Association of baseline serum levels of CXCL5 with the efficacy of nivolumab in advanced melanoma

Taku Fujimura, Yota Sato, Kayo Tanita, Chinbing Lyu, Yumi Kambayashi, Ryo Amagai, Atsushi Otsuka, Yasuhiro Fujisawa, Koji Yoshino, Shigeto Matsushita, Hiroshi Uchi, Yuki Yamamoto, Hiroo Hata, Takeru Funakoshi, Yumi Nonomura, Ryota Tanaka, Hisako Okuhira, Naoko Wada, Akira Hashimoto, Setsuya Aiba

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)

Abstract

Anti-programmed cell death protein 1 (PD1) antibodies are in wide use for the treatment of various cancers. PD1 antibody-based immunotherapy, co-administration of nivolumab and ipilimumab, is one of the optimal immunotherapies, especially in advanced melanoma with high tumor mutation burden. Since this combined therapy leads to a high frequency of serious immune-related adverse events (irAEs) in patients with advanced melanoma, biomarkers are needed to evaluate nivolumab efficacy to avoid serious irAEs caused by ipilimumab. This study analyzed baseline serum levels of CXCL5, CXCL10, and CCL22 in 46 cases of advanced cutaneous melanoma treated with nivolumab. Baseline serum levels of CXCL5 were significantly increased in responders compared to non-responders. In contrast, there were no significant differences of baseline serum levels of CXCL10 and CCL22 between responders and non-responders. These results suggest that baseline serum levels of CXCL5 may be useful as a biomarker for screening patients with advanced cutaneous melanoma most likely to benefit from anti-melanoma immunotherapy.

Original languageEnglish
Article number86
JournalFrontiers in Medicine
Volume6
Issue numberAPR
DOIs
Publication statusPublished - 2019

Keywords

  • Baseline levels of CXCL5
  • Melanoma
  • Nivolumab
  • Nivolumab and ipilimumab combined therapy
  • Prediction of efficacy

ASJC Scopus subject areas

  • Medicine(all)

Fingerprint Dive into the research topics of 'Association of baseline serum levels of CXCL5 with the efficacy of nivolumab in advanced melanoma'. Together they form a unique fingerprint.

Cite this