Antibiotic Usage Reduced Overall Survival by over 70% in Non-small Cell Lung Cancer Patients on Anti-PD-1 Immunotherapy.


Journal

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

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 29 07 2021
revised: 22 08 2021
accepted: 23 08 2021
entrez: 1 10 2021
pubmed: 2 10 2021
medline: 13 10 2021
Statut: ppublish

Résumé

There is an increasing use of immunotherapy for non-small cell lung cancer (NSCLC) patients. The present study analysed the effect of antibiotic use on the outcome of NSCLC patients undergoing treatment with anti-programmed cell death-1 (anti-PD-1) immunotherapy. This was a retrospective study of 69 NSCLC patients. Eighteen out of 69 patients received antibiotics within 21 days before or within 21 days after start of anti-PD-1 therapy. Patients treated with anti-PD-1 antibodies receiving antibiotics had greatly decreased objective response rate (ORR), overall survival (OS) and progression-free survival (PFS) compared to those who did not use antibiotics. Multivariate analysis showed that antibiotic treatment of patients on anti-PD-1 antibody therapy was an independent negative predictive factor of PFS; however, it was not a significant independent predictive factor of OS. Use of antibiotics within 21 days before and after anti-PD-1 treatment initiation in patients with NSCLC strongly reduced OS and PFS, suggesting the two treatments should not be combined.

Sections du résumé

BACKGROUND/AIM OBJECTIVE
There is an increasing use of immunotherapy for non-small cell lung cancer (NSCLC) patients. The present study analysed the effect of antibiotic use on the outcome of NSCLC patients undergoing treatment with anti-programmed cell death-1 (anti-PD-1) immunotherapy.
PATIENTS AND METHODS METHODS
This was a retrospective study of 69 NSCLC patients. Eighteen out of 69 patients received antibiotics within 21 days before or within 21 days after start of anti-PD-1 therapy.
RESULTS RESULTS
Patients treated with anti-PD-1 antibodies receiving antibiotics had greatly decreased objective response rate (ORR), overall survival (OS) and progression-free survival (PFS) compared to those who did not use antibiotics. Multivariate analysis showed that antibiotic treatment of patients on anti-PD-1 antibody therapy was an independent negative predictive factor of PFS; however, it was not a significant independent predictive factor of OS.
CONCLUSION CONCLUSIONS
Use of antibiotics within 21 days before and after anti-PD-1 treatment initiation in patients with NSCLC strongly reduced OS and PFS, suggesting the two treatments should not be combined.

Identifiants

pubmed: 34593446
pii: 41/10/4985
doi: 10.21873/anticanres.15312
doi:

Substances chimiques

Anti-Bacterial Agents 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4985-4993

Informations de copyright

Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Kazuyuki Hamada (K)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Department of Surgery, University of California, San Diego, CA, U.S.A.
AntiCancer Inc., San Diego, CA, U.S.A.

Kiyoshi Yoshimura (K)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan; kyoshim1@med.showa-u.ac.jp.
Department of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Yuya Hirasawa (Y)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Masahiro Hosonuma (M)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Department of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Masakazu Murayama (M)

Department of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Yoichiro Narikawa (Y)

Department of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Hirotsugu Ariizumi (H)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Ryotaro Ohkuma (R)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Midori Shida (M)

Department of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Yutaro Kubota (Y)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Satoshi Matsukuma (S)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Tomoyuki Ishiguro (T)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Takehiko Sambe (T)

Division of Clinical Pharmacology, Department of Pharmacology, Showa University School of Medicine, Tokyo, Japan.
Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Atsushi Horiike (A)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

Atsuo Kuramasu (A)

Department of Clinical Immuno Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Satoshi Wada (S)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Department of Clinical Diagnostic Oncology, Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Junji Tsurutani (J)

Advanced Cancer Translational Research Institute, Showa University, Tokyo, Japan.

Eisuke Inoue (E)

Research Administration Center, Showa University, Tokyo, Japan.

Naoki Uchida (N)

Division of Clinical Pharmacology, Department of Pharmacology, Showa University School of Medicine, Tokyo, Japan.
Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Yuji Kiuchi (Y)

Department of Pharmacology, Showa University School of Medicine, Tokyo, Japan.

Shinichi Kobayashi (S)

Clinical Research Institute for Clinical Pharmacology and Therapeutics, Showa University, Tokyo, Japan.

Robert M Hoffman (RM)

Department of Surgery, University of California, San Diego, CA, U.S.A.
AntiCancer Inc., San Diego, CA, U.S.A.

Takuya Tsunoda (T)

Division of Medical Oncology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.

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