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Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer

PURPOSE: To determine the long-term efficacy of adjuvant immunotherapy with autologous cytokine-induced killer (CIK) cells for locally advanced gastric cancer patients. EXPERIMENTAL DESIGN: One hundred and fifty-one patients with stage III/IV gastric cancer who had undergone gastrectomy were enrolle...

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Autores principales: Shi, Liangrong, Zhou, Qi, Wu, Jun, Ji, Mei, Li, Guojun, Jiang, Jingting, Wu, Changping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506195/
https://www.ncbi.nlm.nih.gov/pubmed/22674056
http://dx.doi.org/10.1007/s00262-012-1289-2
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author Shi, Liangrong
Zhou, Qi
Wu, Jun
Ji, Mei
Li, Guojun
Jiang, Jingting
Wu, Changping
author_facet Shi, Liangrong
Zhou, Qi
Wu, Jun
Ji, Mei
Li, Guojun
Jiang, Jingting
Wu, Changping
author_sort Shi, Liangrong
collection PubMed
description PURPOSE: To determine the long-term efficacy of adjuvant immunotherapy with autologous cytokine-induced killer (CIK) cells for locally advanced gastric cancer patients. EXPERIMENTAL DESIGN: One hundred and fifty-one patients with stage III/IV gastric cancer who had undergone gastrectomy were enrolled, assigned to two groups (immunotherapy group versus no immunotherapy group/or control group), and followed. RESULTS: The 5-year overall survival (OS) and 5-year disease-free survival (DFS) rates for immunotherapy versus control group were 32.4 versus 23.4 % (P = 0.071) and 28.3 versus 10.4 % (P = 0.044), respectively. For patients with intestinal-type tumors, the 5-year OS and DFS rates were significantly higher for immunotherapy (OS, 46.8 vs. 31.4 % and P = 0.045; DFS, 42.4 vs. 15.7 % and P = 0.023). In the immunotherapy group, the mean CD3(+) level, CD4(+) level, and CD4(+)/CD8(+) ratio increased from 50.8, 26.5, and 0.9 %, respectively, at baseline to 62.6, 35.0, and 1.4 %, respectively, 1 week after the first CIK-cell treatment, returned to baseline after 2 months, and maintained a higher level (60.7 ± 8.2 %, 34.2 ± 7.1 %, and 1.3 ± 0.3 %, respectively) 2 months after 3 cycles of immunotherapy. CONCLUSIONS: Adjuvant immunotherapy with CIK cells prolongs DFS in patients with locally advanced gastric cancer and significantly improves OS in patients with intestinal-type tumors. Intestinal-type tumors could be selected as an important indication for CIK-cell therapy. This treatment may help improve T-lymphocyte subset distribution and improve the host’s immune functions, but multiple cycles are necessary for long-term therapeutic efficacy.
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spelling pubmed-35061952012-11-28 Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer Shi, Liangrong Zhou, Qi Wu, Jun Ji, Mei Li, Guojun Jiang, Jingting Wu, Changping Cancer Immunol Immunother Original Article PURPOSE: To determine the long-term efficacy of adjuvant immunotherapy with autologous cytokine-induced killer (CIK) cells for locally advanced gastric cancer patients. EXPERIMENTAL DESIGN: One hundred and fifty-one patients with stage III/IV gastric cancer who had undergone gastrectomy were enrolled, assigned to two groups (immunotherapy group versus no immunotherapy group/or control group), and followed. RESULTS: The 5-year overall survival (OS) and 5-year disease-free survival (DFS) rates for immunotherapy versus control group were 32.4 versus 23.4 % (P = 0.071) and 28.3 versus 10.4 % (P = 0.044), respectively. For patients with intestinal-type tumors, the 5-year OS and DFS rates were significantly higher for immunotherapy (OS, 46.8 vs. 31.4 % and P = 0.045; DFS, 42.4 vs. 15.7 % and P = 0.023). In the immunotherapy group, the mean CD3(+) level, CD4(+) level, and CD4(+)/CD8(+) ratio increased from 50.8, 26.5, and 0.9 %, respectively, at baseline to 62.6, 35.0, and 1.4 %, respectively, 1 week after the first CIK-cell treatment, returned to baseline after 2 months, and maintained a higher level (60.7 ± 8.2 %, 34.2 ± 7.1 %, and 1.3 ± 0.3 %, respectively) 2 months after 3 cycles of immunotherapy. CONCLUSIONS: Adjuvant immunotherapy with CIK cells prolongs DFS in patients with locally advanced gastric cancer and significantly improves OS in patients with intestinal-type tumors. Intestinal-type tumors could be selected as an important indication for CIK-cell therapy. This treatment may help improve T-lymphocyte subset distribution and improve the host’s immune functions, but multiple cycles are necessary for long-term therapeutic efficacy. Springer-Verlag 2012-06-07 2012 /pmc/articles/PMC3506195/ /pubmed/22674056 http://dx.doi.org/10.1007/s00262-012-1289-2 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Shi, Liangrong
Zhou, Qi
Wu, Jun
Ji, Mei
Li, Guojun
Jiang, Jingting
Wu, Changping
Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
title Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
title_full Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
title_fullStr Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
title_full_unstemmed Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
title_short Efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
title_sort efficacy of adjuvant immunotherapy with cytokine-induced killer cells in patients with locally advanced gastric cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3506195/
https://www.ncbi.nlm.nih.gov/pubmed/22674056
http://dx.doi.org/10.1007/s00262-012-1289-2
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