TY - JOUR
T1 - Pegylated IFN-α2b plus ribavirin as therapy for chronic hepatitis C in HIV-infected patients
AU - Pérez-Olmeda, Mayte
AU - Núñez, Marina
AU - Romero, Miriam
AU - González, Juan
AU - Castro, Angeles
AU - Arribas, José Ramón
AU - Pedreira, José
AU - Barreiro, Pablo
AU - García-Samaniego, Javier
AU - Martín-Carbonero, Luz
AU - Jiménez-Nácher, Inmaculada
AU - Soriano, Vincent
PY - 2003/5/2
Y1 - 2003/5/2
N2 - Background: Treatment of hepatitis C virus (HCV) has become a major challenge in HIV-infected individuals. No data exist on the efficacy and tolerability of pegylated IFN (peg-IFN) plus ribavirin in HIV-co-infected patients. Methods: Subcutaneous peg-IFN (150 μg weekly during the first 12 weeks and 100 μg weekly thereafter) plus ribavirin (400 mg twice a day) was given to 68 HIV-infected patients with chronic hepatitis C, having CD4 cell counts greater than 300 cells/μl, plasma HIV-RNA less than 5000 copies/ml, and elevated aminotransferase levels. All were naive for IFN, and 73% were receiving antiretroviral drugs. Results: Plasma HCV-RNA levels greater than 800000 IU/ml were seen in 50%, and 35% carried HCV genotype 3. Adverse events leading to treatment discontinuation occurred in 10 patients (15%). One patient taking didanosine developed pancreatitis. Severe weight loss occurred in 70% of patients. Clearance of HCV-RNA at the end of therapy (6 months for HCV-3 and 12 months for HCV-1/4) occurred in 50% of patients (81% with HCV-3 versus 30% with HCV-1/4). As 30% relapsed, the overall sustained response rate was 35% (28% in the intent-to-treat analysis). The main predictors of response were infection with HCV-3 and low HCV load. Conclusion: Treatment with peg-IFN and ribavirin is relatively well-tolerated in HIV/HCV-co-infected patients, although new side-effects, including pancreatitis and severe weight loss, may result from the interaction of ribavirin with antiretroviral drugs. Overall, therapy provides cure to one third of patients, a rate significantly lower than that seen in HCV-monoinfected individuals. Given that relapses are common, extended periods of therapy should be investigated.
AB - Background: Treatment of hepatitis C virus (HCV) has become a major challenge in HIV-infected individuals. No data exist on the efficacy and tolerability of pegylated IFN (peg-IFN) plus ribavirin in HIV-co-infected patients. Methods: Subcutaneous peg-IFN (150 μg weekly during the first 12 weeks and 100 μg weekly thereafter) plus ribavirin (400 mg twice a day) was given to 68 HIV-infected patients with chronic hepatitis C, having CD4 cell counts greater than 300 cells/μl, plasma HIV-RNA less than 5000 copies/ml, and elevated aminotransferase levels. All were naive for IFN, and 73% were receiving antiretroviral drugs. Results: Plasma HCV-RNA levels greater than 800000 IU/ml were seen in 50%, and 35% carried HCV genotype 3. Adverse events leading to treatment discontinuation occurred in 10 patients (15%). One patient taking didanosine developed pancreatitis. Severe weight loss occurred in 70% of patients. Clearance of HCV-RNA at the end of therapy (6 months for HCV-3 and 12 months for HCV-1/4) occurred in 50% of patients (81% with HCV-3 versus 30% with HCV-1/4). As 30% relapsed, the overall sustained response rate was 35% (28% in the intent-to-treat analysis). The main predictors of response were infection with HCV-3 and low HCV load. Conclusion: Treatment with peg-IFN and ribavirin is relatively well-tolerated in HIV/HCV-co-infected patients, although new side-effects, including pancreatitis and severe weight loss, may result from the interaction of ribavirin with antiretroviral drugs. Overall, therapy provides cure to one third of patients, a rate significantly lower than that seen in HCV-monoinfected individuals. Given that relapses are common, extended periods of therapy should be investigated.
KW - Antiretroviral therapy
KW - Hepatitis C
KW - HIV
KW - Pegylated interferon
KW - Ribavirin
UR - http://www.scopus.com/inward/record.url?scp=0038555663&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0038555663&partnerID=8YFLogxK
U2 - 10.1097/00002030-200305020-00011
DO - 10.1097/00002030-200305020-00011
M3 - Article
C2 - 12700452
AN - SCOPUS:0038555663
SN - 0269-9370
VL - 17
SP - 1023
EP - 1028
JO - AIDS
JF - AIDS
IS - 7
ER -