Sandlund J T, Pui C-H, Zhou Y, Behm F G, Onciu M, Razzouk B I, Hijiya N, Campana D, Hudson M M, Ribeiro R C
Department of Oncology, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
Leukemia. 2009 Jun;23(6):1127-30. doi: 10.1038/leu.2008.400. Epub 2009 Feb 5.
There has been a steady improvement in cure rates for children with advanced-stage lymphoblastic non-Hodgkin's lymphoma. To further improve cure rates whereas minimizing long-term toxicity, we designed a protocol (NHL13) based on a regimen for childhood T-cell acute lymphoblastic leukemia, which features intensive intrathecal chemotherapy for central -nervous system-directed therapy and excludes prophylactic cranial irradiation. From 1992 to 2002, 41 patients with advanced-stage lymphoblastic lymphoma were enrolled on the protocol. Thirty patients had stage III and 11 had stage IV disease. Thirty-three cases had a precursor T-cell immunophenotype, five had precursor B-cell immunophenotype and in three immunophenotype was not determined. Out of the 41 patients, 39 (95%) achieved a complete remission. The 5-year event-free rate was 82.9+/-6.3% (s.e.), and 5-year overall survival rate was 90.2+/-4.8% (median follow-up 9.3 years (range 4.62-13.49 years)). Adverse events included two induction failures, one death from typhlitis during remission, three relapses and one secondary acute myeloid leukemia. The treatment described here produces high cure rates in children with lymphoblastic lymphoma without the use of prophylactic cranial irradiation.
晚期淋巴细胞性非霍奇金淋巴瘤患儿的治愈率一直在稳步提高。为了进一步提高治愈率并将长期毒性降至最低,我们基于儿童T细胞急性淋巴细胞白血病的治疗方案设计了一个方案(NHL13),该方案的特点是采用强化鞘内化疗进行中枢神经系统定向治疗,且不进行预防性颅脑照射。1992年至2002年,41例晚期淋巴细胞性淋巴瘤患者纳入该方案。30例为Ⅲ期,11例为Ⅳ期。33例具有前体T细胞免疫表型,5例具有前体B细胞免疫表型,3例免疫表型未确定。41例患者中,39例(95%)实现完全缓解。5年无事件生存率为82.9±6.3%(标准误),5年总生存率为90.2±4.8%(中位随访9.3年(范围4.62 - 13.49年))。不良事件包括2例诱导失败、1例缓解期死于盲肠炎、3例复发和1例继发性急性髓系白血病。本文所述的治疗方法在不使用预防性颅脑照射的情况下,可使淋巴细胞性淋巴瘤患儿获得高治愈率。