10.3389/fimmu.2018.01513.s003
Zibing Wang
Zibing
Wang
Xiaoli Liu
Xiaoli
Liu
Brian Till
Brian
Till
Miaomiao Sun
Miaomiao
Sun
Xiang Li
Xiang
Li
Quanli Gao
Quanli
Gao
table_3_Combination of Cytokine-Induced Killer Cells and Programmed Cell Death-1 Blockade Works Synergistically to Enhance Therapeutic Efficacy in Metastatic Renal Cell Carcinoma and Non-Small Cell Lung Cancer.PDF
Frontiers
2018
cytokine-induced killer cells
programmed cell death-1
immunotherapy
lung cancer
renal cell carcinoma
2018-07-05 04:02:53
Dataset
https://frontiersin.figshare.com/articles/dataset/table_3_Combination_of_Cytokine-Induced_Killer_Cells_and_Programmed_Cell_Death-1_Blockade_Works_Synergistically_to_Enhance_Therapeutic_Efficacy_in_Metastatic_Renal_Cell_Carcinoma_and_Non-Small_Cell_Lung_Cancer_PDF/6741974
Introduction<p>Programmed cell death-1 (PD-1) inhibition therapy has changed the treatment paradigm of metastatic renal cell carcinoma (MRCC) and non-small cell lung cancer (NSCLC). However, attempts to use the drug as a single agent have achieved only limited clinical success. To further enhance the clinical benefits of monotherapy, combination therapies will likely be necessary. Cytokine-induced killer (CIK) cells are a heterogeneous subset of ex vivo expanded T lymphocytes that have been shown to prolong the survival of cancer patients. We are conducting a study to evaluate the efficacy of PD-1 inhibitor in combination with CIK cells in relapsed/refractory MRCC and NSCLC and to analyze potential biomarkers to predict which patients will benefit most from the combined therapy.</p>Case presentation<p>The results of two patients treated in an ongoing clinical trial for MRCC and NSCLC are described here. The tumor biopsy from Patient 1 exhibited moderate CD3<sup>+</sup> T cell infiltration, but no PD-1 or PD-L1 expression. The tumor cells from Patient 2 strongly expressed PD-L1, and there was extensive tumor infiltration by CD3<sup>+</sup> T cells; however, no PD-1 staining was seen. Non-synonymous single nucleotide variant (nsSNVs), along with higher indel mutations, in Patient 1 and nsSNVs along with higher tumor mutation burden in Patient 2 correlate with tumor-infiltrating CD3<sup>+</sup> lymphocyte density. Patient 1 achieved a complete response, and Patient 2 achieved a near-complete response.</p>Conclusion<p>A PD-1 inhibitor in combination with CIK cells led to potent antitumor activity in MRCC and NSCLC; CD3<sup>+</sup> T cell infiltration in baseline tumor biopsies is a potential predictive biomarker. This approach is being further investigated in an ongoing phase I trial.</p>