摘要
目的:研究成人急性髓系白血病(acute myeloid leukemia,AML)中淋系抗原的表达及其与预后的关系。方法:对275例成人AML进行细胞形态学、流式细胞免疫表型分析和染色体细胞遗传学(MIC)分型实验研究并对其中的64例M2进行临床治疗结果观察研究。结果:①AML淋系抗原阳性率31.3%,其中t(8;21)者为48.3%,无t(8;21)者为26.5%(P< 0.001)。②CD19+在t(8;21)中占38.3%,无t(8;21)中占1.9%(P<0.001);而其他淋系抗原两组比较均为P>0.05.③治疗结果(CR率):t(8;21)和无t(8;21)M2分别为66.7%和41.9%,CD19+和CD19-M2分别为76.5%和46.8%,CD19+/t(8; 21)和CD19-/无t(8;21)分别为80.0%和41.4%,以上均为P<0.05。而CD19-/t(8;21)和CD19+/无t(8;21)分别为55.6%和50.0%(P>0.05)。结论:成人AML中淋系抗原表达与核型密切相关,t(8;21)AML高表达CD19。t(8;21)和CD19都是M2预后好的标志之一。
Objective:To study the lymphocytic antigen expression in adult acute myeloid leukemia (AMID and its relationship with clinical prognosis. Methods: The morphologic, immunologic, and cytogenetic (MIC) classifications of lymphocytic antigen expression were performed on 275 adult AML patients. We observed the clinical therapeutic effects of 64 cases of AML/M2 and correlated with MIC parameters. Results: ①The positive rate of lymphocytic antigen in AML was 31.3%. t(8;21)/AML was 48.3% and non t(8;21)/AML was 26. 5% (P〈0.001). ②CD19^+ positive rate was 38.3% in t(8;21)/AML and 1.9 % in non t(8;21)/AML, respectively (P〈0. 001). There was no significant difference in the expression of other lymphocytic antigen between the two groups (P〉0.05). ③The complete remission (CR) rates of t(8;21)/M2 and non t(8;21)/M2 were 66.7% and 41.9%, respectively (P-%0.05). TheCR rates of CD19^+/M2 and CD19^+-/M2 were 76.5% and 46.8%, respectively (P 〈0.05). TheCR rates of CD19^+/t(8;21)/M2 and CD19^+/non t(8;21)/M2 patients were 80.0% and 41. 4% ,respectively (P〈0.05). But the CR rates of CD19^+/t(8;21)/M2 and CD19^+/non t(8;21)/M2 patients was 55.6% and 50.0%, respec tively (P〉0.05). Conclusion: Lymphocytic antigen expression in adult AML closely correlated with nuclear type. The expression of CD19 was higher in t(8;21)/AML. Both CD19 and t(8;21) indicate good prognosis of M2.
出处
《肿瘤》
CAS
CSCD
北大核心
2006年第10期944-946,963,共4页
Tumor
关键词
白血病
髓样费城阴性
白血病
髓样
费城阴性
抗原.CD19
药物疗法
预后
Leukemia, myeloid Philadelphia-negative
Leukemia, myeloid, Philadelphia positive
Antigens, CD19
Drug therapy
Prognosis