Breviglieri Carla Nolasco Monteiro, de Almeida Maria Tereza Assis, Neto Gabriele Zampelini, Teixeira Roberto Augusto Plaza, Odone-Filho Vicente, Cristofani Lilian Maria
Instituto da Criança do Instituto do Tratamento do Câncer Infantil, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, (ICr ITACI FMUSP), São Paulo, SP, Brazil.
Instituto da Criança do Instituto do Tratamento do Câncer Infantil, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, (ICr ITACI FMUSP), São Paulo, SP, Brazil.
Hematol Transfus Cell Ther. 2023 Jul;45 Suppl 2(Suppl 2):S126-S130. doi: 10.1016/j.htct.2022.09.1276. Epub 2022 Nov 7.
Acute promyelocytic leukemia currently presents an excellent chance of cure with protocols based on all-trans-retinoic acid (ATRA) and anthracycline or only differentiation agents. However, high early mortality rates continue to be reported METHODS: Between 2000 and 2018, patients were enrolled and retrospectively analyzed by medical records. A modified AIDA protocol, with a 1-year shortening of the treatment duration, reduction in the number of drugs and a strategy to reduce early mortality by the postponement of the initiation of anthracyclines were employed. Overall and event-free survival rates and toxicity were analyzed RESULTS: Thirty-two patients were enrolled, of whom 56% were female, with a median age of 12 years and 34% belonged to the high-risk group. Two patients had the hypogranular variant and three had another cytogenetic alteration, in addition to the t(15;17). The median start of the first anthracycline dose was 7 days. There were two early deaths (6%) due to central nervous system (CNS) bleeding. All patients achieved molecular remission after the consolidation phase. Two children relapsed and were rescued by arsenic trioxide and hematopoietic stem cell transplantation. The presence of disseminated intravascular coagulation (DIC) at diagnosis (p = 0.03) was the only factor with survival impact. The five-year event-free survival (EFS) was 84% and 5-year overall survival (OS) was 90% CONCLUSION: The survival results were comparable to those found in the AIDA protocol, with a low rate of early mortality in relation to the Brazilian reality.
急性早幼粒细胞白血病目前通过基于全反式维甲酸(ATRA)和蒽环类药物或仅使用分化剂的方案,有极佳的治愈机会。然而,仍有高早期死亡率的报道。方法:2000年至2018年期间,对患者进行入组并通过病历进行回顾性分析。采用改良的AIDA方案,将治疗时间缩短1年,减少药物数量,并采取通过推迟蒽环类药物起始使用来降低早期死亡率的策略。分析总生存率、无事件生存率和毒性。结果:入组32例患者,其中56%为女性,中位年龄12岁,34%属于高危组。除t(15;17)外,2例患者有低颗粒变异型,3例有其他细胞遗传学改变。首个蒽环类药物剂量的中位起始时间为7天。有2例(6%)因中枢神经系统(CNS)出血导致早期死亡。所有患者在巩固期后均实现分子缓解。2例儿童复发,通过三氧化二砷和造血干细胞移植获救。诊断时存在弥散性血管内凝血(DIC)(p = 0.03)是唯一影响生存的因素。五年无事件生存率(EFS)为84%,五年总生存率(OS)为90%。结论:生存结果与AIDA方案相当,相对于巴西的实际情况,早期死亡率较低。