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Peri-CAR-T practice patterns and survival predictors for all CAR-T patients and post-CAR-T failure in aggressive B-NHL.
Zurko, Joanna; Nizamuddin, Imran; Epperla, Narendranath; David, Kevin; Cohen, Jonathon B; Moyo, Tamara K; Ollila, Thomas; Hess, Brian; Roy, Ishan; Ferdman, Robert; Liu, Jieqi; Chowdhury, Sayan Mullick; Romancik, Jason; Bhansali, Rahul S; Harris, Elyse I; Sorrell, Mckenzie; Masel, Rebecca; Kittai, Adam S; Denlinger, Nathan; Sigmund, Audrey M; Fitzgerald, Lindsey; Galvez, Carlos; Ma, Shuo; Winter, Jane; Pro, Barbara; Gordon, Leo I; Danilov, Alexey; Stephens, Deborah; Shah, Nirav N; Kenkre, Vaishalee; Barta, Stefan K; Torka, Pallawi; Shouse, Geoffrey; Karmali, Reem.
Afiliación
  • Zurko J; Department of Medicine, Carbone Cancer Center, University of Wisconsin, Madison, WI.
  • Nizamuddin I; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Epperla N; Department of Internal Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
  • David K; Department of Medicine, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, NJ.
  • Cohen JB; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
  • Moyo TK; Atrium Health Carolinas Medical Center, Charlotte, NC.
  • Ollila T; Department of Medicine, Lifespan Cancer Institute, Brown University, Providence, RI.
  • Hess B; Department of Medicine, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC.
  • Roy I; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Ferdman R; Department of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Liu J; Department of Medicine, Rutgers Cancer Institute of New Jersey, Rutgers University, New Brunswick, NJ.
  • Chowdhury SM; Department of Internal Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
  • Romancik J; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University, Atlanta, GA.
  • Bhansali RS; Department of Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
  • Harris EI; Department of Medicine, Carbone Cancer Center, University of Wisconsin, Madison, WI.
  • Sorrell M; Department of Medicine, Hollings Cancer Center, Medical University of South Carolina, Charleston, SC.
  • Masel R; Department of Medicine, Lifespan Cancer Institute, Brown University, Providence, RI.
  • Kittai AS; Department of Internal Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
  • Denlinger N; Department of Internal Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
  • Sigmund AM; Department of Internal Medicine, Arthur G. James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University, Columbus, OH.
  • Fitzgerald L; Department of Internal Medicine, Huntsman Cancer Institute, The University of Utah, Salt Lake City, UT.
  • Galvez C; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Ma S; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Winter J; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Pro B; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Gordon LI; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Danilov A; Department of Hematology & Hematopoietic Cell Transplantation, City of Hope Comprehensive Cancer Center, Duarte, CA.
  • Stephens D; Department of Internal Medicine, Huntsman Cancer Institute, The University of Utah, Salt Lake City, UT.
  • Shah NN; Department of Medicine, MCW Cancer Center, Medical College of Wisconsin, Milwaukee, WI.
  • Kenkre V; Department of Medicine, Carbone Cancer Center, University of Wisconsin, Madison, WI.
  • Barta SK; Department of Medicine, Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA.
  • Torka P; Department of Medicine, Roswell Park Comprehensive Cancer Center, Buffalo, NY.
  • Shouse G; Department of Hematology & Hematopoietic Cell Transplantation, City of Hope Comprehensive Cancer Center, Duarte, CA.
  • Karmali R; Department of Medicine, Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL.
Blood Adv ; 7(12): 2657-2669, 2023 Jun 27.
Article en En | MEDLINE | ID: mdl-36094847
ABSTRACT
Most patients receiving chimeric antigen receptor T-cell therapy (CAR-T) for aggressive B-cell non-Hodgkin lymphoma (B-NHL) do not experience a durable remission. Several novel agents are approved to treat relapsed, refractory aggressive B-NHL; however, it remains unclear how to sequence these therapies pre- and post-CAR-T. We conducted a multicenter retrospective analysis to describe peri-CAR-T practice patterns and survival predictors for patients receiving CD19-directed CAR-T. Patients (n = 514) from 13 centers treated with CAR-T for B-NHL between 2015-2021 were included in the study. Survival curves were constructed using Kaplan-Meier method. Multivariate Cox regression analysis was used to determine the impact of the variables on survival outcomes. For all patients receiving CAR-T, a greater number of lines of therapy pre-CAR-T apheresis and bridging therapy were predictive of inferior progression-free survival (PFS) and overall survival (OS). The median PFS and OS from the time of CAR-T cell infusion were 7.6 and 25.6 months, respectively. From the time of progression post-CAR-T, the median OS was 5.5 months. The median PFS of treatments administered in the first-line post-CAR-T failure was 2.8 months. Patients with refractory disease on day 30 had inferior OS and were less likely to receive subsequent treatment(s) than other patients with CAR-T failure. Allogeneic hematopoietic cell transplantation for selected patients at any time following CAR-T failure led to durable responses in over half of patients at 1 year. These data provide a benchmark for future clinical trials in patients with post-CAR-T cell progression, which remains an unmet clinical need.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfoma de Células B / Receptores Quiméricos de Antígenos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Blood Adv Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Linfoma de Células B / Receptores Quiméricos de Antígenos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Blood Adv Año: 2023 Tipo del documento: Article