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RESEARCH PRODUCT

Effects of Ribavirin Dose Reduction vs Erythropoietin for Boceprevir-Related Anemia in Patients With Chronic Hepatitis C Virus Genotype 1 Infection—A Randomized Trial

Fred PoordadEric LawitzK. Rajender ReddyNezam H. AfdhalChristophe HézodeStefan ZeuzemSamuel LeeJose Luis CallejaRobert BrownAntonio CraxìHeiner WedemeyerL. M. NybergDavid NelsonLorenzo RossaroLuis BalartTimothy MorganBruce BaconSteven FlammKris KowdleyWeiping DengKenneth KouryLisa PediconeFrank DutkoMargaret BurroughsKatia AlvesJanice WahlClifford BrassJanice AlbrechtMark SulkowskiR. BaileyC. CooperS.v. FeinmanP. MarottaE. TamF. WongMarc BourlièreJean-pierre BronowickiChristophe HezodeA. TranTobias GoeserD. KlassR. SchmidM. PirisiM. ZuinM. BennettD. BernsteinT. BoxT. BoyerD. ClainJ. CrippinM. DavisFranco FelizartaBradley FreilichJoseph GalatiG. GallerReem GhalibA. GibasE. GodofskyF. GordonS. GordonJ. GrossS. HarrisonJ. HerreraS. HerrineR. HerringI. JacobsonS. JoshiA. KilbyJ. KingA. KochKris V KowdleyP. KwoE. LebovicsW. LeeJ. LevinXiaojian LiVelimir LuketicM. MailliardJonathan McconeD. MikolichA. MuirK. MullenF. NunesA. NybergP. PandyaM. PaulyC. PeineGary PoleynardJ. PoulosD. PoundM. RabinovitzNatarajan RavendhranR. ReddyRobert ReindollarA. ReubenT. RileyR. RubinM. RussoM. RyanS. SaabJ. SantoroW. SchmidtT. SepeK. ShermanMarketa SjögrenJ. SlimC. SmithL. SteinR. StraussH. VargasJohn VierlingD. WittG. WuZ. Younes

subject

Maleviruses[SDV]Life Sciences [q-bio]Hepacivirusmedicine.disease_causeGastroenterologyPolyethylene Glycolslaw.inventionchemistry.chemical_compound0302 clinical medicineRandomized controlled triallawErythropoiesisIncidenceGastroenterologyDisease Managementvirus diseasesAnemiaMiddle AgedRecombinant Proteins3. Good healthTreatment Outcome030220 oncology & carcinogenesisDrug Therapy CombinationFemale030211 gastroenterology & hepatologyAlgorithmsmedicine.drugmedicine.medical_specialtyGenotypeProlineSide effectAnemiaHepatitis C virusInterferon alpha-2Antiviral Agents03 medical and health sciencesInternal medicineBoceprevirRibavirinmedicineHumansErythropoietinDAADose-Response Relationship DrugHepatologybusiness.industryRibavirinInterferon-alphaHepatitis C Chronicbiochemical phenomena metabolism and nutritionmedicine.diseasedigestive system diseasesSide EffectLogistic ModelschemistryErythropoietinImmunologyHemoglobinbusinessEPO

description

International audience; Background & AimsTreatment of hepatitis C virus (HCV) infection with boceprevir, peginterferon, and ribavirin can lead to anemia, which has been managed by reducing ribavirin dose and/or erythropoietin therapy. We assessed the effects of these anemia management strategies on rates of sustained virologic response (SVR) and safety.MethodsPatients (n = 687) received 4 weeks of peginterferon and ribavirin followed by 24 or 44 weeks of boceprevir (800 mg, 3 times each day) plus peginterferon and ribavirin. Patients who became anemic (levels of hemoglobin approximately ≤10 g/dL) during the study treatment period (n = 500) were assigned to groups that were managed by ribavirin dosage reduction (n = 249) or erythropoietin therapy (n = 251).ResultsRates of SVR were comparable between patients whose anemia was managed by ribavirin dosage reduction (71.5%) vs erythropoietin therapy (70.9%), regardless of the timing of the first intervention to manage anemia or the magnitude of ribavirin dosage reduction. There was a threshold for the effect on rate of SVR: patients who received <50% of the total milligrams of ribavirin assigned by the protocol had a significantly lower rate of SVR (P < .0001) than those who received ≥50%. Among patients who did not develop anemia, the rate of SVR was 40.1%. Eleven thromboembolic adverse events were reported in 9 of 295 patients who received erythropoietin, compared with 1 of 392 patients who did not receive erythropoietin.ConclusionsReduction of ribavirin dosage can be the primary approach for management of anemia in patients receiving peginterferon, ribavirin, and boceprevir for HCV infection. Reduction in ribavirin dosage throughout the course of triple therapy does not affect rates of SVR. However, it is important that the patient receives at least 50% of the total amount (milligrams) of ribavirin assigned by response-guided therapy.

10.1053/j.gastro.2013.07.051https://hal.univ-lorraine.fr/hal-01707324