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侵袭性恶性淋巴瘤的强化序贯联合化疗(方案LNH - 80)

Intensive and sequential combination chemotherapy for aggressive malignant lymphomas (protocol LNH-80).

作者信息

Coiffier B, Bryon P A, Berger F, Archimbaud E, Ffrench M, Extra J M, Guyotat D, Fiere D, Gentilhomme O, Magaud J P

出版信息

J Clin Oncol. 1986 Feb;4(2):147-53. doi: 10.1200/JCO.1986.4.2.147.

DOI:10.1200/JCO.1986.4.2.147
PMID:2418166
Abstract

Ninety-seven patients with aggressive malignant lymphoma (ML) were treated with an intensive and sequential chemotherapy (protocol LNH-80). There were 42 patients with intermediate grade ML, 53 patients with high-grade ML, and two patients with true histiocytic ML. Most of the patients were in advanced stage: 21 stage III and 61 stage IV. The LNH-80 protocol schedule comprised three phases: (1) induction with three courses of an intensified CHOP-Bleo (cyclophosphamide, doxorubicin, vindesine, methylprednisolone, and bleomycin); (2) consolidation with cytarabine, followed by high-dose methotrexate and folinic acid rescue, then asparaginase; and (3) final intensification with two courses of CVAP-Bleo (cyclophosphamide, teniposide, cytarabine, methylprednisolone, and bleomycin). CNS prophylaxis included one injection of methotrexate during each induction course and the drugs of the consolidation phase. In cases of initial CNS localization, cranial radiotherapy was added. Eighty-four patients (87%) went into complete remission (CR), 18 (21%) of whom relapsed, usually during the phase of treatment or within 6 months of completing chemotherapy. Sixty-three patients are alive with an overall median follow-up of 24 months. The median survival time and the median disease-free survival have not been reached, and the survival curve seems to have plateaued at above 60%. There was no statistical difference between intermediate-grade ML (CR 90%, relapse 18%) and high-grade ML (CR 84%, relapse 24%). The toxicity of this treatment is mainly encountered during the induction phase: almost all patients had short-term neutropenia, less than 0.500 g/L in 57, with a documented infection in 25. Overall treatment-related mortality was 6%, with four patients dying during the induction phase.

摘要

97例侵袭性恶性淋巴瘤(ML)患者接受了强化序贯化疗(LNH - 80方案)。其中42例为中级别ML患者,53例为高级别ML患者,2例为真性组织细胞性ML患者。大多数患者处于晚期:21例为Ⅲ期,61例为Ⅳ期。LNH - 80方案疗程包括三个阶段:(1)诱导期,采用三个疗程的强化CHOP - Bleo方案(环磷酰胺、阿霉素、长春地辛、甲基泼尼松龙和博来霉素);(2)巩固期,采用阿糖胞苷,随后进行大剂量甲氨蝶呤及亚叶酸钙解救,然后使用门冬酰胺酶;(3)最终强化期,采用两个疗程的CVAP - Bleo方案(环磷酰胺、替尼泊苷、阿糖胞苷、甲基泼尼松龙和博来霉素)。中枢神经系统预防措施包括在每个诱导疗程期间注射一次甲氨蝶呤以及使用巩固期的药物。对于初始中枢神经系统受累的病例,加用颅脑放疗。84例患者(87%)达到完全缓解(CR),其中18例(21%)复发,通常在治疗阶段或完成化疗后6个月内复发。63例患者存活,总体中位随访时间为24个月。中位生存时间和中位无病生存时间尚未达到,生存曲线似乎在60%以上趋于平稳。中级别ML(CR 90%,复发18%)和高级别ML(CR 84%,复发24%)之间无统计学差异。该治疗的毒性主要出现在诱导期:几乎所有患者都有短期中性粒细胞减少,57例患者中性粒细胞计数低于0.500 g/L,25例有记录的感染。总体治疗相关死亡率为6%,4例患者在诱导期死亡。

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