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侵袭性非霍奇金淋巴瘤的治疗。过去十年的经验教训。

Treatment of aggressive non-Hodgkin' lymphomas. Lessons from the past 10 years.

作者信息

Fisher R I

机构信息

Division of Hematology/Oncology, Loyola University Medical Center, Maywood, Illinois 60153.

出版信息

Cancer. 1994 Nov 1;74(9 Suppl):2657-61. doi: 10.1002/1097-0142(19941101)74:9+<2657::aid-cncr2820741812>3.0.co;2-t.

Abstract

Therapy for aggressive non-Hodgkin's lymphomas has undergone significant evolution in the last 25 years. First generation combination chemotherapy studies produced complete remissions (CRs) of 45-53%, with 30-37% long term survivors. New treatment programs aimed at increasing CR rates were then developed with the assumption that the additional complete responders would also become long term disease free survivors. Initial reports of single institution pilot studies with third generation regimens suggested 68-86% CR and 58-69% survival; however, with longer follow-up, the survival decreased. Furthermore, confirmatory national Phase II trials using these newer regimens produced CR rates of only 49-65% and survival of 50-61%. Thus conclusions concerning the efficacy of these new regimens awaited the results of prospective randomized trials. The Southwest Oncology Group (SWOG) recently conducted a randomized trial comparing standard therapy, CHOP, to the third generation chemotherapy regimens, m-BACOD, ProMACE-CytaBOM, or MACOP-B. There is no difference in response rate, time to treatment failure, or overall survival between CHOP and the third generation regimens. However, the cost and toxicity levels of the new regimens were higher. Thus, CHOP remains the best available standard of care, but based on the finding that fewer than 50% of these patients are cured, SWOG believes that new treatment approaches for patients with advanced-stage aggressive histology non-Hodgkin's lymphoma must be developed.

摘要

在过去25年中,侵袭性非霍奇金淋巴瘤的治疗方法经历了重大演变。第一代联合化疗研究的完全缓解率(CR)为45%-53%,长期生存率为30%-37%。随后,旨在提高CR率的新治疗方案得以开发,其假设是额外的完全缓解者也将成为长期无病生存者。单机构第三代方案试点研究的初步报告显示CR率为68%-86%,生存率为58%-69%;然而,随着随访时间延长,生存率下降。此外,使用这些新方案的全国性II期验证性试验的CR率仅为49%-65%,生存率为50%-61%。因此,关于这些新方案疗效的结论有待前瞻性随机试验的结果。西南肿瘤协作组(SWOG)最近进行了一项随机试验,比较标准疗法CHOP与第三代化疗方案m-BACOD、ProMACE-CytaBOM或MACOP-B。CHOP与第三代方案在缓解率、治疗失败时间或总生存率方面没有差异。然而,新方案的成本和毒性水平更高。因此,CHOP仍然是现有的最佳标准治疗方案,但基于不到50%的患者被治愈这一发现,SWOG认为必须为晚期侵袭性组织学非霍奇金淋巴瘤患者开发新的治疗方法。

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