Evidence map›Paper›PMID 37874913›Full record

ArticleBlood advances2024

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

Hervé Ghesquières, Fanny Cherblanc, Aurélien Belot, Sophie Micon, Krimo K Bouabdallah, Cyril Esnault, Luc-Matthieu Fornecker, Katia Thokagevistk, Maxime Bonjour, Fontanet Bijou and 38 more

Registry-linked trialAbstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03869619 (REAL WORLD DATA IN LYMPHOMA AND SURVIVAL IN ADULTS), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03869619 recruitingnot on this map

Real world data in lymphoma and survival in adults

Typeobservational_patient_registrySponsorHospices Civils de LyonRan2018 to 2027Enrolled6,000ConditionsDiffuse Large B Lymphoma (DLBCL), Follicular Lymphoma (FL), Mantle Cell Lymphoma (MCL), Marginal Zone Lymphoma (MZL)ArmsReal-life epidemiological platform of lymphoma in France
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

48 authors.

Hervé GhesquièresDepartment of Hematology, Hopital Lyon Sud, Claude Bernard Lyon 1 University, Pierre Benite, France.
Fanny CherblancLymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.
Aurélien BelotLymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.ORCID 0000-0003-1410-5172
Sophie MiconRoche SAS, Boulogne-Billancourt, France.
Krimo K BouabdallahHematology and Cell Therapy Department, University Hospital of Bordeaux, Bordeaux, France.
Cyril EsnaultRoche SAS, Boulogne-Billancourt, France.ORCID 0000-0003-2896-6045
Luc-Matthieu ForneckerInstitut de Cancérologie Strasbourg Europe (ICANS) and University of Strasbourg, Strasbourg, France.
Katia ThokagevistkRoche SAS, Boulogne-Billancourt, France.
Maxime BonjourLymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.
Fontanet BijouDepartment of Hematology, Institut Bergonie, Bordeaux, France.ORCID 0000-0001-6768-7175
Corinne HaiounLymphoid Malignancies Unit, Assistante Publique Hôpitaux de Paris APHP, Hopital Henri Mondor, Creteil, France.
Nadine MorineauDepartment of Hematology, Centre Hospitalier Départemental Vendée, La Roche-sur-Yon, France.
Loïc YsebaertInstitut universitaire du cancer de Toulouse Oncopole, Toulouse, France.
Gandhi DamajHematology Institute of Basse Normandie, Centre Hospitalier Universitaire de Caen, Caen, France.ORCID 0000-0002-4689-3882
Benoit TessoulinDepartment of Hematology, Centre Hospitalier Universitaire de Nantes, Nantes, France.ORCID 0000-0001-7600-3329
Stéphanie GuidezDepartment of Hematology, Centre Hospitalier Universitaire de Poitiers, Poitiers, France.
Franck MorschhauserDepartment of Hematology, Universite de Lille, Centre Hospitalier Universitaire de Lille, Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France.ORCID 0000-0002-3714-9824
Catherine ThiéblemontUniversité Paris Cité, Assistante Publique Hôpitaux de Paris, Hôpital Saint-Louis, Service d'Hémato-Oncologie, Paris, France.
Adrien ChauchetDepartment of Hematology, Centre Hospitalier Universitaire de Besançon, Besançon, France.
Rémy GressinDepartment of Hematology, Centre Hospitalier Universitaire de Grenoble, Institute for Advanced Biosciences, INSERM U1209/CNRS UMR 5309/Grenoble Alpes University, Grenoble, France.
Fabrice JardinDepartment of Clinical Hematology, INSERM U1245 Unit, Centre Henri Becquerel, Rouen, France.
Christophe FruchartDepartment of Hematology, Centre Hospitalier de Dunkerque, Dunkirk, France.
Gaëlle LabouréDeparment of Hematology, Centre Hospitalier de Libourne, Libourne, France.
Ludovic FouilletDepartment of Hematology, Centre Hospitalier Universitaire de Saint Etienne, Saint Etienne, France.
Pauline Lionne-HuygheDepartment of Hematology, Centre Hospitalier d'Arras, Arras, France.
Antoine BonnetDepartment of Hematology, Centre Hospitalier de Bretagne Atlantique, Vannes, France.ORCID 0000-0001-6962-3650
Laure LebrasDepartment of Hematology, Leon Berard Cancer Center, Lyon, France.
Sandy AmorimDepartment of Hematology, Hopital Saint Vincent de Paul, Lille, France.
Cécile LeyronnasDepartment of Hematology, Groupe Hospitalier Mutualiste de Grenoble, Grenoble, France.
Gaelle OlivierDepartment of Hematology, Centre Hospitalier de Niort, Niort, France.
Romain GuiezeDepartment of Hematology, Centre Hospitalier Universitaire de Clermont Ferrand, Clermont Ferrand, France.
Roch HouotDepartment of Hematology, Centre Hospitalier Universitaire de Rennes, Rennes, France.
Vincent LaunayDepartment of Hematology, Centre Hospitalier de Saint Brieuc, Saint Brieuc, France.
Bernard DrénouDepartment Hematology, Groupe Hospitalier Mulhouse Sud Alsace, Mulhouse, France.ORCID 0000-0002-2175-6785
Olivier FitoussiDepartment of Hematology, Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France.
Laurence DetourmigniesDepartment of Hematology, Centre Hospitalier de Roubaix, Roubaix, France.
Julie AbrahamDepartment of Hematology, Centre Hospitalier Universitaire de Limoges, Limoges, France.
Carole SoussainDepartment of Hematology, Institut Curie, Saint-Cloud, France.
Florence LachenalDepartment of Hematology, Centre Hospitalier Pierre Oudot, Bourgoin-Jallieu, France.
Gian Matteo PicaDepartment of Hematology, Centre Hospitalier Metropole Savoie, Chambery, France.
Patrick FogartyLymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.
Pascale Cony-MakhoulLymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.
Adeline BernierLymphoma Academic Research Organisation, Hopital Lyon Sud, Pierre Benite, France.ORCID 0000-0003-3023-429X
Sandra Le Guyader-PeyrouRegistre des Hémopathies Malignes de la Gironde, Institut Bergonié, University of Bordeaux, Inserm, Team EPICENE, Bordeaux, France.
Alain MonnereauRegistre des Hémopathies Malignes de la Gironde, Institut Bergonié, University of Bordeaux, Inserm, Team EPICENE, Bordeaux, France.
Frédéric BoissardF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Cédric RossiDepartment of Hematology, Centre Hospitalier Universitaire de Dijon Bourgogne, Dijon, France.ORCID 0000-0003-3717-7961
Vincent CamusDepartment of Clinical Hematology, INSERM U1245 Unit, Centre Henri Becquerel, Rouen, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractReal-world data (RWD) are essential to complement clinical trial (CT) data, but major challenges remain, such as data quality. REal world dAta in LYmphoma and Survival in Adults (REALYSA) is a prospective noninterventional multicentric cohort started in 2018 that included patients newly diagnosed with lymphoma in France. Herein is a proof-of-concept analysis on patients with first-line diffuse large B-cell lymphoma (DLBCL) to (1) evaluate the capacity of the cohort to provide robust data through a multistep validation process; (2) assess the consistency of the results; and (3) conduct an exploratory transportability assessment of 2 recent phase 3 CTs (POLARIX and SENIOR). The analysis population comprised 645 patients with DLBCL included before 31 March 2021 who received immunochemotherapy and for whom 3589 queries were generated, resulting in high data completeness (<4% missing data). Median age was 66 years, with mostly advanced-stage disease and high international prognostic index (IPI) score. Treatments were mostly rituximab, cyclophosphamide, doxorubicin hydrochloride, vincristine, and prednisone (R-CHOP 75%) and reduced dose R-CHOP (13%). Estimated 1-year event-free survival (EFS) and overall survival rates were 77.9% and 90.0%, respectively (median follow-up, 9.9 months). Regarding transportability, when applying the CT's main inclusion criteria (age, performance status, and IPI), outcomes seemed comparable between patients in REALYSA and standard arms of POLARIX (1-year progression-free survival 79.8% vs 79.8%) and SENIOR (1-year EFS, 64.5% vs 60.0%). With its rigorous data validation process, REALYSA provides high-quality RWD, thus constituting a platform for numerous scientific purposes. The REALYSA study was registered at www.clinicaltrials.gov as #NCT03869619.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Large B-Cell, DiffuseAdultAgedCyclophosphamideDoxorubicinHumansPrednisoneProspective StudiesRetrospective StudiesRituximabVincristineCyclophosphamideDoxorubicinPrednisoneRituximabVincristine

Identifiers

PMID37874913
PMCPMC10824688

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.