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Cell-based Immunotherapy for Colorectal Cancer with Cytokine-induced Killer Cells
Immune Network ; : 99-108, 2016.
Article in English | WPRIM | ID: wpr-168218
ABSTRACT
Colorectal cancer is the third leading cancer worldwide. Although incidence and mortality of colorectal cancer are gradually decreasing in the US, patients with metastatic colorectal cancer have poor prognosis with an estimated 5-year survival rate of less than 10%. Over the past decade, advances in combination chemotherapy regimens for colorectal cancer have led to significant improvement in progression-free and overall survival. However, patients with metastatic disease gain little clinical benefit from conventional therapy, which is associated with grade 3~4 toxicity with negative effects on quality of life. In previous clinical studies, cell-based immunotherapy using dendritic cell vaccines and sentinel lymph node T cell therapy showed promising therapeutic results for metastatic colorectal cancer. In our preclinical and previous clinical studies, cytokine-induced killer (CIK) cells treatment for colorectal cancer showed favorable responses without toxicities. Here, we review current treatment options for colorectal cancer and summarize available clinical studies utilizing cell-based immunotherapy. Based on these studies, we recommend the use CIK cell therapy as a promising therapeutic strategy for patients with metastatic colorectal cancer.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Prognosis / Quality of Life / Dendritic Cells / Vaccines / Colorectal Neoplasms / Incidence / Survival Rate / Mortality / Drug Therapy, Combination / Cytokine-Induced Killer Cells Type of study: Incidence study / Prognostic study Limits: Humans Language: English Journal: Immune Network Year: 2016 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Prognosis / Quality of Life / Dendritic Cells / Vaccines / Colorectal Neoplasms / Incidence / Survival Rate / Mortality / Drug Therapy, Combination / Cytokine-Induced Killer Cells Type of study: Incidence study / Prognostic study Limits: Humans Language: English Journal: Immune Network Year: 2016 Type: Article