Abromowitch Minnie, Sposto Richard, Perkins Sherrie, Zwick David, Siegel Stuart, Finlay Jonathan, Cairo Mitchell S
Department of Pediatrics Hematology/Oncology, University of Nebraska Medical Center, Omaha, NE 68198-2168, USA.
Br J Haematol. 2008 Oct;143(2):261-7. doi: 10.1111/j.1365-2141.2008.07320.x. Epub 2008 Aug 28.
Pediatric lymphoblastic lymphoma (LL) has utilized treatment strategies similar to childhood acute lymphoblastic leukaemia (ALL) with prolonged maintenance chemotherapy. We report the results of a pilot study to estimate the feasibility, toxicity and efficacy of a 12-month aggressive multi-agent chemotherapy regimen in children and adolescents with advanced LL. Between July 1994 and June 1997, 85 eligible children and adolescents with advanced LL (Stage III/IV) were enrolled on this pilot study. Patients achieving a complete response following induction and consolidation received six cycles of maintenance chemotherapy for a total duration of 12 months. Grade III/IV toxicities included: hematological (80%), infections (20%), stomatitis and elevated transaminases, (29%). There were a total of 19 events, 13 relapses, two secondary acute myeloid leukaemia and four toxic deaths (5%). The 5-year event-free survival (EFS) and overall survival (OS) was 78 +/- 4.5% and 85 +/- 3.9%, respectively. Relapsed patients had a 5-year OS of only 33 +/- 14%. Multivariate analysis failed to demonstrate age, gender, lactate dehydrogenase level, presence of marrow and/or central nervous system disease to have independent prognostic value. These results suggest that this experimental approach is safe and results in similar outcomes as more prolonged childhood ALL regimens.
小儿淋巴细胞性淋巴瘤(LL)采用了与儿童急性淋巴细胞白血病(ALL)相似的治疗策略,进行延长疗程的维持化疗。我们报告了一项前瞻性研究的结果,以评估一种为期12个月的多药联合强化化疗方案在晚期LL儿童和青少年中的可行性、毒性和疗效。1994年7月至1997年6月,85例符合条件的晚期LL(Ⅲ/Ⅳ期)儿童和青少年被纳入该前瞻性研究。诱导和巩固治疗后达到完全缓解的患者接受6个周期的维持化疗,总疗程为12个月。Ⅲ/Ⅳ级毒性反应包括:血液学毒性(80%)、感染(20%)、口腔炎和转氨酶升高(29%)。共有19例事件发生,13例复发,2例继发急性髓系白血病,4例因毒性反应死亡(5%)。5年无事件生存率(EFS)和总生存率(OS)分别为78±4.5%和85±3.9%。复发患者的5年OS仅为33±14%。多因素分析未能证明年龄、性别、乳酸脱氢酶水平、骨髓和/或中枢神经系统疾病的存在具有独立的预后价值。这些结果表明,这种实验性方法是安全的,并且与更长疗程的儿童ALL方案产生相似的结果。