MP) followed by ATRA alone.
Twenty-three out of 24 patients (96%) completed induction therapy and achieved haematological CR (HCR) as well as molecular remission (MR); however, 1 patient (5%) died from retinoic acid syndrome. Twenty-one out of 23 evaluable patients (91%) completed consolidation chemotherapy, and 2 patients (10%) died, 1 from neutropenic sepsis and the other from relapse following non-compliance to therapy. All 21 surviving patients in the present study received maintenance chemotherapy and are still in HCR and MR at a median follow-up of 23 months. The estimated actuarial 2-year overall survival (OS) and event-free survival (EFS) rates were both 84% +/- 9%.
The combination of ATRA with an anthracycline is an effective remission-induction therapy for newly-diagnosed APL. Maintenance therapy using alternating cycles of MTX plus 6MP followed by ATRA alone is effective in maintaining CR and MR as well as prolonging the survival of patients with APL.
全反式维甲酸(ATRA)与化疗联合应用改善了急性早幼粒细胞白血病(APL)的治疗效果。使用这种抗白血病药物组合可实现对APL有效的诱导治疗以及维持治疗。
24例新诊断的APL患者连续接受ATRA治疗,同时联合柔红霉素或伊达比星。持续进行ATRA治疗直至达到完全缓解(CR);此后,患者接受2个周期的蒽环类药物巩固化疗(柔红霉素或伊达比星)。维持治疗采用5个交替周期的小剂量甲氨蝶呤(MTX)加6-巯基嘌呤(6MP),随后单独使用ATRA。
24例患者中有23例(96%)完成诱导治疗并实现血液学完全缓解(HCR)以及分子学缓解(MR);然而,1例患者(5%)死于维甲酸综合征。23例可评估患者中有21例(91%)完成巩固化疗,2例患者(10%)死亡,1例死于中性粒细胞减少性败血症,另1例死于因未遵医嘱治疗导致的复发。本研究中所有21例存活患者均接受了维持化疗,在中位随访23个月时仍处于HCR和MR状态。估计的2年总生存(OS)率和无事件生存(EFS)率均为84%±9%。
ATRA与蒽环类药物联合是新诊断APL有效的缓解诱导治疗方法。采用MTX加6MP交替周期随后单独使用ATRA的维持治疗在维持CR和MR以及延长APL患者生存期方面有效。