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Early experience using salvage radiotherapy for relapsed/refractory non-Hodgkin lymphomas after CD19 chimeric antigen receptor (CAR) T cell therapy.

Abstract
Radiotherapy is potentially an important salvage strategy post-chimeric antigen receptor T cell therapy (CART), but limited data exist. We reviewed 14 patients treated with salvage radiation post-CART progression (SRT). Most received SRT for first post-CART relapse (71%) to sites previously PET-avid pre-CART (79%). Median overall survival (OS) post-SRT was 10 months. Post-SRT, six localized relapses achieved 100% response (3 = complete, 3 = partial), with improved freedom from subsequent relapse (P = 0·001) and OS (P = 0·004) compared to advanced stage relapses. Three were bridged to allogeneic transplantation; at analysis, all were alive/NED. SRT has diverse utility and can integrate with novel agents or transplantation to attempt durable remissions.
AuthorsBrandon S Imber, Michel Sadelain, Carl DeSelm, Connie Batlevi, Renier J Brentjens, Parastoo B Dahi, Sergio Giralt, Jae H Park, Craig Sauter, Michael Scordo, Gunjan Shah, Miguel-Angel Perales, M Lia Palomba, Joachim Yahalom
JournalBritish journal of haematology (Br J Haematol) Vol. 190 Issue 1 Pg. 45-51 (07 2020) ISSN: 1365-2141 [Electronic] England
PMID32135029 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Copyright© 2020 British Society for Haematology and John Wiley & Sons Ltd.
Chemical References
  • Antigens, CD19
  • Receptors, Chimeric Antigen
Topics
  • Adult
  • Aged
  • Antigens, CD19
  • Female
  • Humans
  • Lymphoma, Non-Hodgkin (radiotherapy)
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local
  • Receptors, Chimeric Antigen (therapeutic use)
  • Salvage Therapy (methods)
  • Young Adult

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