Connors J M, Klimo P
Division of Medical Oncology, Cancer Control Agency of British Columbia, Vancouver, Canada.
Semin Hematol. 1988 Apr;25(2 Suppl 2):41-6.
Between 1981 and 1986, we treated 179 newly diagnosed patients with advanced-stage malignant lymphoma or related conditions with methotrexate, doxorubicin, cyclophosphamide, vincristine, prednisone, bleomycin (MACOP-B). Experience with 12 different histologic subtypes indicates that MACOP-B is acceptably tolerated and effective for diffuse large cleaved cell, diffuse large noncleaved cell, diffuse mixed large and small cleaved cell, immunoblastic, and discordant lymphomas but not for angioimmunoblastic lymphadenopathy or for diffuse small cleaved cell, follicular large cell, follicular mixed large and small cleaved cell, acquired immune deficiency syndrome (AIDS)-related, unclassifiable, or small noncleaved cell lymphomas. Pooled long-term results for the 126 patients with variants of diffuse large cell lymphoma (cleaved, noncleaved, immunoblastic, and mixed) show an actuarial relapse-free survival of 67% for the 86% of patients who had a complete response and an overall survival for all patients of 65% at 78 months of follow-up. Analysis of toxicity reveals a substantially higher risk of lethal toxicity in patients over 59 years of age. MACOP-B should only be used for patients with one of the diagnoses for which it is effective; meticulous care should be taken to prevent severe toxicity in older patients.
1981年至1986年间,我们用甲氨蝶呤、阿霉素、环磷酰胺、长春新碱、强的松、博来霉素(MACOP-B方案)治疗了179例新诊断的晚期恶性淋巴瘤或相关疾病患者。对12种不同组织学亚型的治疗经验表明,MACOP-B方案耐受性良好,对弥漫性大裂细胞型、弥漫性大无裂细胞型、弥漫性大小裂细胞混合型、免疫母细胞型及不典型淋巴瘤有效,但对血管免疫母细胞性淋巴结病、弥漫性小裂细胞型、滤泡性大细胞型、滤泡性大小裂细胞混合型、获得性免疫缺陷综合征(AIDS)相关型、无法分类型或小无裂细胞型淋巴瘤无效。对126例弥漫性大细胞淋巴瘤变异型(裂细胞型、无裂细胞型、免疫母细胞型及混合型)患者的长期汇总结果显示,86%达到完全缓解的患者无病生存率为67%,所有患者在随访78个月时的总生存率为65%。毒性分析显示,59岁以上患者发生致命毒性的风险显著更高。MACOP-B方案仅应用于对其有效的诊断类型的患者;应格外小心预防老年患者发生严重毒性反应。