4.3 Review

Chimeric-antigen receptor T (CAR-T) cell therapy for solid tumors: challenges and opportunities

Journal

ONCOTARGET
Volume 8, Issue 52, Pages 90521-90531

Publisher

IMPACT JOURNALS LLC
DOI: 10.18632/oncotarget.19361

Keywords

chimeric antigen receptor; T cells; cancer; adoptive cell transfer; tumor microenvironment

Funding

  1. National Key Research and Development Program of China [2016YFC0905900]
  2. National Natural Science Foundation [81430062]
  3. Priority Academic Program of Jiangsu Higher Education Institutions

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Chimeric antigen receptor (CAR)-engineered T cells (CAR-T cells) have been shown to have unprecedented efficacy in B cell malignancies, most notably in B cell acute lymphoblastic leukemia (B-ALL) with up to a 90% complete remission rate using anti-CD19 CAR-T cells. However, CAR T-cell therapy for solid tumors currently is faced with numerous challenges such as physical barriers, the immunosuppressive tumor microenvironment and the specificity and safety. The clinical results in solid tumors have been much less encouraging, with multiple cases of toxicity and a lack of therapeutic response. In this review, we will discuss the current stats and challenges of CAR-T cell therapy for solid tumors, and propose possibl e solutions and future perspectives.

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