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Your search keyword '"Lionne-Huyghe P"' showing total 2 results
Start Over Author "Lionne-Huyghe P" Journal blood advances
2 results on '"Lionne-Huyghe P"'

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

Author

Ghesquières, Hervé, Cherblanc, Fanny, Belot, Aurélien, Micon, Sophie, Bouabdallah, Krimo K., Esnault, Cyril, Fornecker, Luc-Matthieu, Thokagevistk, Katia, Bonjour, Maxime, Bijou, Fontanet, Haioun, Corinne, Morineau, Nadine, Ysebaert, Loïc, Damaj, Gandhi, Tessoulin, Benoit, Guidez, Stéphanie, Morschhauser, Franck, Thiéblemont, Catherine, Chauchet, Adrien, Gressin, Rémy, Jardin, Fabrice, Fruchart, Christophe, Labouré, Gaëlle, Fouillet, Ludovic, Lionne-Huyghe, Pauline, Bonnet, Antoine, Lebras, Laure, Amorim, Sandy, Leyronnas, Cécile, Olivier, Gaelle, Guieze, Romain, Houot, Roch, Launay, Vincent, Drénou, Bernard, Fitoussi, Olivier, Detourmignies, Laurence, Abraham, Julie, Soussain, Carole, Lachenal, Florence, Pica, Gian Matteo, Fogarty, Patrick, Cony-Makhoul, Pascale, Bernier, Adeline, Le Guyader-Peyrou, Sandra, Monnereau, Alain, Boissard, Frédéric, Rossi, Cédric, and Camus, Vincent

Abstract

•The REALYSA cohort is a source of RWD of high quality for lymphoma thanks to a multistep rigorous data validation process.•Effectiveness results on patients with first-line DLBCL seem consistent with literature and recent CTs.

Published
2023
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2. Challenges for quality and utilization of real-world data for diffuse large B-cell lymphoma in REALYSA, a LYSA cohort.

Author

Ghesquières H, Cherblanc F, Belot A, Micon S, Bouabdallah KK, Esnault C, Fornecker LM, Thokagevistk K, Bonjour M, Bijou F, Haioun C, Morineau N, Ysebaert L, Damaj G, Tessoulin B, Guidez S, Morschhauser F, Thiéblemont C, Chauchet A, Gressin R, Jardin F, Fruchart C, Labouré G, Fouillet L, Lionne-Huyghe P, Bonnet A, Lebras L, Amorim S, Leyronnas C, Olivier G, Guieze R, Houot R, Launay V, Drénou B, Fitoussi O, Detourmignies L, Abraham J, Soussain C, Lachenal F, Pica GM, Fogarty P, Cony-Makhoul P, Bernier A, Le Guyader-Peyrou S, Monnereau A, Boissard F, Rossi C, and Camus V

Subjects
Adult, Humans, Aged, Prospective Studies, Retrospective Studies, Rituximab therapeutic use, Cyclophosphamide therapeutic use, Prednisone therapeutic use, Vincristine therapeutic use, Doxorubicin therapeutic use, Antineoplastic Combined Chemotherapy Protocols therapeutic use, Lymphoma, Large B-Cell, Diffuse diagnosis, Lymphoma, Large B-Cell, Diffuse drug therapy
Abstract

Abstract: Real-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., (© 2024 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.)

Published
2024
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