Ezdinli E Z, Anderson J R, Melvin F, Glick J H, Davis T E, O'Connell M J
J Clin Oncol. 1985 Jun;3(6):769-75. doi: 10.1200/JCO.1985.3.6.769.
One hundred twenty-eight patients with purely nodular lymphocytic poorly differentiated lymphoma (NLPDL) without any prior therapy, entered on Eastern Cooperative Oncology Group protocol EST 2474, were analyzed for response, progression-free and overall survival. The restaged complete response rates with cyclophosphamide-prednisone (CP) (moderate regimen) of 54% compared favorably with those of the more intensive regimens; cyclophosphamide, vincristine, procarbazine and prednisone (COPP) (56%) and BCNU, cyclophosphamide, vincristine, and prednisone (BCVP) (53%). The toxicity of the regimens decreased from BCVP to COPP to CP. The median survival rate for the entire group was 7.8 years. Estimated progression-free survival at five years by regimen was COPP, 57%; BCVP, 26%; CP, 22% (P = .02). No other prognostic parameter significantly affected progression-free survival. In spite of the better progression-free survival of COPP-treated patients, the overall survival rates with the different induction regimens were similar. Maintenance therapy for patients in complete response at the end of induction therapy with periodic BCVP reinduction did not significantly affect the disease-free or overall survival. Cyclophosphamide-prednisone is a minimally toxic regimen effective in the treatment of NLPDL, but COPP, in view of its acceptable toxicity in this patient population and apparent superiority in providing a longer disease-free state, deserves further testing.
128例未经任何前期治疗的纯结节性淋巴细胞低分化淋巴瘤(NLPDL)患者,按照东部肿瘤协作组方案EST 2474入组,对其缓解情况、无进展生存期和总生存期进行了分析。环磷酰胺-泼尼松(CP)(中等强度方案)的再次分期完全缓解率为54%,与更强的方案相比具有优势;环磷酰胺、长春新碱、丙卡巴肼和泼尼松(COPP)(56%)以及卡莫司汀、环磷酰胺、长春新碱和泼尼松(BCVP)(53%)。这些方案的毒性从BCVP到COPP再到CP逐渐降低。整个组的中位生存期为7.8年。按方案估计的五年无进展生存率为:COPP,57%;BCVP,26%;CP,22%(P = 0.02)。没有其他预后参数对无进展生存期有显著影响。尽管接受COPP治疗的患者无进展生存期更好,但不同诱导方案的总生存率相似。诱导治疗结束时完全缓解的患者采用定期BCVP再诱导进行维持治疗,对无病生存期或总生存期没有显著影响。环磷酰胺-泼尼松是一种毒性最小的方案,对NLPDL治疗有效,但鉴于COPP在该患者群体中的可接受毒性以及在提供更长无病状态方面的明显优势,值得进一步试验。