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[高级别非霍奇金淋巴瘤的治疗]

[Therapy of high-grade non-Hodgkin's lymphoma].

作者信息

Jäger U, Karth G D, Knapp S, Tueni C

机构信息

Abteilung für Hämatologie und Hämostaseologie, Universität Wien.

出版信息

Wien Klin Wochenschr. 1994;106(10):315-20.

PMID:8053199
Abstract

Complete remission can be achieved in 50 to 80% of adult patients with high-grade non-Hodgkin's lymphoma [2, 33]. The average disease-free survival is 40 to 50% at 3 years and 30 to 35% at 5 years [2, 6]. The diagnosis of non-Hodgkin's lymphoma should still be based on the histopathological and immunohistochemical evaluation of a surgical biopsy specimen. Initial staging involves radiological evaluation of tumor mass and lymph-node involvement, bone marrow biopsy, conventional laboratory investigations including LDH and beta 2-microglobulin, as well as chromosome analysis and molecular biology. These methods are also used for monitoring of patients during and after therapy. Established negative risk factors include age over 60 years, clinical stage III or IV, involvement of more than 1 extranodal site, a WHO performance status of 2 or more, and an elevation of the LDH. CHOP remains the standard chemotherapy. Aggressive regimens of the second and third generations, as well as dose-intensification have failed to prove a superior effect on overall survival [7]. Full-dose treatment on schedule can be facilitated by supportive therapy with cytokines such as G-CSF or GM-CSG. High-risk patients may have a favorable outcome after myeloablative chemotherapy and radiation followed by autologous or allogeneic bone marrow transplantation. Co-ordinated planning between conventional centers and transplant units should lead to a risk adjusted treatment of the individual patient.

摘要

50%至80%的成年高级别非霍奇金淋巴瘤患者可实现完全缓解[2, 33]。3年时的无病生存率平均为40%至50%,5年时为30%至35%[2, 6]。非霍奇金淋巴瘤的诊断仍应基于手术活检标本的组织病理学和免疫组织化学评估。初始分期包括对肿瘤肿块和淋巴结受累情况进行放射学评估、骨髓活检、包括乳酸脱氢酶(LDH)和β2-微球蛋白在内的常规实验室检查,以及染色体分析和分子生物学检查。这些方法也用于治疗期间及治疗后的患者监测。已确定的不良风险因素包括年龄超过60岁、临床分期为III期或IV期、累及1个以上结外部位、世界卫生组织体能状态评分为2分或更高,以及LDH升高。CHOP方案仍然是标准的化疗方案。第二代和第三代积极化疗方案以及剂量强化治疗均未证明对总生存期有更好的效果[7]。使用粒细胞集落刺激因子(G-CSF)或粒细胞-巨噬细胞集落刺激因子(GM-CSF)等细胞因子进行支持治疗有助于按计划进行全剂量治疗。高危患者在进行清髓性化疗和放疗后接受自体或异基因骨髓移植可能会有较好的预后。传统中心和移植单位之间的协调规划应能实现对个体患者的风险调整治疗。

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