Magrath I, Adde M, Shad A, Venzon D, Seibel N, Gootenberg J, Neely J, Arndt C, Nieder M, Jaffe E, Wittes R A, Horak I D
Pediatric Branch, National Cancer Institute, Bethesda, MD, USA.
J Clin Oncol. 1996 Mar;14(3):925-34. doi: 10.1200/JCO.1996.14.3.925.
We have used identical treatment protocols for adults and children with small non-cleaved-cell lymphoma (SNCL) for many years and report here the results of two successive treatment regimens in these age groups.
Seventy-two patients (39 adults and 33 children) were treated with protocol 77-04 between 1977 and 1985. All patients, except those with resected abdominal disease, received 15 cycles of a combination of cyclophosphamide (CTX), doxorubicin (ADR), prednisone (PRED), vincristine (VCR), high-dose methotrexate (MTX), and intrathecal (IT) therapy. Forty-one patients (20 adults and 21 children) were treated with protocol 89-C-41, which has been used since 1989. High-risk patients received four alternating cycles (with a total duration of 12 to 15 weeks) of an intensified version of protocol 77-04 without PRED (CODOX-M), and a new drug combination consisting of ifosfamide, etoposide, high-dose cytarabine (ara-C), and IT MTX (IVAC). Low-risk patients received three cycles of the CODOX-M regimen. High-risk patients were randomized to either receive or not receive granulocyte-macrophage colony-stimulating factor (GM-CSF).
Event-free survival (EFS) in protocol 77-04 was 56% at 2 years and beyond. EFS in protocol 89-C-41 was 92% at 2 years and beyond. GM-CSF was associated with increased thrombocytopenia.
Adults and children with SNCL have a similar prognosis when treated with the same chemotherapy. EFS in high-risk patients has been markedly improved by including IVAC in protocol 89-C-41, and excellent results can be achieved with only four cycles of therapy. In protocol 89-C-41, GM-CSF was not beneficial.
多年来我们一直对成人和儿童小无裂细胞淋巴瘤(SNCL)采用相同的治疗方案,在此报告这两个年龄组连续两个治疗方案的结果。
1977年至1985年间,72例患者(39例成人和33例儿童)接受了77 - 04方案治疗。除腹部疾病已切除的患者外,所有患者均接受了15个周期的环磷酰胺(CTX)、阿霉素(ADR)、泼尼松(PRED)、长春新碱(VCR)、大剂量甲氨蝶呤(MTX)联合鞘内(IT)治疗。41例患者(20例成人和21例儿童)接受了自1989年起使用的89 - C - 41方案治疗。高危患者接受了4个交替周期(总疗程12至15周)的强化版77 - 04方案(不含PRED,即CODOX - M),以及由异环磷酰胺、依托泊苷、大剂量阿糖胞苷(ara - C)和鞘内MTX组成的新药联合方案(IVAC)。低危患者接受3个周期的CODOX - M方案。高危患者被随机分为接受或不接受粒细胞 - 巨噬细胞集落刺激因子(GM - CSF)治疗。
77 - 04方案的无事件生存率(EFS)在2年及以后为56%。89 - C - 41方案的EFS在2年及以后为92%。GM - CSF与血小板减少症增加有关。
成人和儿童SNCL患者接受相同化疗时预后相似。89 - C - 41方案中加入IVAC显著改善了高危患者的EFS,仅4个周期的治疗就能取得优异结果。在89 - C - 41方案中,GM - CSF并无益处。