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Subsequent Malignancies After CD19-Targeted Chimeric Antigen Receptor T Cells in Patients With Lymphoma.
Lorenc, Rachel; Shouval, Roni; Flynn, Jessica R; Devlin, Sean M; Saldia, Amethyst; De Abia, Alejandro Luna; De Lapuerta, Magdalena Corona; Tomas, Ana Alarcon; Cassanello, Gulio; Leslie, Lori A; Rejeski, Kai; Lin, Richard J; Scordo, Michael; Shah, Gunjan L; Palomba, M Lia; Salles, Gilles; Park, Jae; Giralt, Sergio A; Perales, Miguel-Angel; Ip, Andrew; Dahi, Parastoo B.
Afiliação
  • Lorenc R; Department of Medicine, Weill Cornell Medical College, New York, New York.
  • Shouval R; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Flynn JR; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Devlin SM; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Saldia A; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • De Abia AL; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York; Adult Bone Marrow Transplantation Unit. Hospital Universitario Ramón y Cajal, Madrid, Spain.
  • De Lapuerta MC; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Tomas AA; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York; Hospital Universitario Gregorio Marañón, Madrid, Spain.
  • Cassanello G; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York; Department of Oncology and Hemato-Oncology, University of Milan, Italy; Lymphoma Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Leslie LA; Lymphoma Service, Hackensack Meridian Health, New Jersey, New Jersey.
  • Rejeski K; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Lin RJ; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Scordo M; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Shah GL; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Palomba ML; Department of Medicine, Weill Cornell Medical College, New York, New York; Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Salles G; Department of Medicine, Weill Cornell Medical College, New York, New York; Lymphoma Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Park J; Department of Medicine, Weill Cornell Medical College, New York, New York; Cellular Therapy Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Giralt SA; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Perales MA; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Ip A; Lymphoma Service, Hackensack Meridian Health, New Jersey, New Jersey.
  • Dahi PB; Department of Medicine, Weill Cornell Medical College, New York, New York; Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, New York. Electronic address: dahip@mskcc.org.
Transplant Cell Ther ; 2024 Jul 06.
Article em En | MEDLINE | ID: mdl-38972512
ABSTRACT
Chimeric antigen receptor (CAR) T cells are an established treatment for B cell non-Hodgkin lymphomas (B-NHL). With the remarkable success in improving survival, understanding the late effects of CAR T cell therapy is becoming more relevant. The aim of this study is to determine the incidence of subsequent malignancies in adult patients with B-NHL. We retrospectively studied 355 patients from 2 different medical centers treated with four different CAR T cell products from 2016 to 2022. The overall cumulative incidence for subsequent malignancies at 36 months was 14% (95% CI 9.2%, 19%). Subsequent malignancies were grouped into 3 primary categories solid tumor, hematologic malignancy, and dermatologic malignancy with cumulative incidences at 36 months of 6.1% (95% CI 3.1%-10%), 4.5% (95% CI 2.1%-8.1%) and 4.2% (95% CI 2.1%-7.5%) respectively. Notably, no cases of T cell malignancies were observed. In univariable analysis, increasing age was associated with higher risk for subsequent malignancy. While the overall benefits of CAR T products continue to outweigh their potential risks, more studies and longer follow ups are needed to further demonstrate the risks, patterns, and molecular pathways that lead to the development of subsequent malignancies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Transplant Cell Ther Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Transplant Cell Ther Ano de publicação: 2024 Tipo de documento: Article