Programmed cell death ligand 1 measurement study in granulocyte colony-stimulating factor-producing lung cancer: an observational study

Background Granulocyte colony-stimulating factor (G-CSF)-producing lung cancer induces severe inflammation and a high white blood cell (WBC) count and is associated with poor prognosis. A recent case of G-CSF-producing lung adenocarcinoma showed high expression of programmed cell death ligand 1 (PD-...

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Veröffentlicht in:BMC cancer 2022-09, Vol.22 (1), p.1-977, Article 977
Hauptverfasser: Miyazaki, Kazuhito, Shiba, Aya, Ikeda, Toshiki, Higashi, Yuko, Aga, Masaharu, Hamakawa, Yusuke, Taniguchi, Yuri, Misumi, Yuki, Agemi, Yoko, Nakamura, Yukiko, Shimokawa, Tsuneo, Okamoto, Hiroaki
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Sprache:eng
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Zusammenfassung:Background Granulocyte colony-stimulating factor (G-CSF)-producing lung cancer induces severe inflammation and a high white blood cell (WBC) count and is associated with poor prognosis. A recent case of G-CSF-producing lung adenocarcinoma showed high expression of programmed cell death ligand 1 (PD-L1) and was treated with pembrolizumab as first-line therapy, which was extremely effective. We hypothesized that G-CSF-producing lung cancers are associated with high PD-L1 expression. Methods This retrospective study included patients diagnosed with lung cancer at Yokohama Municipal Citizen's Hospital (Kanagawa, Japan) between 2009 and 2019. The PD-L1 status of 13 patients with high plasma G-CSF levels ([greater than or equal to]40 pg/mL) was assessed by conducting immunohistochemical analysis of tissue samples. Results Of the total patients, 11 were men and 2 were women, with a median age of 74 years (70-85 years). Four, five, and three patients had adenocarcinoma, squamous cell carcinoma, and others, respectively. The median G-CSF level and WBC count were 85.5 pg/mL (range, 40.8-484 pg/mL) and 15,550/[mu]L (range, 6,190-56,800/[mu]L), respectively. The PD-L1 tumor proportion scores (TPSs) were [greater than or equal to]50%, 1%-49%, and
ISSN:1471-2407
1471-2407
DOI:10.1186/s12885-022-10065-w