Systemic Inflammation/Nutritional Status Scores Are Prognostic but Not Predictive in Metastatic Non-Small-Cell Lung Cancer Treated with First-Line Immune Checkpoint Inhibitors

Author:

Mahiat Cédric1ORCID,Bihin Benoît2ORCID,Duplaquet Fabrice1,Stanciu Pop Claudia3,Dupont Michael4ORCID,Vander Borght Thierry5,Rondelet Benoît6ORCID,Vanderick Jean7,André Bénédicte2,Pirard Lionel1ORCID,Ocak Sebahat18ORCID

Affiliation:

1. Pneumology Division, CHU UCL Namur (Godinne Site), Université Catholique de Louvain (UCLouvain), Avenue Docteur G. Thérasse 1, 5530 Yvoir, Belgium

2. Scientific Support Unit, CHU UCL Namur (Godinne Site), UCLouvain, Avenue Docteur G. Thérasse 1, 5530 Yvoir, Belgium

3. Pathology Department, CHU UCL Namur (Godinne Site), UCLouvain, Avenue Docteur G. Thérasse 1, 5530 Yvoir, Belgium

4. Radiology Division, CHU UCL Namur (Godinne Site), UCLouvain, Avenue Docteur G. Thérasse 1, 5530 Yvoir, Belgium

5. Nuclear Medicine Division, CHU UCL Namur (Godinne Site), UCLouvain, Avenue Docteur G. Thérasse 1, 5530 Yvoir, Belgium

6. Thoracic Surgery Department, CHU UCL Namur (Godinne Site), UCLouvain, Avenue Docteur G. Thérasse 1, 5530 Yvoir, Belgium

7. Radiation Therapy Department, CHU UCL Namur (Sainte Elisabeth Site), UCLouvain, Place Louise Godin 15, 5000 Namur, Belgium

8. Pole of Pneumology, ENT, and Dermatology (PNEU), Institut de Recherche Expérimentale et Clinique (IREC), UCLouvain, Avenue Hippocrate 10, 1200 Brussels, Belgium

Abstract

Biomarkers of systemic inflammation/nutritional status have been associated with outcomes in advanced-stage non-small-cell lung cancer (NSCLC) treated with immune checkpoint inhibitors (ICIs). However, most of them were not tested in cohorts of patients treated with ICIs in combination with chemotherapy (CT) (ICI + CT) or with CT alone, making it impossible to discriminate a predictive from a prognostic effect. We conducted a single-center retrospective study to search for associations between various baseline biomarkers/scores that reflected the systemic inflammation/nutritional status (Lung Immune Prognostic Index, Modified Lung Immune Prognostic Index, Scottish Inflammatory Prognostic Score, Advanced Lung Cancer Inflammation Index, EPSILoN, Prognostic Nutritional Index, Systemic Immune-Inflammation Index, Gustave Roussy Immune Score, Royal Marsden Hospital Prognostic Score, Lung Immuno-oncology Prognostic Score 3, Lung Immuno-oncology Prognostic Score 4, score published by Holtzman et al., and Glasgow Prognostic Score) and outcomes in metastatic NSCLC treated in a first-line setting either with ICI in monotherapy (cohort 1; n = 75), ICI + CT (cohort 2; n = 56), or CT alone (cohort 3; n = 221). In the three cohorts, the biomarkers/scores were moderately associated with overall survival (OS) and progression-free survival (PFS). Their prognostic performance was relatively poor, with a maximum c-index of 0.66. None of them was specific to ICIs and could help to choose the best treatment modality. The systemic inflammation/nutritional status, associated with outcomes independently of the treatment, is therefore prognostic but not predictive in metastatic NSCLC.

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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