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细胞标志物分析在初发急性髓系白血病中的预后价值

Prognostic value of cell marker analysis in de novo acute myeloid leukemia.

作者信息

Del Poeta G, Stasi R, Venditti A, Suppo G, Aronica G, Bruno A, Masi M, Tabilio A, Papa G

机构信息

Division of Hematology, University of Rome Tor Vergata, Ospedale S. Eugenio, Italy.

出版信息

Leukemia. 1994 Mar;8(3):388-94.

PMID:7907393
Abstract

Clinical and cytologic characteristics were correlated to immunologic markers in 154 patients with newly diagnosed acute myeloid leukemia (AML). The panel of monoclonal antibodies (MoAbs) was selected to identify differentiation-associated antigens of both the myeloid and the lymphoid lineages (CD13, CD33, CD14, CD15, CD7, CD34, CD10, HLA-DR, CD19, CD2, CD5, TdT). The expression of multidrug resistance P-glycoprotein (P-170) was also evaluated in 117 patients. Differences in antigenic expression was observed among the various French-American-British (FAB) subgroups. HLA-DR was poorly expressed on the blasts of acute promyelocytic leukemia (M3), and was always found in FAB M5. CD34 was detectable in all M0 cases and only in one M3 (p < 0.001). Lymphoid-associated antigens were positive in 74 cases (48.1%). In particular, CD7 was found in 49 patients (31.8%), and TdT in 30 (21.3%), 15 samples displaying coexpression of these two antigens. The incidence of CD7+ cases was particularly elevated in M0 and M5 AML (p = 0.005). It significantly correlated with the expression of CD34, HLA-DR, P-170 (p < 0.001, p = 0.018 and p = 0.034 respectively), and with a leukocyte count > 50 x 10(9)/l (p = 0.038). Sixty-nine (59%) samples demonstrated P-170 positivity. Again, this phenotype was particularly expressed in the poorly differentiated forms (M5, M0 and M1) and showed significant correlation with the immaturity markers CD34, CD7 and HLA-DR (p = 0.013, p = 0.022 and p = 0.001, respectively). Expression of individual antigens correlated with prognosis. Refractoriness to first line therapy was associated with CD7 expression (p = 0.002) and P-170 (p = 0.001). The CD7 marker was also significantly associated with a very low overall survival (p < 0.001) and continuous complete remission (p < 0.001). CD14 expression also significantly predicted lower survival rates (p = 0.033). The combination (CD7+ CD14+) identified a subset of patients with a particularly adverse outcome. The prognostic value of CD7 expression, alone or in combination with other markers, was confirmed in multivariate analysis.

摘要

对154例新诊断的急性髓系白血病(AML)患者的临床和细胞特征与免疫标志物进行了相关性分析。选择一组单克隆抗体(MoAbs)来识别髓系和淋巴系的分化相关抗原(CD13、CD33、CD14、CD15、CD7、CD34、CD10、HLA-DR、CD19、CD2、CD5、TdT)。还对117例患者评估了多药耐药P-糖蛋白(P-170)的表达。在不同的法国-美国-英国(FAB)亚组中观察到抗原表达的差异。HLA-DR在急性早幼粒细胞白血病(M3)的原始细胞上表达较弱,而在FAB M5中总是可以检测到。CD34在所有M0病例中均可检测到,仅在1例M3中检测到(p<0.001)。74例(48.1%)患者的淋巴系相关抗原呈阳性。特别是,49例(31.8%)患者检测到CD7,30例(21.3%)检测到TdT,15个样本同时表达这两种抗原。CD7+病例的发生率在M0和M5 AML中尤其升高(p = 0.005)。它与CD34、HLA-DR、P-170的表达显著相关(分别为p<0.001、p = 0.018和p = 0.034),并且与白细胞计数>50×10⁹/L相关(p = 0.038)。69例(59%)样本显示P-170阳性。同样,这种表型在低分化形式(M5、M0和M1)中尤其明显,并且与不成熟标志物CD34、CD7和HLA-DR显著相关(分别为p = 0.013、p = 0.022和p = 0.001)。单个抗原的表达与预后相关。一线治疗难治性与CD7表达(p = 0.002)和P-170(p = 0.001)相关。CD7标志物还与极低的总生存率(p<0.001)和持续完全缓解率(p<0.001)显著相关。CD14表达也显著预测较低的生存率(p = 0.033)。(CD7+ CD14+)组合识别出一组预后特别不良的患者。在多变量分析中证实了CD7表达单独或与其他标志物联合的预后价值。

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