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在慢性髓性白血病的一线治疗中,药物治疗优于同种异体移植。

Drug treatment is superior to allografting as first-line therapy in chronic myeloid leukemia.

作者信息

Hehlmann Rüdiger, Berger Ute, Pfirrmann Markus, Heimpel Hermann, Hochhaus Andreas, Hasford Joerg, Kolb Hans-Jochem, Lahaye Tanja, Maywald Ole, Reiter Andreas, Hossfeld Dieter K, Huber Christoph, Löffler Helmut, Pralle Hans, Queisser Wolfgang, Tobler Andreas, Nerl Christoph, Solenthaler Max, Goebeler Mariele E, Griesshammer Martin, Fischer Thomas, Kremers Stephan, Eimermacher Hartmut, Pfreundschuh Michael, Hirschmann Wolf-Dietrich, Lechner Klaus, Wassmann Barbara, Falge Christiane, Kirchner Hartmut H, Gratwohl Alois

机构信息

III Medizinische Universitätsklinik, Medizinische Fakultät Mannheim der Universität Heidelberg, Wiesbadener Strasse 7-11, 63805 Mannheim, Germany.

出版信息

Blood. 2007 Jun 1;109(11):4686-92. doi: 10.1182/blood-2006-11-055186. Epub 2007 Feb 22.

Abstract

Early allogeneic hematopoietic stem cell transplantation (HSCT) has been proposed as primary treatment modality for patients with chronic myeloid leukemia (CML). This concept has been challenged by transplantation mortality and improved drug therapy. In a randomized study, primary HSCT and best available drug treatment (IFN based) were compared in newly diagnosed chronic phase CML patients. Assignment to treatment strategy was by genetic randomization according to availability of a matched related donor. Evaluation followed the intention-to-treat principle. Six hundred and twenty one patients with chronic phase CML were stratified for eligibility for HSCT. Three hundred and fifty four patients (62% male; median age, 40 years; range, 11-59 years) were eligible and randomized. One hundred and thirty five patients (38%) had a matched related donor, of whom 123 (91%) received a transplant within a median of 10 months (range, 2-106 months) from diagnosis. Two hundred and nineteen patients (62%) had no related donor and received best available drug treatment. With an observation time up to 11.2 years (median, 8.9 years), survival was superior for patients with drug treatment (P = .049), superiority being most pronounced in low-risk patients (P = .032). The general recommendation of HSCT as first-line treatment option in chronic phase CML can no longer be maintained. It should be replaced by a trial with modern drug treatment first.

摘要

早期异基因造血干细胞移植(HSCT)已被提议作为慢性髓性白血病(CML)患者的主要治疗方式。这一概念受到了移植死亡率和改进的药物治疗的挑战。在一项随机研究中,对新诊断的慢性期CML患者比较了原发性HSCT和最佳可用药物治疗(基于干扰素)。根据匹配的相关供体的可用性,通过基因随机化分配治疗策略。评估遵循意向性治疗原则。621例慢性期CML患者被分层以确定是否适合HSCT。354例患者(62%为男性;中位年龄40岁;范围11 - 59岁)符合条件并被随机分组。135例患者(38%)有匹配的相关供体,其中123例(91%)在诊断后中位10个月(范围2 - 106个月)内接受了移植。219例患者(62%)没有相关供体,接受了最佳可用药物治疗。观察时间长达11.2年(中位8.9年),药物治疗患者的生存率更高(P = 0.049),在低风险患者中优势最为明显(P = 0.032)。HSCT作为慢性期CML一线治疗选择的一般建议已不能再维持。应首先用现代药物治疗进行试验来取代它。

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