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Research ArticleClinical Studies

RBM17 Expression Is Associated With the Efficacy of ICI Monotherapy in NSCLC With Low PD-L1 Expression

HIROAKI NAGAMINE, MASAKAZU YASHIRO, NAOKI YOSHIMOTO, MOTOHIRO IZUMI, AKIRA SUGIMOTO, KENJI NAKAHAMA, KOICHI OGAWA, YOSHIYA MATSUMOTO, KENJI SAWA, YOKO TANI, HIROYASU KANEDA, SHIGEKI MITSUOKA, KAZUHIRO YAMADA, TETSUYA WATANABE, KAZUHISA AASAI, KAZUHIRO FUKUMURA, AKILA MAYEDA and TOMOYA KAWAGUCHI
Anticancer Research October 2023, 43 (10) 4663-4672; DOI: https://doi.org/10.21873/anticanres.16662
HIROAKI NAGAMINE
1Department of Respiratory Medicine, Osaka City University, Graduate School of Medicine, Osaka, Japan;
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MASAKAZU YASHIRO
2Molecular Oncology and Therapeutics, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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  • For correspondence: i21496f@omu.ac.jp
NAOKI YOSHIMOTO
3Department of Pulmonary Medicine, Ishikiriseiki Hospital, Higashiosaka, Japan;
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MOTOHIRO IZUMI
4Department of Pulmonary Medicine, Bell land General Hospital, Sakai, Japan;
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AKIRA SUGIMOTO
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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KENJI NAKAHAMA
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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KOICHI OGAWA
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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YOSHIYA MATSUMOTO
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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KENJI SAWA
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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YOKO TANI
6Department of Clinical Oncology, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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HIROYASU KANEDA
6Department of Clinical Oncology, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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SHIGEKI MITSUOKA
6Department of Clinical Oncology, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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KAZUHIRO YAMADA
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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TETSUYA WATANABE
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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KAZUHISA AASAI
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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KAZUHIRO FUKUMURA
7Division of Gene Expression Mechanism, Center for Medical Science, Fujita Health University, Toyoake, Japan
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AKILA MAYEDA
7Division of Gene Expression Mechanism, Center for Medical Science, Fujita Health University, Toyoake, Japan
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TOMOYA KAWAGUCHI
5Department of Respiratory Medicine, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
6Department of Clinical Oncology, Osaka Metropolitan University, Graduate School of Medicine, Osaka, Japan;
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Abstract

Background/Aim: Immune checkpoint inhibitors (ICIs) are currently a standard treatment tool for non-small cell lung cancer (NSCLC). RNA-binding motif protein 17 (RBM17), a splicing factor, is frequently over-expressed in NSCLC, but little is known about the role of RBM17 in the efficacy of ICIs for NSCLC. Thus, we investigated the correlation between RBM17 expression and ICI efficacy in NSCLC. Patients and Methods: Biopsy or surgical specimens were collected from patients with advanced or recurrent NSCLC who received ICI monotherapy or chemo-immunotherapy in a first-line setting. RBM17 expression was examined using immunohistochemistry. The correlation between the efficacy of ICI monotherapy or chemo-immunotherapy and RBM17 expression was evaluated. Results: Among the 218 cases, 115 (52.8%) cases were positive for RBM17 expression. RBM17 expression was not associated with the objective response rate (ORR) or progression-free survival (PFS) in either of the ICI monotherapy or chemo-immunotherapy groups. However, among those with a low PD-L1 expression level (PD-L1 <50%; n=86), RBM17 expression was significantly associated with a better ORR (p=0.045) and a better PFS (p<0.001) in the ICI monotherapy group, and was significantly associated with a poor ORR in the chemo-immunotherapy group (p=0.041). Conclusion: RBM17 might be a useful predictive marker for a higher efficacy of ICI monotherapy in NSCLC patients with a low PD-L1 expression level.

Key Words:
  • Splicing factor
  • RBM17/SPF45
  • non-small cell lung cancer
  • immune checkpoint inhibitor
  • chemotherapy
  • predictive marker
  • chemosensitivity
  • Received July 21, 2023.
  • Revision received September 4, 2023.
  • Accepted September 5, 2023.
  • Copyright © 2023 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.
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Anticancer Research: 43 (10)
Anticancer Research
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October 2023
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RBM17 Expression Is Associated With the Efficacy of ICI Monotherapy in NSCLC With Low PD-L1 Expression
HIROAKI NAGAMINE, MASAKAZU YASHIRO, NAOKI YOSHIMOTO, MOTOHIRO IZUMI, AKIRA SUGIMOTO, KENJI NAKAHAMA, KOICHI OGAWA, YOSHIYA MATSUMOTO, KENJI SAWA, YOKO TANI, HIROYASU KANEDA, SHIGEKI MITSUOKA, KAZUHIRO YAMADA, TETSUYA WATANABE, KAZUHISA AASAI, KAZUHIRO FUKUMURA, AKILA MAYEDA, TOMOYA KAWAGUCHI
Anticancer Research Oct 2023, 43 (10) 4663-4672; DOI: 10.21873/anticanres.16662

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RBM17 Expression Is Associated With the Efficacy of ICI Monotherapy in NSCLC With Low PD-L1 Expression
HIROAKI NAGAMINE, MASAKAZU YASHIRO, NAOKI YOSHIMOTO, MOTOHIRO IZUMI, AKIRA SUGIMOTO, KENJI NAKAHAMA, KOICHI OGAWA, YOSHIYA MATSUMOTO, KENJI SAWA, YOKO TANI, HIROYASU KANEDA, SHIGEKI MITSUOKA, KAZUHIRO YAMADA, TETSUYA WATANABE, KAZUHISA AASAI, KAZUHIRO FUKUMURA, AKILA MAYEDA, TOMOYA KAWAGUCHI
Anticancer Research Oct 2023, 43 (10) 4663-4672; DOI: 10.21873/anticanres.16662
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Keywords

  • Splicing factor
  • RBM17/SPF45
  • non-small cell lung cancer
  • immune checkpoint inhibitor
  • chemotherapy
  • predictive marker
  • chemosensitivity
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