Adoptive transfer of activated immune cells against solid tumors: A preliminary study.


Journal

Cellular immunology
ISSN: 1090-2163
Titre abrégé: Cell Immunol
Pays: Netherlands
ID NLM: 1246405

Informations de publication

Date de publication:
12 2022
Historique:
received: 14 07 2022
revised: 22 09 2022
accepted: 22 09 2022
pubmed: 12 10 2022
medline: 7 12 2022
entrez: 11 10 2022
Statut: ppublish

Résumé

This study presents preliminary results concerning the effectiveness of a novel immunotherapy in cancer. The proposed adoptive cellular therapy product contains a mixture of effector immune cells, specifically macrophages, NK cells, dendritic cells, cytotoxic T lymphocytes and monoclonal antibody producing plasma cells. The results were based on both descriptive and inferential statistical analysis of data concerning 17 cancer patients. Particularly, performance scales such as clinical condition, Karnofsky-Index, ECOG index and symptom's scale were evaluated post therapy administration (4 months). Furthermore, circulating tumor cells (CTCs) and a specific tumor marker (EpCAM) were measured pre- and post-cellular therapy. The results revealed a positive evaluation for clinical condition (70.59 %), Karnofsky-Index (88.23 %), ECOG index (94.12 %), and symptoms' scale (64.70 %). In addition, statistically significant reductions were found for both CTCs (p = 0.0016) and EpCAM positive cells (p = 0.0005), post-therapy, which were related to large size effects, namely 0.77 and 0.85, respectively. No cytokine storm, anaphylaxis or severe adverse events were observed with 4 months follow up evaluation. These preliminary results indicate that the proposed cellular therapy can be considered for further studies in clinical trials.

Sections du résumé

BACKGROUND
This study presents preliminary results concerning the effectiveness of a novel immunotherapy in cancer. The proposed adoptive cellular therapy product contains a mixture of effector immune cells, specifically macrophages, NK cells, dendritic cells, cytotoxic T lymphocytes and monoclonal antibody producing plasma cells.
METHODS
The results were based on both descriptive and inferential statistical analysis of data concerning 17 cancer patients. Particularly, performance scales such as clinical condition, Karnofsky-Index, ECOG index and symptom's scale were evaluated post therapy administration (4 months). Furthermore, circulating tumor cells (CTCs) and a specific tumor marker (EpCAM) were measured pre- and post-cellular therapy.
RESULTS
The results revealed a positive evaluation for clinical condition (70.59 %), Karnofsky-Index (88.23 %), ECOG index (94.12 %), and symptoms' scale (64.70 %). In addition, statistically significant reductions were found for both CTCs (p = 0.0016) and EpCAM positive cells (p = 0.0005), post-therapy, which were related to large size effects, namely 0.77 and 0.85, respectively. No cytokine storm, anaphylaxis or severe adverse events were observed with 4 months follow up evaluation.
CONCLUSIONS
These preliminary results indicate that the proposed cellular therapy can be considered for further studies in clinical trials.

Identifiants

pubmed: 36219944
pii: S0008-8749(22)00141-1
doi: 10.1016/j.cellimm.2022.104616
pii:
doi:

Substances chimiques

Epithelial Cell Adhesion Molecule 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

104616

Informations de copyright

Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Panagiotis Parsonidis (P)

Research Genetic Cancer Centre S.A., Florina, Greece.

Georgios Beis (G)

Research Genetic Cancer Centre S.A., Florina, Greece.

Aggelos C Iliopoulos (AC)

Research Genetic Cancer Centre S.A., Florina, Greece.

Ioannis Papasotiriou (I)

Research Genetic Cancer Centre International GmbH, Zug, Switzerland. Electronic address: papasotiriou.ioannis@rgcc-international.com.

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Classifications MeSH