Abstract
All-oral direct-acting antiviral drugs (DAAs) for hepatitis C virus, which have response rates of 95% or more, represent a major clinical advance. However, the high list price of DAAs has led many governments to restrict their reimbursement. We reviewed the availability of, and national criteria for, interferon-free DAA reimbursement among countries in the European Union and European Economic Area, and Switzerland. Reimbursement documentation was reviewed between Nov 18, 2016, and Aug 1, 2017. Primary outcomes were fibrosis stage, drug or alcohol use, prescriber type, and HIV co-infection restrictions. Among the 35 European countries and jurisdictions included, the most commonly reimbursed DAA was ombitasvir, paritaprevir, and ritonavir, with dasabuvir, and with or without ribavirin (33 [94%] countries and jurisdictions). 16 (46%) countries and jurisdictions required patients to have fibrosis at stage F2 or higher, 29 (83%) had no listed restrictions based on drug or alcohol use, 33 (94%) required a specialist prescriber, and 34 (97%) had no additional restrictions for people co-infected with HIV and hepatitis C virus. These findings have implications for meeting WHO targets, with evidence of some countries not following the 2016 hepatitis C virus treatment guidelines by the European Association for the Study of Liver.
Original language | English |
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Pages (from-to) | 125-133 |
Number of pages | 9 |
Journal | The Lancet Gastroenterology and Hepatology |
Volume | 3 |
Issue number | 2 |
DOIs | |
Publication status | Published - Feb 2018 |
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In: The Lancet Gastroenterology and Hepatology, Vol. 3, No. 2, 02.2018, p. 125-133.
Research output: Contribution to journal › Article › Research › peer-review
TY - JOUR
T1 - Restrictions for reimbursement of interferon-free direct-acting antiviral drugs for HCV infection in Europe
AU - Marshall, Alison D.
AU - Cunningham, Evan B.
AU - Nielsen, Stine
AU - Aghemo, Alessio
AU - Alho, Hannu
AU - Backmund, Markus
AU - Bruggmann, Philip
AU - Dalgard, Olav
AU - Seguin-Devaux, Carole
AU - Flisiak, Robert
AU - Foster, Graham R.
AU - Gheorghe, Liana
AU - Goldberg, David
AU - Goulis, Ioannis
AU - Hickman, Matthew
AU - Hoffmann, Patrick
AU - Jancorienė, Ligita
AU - Jarcuska, Peter
AU - Kåberg, Martin
AU - Kostrikis, Leondios G.
AU - Makara, Mihály
AU - Maimets, Matti
AU - Marinho, Rui Tato
AU - Matičič, Mojca
AU - Norris, Suzanne
AU - Ólafsson, Sigurður
AU - Øvrehus, Anne
AU - Pawlotsky, Jean Michel
AU - Pocock, James
AU - Robaeys, Geert
AU - Roncero, Carlos
AU - Simonova, Marieta
AU - Sperl, Jan
AU - Tait, Michele
AU - Tolmane, Ieva
AU - Tomaselli, Stefan
AU - van der Valk, Marc
AU - Vince, Adriana
AU - Dore, Gregory J.
AU - Lazarus, Jeffrey V.
AU - Grebely, Jason
AU - on behalf of the
AU - International Network on Hepatitis in Substance Users (INHSU)
N1 - Funding Information: AA has received a research grant from Gilead Sciences, is on the advisory board for Janssen, Merck Sharp & Dohme, Bristol-Myers Squibb, Gilead Sciences, and AbbVie, and has received personal fees from Janssen, Merck Sharp & Dohme, Bristol-Myers Squibb, Gilead Sciences, and AbbVie, outside the submitted work. PB has received grants and personal fees from AbbVie, Merck Sharp & Dohme, Gilead Sciences, and Bristol-Myers Squibb, outside the submitted work. OD has received grants from Gilead Sciences, and grants and personal fees from AbbVie and Merck Sharp & Dohme, outside the submitted work. CS-D has received grants from Gilead Sciences, outside the submitted work. GJD has received grants from AbbVie, Merck Sharp & Dohme, Bristol-Myers Squibb, Janssen, and Roche, personal fees from Gilead Sciences, AbbVie, Merck Sharp & Dohme, Bristol-Myers Squibb, Janssen, Roche, GlaxoSmithKline, and Abbott Diagnostics, and non-financial support from Gilead Sciences, AbbVie, Merck Sharp & Dohme, Bristol-Myers Squibb, and Roche, outside the submitted work. RF has received grants and personal fees from AbbVie, Gilead Sciences, Merck Sharp & Dohme, and Roche, and personal fees from Janssen, outside the submitted work. GRF has received grants and personal fees from Merck Sharp & Dohme, Gilead Sciences, and AbbVie during the conduct of the study, outside the submitted work, and is the National Clinical Lead for Hepatitis C in England. JG has received grants from AbbVie, Bristol-Myers Squibb, and Cepheid, and grants and personal fees from Gilead Sciences and Merck Sharp & Dohme, outside the submitted work. LG has received personal fees from AbbVie, Bristol-Myers Squibb, Gilead Sciences, and Merck Sharp & Dohme, and is part of the consulting and advisory board for Merck Sharp & Dohme, AbbVie, and Gilead Sciences. DG has received personal fees (honoraria) from Gilead Sciences, AbbVie, and Merck for lectures not related to products, outside the submitted work. MH has received personal fees from Merck Sharp & Dohme, AbbVie, and Gilead Sciences, outside the submitted work. LJ has received personal fees and non-financial support from Merck Sharp & Dohme and AbbVie, outside the submitted work. PJ has received personal fees and non-financial support from AbbVie and Gilead Sciences, and personal fees from Merck Sharp & Dohme, outside the submitted work. MK has received grants and personal fees from Gilead Sciences and personal fees from AbbVie and Merck Sharp & Dohme, outside the submitted work. JVL has received research grants and personal fees from AbbVie, Gilead Sciences, and Merck Sharp & Dohme, outside the submitted work. MMak has been an investigator in clinical trials for Novartis, Bristol-Myers Squibb, Janssen-Cilag, AbbVie, Roche, Boehringer-Ingelheim, Merck Sharp & Dohme, and Regulus, and has received personal fees from Janssen-Cilag, AbbVie, Roche, Boehringer-Ingelheim, Merck Sharp & Dohme, and Gilead Sciences, outside the submitted work. RTM has received personal fees, advisory board fees, and speaker fees from AbbVie, Merck Sharp & Dohme, and Gilead Sciences. SÓ has received personal fees from Merck Sharp & Dohme, outside the submitted work. CR has received speaker fees from Janssen-Cilag, Ferrer-Brainfarma, Pfizer, Reckitt-Benckiser/Indivior, Lundbeck, Otsuka, Servier, Lilly, GlaxoSmithKline, Astra, Sanofi, and Excelsis, received financial compensation for participation as a member of Janseen-Cilag, Indivior, Gilead Sciences, Merck Sharp & Dohme, and Munidipharma advisory boards, and received grants funded by Reckitt-Benckisert/Indivior and Gilead Sciences, outside the submitted work. AØ has received personal, travel, speaker, and consultancy fees from AbbVie, grants, personal fees, travel fees, and consultancy fees from Gilead Sciences, personal fees from Bristol-Myers Squibb, and travel fees from Merck Sharp & Dohme, outside the submitted work. J-MP has received grants and personal fees from Abbvie, grants and personal fees from Gilead Sciences, and personal fees from Merck, outside the submitted work. JP has received non-financial support from Gilead Sciences and AbbVie, outside the submitted work. MS has received speaker fees from AbbVie, Gilead Sciences, and Merck, and has been an advisor for AbbVie, Gilead Sciences, and Merck, outside the submitted work. JS has received grants and personal fees from AbbVie, and personal fees from Merck, Gilead Sciences, Bristol-Myers Squibb, and Herbacos Recordati, outside the submitted work. GR has received research grants from Merck Sharp & Dohme, AbbVie, Janssen Pharmaceuticals, and has acted as a consultant and advisor for Gilead Sciences, AbbVie, Merck Sharp & Dohme, and Bristol-Myers Squibb. IT has received honoraria for lectures from Merck Sharp & Dohme and AbbVie. MvdV has received personal fees from AbbVie, Bristol-Myers Squibb, Johnson & Johnson, and ViiV Healthcare, grants and personal fees from Gilead Sciences, and grants, personal fees, and non-financial support from Merck Sharp & Dohme, outside the submitted work. AV has received personal fees and non-financial support from Gilead Sciences, and personal fees from Merck Sharp & Dohme and AbbVie during the conduct of this study. SNi declares non-financial support from INHSU. ADM, EBC, HA, MB, MMai, MMat, IC, LGK, SNo, and ST declare no competing interests. Funding Information: We thank the following people for their assistance with retrieval and interpretation of documentation: Håvard Midgard (Department of Infectious Diseases, Akershus University Hospital, Norway; Institute for Clinical Medicine, University of Oslo, Norway; Department of Gastroenterology, Oslo University Hospital, Norway), Ecaterina Filep, Gerard Estivill Mercade, Marcel Schulz, Rainer Puhr (The Kirby Institute, UNSW, Sydney, NSW, Australia), Petros Katsioloudes (Ministry of Health, Cyprus), and Ioannis Demetriades (Grigorios Clinic, Larnaca General Hospital, Cyprus). We also thank The All Wales Therapeutics and Toxicology Centre (Penarth, UK), and the National Institute for Health Research Health Protection Research Unit in Evaluation of Interventions (University of Bristol, UK). ADM holds a University International Postgraduate Award from UNSW (Sydney, Australia). ADM and EBC are supported by the CanHepC Trainee Program (Canada). JG and GJD are supported by a National Health and Medical Research Council Career Development Fellowship. The Kirby Institute is funded by the Australian Government Department of Health. The views expressed in this publication do not necessarily represent the position of the Australian Government. Publisher Copyright: © 2018 Elsevier Ltd
PY - 2018/2
Y1 - 2018/2
N2 - All-oral direct-acting antiviral drugs (DAAs) for hepatitis C virus, which have response rates of 95% or more, represent a major clinical advance. However, the high list price of DAAs has led many governments to restrict their reimbursement. We reviewed the availability of, and national criteria for, interferon-free DAA reimbursement among countries in the European Union and European Economic Area, and Switzerland. Reimbursement documentation was reviewed between Nov 18, 2016, and Aug 1, 2017. Primary outcomes were fibrosis stage, drug or alcohol use, prescriber type, and HIV co-infection restrictions. Among the 35 European countries and jurisdictions included, the most commonly reimbursed DAA was ombitasvir, paritaprevir, and ritonavir, with dasabuvir, and with or without ribavirin (33 [94%] countries and jurisdictions). 16 (46%) countries and jurisdictions required patients to have fibrosis at stage F2 or higher, 29 (83%) had no listed restrictions based on drug or alcohol use, 33 (94%) required a specialist prescriber, and 34 (97%) had no additional restrictions for people co-infected with HIV and hepatitis C virus. These findings have implications for meeting WHO targets, with evidence of some countries not following the 2016 hepatitis C virus treatment guidelines by the European Association for the Study of Liver.
AB - All-oral direct-acting antiviral drugs (DAAs) for hepatitis C virus, which have response rates of 95% or more, represent a major clinical advance. However, the high list price of DAAs has led many governments to restrict their reimbursement. We reviewed the availability of, and national criteria for, interferon-free DAA reimbursement among countries in the European Union and European Economic Area, and Switzerland. Reimbursement documentation was reviewed between Nov 18, 2016, and Aug 1, 2017. Primary outcomes were fibrosis stage, drug or alcohol use, prescriber type, and HIV co-infection restrictions. Among the 35 European countries and jurisdictions included, the most commonly reimbursed DAA was ombitasvir, paritaprevir, and ritonavir, with dasabuvir, and with or without ribavirin (33 [94%] countries and jurisdictions). 16 (46%) countries and jurisdictions required patients to have fibrosis at stage F2 or higher, 29 (83%) had no listed restrictions based on drug or alcohol use, 33 (94%) required a specialist prescriber, and 34 (97%) had no additional restrictions for people co-infected with HIV and hepatitis C virus. These findings have implications for meeting WHO targets, with evidence of some countries not following the 2016 hepatitis C virus treatment guidelines by the European Association for the Study of Liver.
UR - http://www.scopus.com/inward/record.url?scp=85041530359&partnerID=8YFLogxK
UR - https://www.ncbi.nlm.nih.gov/pubmed/28986139
U2 - 10.1016/S2468-1253(17)30284-4
DO - 10.1016/S2468-1253(17)30284-4
M3 - Article
C2 - 28986139
AN - SCOPUS:85041530359
SN - 2468-1253
VL - 3
SP - 125
EP - 133
JO - The Lancet Gastroenterology and Hepatology
JF - The Lancet Gastroenterology and Hepatology
IS - 2
ER -