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Chimeric Antigen Receptor T cells for B Cell Neoplasms: Choose the Right CAR for You

Journal

CURRENT HEMATOLOGIC MALIGNANCY REPORTS
Volume 11, Issue 5, Pages 368-384

Publisher

CURRENT MEDICINE GROUP
DOI: 10.1007/s11899-016-0336-z

Keywords

Chimeric antigen receptor Tcells; CART; CTL019; KTE-C19; JCAR; Immunotherapy; Adoptive cell therapy

Funding

  1. Univ. of Pennsylvania-Novartis Alliance
  2. NIH [5R01CA120409]
  3. Parker Institute of Cancer Immunotherapy at the University of Pennsylvania
  4. EMD-Serono Cancer Immunotherapy Clinical Fellowship by the Society for Immunotherapy of Cancer (SITC)
  5. Bristol-Myers Squibb Oncology Fellowship in Clinical Cancer Research by the American Association for Cancer Research (AACR)
  6. Gabrielle's Angel Foundation
  7. SIES-AIL fellowship by the Italian Society for Experimental Hematology
  8. Italian Leukemia Association

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Genetic redirection of T lymphocytes allows us to unleash these potent cellular immune effectors against cancer. Chimeric antigen receptor (CAR) T cells are the best-in-class example that genetic engineering of T cells can lead to deep and durable responses, as has been shown in several clinical trials for CD19+ B cell malignancies. As a consequence, in the last few years, several academic institutions and commercial partners have started developing anti-CD19 CAR T cell products. Although most of these T cell products are highly effective in vivo, basic differences among them can generate different performance characteristics and thereby impact their long-term clinical outcome. Several strategies are being implemented in order to solve the current open issues of CART19 therapy: (i) increasing efficacy against indolent B cell leukemias and lymphomas, (ii) avoiding or preventing antigen-loss relapses, (iii) reducing and managing toxicity, and (iv) bringing this CART therapy to routine clinical practice. The field of CART therapies is thriving, and exciting new avenues are opening for both scientists and patients.

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