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

Author:

Kasajima Masashi,Igawa Satoshi,Manaka Hiroya,Yamada Kaori,Akazawa Yuki,Manabe Hideaki,Yagami Yuri,Yamamoto Hiroki,Ito Hiroki,Kaizuka Nobuki,Nakahara YoshiroORCID,Sato TakashiORCID,Mitshufuji Hisashi,Yokoba Masanori,Kubota Masaru,Sasaki Jiichiro,Naoki Katsuhiko

Abstract

<b><i>Introduction:</i></b> 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. <b><i>Methods:</i></b> 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. <b><i>Results:</i></b> The median follow-up period was 11.1 months. Patients with a BMI ≥20.4 kg/m<sup>2</sup> had significantly longer PFS and OS (3.7 and 22.2 month, respectively) than did those with a BMI &#x3c;20.4 kg/m<sup>2</sup> (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, <i>p</i> = 0.002) and 2 (1.8 months, <i>p</i> = 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, <i>p</i> = 0.002) and 2 (4.7 months, <i>p</i> = 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%, <i>p</i> = 0.03). <b><i>Conclusion:</i></b> The GPS is an independent predictor of PFS and OS in patients with NSCLC who received second- or subsequent-line pembrolizumab or atezolizumab monotherapy.

Publisher

S. Karger AG

Subject

Cancer Research,Oncology,General Medicine

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