TY - JOUR
T1 - Effect of Gender on the Response to Hepatitis C Treatment in an Inner-City Population
AU - Simoes, Priya
AU - Asaad, Adel
AU - Abed, Jean
AU - Engelson, Ellen S.
AU - Kotler, Donald P.
N1 - Funding Information:
Kotler DP: has received research and/or educational grants from Vertex , Merck , Boehringer Ingelheim , Gilead , Janssen and Genentech laboratories. He has also provided training sessions for Abbott and Boehringer Ingelheim. He is an unpaid Medical Director for a community-based program that identifies HCV-infected patients in the community and links them to medical care.
Publisher Copyright:
© 2015 Jacobs Institute of Women's Health.
PY - 2015/5/1
Y1 - 2015/5/1
N2 - Introduction: Hepatitis C virus (HCV) is the leading cause of cirrhosis, hepatocellular carcinoma, and liver transplantation in the United States. Response to treatment has improved with the addition of direct acting protease inhibitors. However, there are limited real-world data on the role of gender in achieving a sustained virologic response (SVR). Methods: We conducted a cross-sectional study in 70 patients treated for HCV, genotype 1 infection with pegylated alpha interferon, ribavirin, and either telaprevir or boceprevir at our inner-city liver clinic. Results: The SVR was significantly lower in women than in men (24% vs. 59%; p<.01). Statistical significance persisted after adjusting for age, race, genotype, prior treatment status, duration of therapy, and stage of fibrosis. The adjusted odds ratio for achieving SVR was significantly lower in women than in men (odds ratio [OR], 0.13; 95% CI, 0.03-0.58; p=01). Relapse after completing treatment was more likely to occur in women (p=02). Thirty-four patients (48%) did not complete therapy. Discontinuation because of loss to follow-up was more likely in women, whereas discontinuation owing to therapy limiting adverse drug events were more common in men. Discontinuation rates owing to failure of therapy were similar in men and women. Conclusions: There was a significant difference in SVR between men and women. Both biological and nonbiological factors, the latter including access to care, adherence to therapy, and attitudes of and toward health care providers all could play a role in contributing to the observed disparity between sexes in treatment response.
AB - Introduction: Hepatitis C virus (HCV) is the leading cause of cirrhosis, hepatocellular carcinoma, and liver transplantation in the United States. Response to treatment has improved with the addition of direct acting protease inhibitors. However, there are limited real-world data on the role of gender in achieving a sustained virologic response (SVR). Methods: We conducted a cross-sectional study in 70 patients treated for HCV, genotype 1 infection with pegylated alpha interferon, ribavirin, and either telaprevir or boceprevir at our inner-city liver clinic. Results: The SVR was significantly lower in women than in men (24% vs. 59%; p<.01). Statistical significance persisted after adjusting for age, race, genotype, prior treatment status, duration of therapy, and stage of fibrosis. The adjusted odds ratio for achieving SVR was significantly lower in women than in men (odds ratio [OR], 0.13; 95% CI, 0.03-0.58; p=01). Relapse after completing treatment was more likely to occur in women (p=02). Thirty-four patients (48%) did not complete therapy. Discontinuation because of loss to follow-up was more likely in women, whereas discontinuation owing to therapy limiting adverse drug events were more common in men. Discontinuation rates owing to failure of therapy were similar in men and women. Conclusions: There was a significant difference in SVR between men and women. Both biological and nonbiological factors, the latter including access to care, adherence to therapy, and attitudes of and toward health care providers all could play a role in contributing to the observed disparity between sexes in treatment response.
UR - http://www.scopus.com/inward/record.url?scp=84929084893&partnerID=8YFLogxK
U2 - 10.1016/j.whi.2015.02.008
DO - 10.1016/j.whi.2015.02.008
M3 - Article
C2 - 25965157
AN - SCOPUS:84929084893
SN - 1049-3867
VL - 25
SP - 289
EP - 293
JO - Women's Health Issues
JF - Women's Health Issues
IS - 3
ER -