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10.18632/oncotarget.19361

http://scihub22266oqcxt.onion/10.18632/oncotarget.19361
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C5685771!5685771!29163850
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suck abstract from ncbi


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pmid29163850      Oncotarget 2017 ; 8 (52): 90521-31
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  • Chimeric-antigen receptor T (CAR-T) cell therapy for solid tumors: challenges and opportunities #MMPMID29163850
  • Xia AL; Wang XC; Lu YJ; Lu XJ; Sun B
  • Oncotarget 2017[Oct]; 8 (52): 90521-31 PMID29163850show ga
  • 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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