Advani S H, Nair R, Bapna A, Gladstone B, Kadam P, Saikia T K, Parekh P M, Gopal R, Nair C N
Department of Medical Oncology, Tata Memorial Hospital, Mumbai, India.
Am J Hematol. 1999 Feb;60(2):87-93. doi: 10.1002/(sici)1096-8652(199902)60:2<87::aid-ajh1>3.0.co;2-5.
This study was conducted to compare the results of treatment of acute promyelocytic leukemia (APL) with all-trans retinoic acid alone (ATRA) or a combination therapy of ATRA followed by chemotherapy. Forty-three patients treated between February 1992 and February 1996 were included in this study. Eighteen patients were treated with ATRA alone and 25 patients were treated with ATRA followed by chemotherapy. The cytogenetic analysis was done in 41 patients at presentation, following treatment, and at follow-up. A complete response (CR) was achieved in 13 (72%) patients on ATRA and 19 (76%) on ATRA followed by chemotherapy. Eleven of 13 patients with response to ATRA alone relapsed with median survival of eight months (range, 1 to 28). One patient died of hepatitis in CR and one patient is alive 2 years after diagnosis. In the combination therapy arm, 10 patients are in CR with a median follow-up of 22 months (range, 6 to 56 months). After achieving a CR, four patients died due to infections during chemotherapy therapy, and only 5 of 19 patients have relapsed. Major cytogenetic response was seen in 8 of the 10 patients in whom cytogenetic data was available after treatment with ATRA at the time of remission. Similarly, 13 of 15 for whom data was available showed a major cytogenetic response after treatment with ATRA plus chemotherapy. Prior to relapse, 80% of the patients had an increase in the percentage of t(15;17) cells in the marrow. Patients with a complete hematological response but no cytogenetic response relapsed within six months. Ten patients died prior to response evaluation. Two patients who received ATRA died of retinoic acid syndrome, one of pneumonia, and one of intracranial hemorrhage. Of the six patients on ATRA and chemotherapy, four died of retinoic acid syndrome (RAS), one of intracranial hemorrhage, and one of left ventricular failure. Only one patient is alive at 24 months following treatment with ATRA alone. The relapse-free survival is 42% at four years for patients treated with ATRA followed by chemotherapy. This trial is a historical comparison of ATRA alone and ATRA with subsequent combination chemotherapy. Nonetheless, the trial shows a significant improvement in the event free survival of patients receiving chemotherapy as consolidation following ATRA.
本研究旨在比较全反式维甲酸(ATRA)单药治疗与ATRA联合化疗治疗急性早幼粒细胞白血病(APL)的效果。本研究纳入了1992年2月至1996年2月期间接受治疗的43例患者。18例患者接受ATRA单药治疗,25例患者接受ATRA联合化疗。对41例患者在初诊时、治疗后及随访时进行了细胞遗传学分析。接受ATRA治疗的13例患者(72%)和接受ATRA联合化疗的19例患者(76%)达到完全缓解(CR)。仅接受ATRA治疗的13例有反应患者中,11例复发,中位生存期为8个月(范围1至28个月)。1例患者在CR期死于肝炎,1例患者在诊断后2年仍存活。在联合治疗组中,10例患者达到CR,中位随访时间为22个月(范围6至56个月)。达到CR后,4例患者在化疗期间死于感染,19例患者中仅5例复发。在缓解期接受ATRA治疗后有细胞遗传学数据的10例患者中,8例出现主要细胞遗传学反应。同样,有数据的15例患者中,13例在接受ATRA加化疗后出现主要细胞遗传学反应。复发前,80%的患者骨髓中t(15;17)细胞百分比增加。血液学完全缓解但无细胞遗传学反应的患者在6个月内复发。10例患者在反应评估前死亡。2例接受ATRA治疗的患者死于维甲酸综合征,1例死于肺炎,1例死于颅内出血。在接受ATRA和化疗的6例患者中,4例死于维甲酸综合征(RAS),1例死于颅内出血,1例死于左心室衰竭。仅1例接受ATRA单药治疗的患者在治疗后24个月仍存活。接受ATRA联合化疗的患者4年无复发生存率为42%。本试验是ATRA单药与ATRA后续联合化疗的历史性比较。尽管如此,该试验表明,接受化疗作为ATRA巩固治疗的患者无事件生存期有显著改善。