Connors J M, Klimo P
Semin Hematol. 1987 Apr;24(2 Suppl 1):35-40.
Seventy-six patients with previously untreated advanced Hodgkin's disease have been treated with the MOPP/ABV (mechlorethamine, vincristine, procarbazine, prednisone/doxorubicin, bleomycin, vincristine) hybrid program. Ten patients also received involved field radiation to the mediastinum for residual nodal disease after six cycles of chemotherapy. Of the 74 evaluable patients, 71 (96%) had a complete response. The actuarial relapse-free survival for the complete responders after 62 months off treatment is 90% (median follow-up from treatment completion was 35 months; range, 4 to 62 months). Actuarial overall survival for all 76 patients including all causes of death is 95% (median follow-up time from diagnosis was 43 months; range, 4 to 70 months). Toxicity was modest. Only one death occurred during treatment, and toxicity-related hospitalization was necessary for only 8% of patients. Failure analysis indicates that a disproportionate number of treatment failures occurred in the sub-group with B symptoms and a mediastinal mass ratio greater than one third the transthoracic diameter. This updated report confirms the efficacy and safety of the MOPP/ABV hybrid program for advanced Hodgkin's disease, which is now being tested in a prospective, randomized, multicenter trial.
76例既往未经治疗的晚期霍奇金淋巴瘤患者接受了MOPP/ABV(氮芥、长春新碱、丙卡巴肼、泼尼松/阿霉素、博来霉素、长春新碱)联合方案治疗。10例患者在接受6个周期化疗后,针对残留淋巴结病灶还接受了纵隔累及野放疗。在74例可评估患者中,71例(96%)获得完全缓解。完成治疗后62个月,完全缓解者的无病生存率为90%(从治疗结束开始计算的中位随访时间为35个月;范围为4至62个月)。包括所有死亡原因在内的76例患者的总生存率为95%(从诊断开始计算的中位随访时间为43个月;范围为4至70个月)。毒性反应较轻。治疗期间仅发生1例死亡,仅8%的患者因毒性反应需要住院治疗。失败分析表明,B症状且纵隔肿块比例大于胸廓横径三分之一的亚组中,治疗失败的比例过高。这份更新报告证实了MOPP/ABV联合方案治疗晚期霍奇金淋巴瘤的有效性和安全性,目前该方案正在一项前瞻性、随机、多中心试验中进行测试。