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儿童和青少年晚期淋巴细胞性淋巴瘤的短疗程强化多药化疗及非交叉耐药维持治疗:儿童肿瘤协作组报告

Shortened intensified multi-agent chemotherapy and non-cross resistant maintenance therapy for advanced lymphoblastic lymphoma in children and adolescents: report from the Children's Oncology Group.

作者信息

Abromowitch Minnie, Sposto Richard, Perkins Sherrie, Zwick David, Siegel Stuart, Finlay Jonathan, Cairo Mitchell S

机构信息

Department of Pediatrics Hematology/Oncology, University of Nebraska Medical Center, Omaha, NE 68198-2168, USA.

出版信息

Br J Haematol. 2008 Oct;143(2):261-7. doi: 10.1111/j.1365-2141.2008.07320.x. Epub 2008 Aug 28.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fa8/3057023/b8b8db2f6c13/nihms107033f1.jpg

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