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Published on: October 19, 2014
The prognostic role of HBV infection in chronic lymphocytic leukemia
Jin-Hua Liang1,2,3, Rui Gao4, Jun-Cheng Dai5
1Department of Hematology, Jiangsu Province Hospital, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Insights
Hepatitis B virus (HBV) infection is a significant independent predictor for chronic lymphocytic leukemia (CLL) prognosis, impacting both time-to-treatment and overall survival. Incorporating HBV status improves prognostic models for CLL patients.
Area of Science:
- Oncology
- Virology
- Epidemiology
Background:
- Chronic lymphocytic leukemia (CLL) is a common B-cell malignancy.
- Hepatitis B virus (HBV) infection is a global health concern with potential implications for various cancers.
- The prognostic role of HBV in CLL remains incompletely understood.
Purpose of the Study:
- To evaluate the impact of Hepatitis B virus (HBV) status on the prognosis of chronic lymphocytic leukemia (CLL).
- To assess HBV as an independent prognostic factor for time-to-treatment (TTT) and overall survival (OS) in CLL patients.
Main Methods:
- A cohort of 501 newly diagnosed CLL patients was analyzed.
- HBV infection was determined by HBsAg or HBcAb positivity.
- Cox regression and receiver-operator characteristic (ROC) curve analyses were employed to identify prognostic factors and assess model discrimination.
Main Results:
- 24% of CLL patients were HBV positive.
- HBV infection independently predicted poorer TTT (HR=1.37) and OS (HR=2.85).
- Combining HBV status with traditional factors significantly improved prognostic model discrimination for both TTT and OS (AUCs increased).
Conclusions:
- HBV infection is an important independent risk predictor for CLL prognosis.
- HBV status should be considered in prognostic assessments for CLL patients.
- Integration of HBV status enhances the accuracy of CLL prognostic models.
Purpose:
We attempt to assess the impact of hepatis-B virus (HBV) status on the prognosis of chronic lymphocytic leukemia (CLL) using a Chinese case cohort.
Methods:
Five hundred and one consecutive newly diagnosed subjects with CLL were enrolled in this case cohort. HBV infection was defined as hepatitis B surface antigen (HBsAg) positive or hepatitis-B core antibody (HBcAb) positive. Univariate and stepwise multivariate Cox regression analyses were used to screen the prognostic risk factors associated with the end point of time-to-treatment (TTT) or overall survival (OS). Bootstrap re-sampling method was used to evaluate the model's internal validity. The discriminative ability of the models was evaluated using time-dependent receiver-operator characteristic (ROC) curves and corresponding areas under the curve (AUC).
Results:
One hundred and twenty-one subjects (24%) among 501 patients were HBV positive. HBV infection was an independent predictor for the prognosis of TTT (HR = 1.37; 95% CI 1.04-1.80) or OS (HR =2.85; 95% CI 1.80-4.52). The AUCs for HBV infection were 0.62 (95% CI 0.58-0.66) for TTT and 0.69 (95% CI 0.66-0.72) for OS, respectively. When we combined HBV infection with the traditional clinical and biological factors, significant improvements for model's discrimination were observed for TTT [AUC: 0.81 (95% CI: 0.77-0.85) vs. 0.78 (95% CI: 0.74-0.82), P < 0.001] and OS [AUC: 0.81 (95% CI 0.76-0.86) vs. 0.76 (95% CI 0.71-0.82), P < 0.001). Further bootstrap re-sampling method revealed good internal consistence for the final optimal models (Average AUC: 0.78 for TTT and 0.79 for OS based on 1000 bootstraps).
Conclusions:
Our results indicated that HBV infection should be served as an important risk predictor for prognosis of CLL (TTT and OS).
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