Health-related Quality of Life in Patients with Previously Treated Advanced Urothelial Carcinoma from EV-301: A Phase 3 Trial of Enfortumab Vedotin Versus Chemotherapy.

Antineoplastic agents Cancer pain Immunoconjugates Patient-reported outcome measures Urinary bladder neoplasms

Journal

European urology
ISSN: 1873-7560
Titre abrégé: Eur Urol
Pays: Switzerland
ID NLM: 7512719

Informations de publication

Date de publication:
27 Feb 2024
Historique:
received: 31 10 2022
revised: 30 11 2023
accepted: 09 01 2024
medline: 29 2 2024
pubmed: 29 2 2024
entrez: 28 2 2024
Statut: aheadofprint

Résumé

In comparison to chemotherapy, enfortumab vedotin (EV) prolonged overall survival in patients with previously treated advanced urothelial carcinoma in EV-301. The objective of the present study was to assess patient experiences of EV versus chemotherapy using patient-reported outcome (PRO) analysis of health-related quality of life (HRQoL). For patients in the phase 3 EV-301 trial randomized to EV or chemotherapy we assessed responses to the validated European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (QLQ-C30) at baseline, weekly for the first 12 wk, and then every 12 wk until discontinuation. We analyzed the QLQ-C30 change from baseline to week 12, the confirmed improvement rate, and the time to improvement or deterioration. Baseline PRO compliance rates were 91% for the EV arm (n = 301) and 89% for the chemotherapy arm (n = 307); the corresponding average rates from baseline to week 12 were 70% and 67%. Patients receiving EV versus chemotherapy had reduced pain (difference in change from baseline to week 12: -5.7, 95% confidence interval [CI] -10.8 to -0.7; p = 0.027) and worsening appetite loss (7.3, 95% CI 0.90-13.69; p = 0.026). Larger proportions of patients in the EV arm reported HRQoL improvement from baseline than in the chemotherapy arm; the odds of a confirmed improvement across ten QLQ-C30 function/symptom scales were 1.67 to 2.76 times higher for EV than for chemotherapy. Patients in the EV arm had a shorter time to first confirmed improvement in global health status (GHS)/QoL, fatigue, pain, and physical, role, emotional, and social functioning (all p < 0.05). EV delayed the time to first confirmed deterioration in GHS/QoL (p = 0.027), but worsening appetite loss occurred earlier (p = 0.009) in comparison to chemotherapy. HRQoL with EV was maintained, and deterioration in HRQoL was delayed with EV in comparison to chemotherapy. Better results with EV were reported for some scales, with the greatest difference observed for pain. These findings reinforce the EV safety and efficacy outcomes and benefits observed in EV-301. Patients with previously treated advanced cancer of the urinary tract receiving the drug enfortumab vedotin maintained their HRQoL in comparison to patients treated with chemotherapy. The EV-301 trial is registered on ClinicalTrials.gov as NCT03474107 and on EudraCT as 2017-003344-21.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
In comparison to chemotherapy, enfortumab vedotin (EV) prolonged overall survival in patients with previously treated advanced urothelial carcinoma in EV-301. The objective of the present study was to assess patient experiences of EV versus chemotherapy using patient-reported outcome (PRO) analysis of health-related quality of life (HRQoL).
METHODS METHODS
For patients in the phase 3 EV-301 trial randomized to EV or chemotherapy we assessed responses to the validated European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 (QLQ-C30) at baseline, weekly for the first 12 wk, and then every 12 wk until discontinuation. We analyzed the QLQ-C30 change from baseline to week 12, the confirmed improvement rate, and the time to improvement or deterioration.
KEY FINDINGS AND LIMITATIONS UNASSIGNED
Baseline PRO compliance rates were 91% for the EV arm (n = 301) and 89% for the chemotherapy arm (n = 307); the corresponding average rates from baseline to week 12 were 70% and 67%. Patients receiving EV versus chemotherapy had reduced pain (difference in change from baseline to week 12: -5.7, 95% confidence interval [CI] -10.8 to -0.7; p = 0.027) and worsening appetite loss (7.3, 95% CI 0.90-13.69; p = 0.026). Larger proportions of patients in the EV arm reported HRQoL improvement from baseline than in the chemotherapy arm; the odds of a confirmed improvement across ten QLQ-C30 function/symptom scales were 1.67 to 2.76 times higher for EV than for chemotherapy. Patients in the EV arm had a shorter time to first confirmed improvement in global health status (GHS)/QoL, fatigue, pain, and physical, role, emotional, and social functioning (all p < 0.05). EV delayed the time to first confirmed deterioration in GHS/QoL (p = 0.027), but worsening appetite loss occurred earlier (p = 0.009) in comparison to chemotherapy.
CONCLUSIONS AND CLINICAL IMPLICATIONS CONCLUSIONS
HRQoL with EV was maintained, and deterioration in HRQoL was delayed with EV in comparison to chemotherapy. Better results with EV were reported for some scales, with the greatest difference observed for pain. These findings reinforce the EV safety and efficacy outcomes and benefits observed in EV-301.
PATIENT SUMMARY RESULTS
Patients with previously treated advanced cancer of the urinary tract receiving the drug enfortumab vedotin maintained their HRQoL in comparison to patients treated with chemotherapy. The EV-301 trial is registered on ClinicalTrials.gov as NCT03474107 and on EudraCT as 2017-003344-21.

Identifiants

pubmed: 38418343
pii: S0302-2838(24)00008-3
doi: 10.1016/j.eururo.2024.01.007
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT03474107']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

Jonathan E Rosenberg (JE)

Memorial Sloan Kettering Cancer Center, New York City, NY, USA. Electronic address: rosenbj1@mskcc.org.

Ronac Mamtani (R)

Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Guru P Sonpavde (GP)

Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.

Yohann Loriot (Y)

Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Ignacio Duran (I)

Hospital Universitario Marques de Valdecilla, IDIVAL, Santander, Spain.

Jae-Lyun Lee (JL)

Asan Medical Center and University of Ulsan College of Medicine, Seoul, South Korea.

Nobuaki Matsubara (N)

National Cancer Center Hospital East, Chiba, Japan.

Christof Vulsteke (C)

Center for Oncological Research, University of Antwerp, Integrated Cancer Center Ghent, Ghent, Belgium.

Daniel Castellano (D)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Srikala S Sridhar (SS)

Princess Margaret Cancer Center, Toronto, Canada.

Helle Pappot (H)

Region Hovedstaden, Hillerød, Denmark.

Howard Gurney (H)

Macquarie University, Sydney, Australia.

Jens Bedke (J)

Faculty of Medicine, Eberhard Karls University Tübingen, Tübingen, Germany.

Michiel S van der Heijden (MS)

Netherlands Cancer Institute, Amsterdam, The Netherlands.

Luca Galli (L)

Azienda Ospedaliero-Universitaria Pisana Spedali Riuniti S. Chiara, Pisa, Italy.

Bhumsuk Keam (B)

Seoul National University Hospital, Seoul, South Korea.

Naoya Masumori (N)

Sapporo Medical University, Sapporo, Japan.

Johannes Meran (J)

Internal Medicine 2, Krankenhaus der Barmherzigen Brüder Wien, Vienna, Austria.

Peter H O'Donnell (PH)

University of Chicago, Chicago, IL, USA.

Se Hoon Park (SH)

Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, South Korea.

Enrique Grande (E)

MD Anderson Cancer Center Madrid, Madrid, Spain.

Lisa Sengeløv (L)

Herlev Gentofte Hospital, Herlev, Denmark.

Hiroji Uemura (H)

Yokohama City University Medical Center, Yokohama, Japan.

Konstantina Skaltsa (K)

IQVIA, Barcelona, Spain.

Mary Campbell (M)

Seagen, Bothell, WA, USA.

Maria Matsangou (M)

Astellas Pharma, Northbrook, IL, USA.

Chunzhang Wu (C)

Astellas Pharma, Northbrook, IL, USA.

Zsolt Hepp (Z)

Seagen, Bothell, WA, USA.

Caroline McKay (C)

Astellas Pharma, Northbrook, IL, USA.

Thomas Powles (T)

Barts Cancer Centre, Queen Mary University of London, London, UK.

Daniel P Petrylak (DP)

Smilow Cancer Center, Yale School of Medicine, New Haven, CT, USA.

Classifications MeSH