Alexander Sarah, Kraveka Jacqueline M, Weitzman Sheila, Lowe Eric, Smith Lynette, Lynch James C, Chang Myron, Kinney Marsha C, Perkins Sherrie L, Laver Joseph, Gross Thomas G, Weinstein Howard
Division of Pediatric Hematology-Oncology, Hospital for Sick Children, Toronto, Ontario.
Pediatr Blood Cancer. 2014 Dec;61(12):2236-42. doi: 10.1002/pbc.25187. Epub 2014 Aug 23.
Optimal therapy for children and adolescents with advanced stage anaplastic large cell lymphoma (ALCL) is unknown. ANHL0131 examined whether a maintenance regimen including vinblastine compared to the standard APO (doxorubicin, prednisone, vincristine, methotrexate, 6-mercaptopurine) regimen would result in superior event-free survival.
One hundred and twenty five eligible patients were enrolled. Induction was identical for both arms. Post induction patients were randomized to receive APO with vincristine every 3 weeks or a regimen that substituted vincristine with weekly vinblastine (APV).
There was no difference between the patients randomized to the APO versus APV arms in either event free survival (EFS) or overall survival (OS) (three year EFS 74% vs. 79%, P = 0.68 and three years OS of 84% vs. 86%, P = 0.87, respectively). Patients in the APV arm required dose reduction secondary to myelosuppression and had a higher incidence of neutropenia as well as infection with neutropenia compared to those in the APO arm (P < 0.001, P = 0.019, respectively).
Treatment with weekly vinblastine instead of every three week vincristine as part of multi-agent maintenance therapy did not result in improvement in EFS or OS. Weekly vinblastine was associated with increased toxicity. (ClinicalTrials.gov Identifier NCT00059839).
晚期间变性大细胞淋巴瘤(ALCL)患儿及青少年的最佳治疗方案尚不清楚。ANHL0131研究了与标准APO(阿霉素、泼尼松、长春新碱、甲氨蝶呤、6-巯基嘌呤)方案相比,包含长春花碱的维持方案是否能带来更好的无事件生存期。
招募了125名符合条件的患者。两组的诱导治疗相同。诱导治疗后,患者被随机分配,每3周接受一次含长春新碱的APO方案,或接受用每周一次长春花碱替代长春新碱的方案(APV)。
随机分配至APO组和APV组的患者在无事件生存期(EFS)或总生存期(OS)方面均无差异(三年EFS分别为74%对79%,P = 0.68;三年OS分别为84%对86%,P = 0.87)。与APO组相比,APV组患者因骨髓抑制需要降低剂量,且中性粒细胞减少症以及中性粒细胞减少相关感染的发生率更高(P分别<0.001和P = 0.019)。
作为多药维持治疗的一部分,每周使用长春花碱而非每三周使用长春新碱进行治疗,并未改善EFS或OS。每周使用长春花碱与毒性增加相关。(ClinicalTrials.gov标识符NCT00059839)