Literature DB >> 29064851

De-novo versus recurrent hepatocellular carcinoma following direct-acting antiviral therapy for hepatitis C virus.

Ashraf O Abdelaziz1, Mohamed M Nabil1, Ahmed H Abdelmaksoud2, Hend I Shousha1, Ahmed A Cordie1, Eman M Hassan1, Dalia A Omran1, Rania Leithy1, Tamer M Elbaz1.   

Abstract

INTRODUCTION: A recent appearance of direct-acting antivirals (DAAs) led to a surge in hepatitis C virus (HCV) management. Nowadays, a large proportion of treated patients have cirrhosis with a retained possibility to develop hepatocellular carcinoma (HCC) even after complete cure. We aimed to study tumoral differences between patients who developed HCC after DAAs as either a recurrence or de-novo HCC.
METHODS: We retrospectively analyzed 89 patients who presented to our HCC multidisciplinary clinic with HCC lesions following DAA therapy. A total of 45 patients had complete response to HCC according to the modified Response Evaluation Criteria in Solid Tumors before DAAs intake. Another 44 patients developed de-novo lesions after DAA treatment. Both groups were compared regarding their baseline characteristics, tumor criteria, response to DAAs as well response to HCC treatment.
RESULTS: Both groups showed no significant difference regarding their baseline characteristics (age, sex, Child-Pugh score, and performance status) or response to DAAs (P=0.5). No significant difference was present between groups according to number, site, and size of lesions. However, time elapsed between the end of DAAs therapy and first diagnosis of HCC was significantly longer in de-novo group (15.22±16.39 months) versus recurrence group (6.76±5.1 months) (P=0.008). In addition, response to ablation was significantly better in de-novo lesions compared with recurrent HCC (P=0.03).
CONCLUSIONS: Although de-novo HCC lesions significantly developed later than recurrent lesions in DAAs-treated patients, their response rates were significantly better. No differences were detected between both groups in their response to DAAs and their tumoral characteristics.

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Year:  2018        PMID: 29064851     DOI: 10.1097/MEG.0000000000001004

Source DB:  PubMed          Journal:  Eur J Gastroenterol Hepatol        ISSN: 0954-691X            Impact factor:   2.566


  10 in total

1.  Recurrence rate of hepatocellular carcinoma in patients with treated hepatocellular carcinoma and hepatitis C virus-associated cirrhosis after ombitasvir/paritaprevir/ritonavir+dasabuvir+ribavirin therapy.

Authors:  Carmen M Preda; Cristian Baicus; Irina Sandra; Alexandru Oproiu; Teodora Manuc; Ileana Constantinescu; Daniel Gavrila; Mircea Diculescu; Radu Dumitru; Catalin Vasilescu; Cristian Tieranu; Doina Istratescu; Theodor Voiosu; Mircea Manuc
Journal:  United European Gastroenterol J       Date:  2019-03-29       Impact factor: 4.623

Review 2.  Hepatocellular carcinoma, hepatitis C virus infection and miRNA involvement: Perspectives for new therapeutic approaches.

Authors:  Ester Badami; Rosalia Busà; Bruno Douradinha; Giovanna Russelli; Vitale Miceli; Alessia Gallo; Giovanni Zito; Pier Giulio Conaldi; Gioacchin Iannolo
Journal:  World J Gastroenterol       Date:  2022-06-14       Impact factor: 5.374

Review 3.  Hepatocellular carcinoma occurrence in DAA-treated hepatitis C virus patients: Correlated or incidental? A brief review.

Authors:  Eleni Gigi; Vasileios I Lagopoulos; Eleni Bekiari
Journal:  World J Hepatol       Date:  2018-09-27

Review 4.  Impact of treating chronic hepatitis C infection with direct-acting antivirals on the risk of hepatocellular carcinoma: The debate continues - A mini-review.

Authors:  Mohamed El Kassas; Tamer Elbaz; Mohamed Salaheldin; Lobna Abdelsalam; Ahmed Kaseb; Gamal Esmat
Journal:  J Adv Res       Date:  2019-03-07       Impact factor: 10.479

5.  The Impact of Direct-Acting Antiviral Therapy on the Risk of Recurrence after Curative Resection in Patients with Hepatitis-C-Virus-Related Early Stage Hepatocellular Carcinoma.

Authors:  Yu-Syuan Chen; Kuo-Hsuan Huang; Pei-Ming Wang; Ching-Hui Chuang; Chee-Chien Yong; Yueh-Wei Liu; Pao-Yuan Huang; Chih-Chien Yao; Yen-Po Lin; Ming-Chao Tsai
Journal:  Medicina (Kaunas)       Date:  2022-02-09       Impact factor: 2.430

Review 6.  Association between direct-acting antiviral agents in hepatitis C virus treatment and hepatocellular carcinoma occurrence and recurrence: The endless debate.

Authors:  Ahmed Kamal; Ahmed Elsheaita; Mahmoud Abdelnabi
Journal:  World J Clin Cases       Date:  2022-02-26       Impact factor: 1.337

7.  Seven gene signature explores the impact of DAAs on the appearance of hepatocellular carcinoma in HCV infected patients.

Authors:  Reham M Dawood; Mai Abd El-Meguid; Hend Ibrahim Shousha; Ahmed Elsayed; Mohamed Mahmoud Nabeel; Ayman Yosry; Ashraf Abdelaziz; Ghada M Salum
Journal:  Heliyon       Date:  2022-08-08

8.  Long-Term Outcomes and Evaluation of Hepatocellular Carcinoma Recurrence after Hepatitis C Virus Eradication by Direct-Acting Antiviral Treatment: All Kagawa Liver Disease Group (AKLDG) Study.

Authors:  Joji Tani; Tomonori Senoh; Akio Moriya; Chikara Ogawa; Akihiro Deguchi; Teppei Sakamoto; Kei Takuma; Mai Nakahara; Kyoko Oura; Tomoko Tadokoro; Shima Mimura; Koji Fujita; Hirohito Yoneyama; Hideki Kobara; Asahiro Morishita; Takashi Himoto; Akemi Tsutsui; Takuya Nagano; Koichi Takaguchi; Tsutomu Masaki
Journal:  Cancers (Basel)       Date:  2021-05-08       Impact factor: 6.639

Review 9.  Towards hepatitis C virus elimination: Egyptian experience, achievements and limitations.

Authors:  Dalia Omran; Mohamed Alboraie; Rania A Zayed; Mohamed-Naguib Wifi; Mervat Naguib; Mohamed Eltabbakh; Mohamed Abdellah; Ahmed Fouad Sherief; Sahar Maklad; Heba Hamdy Eldemellawy; Omar Khalid Saad; Doaa Mohamed Khamiss; Mohamed El Kassas
Journal:  World J Gastroenterol       Date:  2018-10-14       Impact factor: 5.742

Review 10.  Hepatocellular Carcinoma Recurrence in HCV Patients Treated with Direct Antiviral Agents.

Authors:  Marco Sanduzzi-Zamparelli; Loreto Boix; Cassia Leal; María Reig
Journal:  Viruses       Date:  2019-05-01       Impact factor: 5.048

  10 in total

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