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首页> 外文期刊>Cancer: A Journal of the American Cancer Society >Clinical characteristics, response to therapy, and survival of African American patients diagnosed with chronic lymphocytic leukemia: Joint experience of the MD Anderson Cancer Center and Duke University Medical Center
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Clinical characteristics, response to therapy, and survival of African American patients diagnosed with chronic lymphocytic leukemia: Joint experience of the MD Anderson Cancer Center and Duke University Medical Center

机译:被诊断患有慢性淋巴细胞性白血病的非裔美国人的临床特征,对治疗的反应以及生存:MD安德森癌症中心和杜克大学医学中心的共同经验

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Background Little is known regarding racial disparities in characteristics and outcomes among patients with chronic lymphocytic leukemia (CLL). Methods The characteristics and outcomes of untreated African American (AA) patients with CLL (n = 84) were analyzed and compared with a reference nonblack (NB) patient population (n = 1571). Results At the time of presentation, AA patients had lower median hemoglobin levels (12.9 g/dL vs 13.7 g/dL), higher β2 microglobulin levels (2.7 mg/dL vs 2.4 mg/dL), greater frequency of constitutional symptoms (27% vs 10%), unmutated immunoglobulin heavy-chain variable region (IGHV) mutation status (65% vs 47%), ζ-chain-associated protein kinase 70 (ZAP70) expression (58% vs 32%), and deletion of chromosome 17p or chromosome 11q (28% vs 17%; P ≤ 02 for each comparison). Fifty-one percent of AA patients and 39% of NB patients required first-line therapy and 91% and 88%, respectively, received chemoimmunotherapy. Overall response rates to treatment were 85% for AA patients and 94% for NB patients (P =.06); and the complete response rates were 56% and 58%, respectively (P =.87). The median survival of AA patients was shorter compared with that of NB patients (event-free survival: 36 months vs 61 months; P =.007; overall survival: 152 months vs not reached; P =.0001). AA race was an independent predictor of shorter event-free and overall survival in multivariable regression models. Conclusions The current results indicated that AA patients with CLL have more unfavorable prognostic characteristics and shorter survival compared with their NB counterparts.
机译:背景关于慢性淋巴细胞性白血病(CLL)患者在特征和预后方面的种族差异知之甚少。方法分析未经治疗的美国非裔(AA)CLL(n = 84)患者的特征和结局,并与非黑人(NB)参考患者(n = 1571)进行比较。结果在报告时,AA患者的中位血红蛋白水平较低(12.9 g / dL vs 13.7 g / dL),β2微球蛋白水平较高(2.7 mg / dL vs 2.4 mg / dL),体质症状的发生率较高(27%) vs. 10%),未突变的免疫球蛋白重链可变区(IGHV)突变状态(65%vs 47%),ζ链相关蛋白激酶70(ZAP70)表达(58%vs 32%)和17p染色体缺失或11q染色体(每次比较分别为28%和17%; P≤02)。有51%的AA患者和39%的NB患者需要一线治疗,分别有91%和88%接受了化学免疫治疗。 AA患者的总体治疗反应率为85%,NB患者的总体治疗率为94%(P = .06);完全缓解率分别为56%和58%(P = .87)。与NB患者相比,AA患者的中位生存期较短(无事件生存期:36个月对61个月; P = .007;总生存期:152个月对未达到; P = .0001)。在多变量回归模型中,AA种族是较短的无事件生存期和总生存期的独立预测因子。结论当前的结果表明,与NB相比,AA的CLL患者的预后特征更差,生存期更短。

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