Amadori S, Testi A M, Aricò M, Comelli A, Giuliano M, Madon E, Masera G, Rondelli R, Zanesco L, Mandelli F
Department of Human Biopathology, University La Sapienza, Rome, Italy.
J Clin Oncol. 1993 Jun;11(6):1046-54. doi: 10.1200/JCO.1993.11.6.1046.
This study was conducted to assess the comparative values of allogeneic bone marrow transplantation (BMT) and autologous bone marrow transplantation (ABMT) with sequential postremission chemotherapy (SPC) in children with acute myelogenous leukemia (AML) in first remission.
From March 1987 to March 1990, 161 assessable patients younger than 15 years of age with newly diagnosed AML were treated uniformly with two courses of daunorubicin and standard-dose cytarabine. After initial consolidation with a course of daunorubicin, cytarabine, and thioguanine (DAT), patients in complete remission (CR) were randomized to receive either ABMT or SPC, except for those with an HLA-matched sibling who were assigned to undergo BMT. SPC consisted of three additional courses of DAT, followed by three pairs of drugs administered sequentially for a total of six cycles.
Overall, 127 of 161 patients attained CR (79%). The estimated probabilities of survival and event-free survival (EFS) at 5 years for all patients were 42% and 25%, respectively (median follow-up, 28 months). For the 127 complete responders, the 5-year probability of disease-free survival (DFS) was 31%, with a cumulative risk of relapse of 64%. For the purpose of this study, all complete responders were evaluated for analysis of disease outcome according to the intent-to-treat principle, regardless of whether they actually received the intended therapy. The 5-year DFS was 51% for the BMT group (n = 24), significantly higher (P = .03) than that observed for the other cohorts: 21% for ABMT (n = 35), 27% for SPC (n = 37), and 34% for a group of 31 nonrandomized (NR) patients. Bone marrow relapse was the most frequent cause of postremission failure in all therapeutic subgroups, including the BMT cohort, in which no deaths attributable to the toxicity of the procedure were recorded.
The results of this study show that BMT is more effective than ABMT or SPC in preventing leukemia relapse and extending DFS duration in children with AML in first remission.
本研究旨在评估异基因骨髓移植(BMT)和自体骨髓移植(ABMT)联合缓解后序贯化疗(SPC)在首次缓解的急性髓系白血病(AML)儿童患者中的相对价值。
1987年3月至1990年3月,161例年龄小于15岁、新诊断为AML的可评估患者均接受了两个疗程的柔红霉素和标准剂量阿糖胞苷治疗。在接受一个疗程的柔红霉素、阿糖胞苷和硫鸟嘌呤(DAT)进行初始巩固治疗后,完全缓解(CR)的患者被随机分配接受ABMT或SPC,但有 HLA 匹配同胞供者的患者被指定接受BMT。SPC包括另外三个疗程的DAT,随后依次给予三对药物,共六个周期。
总体而言,161例患者中有127例达到CR(79%)。所有患者5年时的估计生存率和无事件生存率(EFS)分别为42%和25%(中位随访时间,28个月)。对于127例完全缓解者,5年无病生存率(DFS)为31%,累积复发风险为64%。为了本研究的目的,所有完全缓解者均根据意向性治疗原则进行疾病转归分析,无论他们是否实际接受了预期的治疗。BMT组(n = 24)的5年DFS为51%,显著高于其他队列观察到的结果:ABMT组为21%(n = 35),SPC组为27%(n = 37),31例非随机(NR)患者组为34%(P = .03)。骨髓复发是所有治疗亚组缓解后失败的最常见原因,包括BMT队列,该队列中未记录到因手术毒性导致的死亡。
本研究结果表明,在预防首次缓解的AML儿童患者白血病复发和延长DFS持续时间方面,BMT比ABMT或SPC更有效。