Preference for the fixed-dose combination of pertuzumab and trastuzumab for subcutaneous injection in patients with HER2-positive early breast cancer (PHranceSCa): A randomised, open-label phase II study.
Adult
Aged
Aged, 80 and over
Antibodies, Monoclonal, Humanized
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Breast Neoplasms
/ diagnosis
Chemotherapy, Adjuvant
/ methods
Cross-Over Studies
Drug Combinations
Female
Humans
Infusions, Intravenous
/ adverse effects
Injections, Subcutaneous
/ adverse effects
Middle Aged
Neoadjuvant Therapy
/ methods
Neoplasm Staging
Patient Preference
/ statistics & numerical data
Patient Satisfaction
Receptor, ErbB-2
/ analysis
Trastuzumab
/ administration & dosage
Young Adult
Adjuvant
Early breast cancer
Fixed dose
Healthcare resource
Patient preference
Patient-reported outcomes
Pertuzumab
Quality of life
Subcutaneous
Trastuzumab
Journal
European journal of cancer (Oxford, England : 1990)
ISSN: 1879-0852
Titre abrégé: Eur J Cancer
Pays: England
ID NLM: 9005373
Informations de publication
Date de publication:
07 2021
07 2021
Historique:
received:
05
01
2021
revised:
04
03
2021
accepted:
16
03
2021
pubmed:
20
6
2021
medline:
11
11
2021
entrez:
19
6
2021
Statut:
ppublish
Résumé
The aim of the study was to assess patient preference for the fixed-dose combination of pertuzumab and trastuzumab for subcutaneous injection (PH FDC SC) in patients with HER2-positive early breast cancer in PHranceSCa (NCT03674112). Patients who completed neoadjuvant P + H + chemotherapy + surgery were randomised 1:1 to three intravenous (IV) P + H cycles followed by three cycles of PH FDC SC or vice versa (crossover) and then chose subcutaneous (SC) injection or IV infusion to continue up to 18 cycles (continuation). Assessments were via patient and healthcare professional (HCP) questionnaires. One hundred and sixty patients were randomised (cut-off: 24 February 2020); 136 (85.0%, 95% confidence interval: 78.5-90.2%) preferred SC; 22 (13.8%) preferred IV; 2 (1.3%) had no preference. The main reasons for SC preference were reduced clinic time (n = 119) and comfort during administration (n = 73). One hundred and forty-one patients (88.1%) were very satisfied/satisfied with SC injection versus 108 (67.5%) with IV infusion; 86.9% chose PH FDC SC continuation. HCP perceptions of median patient treatment room time ranged from 33.0-50.0 min with SC and 130.0-300.0 min with IV. Most adverse events (AEs) were grade 1/2 (no 4/5s); serious AE rates were low. AE rates before and after switching were similar (cycles 1-3 IV → cycles 4-6 SC: 77.5% → 72.5%; cycles 1-3 SC → cycles 4-6 IV: 77.5% → 63.8%). Most patients strongly preferred PH FDC SC over P + H IV. PH FDC SC was generally well tolerated, with no new safety signals (even when switching), and offers a quicker alternative to IV infusion.
Identifiants
pubmed: 34147014
pii: S0959-8049(21)00214-8
doi: 10.1016/j.ejca.2021.03.047
pii:
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Drug Combinations
0
ERBB2 protein, human
EC 2.7.10.1
Receptor, ErbB-2
EC 2.7.10.1
pertuzumab
K16AIQ8CTM
Trastuzumab
P188ANX8CK
Banques de données
ClinicalTrials.gov
['NCT03674112']
Types de publication
Clinical Trial, Phase II
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
223-232Investigateurs
Ernesto Korbenfeld
(E)
Jorge Nadal
(J)
Helio Pinczowski
(H)
Felipe J Cruz
(FJ)
Gustavo Sousa
(G)
Aline C Goncalves
(AC)
Gisah Guilgen
(G)
Mauricio Burotto
(M)
Antti Jekunen
(A)
Päivi Auvinen
(P)
Winne Yeo
(W)
Chi K Cheng
(CK)
Hikmat A Razeq
(HA)
Fadi Karak
(F)
Fadi Farhat
(F)
Servando C Huerta
(SC)
Brizio M Jaime
(BM)
Juan Feregrino
(J)
Omar Castillo-Fernandez
(O)
Juan C Alcedo
(JC)
Leonor Ribeiro
(L)
Maria Dionisio
(M)
Susana Sousa
(S)
Catarina Pulido
(C)
Salha Bujassoum
(S)
Hatoon Bakhraibah
(H)
Ana Cvetanovic
(A)
Ljiljana Stamatovic
(L)
Alvaro R Lescure
(AR)
Josefina Cruz
(J)
Camilla Wendt
(C)
Sara Margolin
(S)
Helena G Björneklett
(HG)
Michelina Cairo
(M)
Shaker Dakhil
(S)
Nguyet Le-Lindqwister
(N)
Ling Ma
(L)
Kristi J McIntyre
(KJ)
Joyce O'Shaughnessy
(J)
Svetislava J Vukelja
(SJ)
Donald Richards
(D)
Sharon Wilks
(S)
John Wallmark
(J)
Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.
Déclaration de conflit d'intérêts
Conflict of interest statement J.O.'S. reports consultancy/advisory roles for AbbVie, Agendia, Amgen, AstraZeneca, BMS, Celgene, Eisai, Genentech, Inc., Immunomedics, Ipsen, Lilly, Merck, Novartis, Odonate, Pfizer, Puma, Prime Oncology, F. Hoffmann-La Roche Ltd, Seattle Genetics and Daiichi Sankyo. S.S. reports funding for travelling, congresses, lectures and advisory boards from F. Hoffmann-La Roche Ltd, Novartis, Pfizer, Tesaro, AstraZeneca, MSD, Pierre Fabre and Eisai. J.C. reports speaker honoraria from GSK, AstraZeneca, F. Hoffmann-La Roche Ltd, Novartis, PharmaMar, Eisai, Lilly, Celgene, Astellas, Amgen and Pfizer and consultant/advisory roles for GSK, AstraZeneca, F. Hoffmann-La Roche Ltd, Novartis, PharmaMar, Eisai, Lilly, Celgene, Astellas, Amgen and Pfizer. L.F. reports honoraria from Pfizer, AstraZeneca, BMS, Lilly, Novartis, Exact Sciences and Veracyte. P.A. reports funding for the ESMO Breast Cancer Congress 2019. C.P. reports public speaking for AstraZeneca, Grunenthal and Novartis and writing engagements from AstraZeneca. A.C. reports speaker honoraria from Novartis, Pfizer, AstraZeneca and F. Hoffmann-La Roche Ltd. S.W. reports payment for an advisory board from Seattle Genetics. L.R. reports payments for speaking and advisory boards from Roche Pharmaceuticals, Merck Serono, MSD, BMS, AstraZeneca and Pfizer and for personal medical education and participation in congresses from BMS, Roche Pharmaceuticals, Merck Serono, Pfizer, Amgen and Pierre Fabre. M.B. reports payments for advisory boards, speaking at industry symposiums and consulting roles from F. Hoffmann-La Roche Ltd, MSD, BMS, AstraZeneca and Novartis. D.K. is an employee of, and owns stocks in, F. Hoffmann-La Roche Ltd. D.M. is an employee of F. Hoffmann-La Roche Ltd. A.A. is an employee of Roche Products Limited and owns stocks in F. Hoffmann-La Roche Ltd. P.T. is an employee of, and owns stocks in, Genentech, Inc. J.F. is an employee of F. Hoffmann-La Roche Ltd. Z.M. is an employee of, and owns stocks in, F. Hoffmann-La Roche Ltd. L.S. reports speaker honoraria from AstraZeneca, Novartis, Pfizer and F. Hoffmann-La Roche Ltd. All authors have received research support in the form of third-party writing assistance for this manuscript from F. Hoffmann-La Roche Ltd.