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Analysis of the Clinical Efficacy of Dendritic Cell -cytokine Induced Killer Cell-based Adoptive Immunotherapy for Colorectal Cancer.
Xu, Huiru; Qin, Weishan; Feng, Huijing; Song, Dong; Yang, Xiaoling; Zhang, Junping.
Afiliación
  • Xu H; Department of Thoracic Oncology, Cancer Center, Shanxi Academy of Medical Sciences (Shanxi Bethune Hospital), Taiyuan, China.
  • Qin W; Department of Ophthalmology, Shanxi Medical University Second Affiliated Hospital, Taiyuan, China.
  • Feng H; Department of Thoracic Oncology, Cancer Center, Shanxi Academy of Medical Sciences (Shanxi Bethune Hospital), Taiyuan, China.
  • Song D; Department of Thoracic Oncology, Cancer Center, Shanxi Academy of Medical Sciences (Shanxi Bethune Hospital), Taiyuan, China.
  • Yang X; Department of Thoracic Oncology, Cancer Center, Shanxi Academy of Medical Sciences (Shanxi Bethune Hospital), Taiyuan, China.
  • Zhang J; Department of Thoracic Oncology, Cancer Center, Shanxi Academy of Medical Sciences (Shanxi Bethune Hospital), Taiyuan, China.
Immunol Invest ; 50(6): 622-633, 2021 Aug.
Article en En | MEDLINE | ID: mdl-32718264
Background: To analyze the efficacy and safety of dendritic cell - cytokine - induced killer (DC-CIK) immunotherapy combined with chemotherapy for colorectal cancer. Method: A retrospective analysis was conducted in 116 patients from February 2012 to December 2017, who were divided into postoperative adjuvant chemotherapy group alone, combined DC-CIK immunotherapy group, advanced cancer palliative care group, and palliative care + DC-CIK immunotherapy group, to evaluate cellular immune function, disease-free survival(DFS) and overall survival(OS). Results: In the adjuvant therapy and palliative care group, the percentages of CD3+, CD8+ and NK cells after treatment were significantly lower than before, whereas in the other two groups given DC-CIK immunotherapy, the percentages of CD3+, CD8+, NK and NKT cells after treatment were all higher than before, with a significant increase compared with the chemotherapy group (P < .05). DFS (42.4 ± 5.26 m) in the group receiving postoperative adjuvant chemotherapy + DC-CIK immunotherapy was significantly longer than that (23.5 ± 2.79 m) in the group only given postoperative adjuvant chemotherapy (P < .05). OS in the group receiving palliative care + DC-CIK immunotherapy was slightly longer than that in the group only given palliative care for advanced cancer (29 m vs 26 m, P > .05).Conclusion: Combination with DC-CIK immunotherapy could effectively improve cellular immune function. Postoperative adjuvant chemotherapy in combination with DC-CIK immunotherapy could significantly prolong DFS, but palliative care in combination with DC-CIK immunotherapy did not significantly prolong OS in patients with advanced cancer.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Dendríticas / Neoplasias Colorrectales / Inmunoterapia Adoptiva / Células Asesinas Inducidas por Citocinas / Recurrencia Local de Neoplasia Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Immunol Invest Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Células Dendríticas / Neoplasias Colorrectales / Inmunoterapia Adoptiva / Células Asesinas Inducidas por Citocinas / Recurrencia Local de Neoplasia Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Immunol Invest Asunto de la revista: ALERGIA E IMUNOLOGIA Año: 2021 Tipo del documento: Article País de afiliación: China