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侵袭性组织学类型恶性淋巴瘤的序贯化疗和晚期强化治疗

Sequential chemotherapy and late intensification for malignant lymphomas of aggressive histologic type.

作者信息

Cabanillas F, Burgess M A, Bodey G P, Freireich E J

出版信息

Am J Med. 1983 Mar;74(3):382-8. doi: 10.1016/0002-9343(83)90955-5.

Abstract

Fifty-six patients with malignant lymphoma of aggressive histologic type (51 large cell, three diffuse undifferentiated, and two nodular mixed) were treated with three non-cross-resistant combination chemotherapy regimens that were introduced sequentially according to the response to therapy. The objective was to increase the complete remission rate by changing the chemotherapy regimen early if the patient did not attain a complete remission after three courses of treatment. Late intensification was also used with the aim of prolonging the duration of complete remission. The overall complete remission rate obtained with this approach was 82 percent (100 percent in stages I to III and 66 percent in stage IV). The projected survival at four years is 71 percent (93 percent for stages I to III and 55 percent for stage IV). Eighty percent of patients with complete remission are projected to have continued remission at four years. Compared with previous experience with Adriamycin-based combination regimens, these results represent an improvement in remission and survival parameters. The most significant gains occurred in the prolongation of survival of patients with stages I to III disease and in the improved duration of complete remission of patients with stage IV disease. Toxicity included 15 documented infections among 320 courses of therapy, four cases of congestive heart failure, one case of bleomycin lung toxicity, and two cases of liver dysfunction. This multiple combination regimen represents an improvement over previous results utilizing Adriamycin-based combination chemotherapy.

摘要

56例组织学类型为侵袭性的恶性淋巴瘤患者(51例大细胞型、3例弥漫性未分化型和2例结节混合型)接受了三种无交叉耐药性的联合化疗方案治疗,这些方案根据治疗反应依次采用。目的是如果患者在三个疗程治疗后未达到完全缓解,则尽早更换化疗方案以提高完全缓解率。还采用了后期强化治疗,目的是延长完全缓解的持续时间。采用这种方法获得的总体完全缓解率为82%(I至III期为100%,IV期为66%)。预计四年生存率为71%(I至III期为93%,IV期为55%)。预计80%的完全缓解患者四年后仍持续缓解。与以往基于阿霉素的联合方案的经验相比,这些结果在缓解和生存参数方面有所改善。最显著的改善在于I至III期疾病患者的生存期延长以及IV期疾病患者完全缓解的持续时间延长。毒性反应包括320个疗程治疗中有15例记录在案的感染、4例充血性心力衰竭、1例博来霉素肺毒性和2例肝功能障碍。这种多药联合方案比以往基于阿霉素的联合化疗结果有所改善。

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