Changes in Immunological Status in Patients With Metastatic Colorectal Cancer Treated With First-line Chemoimmunotherapy.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 23 05 2020
revised: 21 06 2020
accepted: 22 06 2020
entrez: 31 7 2020
pubmed: 31 7 2020
medline: 11 8 2020
Statut: ppublish

Résumé

Chemoimmunotherapy is a promising treatment for various malignant diseases. In this study, we examined whether first-line chemoimmunotherapy using adoptive immune-cell therapy was effective for metastatic colorectal cancer (mCRC). The therapeutic efficacy and safety of the standard first-line chemoimmunotherapy with adoptive αβ T cell therapy and bevacizumab were assessed using thirty-two patients with mCRC in our hospital. Immunological status after this chemoimmunotherapy was also evaluated. The response and disease control rates were 68.8% and 87.5%, respectively. Further, median progression-free and overall survival were 14.2 and 35.3 months. Immunotherapy-associated toxicity was minimal. Significant decrease in the change of monocyte number (p=0.006) and increase in the change of rate of lymphocyte-to-monocyte ratio (p=0.039) were seen in the complete response group. First-line chemoimmunotherapy with adoptive αβ T cell therapy may be useful for mCRC.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
Chemoimmunotherapy is a promising treatment for various malignant diseases. In this study, we examined whether first-line chemoimmunotherapy using adoptive immune-cell therapy was effective for metastatic colorectal cancer (mCRC).
PATIENTS AND METHODS METHODS
The therapeutic efficacy and safety of the standard first-line chemoimmunotherapy with adoptive αβ T cell therapy and bevacizumab were assessed using thirty-two patients with mCRC in our hospital. Immunological status after this chemoimmunotherapy was also evaluated.
RESULTS RESULTS
The response and disease control rates were 68.8% and 87.5%, respectively. Further, median progression-free and overall survival were 14.2 and 35.3 months. Immunotherapy-associated toxicity was minimal. Significant decrease in the change of monocyte number (p=0.006) and increase in the change of rate of lymphocyte-to-monocyte ratio (p=0.039) were seen in the complete response group.
CONCLUSION CONCLUSIONS
First-line chemoimmunotherapy with adoptive αβ T cell therapy may be useful for mCRC.

Identifiants

pubmed: 32727803
pii: 40/8/4763
doi: 10.21873/anticanres.14478
doi:

Substances chimiques

Bevacizumab 2S9ZZM9Q9V
Fluorouracil U3P01618RT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4763-4771

Informations de copyright

Copyright© 2020, International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Teppei Yamada (T)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan yamatetsu2013@gmail.com.
Department of Regenerative Medicine & Transplantation, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Yoichiro Yoshida (Y)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Toshiki Maeda (T)

Department of Preventive Medicine and Public Health, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Gumpei Yoshimatsu (G)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.
Department of Regenerative Medicine & Transplantation, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Naoya Aisu (N)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Kanefumi Yamashita (K)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Akira Komono (A)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Ryuji Kajitani (R)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Yoshiko Matsumoto (Y)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Hideki Nagano (H)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Keiko Naito (K)

Fukuoka Medical Clinic, Fukuoka, Japan.

Kosei Yasumoto (K)

Fukuoka Medical Clinic, Fukuoka, Japan.

Rishu Takimoto (R)

Seta Clinic Group, Tokyo, Japan.
Department of Next Generation Cell and Immune Therapy, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Takashi Kamigaki (T)

Seta Clinic Group, Tokyo, Japan.
Department of Next Generation Cell and Immune Therapy, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Shigenori Goto (S)

Seta Clinic Group, Tokyo, Japan.
Department of Next Generation Cell and Immune Therapy, Graduate School of Medicine, Juntendo University, Tokyo, Japan.

Fumihiro Yoshimura (F)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Naoaki Sakata (N)

Department of Regenerative Medicine & Transplantation, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Shohta Kodama (S)

Department of Regenerative Medicine & Transplantation, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

Suguru Hasegawa (S)

Department of Gastroenterological Surgery, Fukuoka University Faculty of Medicine, Fukuoka, Japan.

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