Screening for Chronic Hepatitis B Virus Infection in Patients With Malignancies and Assessment of the Impact of Malignancies on the Response To Preemptive Treatment of Chronic Hepatitis B Virus
Creators
- 1. Tropical Medicine Department, Alexandria University.
- 2. Clinical Oncology and Nuclear Medicine Department, Alexandria University.
Description
ABSTRACT
The prevalence of hepatitis B virus (HBV) infection in patients with malignancies especially haematological malignancies is increased compared with the general population worldwide. HBV reactivation is common following chemotherapy and is associated with a high mortality despite prompt anti-viral treatment. HBV reactivation may necessitate interruption of chemotherapy with adverse prognostic consequences for the haematological disease. All candidates for chemotherapy and immunosuppressive therapy should be tested for HBV markers prior to immunosuppression, All HBsAg-positive patients should receive ETV or TDF or TAF as treatment or prophylaxis, HBsAg-negative, anti-HBc positive subjects should receive anti-HBV prophylaxis if they are at high risk of HBV reactivation according to EASL guidelines 2017. The aim of this study was to screen for chronic Hepatitis B virus infection in patients with Malignancies recruited from Oncology department in Main Alexandria University Hospital and assessment of the impact of malignancy on the response to preemptive treatment of chronic Hepatitis B virus with Nucleoside analogue (Entecavir 0.5mg). The study was conducted on 500 patients recruited from Oncology department screened for CHB virus infection and those who suffered from CHB were called group I and treated with Entecavir 0.5mg tab and treatment response was compared to group II patients which included 20 control patients suffering from chronic Hepatitis B virus being treated with Nucleoside analogue (Entecavir 0.5mg). In both groups 100% patients was successfully treated with Entecavir 0.5mg tab daily and all the patients met the criteria of virological response to treatment (undetectable PCR after 6 months of treatment) and no virological breakthrough or treatment failure was reported. Also there was statistically significant reduction in AST, ALT, Total and Direct bilirubin levels in both groups with Entecavir 0.5mg tab treatment daily. Percentage of patients suffering from chronic HBV in Oncology department at Alexandria Main University Hospital is 4.6 % and the effectiveness of Entecavir 0.5mg tab in treatment of chronic HBV in patients with malignancies is comparable to patients without malignancies.
Keywords: Hepatitis B virus, Preemptive treatment, Entecavir, Malignancies.
REFERENCES
- Kowdley KV, Wang CC, Welch S, et al. Prevalence of chronic hepatitis B among foreign-born persons living in the United States by country of origin. Hepatology 2012; 56:422-33.
- Myers RP, Tainturier MH, Ratziu V, Piton A, Thibault V, Imbert-Bismut F, et al. Prediction of liver histological lesions with biochemical markers in patients with chronic hepatitis B. J Hepatol 2003;39:222–30.
- Poynard T, Morra R, Halfon P, Castera L, Ratziu V, Imbert-Bismut F, et al. Meta-analyses of FibroTest diagnostic value in chronic liver disease. BMC Gastroenterol 2007;7:40.
- Marcellin P, Ziol M, Bedossa P, Douvin C, Poupon R, De LV, et al. Noninvasive assessment of liver fibrosis by stiffness measurement in patients with chronic hepatitis B. Liver Int 2009;29:242–7.
- Cardoso AC, Carvalho-Filho RJ, Stern C, Dipumpo A, Giuily N, Ripault MP, et al. Direct comparison of diagnostic performance of transient elastography in patients with chronic hepatitis B and chronic hepatitis C. Liver Int 2012;32:612–21.
- Arena U, Vizzutti F, Corti G, Ambu S, Stasi C, Bresci S, et al. Acute viral hepatitis increases liver stiffness values measured by transient elastography. Hepatology 2008;47:380 384.
- Tassopoulos NC, Volpes R, Pastore G, Heathcote J, Buti M, Goldin RD, et al. Efficacy of lamivudine in patients with hepatitis B e antigen-negative/ hepatitis B virus DNA-p ositive (precore mutant) chronic hepatitis B. Hepatology 1999;29:889–96.
- Marcellin P, Lau GK, Bonino F, Farci P, Hadziyannis S, Jin R, et al. Peginterferon alfa-2a alone, lamivudine alone, and the two in combination in patients with HBeAg-negative chronic hepatitis B. N Engl J Med 2004;351:1206–17.
- Lai CL, Shouval D, Lok AS, Chang TT, Cheinquer H, Goodman Z, et al. Entecavir versus lamivudine for patients with HBeAg-negative chronic hepatitis B. N Engl J Med 2006;354:1011–20.
- Menéndez-Arias L, Álvarez M, Pacheco B. 217. Volz T, Allweiss L, Ben MM, et al. The entry inhibitor Myrcludex-B efficiently blocks intrahepatic virus spreading in humanized mice previously infected with hepatitis B virus. J Hepatol 2013; 58: 861–7.
- Maepa MB, Roelofse I, Ely A, Arbuthnot P. Progress and prospects of ant-HBV gene therapy development. Int J Mol Sci 2015; 16: 17589–610.
- Cradick TJ, Keck K, Bradshaw S, Jamieson AC, McCaffrey AP. Zincfinger nucleases as a novel therapeutic strategy for targeting hepatitis B virus DNAs. Mol Ther 2010; 18: 947–54.
- Bloom K, Ely A, Mussolino C, Cathomen T, Arbuthnot P. Inactivation of hepatitis B virus replication in cultured cells and in vivo with engineered transcription activator-like effector nucleases. Mol Ther 2013; 21: 1889–97.
- Chen J, Zhang W, Lin J, et al. An efficient antiviral strategy for targeting hepatitis B virus genome using transcription activator-like effector nucleases. Mol Ther 2014; 22: 303–11.
- Boni C, Laccabue D, Lampertico P, et al. Restored function of HBV-specific T cells after long-term effective therapy with nucleos (t) ide analogues. Gastroenterology 2012; 143: 963–73.
- Giladi H, Ketzinel-Gilad M, Rivkin L, Felig Y, Nussbaum O, Galun E. Small interfering RNA inhibits hepatitis B virus replication in mice. Mol Ther 2003; 8: 769–76.
- EASL 2017 Clinical Practice Guidelines on the management of hepatitis B virus infection. J Hepatol (2017). Curr Opin Virol 2014; 8: 1–9.
- Swapna Gurrapu and Estari Mamidala. Medicinal Plants Used By TraditionalMedicinePractitioners in the Management of HIV/AIDS-Related Diseases in Tribal Areas of Adilabad
District, Telangana Region. The Ame J Sci & Med Res. 2016:2(1):239-245.
doi:10.17812/ajsmr2101. - Hsu C, Tsou HH, Lin SJ, Wang MC, Yao M, Hwang WL, Kao WY, Chiu CF, Lin SF, Lin J, et al. Chemotherapy-induced hepatitis B reactivation in lymphoma patients with resolved HBV infection: a prospective study. Hepatology. 2014;59:2092–100.
- Dong HJ, Ni LN, Sheng GF, Song HL, Xu JZ, Ling Y. Risk of hepatitis B virus (HBV) reactivation in non-Hodgkin lymphoma patients receiving rituximab-chemotherapy: a meta-analysis. J Clin Virol. 2013;57:209–14.
- Matsui T, Kang JH, Nojima M, Tomonari A, Aoki H, Yamazaki H, Yane K, Tsuji K, Andoh S, Andoh S, et al. Reactivation of hepatitis B virus in patients with undetectable HBsAg undergoing chemotherapy for malignant lymphoma or multiple myeloma. J Med Virol. 2013;85:1900–6.
- Zurawska U, Hicks LK, Woo G, Bell CM, Krahn M, Chan KK, Feld JJ. Hepatitis B virus screening before chemotherapy for lymphoma: a cost-effectiveness analysis. J Clin Oncol. 2012;30:3167–73.
- Terrault NA, Bzowej NH, Chang KM, Hwang JP, Jonas MM, Murad MH; American Association for the Study of Liver Diseases. AASLD Guidelines for Treatment of Chronic Hepatitis B. Hepatology. 2016;63:261-283.
- Reddy KR, Beavers KL, Hammond SP, Lim JK, Falck-Ytter YT; American Gastroenterological Association Institute. American Gastroenterological Association Institute guideline on the prevention and treatment of hepatitis B virus reactivation during immunosuppressive drug therapy.Gastroenterology. 2015;148:215-219.
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