Administration of low‐dose epoetin‐alpha facilitates adherence to ribavirin in triple therapy with pegylated interferon‐alpha‐2b and telaprevir. Issue 10 (7th January 2014)
- Record Type:
- Journal Article
- Title:
- Administration of low‐dose epoetin‐alpha facilitates adherence to ribavirin in triple therapy with pegylated interferon‐alpha‐2b and telaprevir. Issue 10 (7th January 2014)
- Main Title:
- Administration of low‐dose epoetin‐alpha facilitates adherence to ribavirin in triple therapy with pegylated interferon‐alpha‐2b and telaprevir
- Authors:
- Ishida, Hisashi
Sakane, Sadatsugu
Toyama, Takashi
Fukutomi, Keisuke
Kimura, Keiichi
Sugimoto, Aya
Hibino, Kenji
Tamura, Takeshi
Iwasaki, Tetsuya
Iwasaki, Ryuichiro
Hasegawa, Hiroko
Sakakibara, Yuko
Yamada, Takuya
Nakazuru, Shoichi
Mita, Eiji - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12224-sec-0001" sec-type="section"> <title>Aim</title> <p>Anemia frequently develops in patients given pegylated interferon, ribavirin (RBV), telaprevir (TVR) triple therapy and restricts treatment by forcing reduction or discontinuation of RBV administration. We investigated whether erythropoietin (EPO) could alleviate RBV‐induced anemia to help maintain the RBV dose during the first 12 weeks, the triple therapy phase.</p> </sec> <sec id="hepr12224-sec-0002" sec-type="section"> <title>Methods</title> <p>Twenty‐two patients with hepatitis C virus (HCV) genotype 1 were enrolled. Hemoglobin (Hb) concentration was measured every week. If Hb reduction from the baseline was 2 g/dL or more, 12 000 IU of epoetin‐α was administrated. When further reduction (≥3 g/dL) was observed, 24 000 IU of epoetin‐α was used. Inosine triphosphatase (ITPA) single nucleotide polymorphism (rs1127354) was genotyped for all patients.</p> </sec> <sec id="hepr12224-sec-0003" sec-type="section"> <title>Results</title> <p>Among the 22 patients enrolled in this study, three required RBV dose reduction due to anemia, two had to discontinue or reduce TVR and RBV due to creatinine elevation. The remaining 17 patients completed the treatment during the triple therapy phase without reduction of the RBV dose or adverse events attributable to EPO. Regardless of ITPA genotype, Hb decline was well controlled by EPO<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12224-sec-0001" sec-type="section"> <title>Aim</title> <p>Anemia frequently develops in patients given pegylated interferon, ribavirin (RBV), telaprevir (TVR) triple therapy and restricts treatment by forcing reduction or discontinuation of RBV administration. We investigated whether erythropoietin (EPO) could alleviate RBV‐induced anemia to help maintain the RBV dose during the first 12 weeks, the triple therapy phase.</p> </sec> <sec id="hepr12224-sec-0002" sec-type="section"> <title>Methods</title> <p>Twenty‐two patients with hepatitis C virus (HCV) genotype 1 were enrolled. Hemoglobin (Hb) concentration was measured every week. If Hb reduction from the baseline was 2 g/dL or more, 12 000 IU of epoetin‐α was administrated. When further reduction (≥3 g/dL) was observed, 24 000 IU of epoetin‐α was used. Inosine triphosphatase (ITPA) single nucleotide polymorphism (rs1127354) was genotyped for all patients.</p> </sec> <sec id="hepr12224-sec-0003" sec-type="section"> <title>Results</title> <p>Among the 22 patients enrolled in this study, three required RBV dose reduction due to anemia, two had to discontinue or reduce TVR and RBV due to creatinine elevation. The remaining 17 patients completed the treatment during the triple therapy phase without reduction of the RBV dose or adverse events attributable to EPO. Regardless of ITPA genotype, Hb decline was well controlled by EPO administration, whereas the total EPO dose tended to be higher in the CC genotype group. The average adherence to RBV during the triple therapy phase was 97.5%. SVR was achieved in 17 patients; two patients had viral breakthrough and three patients had relapse of HCV RNA.</p> </sec> <sec id="hepr12224-sec-0004" sec-type="section"> <title>Conclusion</title> <p>EPO can be a favorable alternative to reduction of RBV to facilitate the adherence of patients on TVR‐based triple therapy.</p> </sec> </abstract> … (more)
- Is Part Of:
- Hepatology research. Volume 44:Issue 10(2014:Oct.)
- Journal:
- Hepatology research
- Issue:
- Volume 44:Issue 10(2014:Oct.)
- Issue Display:
- Volume 44, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 44
- Issue:
- 10
- Issue Sort Value:
- 2014-0044-0010-0000
- Page Start:
- E84
- Page End:
- E91
- Publication Date:
- 2014-01-07
- Subjects:
- Liver -- Diseases -- Periodicals
Liver Diseases -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09284346 ↗
http://firstsearch.oclc.org/journal=1386-6346;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1872-034X ↗
http://www.sciencedirect.com/science/journal/13866346 ↗
http://www3.interscience.wiley.com/journal/118507311/home ↗
http://www.blackwell-synergy.com/rd.asp?goto=journal&code=hep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hepr.12224 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4235.xml