Philip T, Pinkerton R, Biron P, Ladjadj Y, Bouffet E, Souillet G, Philippe N, Frappaz D, Freycon F, Chauvin F
Br J Haematol. 1987 Feb;65(2):159-64. doi: 10.1111/j.1365-2141.1987.tb02258.x.
Between 1981 and 1985, 50 patients, mainly children and adolescents, with advanced B-cell lymphoma were entered on a protocol comprising eight drugs: cyclophosphamide, vincristine, prednisolone, high dose methotrexate, adriamycin, BCNU, cytosine arabinoside and thioguanine. Treatment to the central nervous system consisted of intrathecal methotrexate and cytosine-arabinoside in association with high dose methotrexate without irradiation. Data was collected prospectively with regard to response rate, treatment related complications and survival. Histology was reviewed in all referred cases and in 21 there was supportive evidence from immunological and cytogenetic studies. The overall complete response rate was 86%: 31/36 stage III and 12/14 stage IV. There were four treatment related deaths. The overall disease-free survival is 75% with a median follow up of 32 months. In the group of stage IV patients 5/7 with only marrow involvement, 2/4 with isolated CNS involvement and 1/3 with combined CNS and marrow infiltration survive. All the patients with CNS involvement at presentation underwent consolidation treatment with high dose chemotherapy and bone marrow transplant. These results demonstrate the very high curability of B-cell lymphoma using intensive multiagent therapy even with advanced abdominal disease. Bone marrow infiltration does not appear to be an adverse prognostic factor in isolation from bulk disease or CNS involvement. There remain, however, two groups of patients in whom further intensification of therapy is indicated, namely, those with initial CNS involvement, especially in combination with marrow infiltration, and those with extensive multiorgan involvement at presentation who fail to achieve remission with initial therapy. For the other patients, the large majority, a reduction in the intensity and duration of therapy is currently under study.
1981年至1985年间,50例主要为儿童和青少年的晚期B细胞淋巴瘤患者进入了一项包含8种药物的方案治疗:环磷酰胺、长春新碱、泼尼松龙、高剂量甲氨蝶呤、阿霉素、卡氮芥、阿糖胞苷和硫鸟嘌呤。中枢神经系统的治疗包括鞘内注射甲氨蝶呤和阿糖胞苷,并联合高剂量甲氨蝶呤,不进行放疗。前瞻性收集了有关缓解率、治疗相关并发症和生存率的数据。对所有转诊病例的组织学进行了复查,其中21例有免疫和细胞遗传学研究的支持证据。总体完全缓解率为86%:III期31/36例,IV期12/14例。有4例治疗相关死亡。总体无病生存率为75%,中位随访时间为32个月。在IV期患者组中,仅骨髓受累的7例中有5例、孤立中枢神经系统受累的4例中有2例、中枢神经系统和骨髓联合浸润的3例中有1例存活。所有初诊时有中枢神经系统受累的患者均接受了高剂量化疗和骨髓移植的巩固治疗。这些结果表明,即使是晚期腹部疾病,使用强化多药联合治疗,B细胞淋巴瘤的治愈率也非常高。孤立于大块疾病或中枢神经系统受累之外,骨髓浸润似乎不是一个不良预后因素。然而,仍有两组患者需要进一步强化治疗,即初诊时有中枢神经系统受累,尤其是合并骨髓浸润的患者,以及初诊时有多器官广泛受累且初始治疗未能缓解的患者。对于其他大多数患者,目前正在研究降低治疗强度和持续时间。