Novel tumor markers provide improved prediction of survival after diagnosis of human immunodeficiency virus (HIV)-related diffuse large B-cell lymphoma

被引:14
作者
Chao, Chun [1 ]
Silverberg, Michael J. [2 ]
Chen, Lie-Hong [1 ]
Xu, Lanfang [1 ,10 ]
Martinez-Maza, Otoniel [3 ,4 ,5 ]
Abrams, Donald I. [6 ,7 ]
Zha, Hongbin D. [8 ]
Haque, Reina [1 ]
Said, Jonathan [9 ]
机构
[1] Kaiser Permanente Southern Calif, Dept Res & Evaluat, 100 S Los Robles Ave,2nd Floor, Pasadena, CA 91101 USA
[2] Kaiser Permanente Northern Calif, Div Res, Pasadena, CA USA
[3] UCLA, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA USA
[4] UCLA, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA USA
[5] UCLA, Fielding Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA USA
[6] Univ Calif San Francisco, San Francisco Gen Hosp, San Francisco, CA USA
[7] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[8] Kaiser Permanente Southern Calif, Los Angeles Med Ctr, Los Angeles, CA USA
[9] Univ Calif Los Angeles, Sch Med, Dept Pathol & Lab Med, Los Angeles, CA USA
[10] MedHlth Stat Consulting Inc, Solon, OH 44139 USA
关键词
Lymphoma; HIV; diffuse large B-cell lymphoma; prognosis; CD4; AIDS; ACTIVE ANTIRETROVIRAL THERAPY; NON-HODGKINS-LYMPHOMA; PROGNOSTIC-SIGNIFICANCE; P53; EXPRESSION; RITUXIMAB-ERA; INFECTION; CD44; DISSEMINATION; CHEMOTHERAPY; MUTATIONS;
D O I
10.1080/10428194.2017.1334121
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Existing prognostic tools for HIV + diffuse large B-cell lymphoma (DLBCL) fail to accurately predict patient outcomes. To develop a novel prognostic algorithm incorporating molecular tumor characteristics and HIV disease factors, we included 80 patients with HIV-related DLBCL diagnosed between 1996 and 2007. Immunohistochemistry staining was used to analyze the expression of 26 tumor markers. Clinical data were collected from medical records. Logistic regression and bootstrapping were used to select and assess stability of the prognostic model, respectively. Of the tumor markers examined, expression of cMYC, Ki 67, CD44, EBV, SKP2, BCL6, p53, CD20 and IgM were associated with two-year mortality. The final prognostic model, confirmed in bootstrapped samples, included IPI, circulating CD4 cell count, history of clinical AIDS, and expression of CD44, p53, IgM and EBV. This model incorporating HIV disease history and tumor markers, achieved better prediction for two-year mortality [AUC = 0.87, 95% CI: 0.78-0.96] compared with IPI alone [AUC = 0.63 (0.51-0.75)].
引用
收藏
页码:321 / 329
页数:9
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