Bessell E M, Graus F, Punt J A, Firth J L, Hope D T, Moloney A J, Lopez-Guillermo A, Villa S
Department of Clinical Oncology, Nottingham City Hospital, United Kingdom.
J Clin Oncol. 1996 Mar;14(3):945-54. doi: 10.1200/JCO.1996.14.3.945.
To assess whether chemotherapy that includes drugs that cross the blood-brain barrier improves survival in primary CNS non-Hodgkin's lymphoma (PCNSL) when combined with radiotherapy.
Thirty-four patients, with no evidence of human immunodeficiency virus type 1 (HIV-1) infection, were treated with the related chemotherapy regimens of carmustine (BCNU), vincristine, cytarabine, and methotrexate (BVAM; 12 patients), cyclophosphamide, doxorubicin, vincristine, and dexamethasone (CHOD)/BVAM (17 patients) and intensified CHOD/BVAM (five patients) between 1986 and 1994. The median age was 60 years (range, 16 to 73) and 47% had a performance status of 3 or 4 (Eastern Cooperative Oncology Group [ECOG]/World Health Organization [WHO]). Ten patients were treated with BVAM chemotherapy between 1986 and 1989, and subsequently 17 patients were treated with CHOD/BVAM (cytarabine 3 g/m2). Twenty of these 27 patients received whole-brain radiotherapy (craniospinal in four).
The complete response (CR) rate at the completion of chemotherapy was 63% for BVAM and 67% for CHOD/BVAM; more neutropenia occurred with CHOD/BVAM. The 5-year actuarial probability of survival of all 34 patients was 33% (95% confidence interval [CI], 14% to 52%), with so far only one recurrence after 2 years. Using multivariate analysis, age (P = .0005) and number of tumors at diagnosis (P = .0358) were prognostic factors. All five patients aged > or = 70 years died during or shortly after chemotherapy. Performance status was not an independent variable.
The BVAM or CHOD/BVAM regimens can be delivered despite neutropenia without significant treatment delay or dose reduction in patients less than 70 years of age. Further intensification of this type of chemotherapy is probably not possible with patients of this age, many of whom have a poor performance status.
评估包含能穿过血脑屏障药物的化疗方案与放疗联合应用时,是否能提高原发性中枢神经系统非霍奇金淋巴瘤(PCNSL)患者的生存率。
1986年至1994年间,34例无人类免疫缺陷病毒1型(HIV-1)感染证据的患者接受了卡莫司汀(BCNU)、长春新碱、阿糖胞苷和甲氨蝶呤相关化疗方案(BVAM;12例患者)、环磷酰胺、多柔比星、长春新碱和地塞米松(CHOD)/BVAM(共17例患者)以及强化CHOD/BVAM(5例患者)治疗。中位年龄为60岁(范围16至73岁),47%的患者东部肿瘤协作组(ECOG)/世界卫生组织(WHO)体能状态评分为3或4分。1986年至1989年间,10例患者接受BVAM化疗,随后17例患者接受CHOD/BVAM(阿糖胞苷3 g/m²)治疗。这27例患者中有20例接受了全脑放疗(4例为全脑脊髓放疗)。
化疗结束时,BVAM方案的完全缓解(CR)率为63%,CHOD/BVAM方案为67%;CHOD/BVAM方案导致更多的中性粒细胞减少。34例患者的5年总生存率为33%(95%置信区间[CI],14%至52%),到目前为止,仅2年后有1例复发。多因素分析显示,年龄(P = 0.0005)和诊断时肿瘤数量(P = 0.0358)是预后因素。所有5例年龄≥70岁的患者在化疗期间或化疗后不久死亡。体能状态不是一个独立变量。
对于年龄小于70岁的患者,尽管存在中性粒细胞减少,BVAM或CHOD/BVAM方案仍可实施,且不会导致明显的治疗延迟或剂量减少。对于这个年龄段的患者,进一步强化此类化疗可能不可行,因为许多患者体能状态较差。