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环磷酰胺、长春新碱和泼尼松联合用药,随后进行维持化疗,并联合或不联合放疗,用于非霍奇金淋巴瘤患者的治疗。

Combination of cyclophosphamide, vincristine, and prednisone, followed by maintenance chemotherapy, with and without radiotherapy, in the management of patients with non-Hodgkin's lymphomas.

作者信息

Gorin N C, David R, Stachowiak J, Najman A, Duhamel G

出版信息

Med Pediatr Oncol. 1977;3(1):41-51. doi: 10.1002/mpo.2950030107.

Abstract

Sixty patients with non-Hodgkin's lymphomas were treated with a cyclophosphamide, vincristine, and prednisone (CVP) induction regimen, either alone (stage IV) or in combination with radiotherapy (stages I, II, III). The response rates for lymphocytic and histiocytic lymphomas were 82 and 86%. The complete remission (CR) rates were 66 and 71% with a median duration of 13 and 5.5 months respectively. Nodular types responded better than diffuse ones in both lymphocytic (CR rate 85% vs 45%; median duration 24+ months vs 2.5 months) and histiocytic lymphoma (CR rate 100% vs 0%). In lymphocytic lymphomas, survival in the responder group was 90% at 24 months vs only 20% in the nonresponder group (median survival 14.2 months). In the group with nodular lymphocytic lymphoma responding to therapy, there was a 100% survival rate at 24 months. The median survival for patients treated with chemotherapy alone (stage IV) and not responding to therapy, was 22 months vs 14.5 months in the whole nonresponder group (stages I, II, III, IV), suggesting a detremental effect of rediotherapy in the nonresponder group. In histiocytic lymphomas, the median survivals in the responder and nonresponder groups were 19 months and 3 months respectively. These results corroborate the excellent efficacy of the CVP regimen. They also indicate that, after CVP induction, 2 major prognostic factors are the histologic type and the nature of the response to therapy.

摘要

60例非霍奇金淋巴瘤患者接受了环磷酰胺、长春新碱和泼尼松(CVP)诱导方案治疗,IV期患者单独使用该方案,I、II、III期患者则联合放疗。淋巴细胞性淋巴瘤和组织细胞性淋巴瘤的缓解率分别为82%和86%。完全缓解(CR)率分别为66%和71%,中位缓解持续时间分别为13个月和5.5个月。在淋巴细胞性淋巴瘤和组织细胞性淋巴瘤中,结节型的缓解情况均优于弥漫型(淋巴细胞性淋巴瘤CR率85%对45%;中位缓解持续时间24 +个月对2.5个月;组织细胞性淋巴瘤CR率100%对0%)。在淋巴细胞性淋巴瘤中,缓解组24个月生存率为90%,未缓解组仅为20%(中位生存期14.2个月)。在接受治疗有反应的结节性淋巴细胞性淋巴瘤组中,24个月生存率为100%。单独接受化疗(IV期)且治疗无反应患者的中位生存期为22个月,而整个未缓解组(I、II、III、IV期)为14.5个月,提示放疗对未缓解组有不利影响。在组织细胞性淋巴瘤中,缓解组和未缓解组的中位生存期分别为19个月和3个月。这些结果证实了CVP方案的卓越疗效。它们还表明,CVP诱导治疗后,两个主要的预后因素是组织学类型和对治疗的反应性质。

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