4.5 Review

Review: Current clinical applications of chimeric antigen receptor (CAR) modified T cells

期刊

CYTOTHERAPY
卷 18, 期 11, 页码 1393-1409

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.jcyt.2016.07.003

关键词

acute lymphoblastic leukemia; adoptive cellular therapy; CART cells; chimeric antigen receptors; cytokine release syndrome

资金

  1. Leukemia and Lymphoma Society Career Development Grant [GC6840]
  2. National Comprehensive Cancer CenterYoung Investigator Award [CA13873801]
  3. Damon Runyon Clinical Investigator Award [GC3222]
  4. Translational and Integrative Medicine Fund Research Grant (MSKCC)
  5. Annual Terry Fox Run for Cancer Research (NewYork, NY) [GC7009]
  6. Carson Family Charitable Trust, Kate's Team
  7. Mr. William H. Goodwin and Mrs. Alice Goodwin and the Commonwealth Cancer Foundation for Research and the Experimental Therapeutics Center of MSKCC
  8. Geoffrey Beene Cancer Foundation [GC4035]
  9. Bocina Cancer Research Fund [GC7003]
  10. National Institutes of Health/National Center for Advancing Translational Sciences [UL1TR0045]

向作者/读者索取更多资源

The past several years have been marked by extraordinary advances in clinical applications of immunotherapy. In particular, adoptive cellular therapy utilizing chimeric antigen receptor (CAR)-modified T cells targeted to CD19 has demonstrated substantial clinical efficacy in children and adults with relapsed or refractory B-cell acute lymphoblastic leukemia (B-ALL) and durable clinical benefit in a smaller subset of patients with relapsed or refractory chronic lymphocytic leukemia (CLL) or B-cell non-Hodgkin lymphoma (B-NHL). Early-phase clinical trials are currently assessing CAR T-cell safety and efficacy in additional malignancies. Here, we discuss clinical results from the largest series to date investigating CD19-targeted CART cells in B-ALL, CLL, and B-NHL, including discussion of differences in CART-cell design and production and treatment approach, as well as clinical efficacy, nature of severe cytokine release syndrome and neurologic toxicities, and CART-cell expansion and persistence. We additionally review the current and forthcoming use of CART cells in multiple myeloma and several solid tumors and highlight challenges and opportunities afforded by the current state of CAR T-cell therapies, including strategies to overcome inhibitory aspects of the tumor microenvironment and enhance antitumor efficacy.

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