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Clin Mol Hepatol. 2023;29(3):794-809.

Treated chronic hepatitis B is a good prognostic factor of diffuse large B-cell lymphoma.

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제1저자 박제연, 정성원, 이윤빈 · 교신저자 김태민, 이정훈

소속 (3)
  1. Department of Internal Medicine and Liver Research Institute, Seoul National University Hospital, Seoul, Korea.
  2. Department of Internal Medicine, Seoul National University Hospital, Seoul National University Cancer Research Institute, Seoul, Korea.
  3. Division of Hematology-Oncology, Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.

Abstract

BACKGROUND/AIMS Chronic hepatitis B (CHB) is a risk factor for non-Hodgkin lymphoma (NHL). Our recent study suggested that antiviral treatment may reduce the incidence of NHL in CHB patients. This study compared the prognoses of hepatitis B virus (HBV)-associated diffuse large B-cell lymphoma (DLBCL) patients receiving antiviral treatment and HBV-unassociated DLBCL patients.

METHODS This study comprised 928 DLBCL patients who were treated with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) at two referral centers in Korea. All patients with CHB received antiviral treatment. Time-to-progression (TTP) and overall survival (OS) were the primary and secondary endpoints, respectively.

RESULTS Among the 928 patients in this study, 82 were hepatitis B surface antigen (HBsAg)-positive (the CHB group) and 846 were HBsAg-negative (the non-CHB group). The median follow-up time was 50.5 months (interquartile range [IQR]=25.6-69.7 months). Multivariable analyses showed longer TTP in the CHB group than the non-CHB group both before inverse probability of treatment weighting (IPTW; adjusted hazard ratio [aHR]=0.49, 95% confidence interval [CI]=0.29-0.82, p=0.007) and after IPTW (aHR=0.42, 95% CI=0.26-0.70, p<0.001). The CHB group also had a longer OS than the non-CHB group both before IPTW (HR=0.55, 95% CI=0.33-0.92, log-rank p=0.02) and after IPTW (HR=0.53, 95% CI=0.32-0.99, log-rank p=0.02). Although liver-related deaths did not occur in the non-CHB group, two deaths occurred in the CHB group due to hepatocellular carcinoma and acute liver failure, respectively.

CONCLUSION Our findings indicate that HBV-associated DLBCL patients receiving antiviral treatment have significantly longer TTP and OS after R-CHOP treatment than HBV-unassociated DLBCL patients.

Keywords

Antiviral agentChemotherapyHepatitis B virusNon-Hodgkin lymphomaRituximab

Figures

Figure 1.
Figure 1. Flow diagram of patient selection for the study. A total of 1,170 patients was identified, and 242 patients were excluded. Finally, 928 patients were included and classified into two groups based on current HBV infection. CHB, chronic hepatitis B; DLBCL, diffuse large B-cell lymphoma; R-CHOP, rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone; HBV, hepatitis B virus; HCV, hepatitis C virus; HIV, human immunodeficiency virus. *Among the CHB patients, 5 were excluded from thisstudy due to previous or concurrent malignancy.
Figure 2.
Figure 2. Kaplan–Meier estimates of TTP based on HBV infection status (A) before and (B) after IPTW. PSs of IPTW were computed using age, sex, Ann Arbor classification, IPI risk, GCB cell subtype, lactate dehydrogenase, presence of extranodal lesions, bone marrow involvement, and cirrhosis. CHB, chronic hepatitis B; HBV, hepatitis B virus; TTP, time-to-progression; PSs, propensity scores; IPTW, inverse probability of treatment weighting; IPI, International Prognostic Index; GCB, germinal center B.
Figure 3.
Figure 3. Kaplan–Meier estimates of OS based on HBV infection status (A) before and (B) after IPTW. PSs of IPTW were computed using age, sex, Ann Arbor classification, IPI risk, GCB cell subtype, lactate dehydrogenase, presence of extranodal lesions, bone marrow involvement, and cirrhosis. CHB, chronic hepatitis B; HBV, hepatitis B virus; OS, overallsurvival; GCB, germinal center; PSs, propensity scores; IPTW, inverse probability of treatment weighting; IPI, International Prognostic Index.

그림 출처: PubMed Central 공개 논문 (PMC10366791)

Comment · 정정

Conflict of interest statement

Conflicts of Interest . Dr. Yun Bin Lee reportsreceiving research grantsfrom Samjin Pharmaceuticals and Yuhan Pharmaceuticals; Dr. Su Jong Yu reports receiving research grants from Yuhan Pharmaceuticals and Daewoong Pharmaceuticals; Dr. Yoon Jun Kim reports receiving research grants from Yuhan Pharmaceuticals, AstraZeneca, Boston Scientific, Daewoong Pharmaceuticals, and Samjin Pharmaceuticals and lecture fees from Bayer HealthCare Pharmaceuticals, Gilead Science, MSD Korea, Yuhan Pharmaceuticals, Samil Pharmaceuticals, CJ Pharmaceuticals, Bukwang Pharmaceuticals, and Handok Pharmaceuticals; Dr. Jung-Hwan Yoon reports receiving research grants from Dicerna Pharmaceuticals, Roche, GlaxoSmithKline, AstraZeneca, Daewoong Pharmaceuticals, and Hanmi Pharmaceuticals; Dr. Tae Min Kim reports receiving research grants from AstraZeneca-Korea Health Industry Development Institute and honoraria or advisory role in AstraZeneca, Boryung, F. Hoffmann-La Roche Ltd/Genentech, Inc, Janssen, Novartis, Regeneron, Sanofi, Takeda, and Yuhan; Dr. Jeong-Hoon Lee reports receiving research grants from Yuhan Pharmaceuticals, and lecture fee from GreenCross Cell, Daewoong Pharmaceuticals, and Gilead Korea. No other potential conflict of interest relevant to this articlewasreported.

그 밖의 정보
출판 형태
Journal Article
저널
Clinical and molecular hepatology · eISSN 2287-285X
전자 출판
2023-05-17
MeSH
Humans · Hepatitis B Surface Antigens · Prognosis · Hepatitis B, Chronic* / complications / drug therapy · Rituximab / therapeutic use · Vincristine / therapeutic use · Cyclophosphamide / therapeutic use · Prednisone / therapeutic use · Doxorubicin / therapeutic use · Lymphoma, Large B-Cell, Diffuse* / complications / diagnosis / drug therapy · Antiviral Agents / therapeutic use · Antineoplastic Combined Chemotherapy Protocols / therapeutic use
Substances
Hepatitis B Surface Antigens · Rituximab · Vincristine · Cyclophosphamide · Prednisone · Doxorubicin · Antiviral Agents
연구비
National IT Industry Promotion Agency · Ministry of Science and ICT S0252-21-1001 · Liver Research Foundation of Korea
참고문헌
49편