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Sorafenib tosylate, Ribavirn and Sofosbuvir combination therapy for HCV virus infected patients with decompensated liver cancer

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dc.contributor.author Munir, Bushra
dc.contributor.author Ahmed, Bilal
dc.contributor.author Kiran, Shumaila
dc.contributor.author Jalal, Fatima
dc.contributor.author Zahoor, Muhammad Kashif
dc.contributor.author Shehzadi, Saba
dc.contributor.author Oranab, Sadaf
dc.contributor.author Kamran, Sayed Kashif Shahid
dc.contributor.author Ghaffar, Abdul
dc.date.accessioned 2022-12-15T05:16:41Z
dc.date.available 2022-12-15T05:16:41Z
dc.date.issued 2017-11-09
dc.identifier.citation Munir, B., Ahmed, B., Kiran, S., Jalal, F., Zahoor, M. K., Shehzadi, S., ... & Ghaffar, A. (2017). Sorafenib tosylate, Ribavirn and Sofosbuvir combination therapy for HCV virus infected patients with decompensated liver cancer. Pak J Pharm Sci, 30(6), 2383-2387. en_US
dc.identifier.issn 1011-601X
dc.identifier.uri http://142.54.178.187:9060/xmlui/handle/123456789/15130
dc.description.abstract : Hepatitis C is the most common health problem worldwide and is major cause of death due to proliferation of hepatocellular carcinoma. The medicines available for HCV treatment overcome up-to 95% complications of HCV. However, liver cancer needs some additional care. Normally Sorafenib tosylate 200 mg is recommended for liver cancer. There is no such trial in which this drug could effectively be used in combination of direct acting antivirals for HCV. The study was conducted for HCV patients (n=30) with liver cancer having decompensated stage. Combination of Sorafenib tosylate, Ribavirn and Sofosbuvir were used for the pharmacokinetics of these medicines. Child pugh score less then 7 (CP A) in adults during treatment phase (received 12 weeks of Sorafenib tosylate 200 mg, Ribavirn and Sofosbuvir 400 mg once daily) have no side effect while child pugh score 7-9 (CP B) have evidence of hypertension. The main efficiency end point sustained virology response with overcoming liver cancer as well in 12 weeks after end treatment (SVR-LLC 12). Mean pharmacokinetic exposure to Sorafenib tosylate 200 mg, Ribavirn and Sofosbuvir at week 8th was 2.1, 1.5,1.2 times greater in CP B than in CP A. Adverse effects (AEs) were observed in 12 out of 30 patients but not severe as lethal for life. Treatment with Sorafenib tosylate, Ribavirn and Sofosbuvir for twelve weeks was harmless and well accepted, 100 % patients achieve (SVR LLC 12) with 10-fold cure rate more than previous ones. The combination therapy of Sorafenib tosylate, Ribavirn and Sofosbuvir was found helpful for the management of decompensated liver cancer. en_US
dc.language.iso en en_US
dc.publisher Karachi: Faculty of Pharmacy & Pharmaceutical Sciences University of Karachi en_US
dc.subject Child pugh (CP) en_US
dc.subject sustained virologic response (SVR) en_US
dc.subject adverse effects (AEs) en_US
dc.title Sorafenib tosylate, Ribavirn and Sofosbuvir combination therapy for HCV virus infected patients with decompensated liver cancer en_US
dc.type Article en_US


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