SOFOSBUVIR AND RIBAVIRIN

RESPONSE TO 16-WEEKS VERSUS 24-WEEKS DUAL THERAPY INCLUDING SOFOSBUVIR AND RIBAVIRIN, IN ALL CIRRHOTIC AND NON-CIRRHOTIC PATIENTS WITH HCV GENOTYPE- 3A INFECTION IN POPULATION OF KPKPAKISTAN

Authors

  • Nizamud din Khyber Medical College Peshawar.
  • Jamalud din Khyber Medical College Peshawar.
  • Abid Shah Khyber Medical College Peshawar.
  • Waheed Iqbal Khyber Medical College Peshawar.

DOI:

https://doi.org/10.29309/TPMJ/18.4587

Keywords:

Chronic Hepatitis-C, End of Treatment Response, Sofosbuvir

Abstract

Objectives: This study was conducted to evaluate the 16-weeks versus 24-weeks efficacy of sofosbuvir and ribavirin in HCV genotype-3a infection. Study Design: Open labeled, single center, longitudinal study. Setting: Khyber Medical College and Khyber Teaching Hospital, Peshawar. Period: The total duration of study was 6-months, starting from January 2017 to July 2017. Methods: Eighty patients with HCV genotype-3a infection were
enrolled. Patients were assigned into 4-groups (20 patients in each group), including group-A as treatment naïve non-cirrhotic, group-B as treatment naïve with liver cirrhosis, group-C as non-cirrhotic but non-responder to peg-interferon and ribavirin and group-D as non-responder
cirrhotic cases. Sofosbuvir plus ribavirin was given for 16-weeks and then extended to 24-weeks. The primary end point was end of treatment response with 16-weeks or 24-weeks therapy (EOT-16 or EOT-24), which is defined as HCV RNA level<40IU/ml after 16-weeks or 24-weeks of
therapy. Results: Out of all 80-patients, 50% (n=40) were male and 50% (n=40) were female, with mean age of 49±2 years. In all 80 cases, 67.5% (n=54/80) of patients have responded at 16 weeks, while 82.5% (n=66/80) of patients have responded to 24-weeks of therapy. In all 40 treatment naïve patients (group A and group B), 72.5% (n=29/40) have responded at 16 weeks, while 85% (n=34/40) of patients have responded to 24-weeks of therapy. Similarly, in all 40-previously non-responder cases (group C and group D), 62.5% (n=25/40) of patients have responded at 16 weeks, while 77.5% (n=31/40) of patients have responded to 24-weeks of therapy. Conclusion: Results of this study confirm that dual therapy given for 24-weeks is more effective compare to 16-weeks therapy in both treatment naïve and previously non-responder cases, which may be either cirrhotic or non-cirrhotic, with chronic hepatitis-C genotype-3a infections.

Author Biographies

Nizamud din, Khyber Medical College Peshawar.

MBBS, MPH, M.Phil, FCPS
Assistant Professor Pharmacology
and Consultant Physician

Jamalud din, Khyber Medical College Peshawar.

MBBS, FCPS,
Associate Professor
Department of Medicine

Abid Shah, Khyber Medical College Peshawar.

MBBS, FCPS (Medicine)
Assistant Professor
Department of Pharmacology

Waheed Iqbal, Khyber Medical College Peshawar.

BSc and M.Phil (Pharmacology
Chemist and Microbiologist

Downloads

Published

2018-12-08