Tertiary lymphoid structure and neutrophil–lymphocyte ratio coordinately predict outcome of pembrolizumab

Author:

Komura Kazumasa12ORCID,Tokushige Satoshi1,Ishida Mitsuaki3,Hirosuna Kensuke4,Yamazaki Shogo1,Nishimura Kazuki15,Ajiro Masahiko5,Ohno Takaya1,Nakamori Keita1,Kinoshita Shoko1,Tsujino Takuya1ORCID,Maenosono Ryoichi1,Yoshikawa Yuki1,Takai Tomoaki1,Tsutsumi Takeshi1,Taniguchi Kohei2ORCID,Tanaka Tomohito2ORCID,Takahara Kiyoshi6,Inamoto Teruo1,Hirose Yoshinobu3,Ono Fumihito2,Shiraishi Yuichi7,Yoshimi Akihide5ORCID,Azuma Haruhito1

Affiliation:

1. Department of Urology Osaka Medical and Pharmaceutical University Takatsuki City, Osaka Japan

2. Division of Translational Research Osaka Medical and Pharmaceutical Takatsuki City, Osaka Japan

3. Department of Pathology Osaka Medical and Pharmaceutical University Takatsuki City, Osaka Japan

4. Graduate School of Medicine Okayama University Okayama Japan

5. Division of Cancer RNA Research National Cancer Center Research Institute Chuo‐ku, Tokyo Japan

6. Department of Urology Fujita‐Health University School of Medicine Toyoake City Japan

7. Division of Genome Analysis Platform Development National Cancer Center Research Chuo‐ku, Tokyo Japan

Abstract

AbstractEmerging evidence suggests that the presence of tertiary lymphoid structures (TLS) and neutrophil–lymphocyte ratio (NLR) in peripheral blood is associated with the treatment response to checkpoint inhibitors (CPIs), whereas there is limited knowledge regarding whether these factors reciprocally impact the treatment outcomes of CPIs in metastatic urothelial carcinoma (mUC). Herein, we investigated treatment outcomes of platinum‐refractory mUC patients (50 cases with whole‐exome and transcriptome sequencing) treated with pembrolizumab. The pathological review identified 24% of cases of TLS in the specimens. There was no significant difference in the NLR between the TLS− and TLS+ groups (p = 0.153). In the lower NLR group, both overall survival and progression‐free survival were significantly longer in patients with TLS than in those without TLS, whereas the favorable outcomes associated with TLS were not observed in patients in the higher NLR group. We explored transcriptomic differences in UC with TLS. The TLS was comparably observed between luminal (20%) and basal (25%) tumor subtypes (p = 0.736). Exploring putative immune‐checkpoint genes revealed that ICOSLG (B7‐H2) was significantly increased in tumors with lower NLR. KRT expression levels exhibited higher basal cell markers (KRT5 and KRT17) in the higher NLR group and lower differentiated cell markers (KRT8 and KRT18) in patients with TLS. In conclusion, the improved outcomes of pembrolizumab treatment in mUC are restricted to patients with lower NLR. Our findings begin to elucidate a distinct molecular pattern for the presence of TLS according to the NLR in peripheral blood.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Japanese Urological Association

Naito Science and Engineering Foundation

SGH Foundation

Takeda Science Foundation

Publisher

Wiley

Subject

Cancer Research,Oncology,General Medicine

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