Challenges for quality and utilization of real-world data for diffuse large B-cell lymphoma in REALYSA, a LYSA cohort.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
24 Oct 2023
Historique:
accepted: 01 10 2023
received: 30 05 2023
revised: 05 09 2023
medline: 24 10 2023
pubmed: 24 10 2023
entrez: 24 10 2023
Statut: aheadofprint

Résumé

Real-world data are essential to complement clinical trial (CT) data, but major challenges remain, like data quality. REal world dAta in LYmphoma and Survival in Adults (REALYSA) is a prospective non-interventional multicentric cohort started in 2018 (NCT03869619) including patients newly diagnosed with lymphoma in France. Herein is a proof-of-concept analysis on first-line DLBCL patients to (i) evaluate the capacity of the cohort to provide robust data through a multi-step validation process; (ii) assess the consistency of the results; (iii) conduct an exploratory transportability assessment of two recent phase 3 CT (POLARIX, SENIOR). The analysis population comprised DLBCL patients included before March 31st 2021, who received immunochemotherapy. 645 patients were included, for whom 3589 queries were generated, resulting in high data completeness (<4% missing data). Median age was 66 years (19-98) with mostly advanced-stage disease (472; 73%) and high international prognostic index (IPI) score (IPI 2-5, 486; 76%). Treatments were mostly R-CHOP (482; 75%) and R-miniCHOP (86; 13%). Estimated 1-year EFS and OS were 77.9% (95% CI: 73.8-81.4) and 90.0% (95% CI: 86.5-92.5), respectively (median follow-up: 9.9 months). Regarding transportability, when applying trials' main inclusion criteria (age, PS, IPI), outcomes seemed comparable between REALYSA patients and standard arms of POLARIX (1-year PFS 79.8% (95% CI, 75.9-83.6) vs. 79.8% (95% CI, 73.9-84.4)) and SENIOR (1-year EFS à 64.5% (95% CI: 47.8-77.0) vs. 60.0% (95% CI: 50.8-68.1)). With its rigorous data validation process, REALYSA program provides high-quality RWD, thus constituting a platform for numerous scientific purposes.

Identifiants

pubmed: 37874913
pii: 498406
doi: 10.1182/bloodadvances.2023010798
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 American Society of Hematology.

Auteurs

Herve Ghesquieres (H)

Hopital Lyon Sud, Claude Bernard Lyon 1 University, Pierre-Benite, France.

Fanny Cherblanc (F)

Lymphoma Academic Research Organisation, Pierre-Bénite, France.

Aurelien Belot (A)

Lymphoma Academic Research Organisation, Pierre-Benite, France.

Sophie Micon (S)

Roche S.A.S, Boulogne Billancourt, France.

Krimo Bouabdallah (K)

Service d'Hématologie clinique et Thérapie cellulaire, PESSAC, France.

Cyril Esnault (C)

Roche S.A.S., Boulogne Billancourt, France.

Luc-Matthieu Fornecker (LM)

University of Strasbourg, France.

Katia Thokagevistk (K)

Roche S.A.S., Boulogne Billancourt, France.

Maxime Bonjour (M)

Service de Biostatistique-Bioinformatique, Pôle Santé Publique, Hospices Civils de Lyon, France.

Fontanet Bijou (F)

Institut Bergonie, Bordeaux, France.

Corinne Haioun (C)

CHU Henri Mondor, Créteil, France.

Nadine Morineau (N)

HOSPITAL OF LA ROCHE SUR YON, La Roche Sur Yon, France.

Loïc Ysebaert (L)

Institut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France.

Gandhi Damaj (G)

Normandy University, Hematology Institute, Caen, France.

Benoit Tessoulin (B)

Nantes University Hospital, Nantes, France.

Stéphanie Guidez (S)

CHU de Poitiers.

Franck Morschhauser (F)

CHU Lille, ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France.

Catherine Thieblemont (C)

AP-HP, Hôpital Saint-Louis, Hemato-oncologie, DMU DHI,F-75010 Paris, France, Paris, France.

Adrien Chauchet (A)

CHU, Besancon, France.

Remy Gressin (R)

Institute for Advanced Biosciences, INSERM U1209/CNRS UMR 5309/Grenoble Alpes University, France.

Fabrice Jardin (F)

INSERM U1245 Unit, Rouen, France.

Christophe Fruchart (C)

Service d'Hématologie, DUNKERQUE, France.

Gaelle Labouré (G)

CH Libourne, Libourne, France.

Ludovic Fouillet (L)

CHU Saint-Etienne, Saint-Priest-en-Jarez, France.

Pauline Lionne-Huyghe (P)

CH Arras, Arras, France.

Antoine Bonnet (A)

CH Bretagne Atlantique, Vannes, France.

Laure Lebras (L)

Centre Léon Bérard, lyon, France.

Sandy Amorim (S)

Hopital Saint Vincent, Lille, Alabama, France.

Cecile Leyronnas (C)

Institut Daniel Hollard, Grenoble, France.

Gaelle Olivier (G)

CH niort, NIORT, France.

Romain Guieze (R)

CHU Clermont-Ferrand, Clermont-ferrand, France.

Roch Houot (R)

CHU Rennes, Rennes, France.

Vincent Launay (V)

CH st brieuc, saint brieuc, France.

Bernard Drénou (B)

CH Mulhouse (GHRMSA), Mulhouse, France.

Olivier Fitoussi (O)

Polyclinique Bordeaux Nord Aquitaine, BORDEAUX cedex, France.

Laurence Detourmignies (L)

CH Roubaix, Roubaix, France.

Julie Abraham (J)

CHU Limoges, Limoges, France.

Carole Soussain (C)

Institut Curie, saint-cloud, France.

Florence Lachenal (F)

CH Pierre Oudot, Bourgoin-Jallieu, France.

Gian Matteo Pica (GM)

Centre Hospitalier Métropole Savoie Chambéry, Chambéry, France.

Patrick Fogarty (P)

Lysarc, Lyon, France.

Pascale Cony-Makhoul (P)

LYSARC, Pierre-Benite cedex, France.

Adeline Bernier (A)

Lymphoma Academic Research Organisation, Pierre-Bénite, France.

Sandra Le Guyader-Peyrou (S)

University of Bordeaux, INSERM, Team EPICENE, UMR1219, France.

Alain Monnereau (A)

University of Bordeaux, INSERM, Team EPICENE, UMR 1219, France.

Frédéric Boissard (F)

F. Hoffman-La Roche Ltd, Basel, Switzerland.

Vincent Camus (V)

INSERM U1245 Unit, France.

Classifications MeSH