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The Glasgow Prognostic Score Predicts Outcomes of Pembrolizumab or Atezolizumab Monotherapy in Patients with Pretreated Non-small Cell Lung Cancer

Authors :
Masashi Kasajima
Satoshi Igawa
Hiroya Manaka
Kaori Yamada
Yuki Akazawa
Hideaki Manabe
Yuri Yagami
Hiroki Yamamoto
Hiroki Ito
Nobuki Kaizuka
Yoshiro Nakahara
Takashi Sato
Hisashi Mitshufuji
Masanori Yokoba
Masaru Kubota
Jiichiro Sasaki
Katsuhiko Naoki
Source :
Oncology.
Publication Year :
2022

Abstract

Introduction: Predictors of the effectiveness of immune checkpoint inhibitor (ICI) monotherapy in previously treated patients with non-small cell lung cancer (NSCLC) remain ill-defined. We investigated whether the Glasgow prognostic score (GPS) could serve as such predictors. Methods: Eighty patients treated with pembrolizumab or atezolizumab monotherapy as second- or subsequent-line therapy for NSCLC were retrospectively reviewed, and the associations between GPS, body mass index (BMI), and each of progression-free survival (PFS) and overall survival (OS) were assessed. Results: The median follow-up period was 11.1 months. Patients with a BMI ≥20.4 kg/m2 had significantly longer PFS and OS (3.7 and 22.2 month, respectively) than did those with a BMI 2 (2.2 and 11.5 months, respectively). Patients with a GPS of 0 had a significantly longer PFS (6.6 months) than did those with a GPS of 1 (2.2 months, p = 0.002) and 2 (1.8 months, p = 0.029). Patients with a GPS of 0 also had a significantly longer OS (22.2 month) than did those with a GPS of 1 (9.2 months, p = 0.002) and 2 (4.7 months, p = 0.002). Notably, the GPS, BMI, and clinical stage were independent predictors of PFS, while the GPS and performance status were independent predictors of OS. The response rate of patients with a GPS of 0 was significantly higher than that of patients with a GPS of 1–2 (26.2% vs. 7.9%, p = 0.03). Conclusion: The GPS is an independent predictor of PFS and OS in patients with NSCLC who received second- or subsequent-line pembrolizumab or atezolizumab monotherapy.

Details

ISSN :
14230232
Database :
OpenAIRE
Journal :
Oncology
Accession number :
edsair.doi.dedup.....0aeb6bd2744ef064ddae4f5362de4457