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全反式维甲酸与伊达比星联合治疗(AIDA)诱导PML/RARα阳性急性早幼粒细胞白血病分子缓解。意大利成人恶性血液病研究组及意大利儿科血液学与肿瘤学协会合作组

Molecular remission in PML/RAR alpha-positive acute promyelocytic leukemia by combined all-trans retinoic acid and idarubicin (AIDA) therapy. Gruppo Italiano-Malattie Ematologiche Maligne dell'Adulto and Associazione Italiana di Ematologia ed Oncologia Pediatrica Cooperative Groups.

作者信息

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

机构信息

Ematologia, Dipartimento di Biotecnologie Cellulari ed Ematologia, University La Sapienza, Rome, Italy.

出版信息

Blood. 1997 Aug 1;90(3):1014-21.

PMID:9242531
Abstract

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.

摘要

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。

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