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成人急性淋巴细胞白血病的治疗

Treatment of adult acute lymphoblastic leukemia.

作者信息

Gökbuget Nicola, Hoelzer Dieter

机构信息

J.W. Goethe University Hospital, Medical Department II, Frankfurt am Main, Germany.

出版信息

Semin Hematol. 2009 Jan;46(1):64-75. doi: 10.1053/j.seminhematol.2008.09.003.

Abstract

Treatment results in adult acute lymphoblastic leukemia (ALL) have improved considerably in the past decade, with an increase of complete remission rates to 85% to 90% and overall survival rates to 40% to 50%. Superior chemotherapy and supportive care, the integration of stem cell transplantation (SCT) into frontline therapy, and optimized risk stratification were important developments. Even more impressive is the success of targeted therapies in subgroups of ALL. In the formerly most unfavorable subgroup, Philadelphia chromosome (Ph)/BCR-ABL-positive ALL, survival now ranges from 40% to 50% after incorporating imatinib in combination chemotherapy. In mature B-ALL, survival rates increased above 80% with the combination of short intensive chemotherapy and rituximab. The prerequisite for comprehensive therapy is standardized and rapid diagnosis and classification as the basis for treatment stratification. Historically, the major aim of original risk stratification was to identify patients with a poor prognosis who would benefit from treatment intensification with SCT; currently stratification has become more complex. Subgroup-specific approaches include age-adapted therapy, subgroup-adjusted therapy, targeted therapy, and individualized therapy based on the presence of minimal residual disease (MRD).

摘要

在过去十年中,成人急性淋巴细胞白血病(ALL)的治疗效果有了显著改善,完全缓解率提高到85%至90%,总生存率提高到40%至50%。先进的化疗和支持性治疗、将干细胞移植(SCT)纳入一线治疗以及优化风险分层是重要进展。更令人瞩目的是靶向治疗在ALL亚组中的成功。在以前最不利的亚组——费城染色体(Ph)/BCR-ABL阳性ALL中,将伊马替尼纳入联合化疗后,生存率目前在40%至50%之间。在成熟B-ALL中,短期强化化疗与利妥昔单抗联合使用,生存率超过80%。综合治疗的前提是标准化和快速诊断及分类,作为治疗分层的基础。从历史上看,最初风险分层的主要目的是识别预后不良的患者,这些患者将从SCT强化治疗中获益;目前分层变得更加复杂。亚组特异性方法包括年龄适应性治疗、亚组调整治疗、靶向治疗以及基于微小残留病(MRD)存在情况的个体化治疗。

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