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甲磺酸伊马替尼与异基因骨髓移植治疗慢性髓性白血病慢性期患者的疗效比较

Imatinib mesylate versus allogeneic BMT for patients with chronic myeloid leukemia in first chronic phase.

作者信息

Bittencourt H, Funke V, Fogliatto L, Magalhães S, Setubal D, Paz A, Macedo A V, Ruiz J, Azambuja A P, Silla L, Clementino N, Pasquini R

机构信息

Hematology and Stem Cell Transplantation Service, Hospital das Clinicas da Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.

出版信息

Bone Marrow Transplant. 2008 Nov;42(9):597-600. doi: 10.1038/bmt.2008.218. Epub 2008 Aug 4.

DOI:10.1038/bmt.2008.218
PMID:18679373
Abstract

Imatinib mesylate (IM) is now first-line treatment for CML. To study the results of treatment with IM after IFN failure/intolerance versus allogeneic BMT (allo-BMT), we retrospectively analyzed 264 patients treated for CML in first chronic phase in three different institutions. Over a 6-year period (2001-2006), 174 patients received IM after failure of or intolerance to IFN. During the same period of time, 90 patients received an allo-BMT from an HLA-matched sibling (n=83) or an unrelated donor (n=7). The IM group was older (41 versus 33 years, P<0.001). Five-year EFS was 62% among patients receiving IM and 52% among patients undergoing allo-BMT (P=0.0002). OS at 5 years was 93% for IM-treated patients and 59% for patients undergoing allo-BMT (P<0.0001). Allo-BMT cannot be considered as first-line treatment for CML patients in first chronic phase.

摘要

甲磺酸伊马替尼(IM)目前是慢性粒细胞白血病(CML)的一线治疗药物。为了研究在干扰素(IFN)治疗失败/不耐受后使用IM治疗与异基因骨髓移植(allo - BMT)的疗效,我们回顾性分析了在三个不同机构接受首次慢性期CML治疗的264例患者。在6年期间(2001 - 2006年),174例患者在IFN治疗失败或不耐受后接受了IM治疗。在同一时期,90例患者接受了来自HLA匹配同胞(n = 83)或无关供体(n = 7)的allo - BMT。IM组患者年龄更大(41岁对33岁,P < 0.001)。接受IM治疗的患者5年无事件生存率(EFS)为62%,接受allo - BMT的患者为52%(P = 0.0002)。接受IM治疗的患者5年总生存率(OS)为93%,接受allo - BMT的患者为59%(P < 0.0001)。对于处于首次慢性期的CML患者,allo - BMT不能被视为一线治疗方法。

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