TREATMENT OF CHRONIC HEPATITIS C IN THALASSAEMIA MAJOR

Li CK1, Chan PKS1, Ling SC2, Luk CW3, Ha SY5

1Prince of Wales Hospital, The Chinese University of Hong Kong, 2Princess Margaret Hospital, 3Queen Elizabeth Hospital, 4Queen Mary Hospital, Hong Kong, China

 

Objectives: To study the efficacy and side effects of combination treatment for chronic hepatitis C (HCV) infection in Chinese thalassaemia major (TM).

Methods: A multicentre prospective single arm study of using standard treatment protocol for HCV was conducted in Hong Kong. TM patients were eligible if they were positive for anti-HCV and HCV-RNA, with persistent elevation of liver enzyme (ALT) for at least 6 months, and liver biopsy showed chronic hepatitis. Patients were treated with interferon a (Intron A) at 3 miu/m2 subcutaneous 3 times per week, and ribavirin 16 mg/kg/day oral (round up to nearest 200 mg tablets). The treatment lasted for one year. Liver enzymes were monitored monthly before regular blood transfusion (biochemical response) and HCV RNA was monitored 3 monthly during and up to 6 months after stopping treatment (virological response).

Results: 18 TM patients were recruited with median age 16.4 years (range 7.2 ¨C 28.8), 10 males and 8 females. Genotype study showed 15 were of genotype 1b and 3 of genotype 6a. The HCV RNA levels at start of treatment were <5000 copies/ml in 6 patient, and >100000 copies/ml in 6 patients, and the others were in between. Biochemical response with normalisation of ALT were noted in 15 patients (83%) and mostly at 4 weeks of treatment and 3 non-responders all had persistent HCV infection. 17 patients had completed one year treatment and 12 had been followed up to 6 months after stopping treatment. The virological response at 3, 6, 12 months during treatment and 6 months after stopping treatment were 73%, 75%, 70% and 75% respectively. The blood consumption during treatment was increased by 30% and the body weight decreased by 6.6%. Leukopenia occurred in 39% and thrombocytopenia in 17%, dose reduction was required in 22%. Other common side effects included fever, fatigue, headache, bone pain and anorexia.

Conclusion: Interferon and ribavirin combination achieved a high biochemical and sustained virological response in Chinese TM patients. Ribavirin treatment was associated with a significant haemolysis requiring increased blood transfusion requirement.

 

 

 

 
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