Identification of serum microRNAs predicting the response of esophageal squamous-cell carcinoma to nivolumab.


Journal

Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225

Informations de publication

Date de publication:
17 Feb 2020
Historique:
received: 20 03 2019
accepted: 23 08 2019
pubmed: 16 10 2019
medline: 9 4 2020
entrez: 16 10 2019
Statut: ppublish

Résumé

Nivolumab, a programmed cell death protein 1 (PD-1) inhibitor, showed promising activity for the treatment of advanced esophageal squamous-cell carcinoma in a phase II study (ONO-4538-07; JapicCTI-No.142422). We explored serum microRNA (miRNA) candidate predictive markers of the response to nivolumab. In the phase II study, 19 patients received nivolumab (3 mg/kg IV Q2W) at National Cancer Center Hospital. The expression of 2565 serum miRNAs before and during treatment was analyzed using a 3D-Gene Human miRNA Oligo Chip (Toray Industries, Inc.). Immune-related response evaluation criteria used to evaluate response and miRNA expression were compared between responders and non-responders. The top 20 miRNAs by accuracy in receiver operating characteristic curve analysis were identified by leave-one-out cross-validation, and those with the area under curve values > 0.8, cross-validated accuracy > 0.8, and a 0.5 difference in the average log2 expression level between responders and non-responders were further analyzed. Of the 19 patients, five responded to nivolumab. We identified miRNAs related to the response to nivolumab, including one detected in the serum before treatment (miR-1233-5p; AUC = 0.895) and three present after treatment (miR-6885-5p, miR-4698 and miR-128-2-5p; AUC = 0.93, 0.97 and 0.93, respectively). Candidate miRNAs capable of predicting the response to nivolumab were identified in the serum of patients with advanced esophageal squamous-cell carcinoma in ONO-4538-07.

Sections du résumé

BACKGROUND BACKGROUND
Nivolumab, a programmed cell death protein 1 (PD-1) inhibitor, showed promising activity for the treatment of advanced esophageal squamous-cell carcinoma in a phase II study (ONO-4538-07; JapicCTI-No.142422). We explored serum microRNA (miRNA) candidate predictive markers of the response to nivolumab.
METHODS METHODS
In the phase II study, 19 patients received nivolumab (3 mg/kg IV Q2W) at National Cancer Center Hospital. The expression of 2565 serum miRNAs before and during treatment was analyzed using a 3D-Gene Human miRNA Oligo Chip (Toray Industries, Inc.). Immune-related response evaluation criteria used to evaluate response and miRNA expression were compared between responders and non-responders. The top 20 miRNAs by accuracy in receiver operating characteristic curve analysis were identified by leave-one-out cross-validation, and those with the area under curve values > 0.8, cross-validated accuracy > 0.8, and a 0.5 difference in the average log2 expression level between responders and non-responders were further analyzed.
RESULTS RESULTS
Of the 19 patients, five responded to nivolumab. We identified miRNAs related to the response to nivolumab, including one detected in the serum before treatment (miR-1233-5p; AUC = 0.895) and three present after treatment (miR-6885-5p, miR-4698 and miR-128-2-5p; AUC = 0.93, 0.97 and 0.93, respectively).
CONCLUSIONS CONCLUSIONS
Candidate miRNAs capable of predicting the response to nivolumab were identified in the serum of patients with advanced esophageal squamous-cell carcinoma in ONO-4538-07.

Identifiants

pubmed: 31612917
pii: 5587299
doi: 10.1093/jjco/hyz146
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
MicroRNAs 0
PDCD1 protein, human 0
Programmed Cell Death 1 Receptor 0
Nivolumab 31YO63LBSN

Types de publication

Clinical Trial, Phase II Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

114-121

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permission@oup.com.

Auteurs

Kazuki Sudo (K)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.
Department of Breast and Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Ken Kato (K)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Juntaro Matsuzaki (J)

Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.

Satoko Takizawa (S)

Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.
Toray Industries, Inc., Tokyo, Japan.

Yoshiaki Aoki (Y)

Dynacom Co., Chiba, Japan.

Hirokazu Shoji (H)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Satoru Iwasa (S)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Yoshitaka Honma (Y)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Atsuo Takashima (A)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Hiromi Sakamoto (H)

Department of Biobank and Tissue Resources, National Cancer Center Research Institute, Tokyo, Japan.

Tomoaki Naka (T)

Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan.

Shigeki Sekine (S)

Department of Pathology and Clinical Laboratories, National Cancer Center Hospital, Tokyo, Japan.

Narikazu Boku (N)

Department of Gastrointestinal Medical Oncology, National Cancer Center Hospital, Tokyo, Japan.

Takahiro Ochiya (T)

Division of Molecular and Cellular Medicine, National Cancer Center Research Institute, Tokyo, Japan.

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Classifications MeSH