Hepatitis B Surface Antigen Positivity is An Independent Unfavorable Prognostic Factor in Diffuse Large B-cell Lymphoma in The Rituximab Era.

BACKGROUND Diffuse large B-cell lymphoma (DLBCL) patients with concurrent hepatitis B surface antigen (HBsAg)-positive hepatitis B virus (HBV) infection have distinct clinical features. Nevertheless, the prognostic value of HBsAg in DLBCL in the rituximab era remains unclear. PATIENTS AND METHODS We conducted a retrospective cohort study to investigate the clinical relevance of HBsAg in immunocompetent patients with DLBCL treated with homogeneous rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone between 2002 and 2016. RESULTS Among 416 analyzed patients, 98 (23.6%) were HBsAg-positive. HBsAg positivity was associated with a younger age and more advanced stage at diagnosis, more frequent hepatic impairment during perichemotherapy, and a trend of higher National Comprehensive Cancer Network-International Prognostic Index (NCCN-IPI) score at diagnosis. Compared with the HBsAg-negative patients, the HBsAg-positive patients had a lower overall response rate (76.5% vs. 85.5%, P = 0.043), poorer 5-year overall survival (OS) rate (57.2% vs. 73.5%, P < 0.001), and shorter 5-year progression-free survival (PFS) rate (47.2% vs. 60.7%, P = 0.013). Multivariate analyses showed HBsAg positivity was an independent unfavorable prognostic indicator for OS and PFS. A scoring system incorporating HBsAg positivity, the NCCN-IPI score, and serum albumin levels proved to be useful for stratifying prognostically relevant subgroups of patients with DLBCL. CONCLUSION This study demonstrated that HBV infection is uniquely relevant to DLBCL. HBsAg might serve as a novel biomarker to improve clinical risk stratification of patients with DLBCL in areas with high prevalence of HBV infection. Further research investigating the etiopathogenesis of HBV infection in DLBCL is imperative. IMPLICATIONS FOR PRACTICE A considerable disparity exists regarding the prognostic relevance of hepatitis B surface antigen (HBsAg)-positive hepatitis B virus (HBV) infection in patients with diffuse large B-cell lymphoma (DLBCL). In this large, retrospective cohort study from an area with high prevalence of HBV infection, the authors demonstrated that HBsAg was an independent unfavorable factor significantly associated with survival, highlighting its potential as a novel prognostic indicator to improve the risk stratification of patients with DLBCL in the rituximab era.

[1]  D. Carrick,et al.  The Impact: , 2020, Call My Name, Clemson.

[2]  Ding‐Shinn Chen,et al.  Chronic hepatitis B is associated with an increased risk of B‐cell non‐Hodgkin's lymphoma and multiple myeloma , 2019, Alimentary pharmacology & therapeutics.

[3]  C. Fan,et al.  Hepatitis B virus and risk of non‐Hodgkin lymphoma: An updated meta‐analysis of 58 studies , 2018, Journal of viral hepatitis.

[4]  Kui Wu,et al.  Genetic landscape of hepatitis B virus-associated diffuse large B-cell lymphoma. , 2018, Blood.

[5]  Mubarak M. Al-Mansour,et al.  Negative effect of hepatitis in overall and progression-free survival among patients with diffuse large B-cell lymphoma , 2018, Infectious Agents and Cancer.

[6]  Hui Zheng,et al.  Capable Infection of Hepatitis B Virus in Diffuse Large B-cell Lymphoma , 2018, Journal of Cancer.

[7]  Q. Mu,et al.  Diffuse large B-cell lymphoma with concurrent hepatitis B virus infection in the MabThera era: Unique clinical features and worse outcomes , 2018, Journal of cancer research and therapeutics.

[8]  Jianmin Yang,et al.  HBV infection potentiates resistance to S-phase arrest-inducing chemotherapeutics by inhibiting CHK2 pathway in diffuse large B-cell lymphoma , 2018, Cell Death & Disease.

[9]  W. Guo,et al.  MYC Gene Rearrangements Are Closely Associated with Poor Survival of Diffuse Large B Cell Lymphoma with Hepatitis B Virus Infection , 2017, BioMed research international.

[10]  W. Guo,et al.  PD1 is highly expressed in diffuse large B-cell lymphoma with hepatitis B virus infection , 2017, PloS one.

[11]  K. Young,et al.  Hepatitis B virus-associated diffuse large B-cell lymphoma: unique clinical features, poor outcome, and hepatitis B surface antigen-driven origin , 2015, Oncotarget.

[12]  R. Greil,et al.  A modified scoring of the NCCN‐IPI is more accurate in the elderly and is improved by albumin and β2‐microglobulin , 2015, British journal of haematology.

[13]  R. Gascoyne,et al.  An enhanced International Prognostic Index (NCCN-IPI) for patients with diffuse large B-cell lymphoma treated in the rituximab era. , 2014, Blood.

[14]  Junmin Li,et al.  HBsAg is an independent prognostic factor in diffuse large B cell lymphoma patients in rituximab era: result from a multicenter retrospective analysis in China , 2014, Medical Oncology.

[15]  Chiun Hsu,et al.  Hepatitis B virus reactivation in B-cell lymphoma patients treated with rituximab: analysis from the Asia Lymphoma Study Group. , 2013, European journal of cancer.

[16]  J. Castillo,et al.  Hepatitis B infection increases the risk of non-Hodgkin lymphoma: a meta-analysis of observational studies. , 2013, Leukemia research.

[17]  He Huang,et al.  Clinical analysis and prognostic significance of hepatitis B virus infections for diffuse large B-cell lymphoma with or without rituximab therapy , 2013, Experimental and therapeutic medicine.

[18]  T. Habermann,et al.  The absolute monocyte and lymphocyte prognostic score predicts survival and identifies high-risk patients in diffuse large-B-cell lymphoma , 2011, Leukemia.

[19]  S. Kimura,et al.  Reactivation of hepatitis B virus after rituximab‐containing treatment in patients with CD20‐positive B‐cell lymphoma , 2010, Cancer.

[20]  B. Coiffier,et al.  Long-term outcome of patients in the LNH-98.5 trial, the first randomized study comparing rituximab-CHOP to standard CHOP chemotherapy in DLBCL patients: a study by the Groupe d'Etudes des Lymphomes de l'Adulte. , 2010, Blood.

[21]  S. Jee,et al.  Hepatitis B virus infection and risk of non-Hodgkin lymphoma in South Korea: a cohort study. , 2010, The Lancet. Oncology.

[22]  G. Weiner,et al.  Rituximab: mechanism of action. , 2010, Seminars in hematology.

[23]  Chien-Hung Chen,et al.  Reactivation of hepatitis B virus following rituximab-based regimens: a serious complication in both HBsAg-positive and HBsAg-negative patients , 2010, Annals of Hematology.

[24]  P. Pontisso,et al.  Biological and clinical implications of HBV infection in peripheral blood mononuclear cells. , 2008, Autoimmunity reviews.

[25]  Wen-Qi Jiang,et al.  Clinical and prognostic analysis of hepatitis B virus infection in diffuse large B-cell lymphoma , 2008, BMC Cancer.

[26]  L. Ruco,et al.  Absolute lymphocyte count is a prognostic factor in diffuse large B‐cell lymphoma , 2008, British journal of haematology.

[27]  Ming-Huang Chen,et al.  High prevalence of occult hepatitis B virus infection in patients with B cell non-Hodgkin’s lymphoma , 2008, Annals of Hematology.

[28]  S. Lim,et al.  The relationship of hepatitis B virus infection and non‐Hodgkin’s lymphoma and its impact on clinical characteristics and prognosis , 2007, European journal of haematology.

[29]  Y. Chae,et al.  Absolute lymphocyte counts predicts response to chemotherapy and survival in diffuse large B-cell lymphoma , 2007, Leukemia.

[30]  Sigrid Stroobants,et al.  Revised response criteria for malignant lymphoma. , 2007, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[31]  Randy D Gascoyne,et al.  Rituximab-CHOP versus CHOP alone or with maintenance rituximab in older patients with diffuse large B-cell lymphoma. , 2006, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[32]  R. Gascoyne,et al.  Introduction of combined CHOP plus rituximab therapy dramatically improved outcome of diffuse large B-cell lymphoma in British Columbia. , 2005, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[33]  H. Seno,et al.  Hepatitis B virus infection in lymphatic tissues in inactive hepatitis B carriers. , 2005, Journal of hepatology.

[34]  S. Markovic,et al.  Timely reconstitution of immune competence affects clinical outcome following autologous stem cell transplantation , 2004, Clinical and Experimental Medicine.

[35]  Ding-Shinn Chen,et al.  Global control of hepatitis B virus infection. , 2002, The Lancet. Infectious diseases.

[36]  Y. Bang,et al.  Hepatitis B Virus Infection and B‐Cell Non‐Hodgkin's Lymphoma in a Hepatitis B Endemic Area: A Case‐control Study , 2002, Japanese journal of cancer research : Gann.

[37]  H. Hsu,et al.  Baseline seroepidemiology of hepatitis B virus infection in children in Taipei, 1984: A study just before mass hepatitis B vaccination program in Taiwan , 1986, Journal of medical virology.

[38]  S. Yip,et al.  The impact of hepatitis B virus (HBV) infection on clinical outcomes of patients with diffuse large B-cell lymphoma. , 2015, European journal of cancer care.

[39]  E. Iannitto,et al.  High prevalence of hepatitis B virus infection in B-cell non-Hodgkin's lymphoma. , 2006, Haematologica.

[40]  L. Staudt,et al.  Confirmation of the molecular classification of diffuse large B-cell lymphoma by immunohistochemistry using a tissue microarray. , 2004, Blood.