@article{8dd66f676f6843ec9efd36a7562af064,
title = "Improving eligibility criteria for first-line trials for patients with DLBCL using a US-based Delphi-method survey",
abstract = "Recent first-line randomized controlled trials (RCTs) for patients with diffuse large B-cell lymphoma (DLBCL) have shown negative results, which may be due in part to onerous eligibility criteria limiting enrollment of poor-risk patients who require immediate treatment. We conducted a Delphi-method survey with lymphoma experts in the United States to define recommendations for essential and potentially unnecessary enrollment criteria for modern first-line DLBCL RCTs aimed at increasing clinical diversity of ensuing study groups. We first tabulated enrollment criteria from 19 DLBCL RCTs spanning the rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP) era to identify common eligibility criteria from prior DLBCL RCTs for inclusion in the Delphi-method survey. We tabulated 451 total eligibility criteria comprising 51 criterion categories across 19 first-line DLBCL RCTs in the R-CHOP era. We then surveyed lymphoma clinical trial experts representing 8 academic medical centers in the United States regarding essential and unnecessary eligibility criteria for modern DLBCL RCTs. Seventeen of 29 invited clinical investigators completed the round-1 questionnaire (response rate, of 58.6%), 15 of 17 round-1 participants (88.2%) completed the round-2 survey, and all round-1 participants reviewed finalized recommendations for eligibility criteria for modern first-line DLBCL RCTs. We defined consensus recommendations for 31 modernized eligibility criteria including threshold values for 10 quantitative eligibility criteria aimed at facilitating enrollment of a clinically diverse study population in first-line DLBCL RCTs designed to improve standard-of-care therapy.",
author = "Harkins, {R. Andrew} and Patel, {Sharvil P.} and Lee, {Michelle J.} and Switchenko, {Jeffrey M.} and Ansell, {Stephen M.} and Bartlett, {Nancy L.} and Blum, {Kristie A.} and Cashen, {Amanda F.} and Carla Casulo and Friedberg, {Jonathan W.} and Johnston, {Patrick B.} and Kahl, {Brad S.} and Leonard, {John P.} and Link, {Brian K.} and Lossos, {Izidore S.} and Peter Martin and Maurer, {Matt J.} and Neha Mehta-Shah and Reagan, {Patrick M.} and Westin, {Jason R.} and Koff, {Jean L.} and Flowers, {Christopher R.}",
note = "Funding Information: Conflict-of-interest disclosure: C.C. receives research funding from Gilead, BMS, Genentech, and Verastem. J.W.F. discloses data safety monitoring committee participation for Acerta and Novartis. Funding Information: B.S.K. receives research funding from Genentech, ADC Therapeutics, Abbvie, AstraZeneca, and Beigene and provides consulting for Genentech, ADC Therapeutics, Abbvie, AstraZeneca, BeiGene, Pharmacyclics, Celgene/BMS, TG Therapeutics, Teva, Janssen, and MEI. J.P.L. provided consulting advice to Sutro, Epizyme, BMS/Cel-gene, Bayer, Gilead/Kite, GenMab, Genentech/Roche, Abbvie, Incyte, Janssen, Eisai, Mustang Bio, and Second Genome, and received research support from Genentech. I.S.L. has served on the advisory boards of Seattle Genetics, Janssen Scientific, and Vera-stem. P.M. is a consultant for ADCT, AstraZeneca, Bayer, Beigene, BMS, Cellectar, Epizyme, Gilead, Incyte, Janssen, Karyopharm, Mor-phosys, Regeneron, and Verastem. M.J.M. discloses consulting or advisory roles with MorphoSys, Kite Pharma, and Pfizer and research funding from Celgene, NanoString Technologies, Genen-tech, and Morphosys. P.M.R. has consultancy for Kite Pharma and research funding from SeaGen and Genentech. J.R.W. discloses consulting work with Novartis, Kite/Gilead, BMS, Morphosys, Astra-Zeneca, Janssen, Genentech, Iksuda, Umoja, and ADC Therapeutics and research funding from Novartis, Kite/Gilead, BMS, Morphosys, AstraZeneca, Janssen, Genentech, Curus, Unum, and ADC Therapeutics. J.L.K. has participated on advisory boards for Janssen, MorphoSys, TG Therapeutics, and Gamida Cell and received research funding from Oncternal Therapeutics, Viracta Therapeutics, and Atara Biotherapeutics. C.R.F. is a consultant for Abbvie, Bayer, BeiGene, Celgene, Denovo Biopharma, Genentech/ Roche, Genmab, Gilead, Karyopharm, Pharmacyclics/Janssen, Sea-Gen, and Spectrum and has received research funding from 4D, Abbvie, Acerta, Adaptimmune, Allogene, Amgen, Bayer, Celgene, Cellectis, EMD, Gilead, Genentech/Roche, Guardant, Iovance, Funding Information: This work was supported by grants from the National Center for Advancing Translational Sciences of the National Institutes of Health (NIH) (grants TL1TR002382 and UL1TR002378) (R.A.H.). C.R.F. is a Cancer Prevention and Research Institute of Texas (CPRIT) Scholar of Cancer Research. The project described was supported in part by the National Cancer Institute (NCI) (K24 CA208132 award for mentored patient-oriented research in lymphoma) and CPRIT Award RR190079 (C.R.F.). Research reported in this publication was supported in part by the Biostatistics Shared Resource of Winship Cancer Institute of Emory University and NIH/NCI under award number P30CA138292. Publisher Copyright: {\textcopyright} 2022 by The American Society of Hematology.",
year = "2022",
month = may,
day = "10",
doi = "10.1182/bloodadvances.2021006504",
language = "English",
volume = "6",
pages = "2745--2756",
journal = "Blood Advances",
issn = "2473-9529",
number = "9",
}