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Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis
BACKGROUND: The number of clinical studies evaluating the benefit of cytokine-induced killer cell (CIK) therapy, an adoptive immunotherapy, for colorectal cancer (CRC) is increasing. In many of these trials, CIK therapy was coadministered with conventional cancer therapy. The aim of this review is t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152003/ https://www.ncbi.nlm.nih.gov/pubmed/37117007 http://dx.doi.org/10.1136/jitc-2023-006764 |
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author | Li, Celine Man Ying Tomita, Yoko Dhakal, Bimala Li, Runhao Li, Jun Drew, Paul Price, Timothy Smith, Eric Maddern, Guy J Fenix, Kevin Aaron |
author_facet | Li, Celine Man Ying Tomita, Yoko Dhakal, Bimala Li, Runhao Li, Jun Drew, Paul Price, Timothy Smith, Eric Maddern, Guy J Fenix, Kevin Aaron |
author_sort | Li, Celine Man Ying |
collection | PubMed |
description | BACKGROUND: The number of clinical studies evaluating the benefit of cytokine-induced killer cell (CIK) therapy, an adoptive immunotherapy, for colorectal cancer (CRC) is increasing. In many of these trials, CIK therapy was coadministered with conventional cancer therapy. The aim of this review is to systematically assess the available literature, in which the majority were only in Chinese, on CIK therapy for the management of CRC using meta-analysis and to identify parameters associated with successful CIK therapy implementation. METHODS: Prospective and retrospective clinical studies which compared CIK therapy to non-CIK therapy in patients with CRC were searched for electronically on MEDLINE, Embase, China National Knowledge Infrastructure, and Wanfang Data databases. The clinical endpoints of overall survival (OS), progression-free survival (PFS), OS and PFS rates, overall response rate (ORR), and toxicity were meta-analyzed using HR and relative ratio (RR), and subgroup analyses were performed using chi-square (χ(2)) test and I-squared (I(2)) statistics for study design, disease stage, cotherapy type, and timing of administration. RESULTS: In total, 70 studies involving 6743 patients were analyzed. CIK therapy was favored over non-CIK therapy for OS (HR=0.59, 95% CI: 0.53 to 0.65), PFS (HR=0.55, 95% CI: 0.47 to 0.63), and ORR (RR=0.65, 95% CI: 0.57 to 0.74) without increasing toxicity (HR=0.59, 95% CI: 0.16 to 2.25). Subgroup analyses on OS and PFS by study design (randomized vs non-randomized study design), disease stage (Stage I–III vs Stage IV), cotreatment with dendritic cells (DCs) (CIK vs DC-CIK therapy), or timing of therapy administration (concurrent vs sequential with coadministered anticancer therapy) also showed that the clinical benefit of CIK therapy was robust in any subgroup analysis. Furthermore, cotreatment with DCs did not improve clinical outcomes over CIK therapy alone. CONCLUSION: Compared with standard therapy, patients who received additional CIK cell therapy had favorable outcomes without increased toxicity, warranting further investigation into CIK therapy for the treatment of CRC. |
format | Online Article Text |
id | pubmed-10152003 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-101520032023-05-03 Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis Li, Celine Man Ying Tomita, Yoko Dhakal, Bimala Li, Runhao Li, Jun Drew, Paul Price, Timothy Smith, Eric Maddern, Guy J Fenix, Kevin Aaron J Immunother Cancer Immune Cell Therapies and Immune Cell Engineering BACKGROUND: The number of clinical studies evaluating the benefit of cytokine-induced killer cell (CIK) therapy, an adoptive immunotherapy, for colorectal cancer (CRC) is increasing. In many of these trials, CIK therapy was coadministered with conventional cancer therapy. The aim of this review is to systematically assess the available literature, in which the majority were only in Chinese, on CIK therapy for the management of CRC using meta-analysis and to identify parameters associated with successful CIK therapy implementation. METHODS: Prospective and retrospective clinical studies which compared CIK therapy to non-CIK therapy in patients with CRC were searched for electronically on MEDLINE, Embase, China National Knowledge Infrastructure, and Wanfang Data databases. The clinical endpoints of overall survival (OS), progression-free survival (PFS), OS and PFS rates, overall response rate (ORR), and toxicity were meta-analyzed using HR and relative ratio (RR), and subgroup analyses were performed using chi-square (χ(2)) test and I-squared (I(2)) statistics for study design, disease stage, cotherapy type, and timing of administration. RESULTS: In total, 70 studies involving 6743 patients were analyzed. CIK therapy was favored over non-CIK therapy for OS (HR=0.59, 95% CI: 0.53 to 0.65), PFS (HR=0.55, 95% CI: 0.47 to 0.63), and ORR (RR=0.65, 95% CI: 0.57 to 0.74) without increasing toxicity (HR=0.59, 95% CI: 0.16 to 2.25). Subgroup analyses on OS and PFS by study design (randomized vs non-randomized study design), disease stage (Stage I–III vs Stage IV), cotreatment with dendritic cells (DCs) (CIK vs DC-CIK therapy), or timing of therapy administration (concurrent vs sequential with coadministered anticancer therapy) also showed that the clinical benefit of CIK therapy was robust in any subgroup analysis. Furthermore, cotreatment with DCs did not improve clinical outcomes over CIK therapy alone. CONCLUSION: Compared with standard therapy, patients who received additional CIK cell therapy had favorable outcomes without increased toxicity, warranting further investigation into CIK therapy for the treatment of CRC. BMJ Publishing Group 2023-04-28 /pmc/articles/PMC10152003/ /pubmed/37117007 http://dx.doi.org/10.1136/jitc-2023-006764 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Immune Cell Therapies and Immune Cell Engineering Li, Celine Man Ying Tomita, Yoko Dhakal, Bimala Li, Runhao Li, Jun Drew, Paul Price, Timothy Smith, Eric Maddern, Guy J Fenix, Kevin Aaron Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
title | Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
title_full | Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
title_fullStr | Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
title_full_unstemmed | Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
title_short | Use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
title_sort | use of cytokine-induced killer cell therapy in patients with colorectal cancer: a systematic review and meta-analysis |
topic | Immune Cell Therapies and Immune Cell Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10152003/ https://www.ncbi.nlm.nih.gov/pubmed/37117007 http://dx.doi.org/10.1136/jitc-2023-006764 |
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