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[CD7表达在成人急性髓系白血病中的预后意义]

[Prognostic significance of CD7 expression in adult acute myeloid leukemia].

作者信息

Saito T, Usui N, Dobashi N, Maki N, Asai O, Yano S, Kato A, Watanabe H, Katori M, Nagamine M, Ogihara A, Yamazaki H, Kobayashi T, Tajima N, Kuraishi Y

机构信息

Department of Hematology/Oncology, Jikei University Hospital.

出版信息

Rinsho Ketsueki. 1998 Jul;39(7):481-6.

PMID:9750454
Abstract

To evaluate the prognostic significance of CD7 expression in de novo acute myeloid leukemia (AML), we studied 63 patients with AML who had been admitted to our hospital between September 1989 and January 1996. Even of the patients were later eliminated from the study (9 due to insufficient surface marker analyses, and 2 due to early death). The remaining 52 patients (median age: 42.5 years) were evaluated for morphologic subtype, immunophenotypic classification, complete remission (CR), disease-free survival (DFS) and overall survival (OS). All 52 patients were grouped by the French-American-British classification system: 10 as M1, 16 as M2, 11 as M3, 8 as M4, 5 as M5, and 2 as M6. Ten of the patients expressed CD7 on their leukemia cells (positive rate > or = 25) and were classified as CD7(+)AML, with morphological subtypes as follows: 3 as M1, 6 as M2, and 1 as M3. Thirty-three of the 42 patients with CD7 + AML (78.6%) and 6 of the 10 patients with CD7 + AML (40%) achieved CR. DFS and OS rates for the patients with CD7(+)AML were 22.1% and 35.4%, respectively; those for the CD7(+)AML patients were 53.3% and 44.4%, respectively. No significant differences in gender hematological findings, clinical manifestations such as hepatosplenomegaly, lymphadenopathy, or incidence of central nervous system involvement, CR rate, and DFS distinguished patients with CD7(+)AML from those with CD7(+)AML. These suggest that CD7 expression is unlikely to be a prognostic factor in AML.

摘要

为评估CD7表达在初发急性髓系白血病(AML)中的预后意义,我们研究了1989年9月至1996年1月期间收治于我院的63例AML患者。部分患者后来被排除在研究之外(9例因表面标志物分析不足,2例因早期死亡)。对其余52例患者(中位年龄:42.5岁)进行了形态学亚型、免疫表型分类、完全缓解(CR)、无病生存期(DFS)和总生存期(OS)评估。所有52例患者均按照法美英分类系统分组:M1型10例,M2型16例,M3型11例,M4型8例,M5型5例,M6型2例。其中10例患者白血病细胞表达CD7(阳性率≥25%),被归类为CD7(+)AML,其形态学亚型如下:M1型3例,M2型6例,M3型1例。42例CD7 + AML患者中有33例(78.6%)达到CR,10例CD7 + AML患者中有6例(40%)达到CR。CD7(+)AML患者的DFS率和OS率分别为22.1%和35.4%;CD7(+)AML患者的DFS率和OS率分别为53.3%和44.4%。在性别、血液学检查结果、肝脾肿大、淋巴结病等临床表现或中枢神经系统受累发生率、CR率和DFS方面,CD7(+)AML患者与CD7(+)AML患者之间无显著差异。这些结果表明,CD7表达不太可能是AML的预后因素。

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