Mandelli F, Diverio D, Avvisati G, Luciano A, Barbui T, Bernasconi C, Broccia G, Cerri R, Falda M, Fioritoni G, Leoni F, Liso V, Petti M C, Rodeghiero F, Saglio G, Vegna M L, Visani G, Jehn U, Willemze R, Muus P, Pelicci P G, Biondi A, Lo Coco F
Ematologia, Dipartimento di Biotecnologie Cellulari ed Ematologia, University La Sapienza, Rome, Italy.
Blood. 1997 Aug 1;90(3):1014-21.
Two hundred fifty-three patients with newly diagnosed acute promyelocytic leukemia (APL) were eligible to enter the multicentric GIMEMA-AIEOP "AIDA" trial during the period July 1993 to February 1996. As a mandatory prerequisite for eligibility, all patients had genetic evidence of the specific t(15;17) lesion in their leukemic cells confirmed by karyotyping or by reverse transcription-polymerase chain reaction (RT-PCR) of the PML/RAR alpha fusion gene (the latter available in 247 cases). Median age was 37.8 years (range, 2.2 to 73.9). Induction treatment consisted of oral all-trans retinoic acid (ATRA), 45 mg/m2/d until complete remission (CR), given with intravenous Idarubicin, 12 mg/m2/d on days 2, 4, 6, and 8. Three polychemotherapy cycles were given as consolidation. Hematologic and molecular response by RT-PCR was assessed after induction and after consolidation. At the time of analysis, 240 of the 253 eligible patients were evaluable for induction. Of these, 11 (5%) died of early complications and 229 (95%) achieved hematologic remission. No cases of resistant leukemia were observed. Of 139 cases studied by RT-PCR after induction, 84 (60.5%) were PCR-negative and 55 (39.5%) PCR-positive. One hundred sixty-two patients were evaluable by RT-PCR at the end of consolidation. Of these, 159 (98%) tested PCR-negative and 3 (2%), PCR-positive. After a median follow up of 12 months (range, 0 to 33), the estimated actuarial event-free survival for the whole series of 253 eligible patients was 83% +/- 2.6% and 79% +/- 3.2% at 1 and 2 years, respectively. This study indicates that the AIDA protocol is a well-tolerated regimen that induces molecular remission in almost all patients with PML/RAR alpha-positive APL. Preliminary survival data suggest that a remarkable cure rate can be obtained with this treatment.
1993年7月至1996年2月期间,253例新诊断的急性早幼粒细胞白血病(APL)患者符合进入多中心GIMEMA - AIEOP “AIDA”试验的条件。作为入选的强制性先决条件,所有患者白血病细胞中均有特定t(15;17)病变的遗传学证据,通过核型分析或PML/RARα融合基因的逆转录 - 聚合酶链反应(RT-PCR)得以证实(后者在247例中可用)。中位年龄为37.8岁(范围2.2至73.9岁)。诱导治疗包括口服全反式维甲酸(ATRA),45 mg/m²/d直至完全缓解(CR),同时静脉给予伊达比星,在第2、4、6和8天为12 mg/m²/d。给予三个多药化疗周期作为巩固治疗。诱导治疗后及巩固治疗后通过RT-PCR评估血液学和分子反应。在分析时,253例符合条件的患者中有240例可进行诱导治疗评估。其中,11例(5%)死于早期并发症,229例(95%)实现血液学缓解。未观察到耐药白血病病例。诱导治疗后通过RT-PCR研究的139例病例中,84例(60.5%)PCR阴性,55例(39.5%)PCR阳性。巩固治疗结束时162例患者可通过RT-PCR评估。其中,159例(98%)检测为PCR阴性,3例(2%)PCR阳性。中位随访12个月(范围0至33个月)后,253例符合条件患者整个系列的估计无事件生存概率在1年和2年时分别为83%±2.6%和79%±3.2%。本研究表明,AIDA方案是一种耐受性良好的方案,几乎可使所有PML/RARα阳性APL患者实现分子缓解。初步生存数据表明,该治疗可获得显著的治愈率。