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Autologous HER2-specific CAR T cells after lymphodepletion for advanced sarcoma: a phase 1 trial.
Hegde, Meenakshi; Navai, Shoba; DeRenzo, Christopher; Joseph, Sujith K; Sanber, Khaled; Wu, Mengfen; Gad, Ahmed Z; Janeway, Katherine A; Campbell, Matthew; Mullikin, Dolores; Nawas, Zeid; Robertson, Catherine; Mathew, Pretty R; Zhang, Huimin; Mehta, Birju; Bhat, Raksha R; Major, Angela; Shree, Ankita; Gerken, Claudia; Kalra, Mamta; Chakraborty, Rikhia; Thakkar, Sachin G; Dakhova, Olga; Salsman, Vita S; Grilley, Bambi; Lapteva, Natalia; Gee, Adrian; Dotti, Gianpietro; Bao, Riyue; Salem, Ahmed Hamed; Wang, Tao; Brenner, Malcolm K; Heslop, Helen E; Wels, Winfried S; Hicks, M John; Gottschalk, Stephen; Ahmed, Nabil.
Afiliación
  • Hegde M; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA. mghegde@bcm.edu.
  • Navai S; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA. mghegde@bcm.edu.
  • DeRenzo C; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA. mghegde@bcm.edu.
  • Joseph SK; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA. mghegde@bcm.edu.
  • Sanber K; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Wu M; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Gad AZ; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Janeway KA; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Campbell M; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Mullikin D; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Nawas Z; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Robertson C; Department of Bone Marrow Transplantation and Cellular Therapy, St. Jude Children's Research Hospital, Memphis, TN, USA.
  • Mathew PR; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Zhang H; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Mehta B; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Bhat RR; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Major A; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Shree A; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Gerken C; Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
  • Kalra M; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Chakraborty R; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Thakkar SG; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Dakhova O; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Salsman VS; Interdepartmental Program in Translational Biology and Molecular Medicine, Baylor College of Medicine, Houston, TX, USA.
  • Grilley B; Department of Pediatrics, Boston Children's Hospital, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
  • Lapteva N; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Gee A; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Dotti G; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Bao R; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Salem AH; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Wang T; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Brenner MK; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Heslop HE; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Wels WS; Department of Pediatrics, Baylor College of Medicine, Houston, TX, USA.
  • Hicks MJ; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Gottschalk S; Texas Children's Cancer and Hematology Center, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
  • Ahmed N; Center for Cell and Gene Therapy, Texas Children's Hospital, Houston Methodist Hospital, Baylor College of Medicine, Houston, TX, USA.
Nat Cancer ; 5(6): 880-894, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38658775
ABSTRACT
In this prospective, interventional phase 1 study for individuals with advanced sarcoma, we infused autologous HER2-specific chimeric antigen receptor T cells (HER2 CAR T cells) after lymphodepletion with fludarabine (Flu) ± cyclophosphamide (Cy) 1 × 108 T cells per m2 after Flu (cohort A) or Flu/Cy (cohort B) and 1 × 108 CAR+ T cells per m2 after Flu/Cy (cohort C). The primary outcome was assessment of safety of one dose of HER2 CAR T cells after lymphodepletion. Determination of antitumor responses was the secondary outcome. Thirteen individuals were treated in 14 enrollments, and seven received multiple infusions. HER2 CAR T cells expanded after 19 of 21 infusions. Nine of 12 individuals in cohorts A and B developed grade 1-2 cytokine release syndrome. Two individuals in cohort C experienced dose-limiting toxicity with grade 3-4 cytokine release syndrome. Antitumor activity was observed with clinical benefit in 50% of individuals treated. The tumor samples analyzed showed spatial heterogeneity of immune cells and clustering by sarcoma type and by treatment response. Our results affirm HER2 as a CAR T cell target and demonstrate the safety of this therapeutic approach in sarcoma. ClinicalTrials.gov registration NCT00902044 .
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sarcoma / Inmunoterapia Adoptiva / Receptor ErbB-2 / Receptores Quiméricos de Antígenos Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Sarcoma / Inmunoterapia Adoptiva / Receptor ErbB-2 / Receptores Quiméricos de Antígenos Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Nat Cancer Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos