Recombinant Zoster Vaccine Significantly Reduces the Impact on Quality of Life Caused by Herpes Zoster in Adult Autologous Hematopoietic Stem Cell Transplant Recipients: A Randomized Placebo-Controlled Trial (ZOE-HSCT).


Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
12 2019
Historique:
received: 17 06 2019
revised: 26 07 2019
accepted: 28 07 2019
pubmed: 9 8 2019
medline: 9 9 2020
entrez: 9 8 2019
Statut: ppublish

Résumé

Herpes zoster (HZ) can have a substantial impact on quality of life (QoL). The vaccine efficacy (VE) of a recombinant zoster vaccine (RZV) was 68.2% (95% confidence interval [CI], 55.6% to 77.5%) in a phase 3 study in adult autologous hematopoietic stem cell transplant (HSCT) recipients (NCT01610414). Herein, we report the impact of RZV on patients' QoL. Autologous HSCT recipients were randomized 1:1 to receive 2 doses of RZV or placebo, given 1 to 2 months apart. QoL was measured by the Short Form Survey-36 and Euro-QoL-5 Dimension at baseline, 1 month, and 1 year postdose 2 and during suspected HZ episodes with the Zoster Brief Pain Inventory (ZBPI). The RZV impact on ZBPI burden of illness and burden of interference scores was estimated. The 2 scores were calculated from the area under the curve (days 0 to 182) of the ZBPI worst pain and ZBPI activities of daily living scores, respectively, assuming a score of 0 for patients not having a confirmed HZ episode. The ZBPI maximum worst pain score was significantly lower in the RZV than placebo group (mean: 5.8 versus 7.1, P = .011). Consequently, the VE estimates for HZ burden of illness (82.5%; 95% CI, 73.6 to 91.4) and burden of interference (82.8%; 95% CI, 73.3 to 92.3) were higher than the HZ VE estimate (ie, 68.2%). RZV showed significantly better QoL scores than placebo 1 week following rash onset among patients with confirmed HZ. In addition to reducing the risk of HZ and its complications, RZV significantly reduced the impact of HZ on patients' QoL in those who developed breakthrough disease.

Identifiants

pubmed: 31394276
pii: S1083-8791(19)30508-7
doi: 10.1016/j.bbmt.2019.07.036
pii:
doi:

Substances chimiques

Chickenpox Vaccine 0
Vaccines, Synthetic 0

Banques de données

ClinicalTrials.gov
['NCT01610414']

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2474-2481

Informations de copyright

Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Desmond Curran (D)

GSK, Wavre, Belgium. Electronic address: desmond.x.curran@gsk.com.

Sean Matthews (S)

Freelance c/o GSK, Wavre, Belgium.

Scott D Rowley (SD)

Hackensack University Medical Center, Hackensack, New Jersey.

Jo-Anne H Young (JH)

University of Minnesota, Minneapolis, Minnesota.

Adriana Bastidas (A)

GSK, Wavre, Belgium.

Achilles Anagnostopoulos (A)

Haematology Department, G. Papanikolaou General Hospital of Thessaloniki, Thessaloniki, Greece.

Ibrahim Barista (I)

Hacettepe University Medical Faculty, Ankara, Turkey.

Pranatharthi Haran Chandrasekar (PH)

Karmanos Cancer Center, Wayne State University, Detroit, Michigan.

Michael Dickinson (M)

Clinical Haematology, Peter MacCallum Cancer Centre and Royal Melbourne Hospital, Melbourne, Victoria, Australia; Sir Peter MacCallum Department of Oncology, University of Melbourne, Melbourne, Victoria, Australia.

Mohamed El Idrissi (M)

GSK, Rixensart, Belgium.

Inmaculada Heras (I)

Hospital General Universitario J. M. Morales Meseguer, Murcia, Spain.

Samuel T Milliken (ST)

Department of Haematology, St Vincent's Hospital, Darlinghurst, New South Wales, Australia.

Jorge Monserrat Coll (J)

Hospital Virgen de la Arrixaca, Murcia (El Palmar), Spain.

María Belén Navarro Matilla (MB)

Hospital Puerta de Hierro, Majadahonda (Madrid), Spain.

Lidia Oostvogels (L)

GSK, Wavre, Belgium.

Beata Piątkowska-Jakubas (B)

Department of Haematology, Jagiellonian University Medical College, Cracow, Poland.

Dimas Quiel (D)

Complejo Hospitalario Dr. Arnulfo Arias Madrid, Panama, Panama.

Waleed Sabry (W)

Saskatoon Cancer Centre, Saskatoon, Saskatchewan, Canada.

Stefan Schwartz (S)

Department of Hematology and Oncology, Charité University Medical Center, Berlin, Germany.

Dominik L D Selleslag (DLD)

Hematologie, AZ Sint-Jan Brugge-Oostende AV-Campus Sint-Jan, Brugge, Belgium.

Keith M Sullivan (KM)

Duke University Medical Center, Durham, North Carolina.

Koen Theunissen (K)

Jessa Ziekenhuis-Campus Virga Jesse, Hasselt, Belgium.

Zeynep Arzu Yegin (ZA)

Gazi University Medical Faculty, Ankara, Turkey.

Su-Peng Yeh (SP)

Department of Hematology, China Medical University Hospital, Taichung, Taiwan.

Francesco Zaja (F)

Clinica Ematologica, Azienda Ospedaliero Universitaria S. Maria Misericordia, Friuli-Venezia-Giulia, Udine, Italy.

Jeff Szer (J)

Royal Melbourne Hospital, Melbourne, Victoria, Australia.

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Classifications MeSH