Suppression of Blood Cell Formation during Chronic Hepatitis C Therapy with Different Interferon Alfa Mono- and Combination Therapy Regimens

Suppression of the formation of blood cells is a serious adverse event that results from the use of interferon alfa in chronic hepatitis C. Researchers at the University of Vienna evaluated the effects of four different IFN/IFN plus ribavirin treatment regimens on hematopoiesis (blood cell formation).

Hematopoiesis was studied in 133 patients with chronic hepatitis C receiving IFN-alfa-2b (Intron A) alone (group A) or in combination with ribavirin (group B), pegylated IFN-alfa-2a (Pegasys) alone (group C), or pegylated IFN-alfa-2b (group D) in combination with ribavirin.

Results

· At week 4, hemoglobin levels were diminished in all groups receiving combination therapy.

·  In the monotherapy group, hemoglobin decreased slightly after eight weeks.

· In all groups, hemoglobin remained diminished throughout therapy.

· In all patients, leucocytes (while blood cells) decreased after four weeks and remained low during treatment.

· Platelets (peripheral platelet count (PPC)) were decreased in all groups after four weeks and remained below baseline levels during therapy in group A, C, and D whereas in group B PPC recovered early and reached baseline levels at week 16 of therapy.

· Concomitantly with the decreases in hemoglobin and PPC, erythropoietin increased in all groups receiving combination therapy and thrombopoietin in all groups.

· Patients treated with pegylated IFN-alfa-2a (Pegasys) and those who received pegylated IFN-alfa-2b (PegIntron) combination therapy differed only in leucopoiesis, whereas erythropoiesis and thrombopoiesis were comparable.

In closing the authors conclude:

· IFN-alfa-based therapies are associated with a decrease in all three hematopoietic lineages, irrespective of the type of therapy used.

· The stronger suppressive effect of pegylated IFN-alfa-2a on leucopoiesis could be due to a dose effect.

· Overall, concentrations of endogenous hematopoietic growth factors are increased but can only partially alleviate hematotoxicity.

· Potential uses of exogenous hematopoietic growth factors and their impact on the virological response need to be explored.

Department of Internal Medicine IV, Division of Gastroenterology and Hepatology, University of Vienna, Wahringergurtel 18-20, A-1090 Vienna, Austria.

07/15/05

Reference
M Schmidt and others. Gut 54(7):1014-1020. July 2005.



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