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Two-year follow-up of KTE-X19 in patients with relapsed or refractory adult B-cell acute lymphoblastic leukemia in ZUMA-3 and its contextualization with SCHOLAR-3, an external historical control study.
Shah, Bijal D; Ghobadi, Armin; Oluwole, Olalekan O; Logan, Aaron C; Boissel, Nicolas; Cassaday, Ryan D; Leguay, Thibaut; Bishop, Michael R; Topp, Max S; Tzachanis, Dimitrios; O'Dwyer, Kristen M; Arellano, Martha L; Lin, Yi; Baer, Maria R; Schiller, Gary J; Park, Jae H; Subklewe, Marion; Abedi, Mehrdad; Minnema, Monique C; Wierda, William G; DeAngelo, Daniel J; Stiff, Patrick; Jeyakumar, Deepa; Dong, Jinghui; Adhikary, Sabina; Zhou, Lang; Schuberth, Petra C; Faghmous, Imi; Masouleh, Behzad Kharabi; Houot, Roch.
Afiliación
  • Shah BD; Moffitt Cancer Center, Tampa, FL, 33612, USA. bijal.shah@moffitt.org.
  • Ghobadi A; Washington University School of Medicine, St Louis, MO, USA.
  • Oluwole OO; Vanderbilt University Cancer Center, Nashville, TN, USA.
  • Logan AC; UCSF Medical Center, San Francisco, CA, USA.
  • Boissel N; Hôpital Saint-Louis, Paris, France.
  • Cassaday RD; University of Washington, Fred Hutchinson Cancer Center, Seattle, WA, USA.
  • Leguay T; Service d'hématologie Clinique Et Thérapie Cellulaire, Hopital du Haut-Leveque CHU de Bordeaux, Bordeaux, France.
  • Bishop MR; The University of Chicago Medicine, Chicago, IL, USA.
  • Topp MS; Medizinische Klinik Und Poliklinik II, Universitätsklinikum Würzburg, Würzburg, Germany.
  • Tzachanis D; University of California San Diego, San Diego, CA, USA.
  • O'Dwyer KM; Wilmot Cancer Institute of University of Rochester, Rochester, NY, USA.
  • Arellano ML; Winship Cancer Institute of Emory University, Atlanta, GA, USA.
  • Lin Y; Mayo Clinic, Rochester, MN, USA.
  • Baer MR; University of Maryland Marlene and Stewart Greenebaum Comprehensive Cancer Center, Baltimore, MD, USA.
  • Schiller GJ; David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
  • Park JH; Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Subklewe M; Ludwig-Maximilians-Universität München, Munich, Germany.
  • Abedi M; University of California Davis Comprehensive Cancer Center, Sacramento, CA, USA.
  • Minnema MC; University Medical Center Utrecht (on behalf of HOVON/LLPC), Utrecht, The Netherlands.
  • Wierda WG; The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
  • DeAngelo DJ; Dana-Farber Cancer Institute, Boston, MA, USA.
  • Stiff P; Loyola University Chicago Stritch School of Medicine, Maywood, IL, USA.
  • Jeyakumar D; University of California Irvine Medical Center, Orange, CA, USA.
  • Dong J; Kite, a Gilead Company, Santa Monica, CA, USA.
  • Adhikary S; Kite, a Gilead Company, Santa Monica, CA, USA.
  • Zhou L; Kite, a Gilead Company, Santa Monica, CA, USA.
  • Schuberth PC; Kite, a Gilead Company, Santa Monica, CA, USA.
  • Faghmous I; Kite, a Gilead Company, Santa Monica, CA, USA.
  • Masouleh BK; Kite, a Gilead Company, Santa Monica, CA, USA.
  • Houot R; CHU Rennes, Univ Rennes, Inserm & EFS, Rennes, France.
J Hematol Oncol ; 15(1): 170, 2022 12 10.
Article en En | MEDLINE | ID: mdl-36494725
BACKGROUND: Brexucabtagene autoleucel (KTE-X19) is an autologous anti-CD19 CAR T-cell therapy approved in the USA to treat adult patients with relapsed or refractory B-precursor acute lymphoblastic leukemia (R/R B-ALL) based on ZUMA-3 study results. We report updated ZUMA-3 outcomes with longer follow-up and an extended data set along with contextualization of outcomes to historical standard of care. METHODS: Adults with R/R B-ALL received a single infusion of KTE-X19 (1 × 106 CAR T cells/kg). Long-term post hoc subgroup assessments of ZUMA-3 were conducted. Outcomes from matched patients between historical clinical trials and ZUMA-3 patients were assessed in the retrospective historical control study SCHOLAR-3. RESULTS: After 26.8-months median follow-up, the overall complete remission (CR) rate (CR + CR with incomplete hematological recovery) among treated patients (N = 55) in phase 2 was 71% (56% CR rate); medians for duration of remission and overall survival (OS) were 14.6 and 25.4 months, respectively. Most patients responded to KTE-X19 regardless of age or baseline bone marrow blast percentage, but less so in patients with > 75% blasts. No new safety signals were observed. Similar outcomes were observed in a pooled analysis of phase 1 and 2 patients (N = 78). In SCHOLAR-3, the median OS for treated patients from ZUMA-3 (N = 49) and matched historical controls (N = 40) was 25.4 and 5.5 months, respectively. CONCLUSIONS: These data, representing the longest follow-up of CAR T-cell therapy in a multicenter study of adult R/R B-ALL, suggest that KTE-X19 provides a clinically meaningful survival benefit with manageable toxicity in this population. TRIAL REGISTRATION: NCT02614066.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras / Receptores Quiméricos de Antígenos Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Revista: J hematol oncol Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Leucemia-Linfoma Linfoblástico de Células Precursoras / Receptores Quiméricos de Antígenos Tipo de estudio: Observational_studies / Prognostic_studies Límite: Adult / Humans Idioma: En Revista: J hematol oncol Asunto de la revista: HEMATOLOGIA / NEOPLASIAS Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos