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. 2019 Dec;8(6):1078-1085.
doi: 10.21037/tlcr.2019.11.07.

Evaluation of the lung immune prognostic index in advanced non-small cell lung cancer patients under nivolumab monotherapy

Affiliations

Evaluation of the lung immune prognostic index in advanced non-small cell lung cancer patients under nivolumab monotherapy

Juan Ruiz-Bañobre et al. Transl Lung Cancer Res. 2019 Dec.

Abstract

The lung immune prognostic index (LIPI) has been proposed as a new categorical blood-based biomarker to select advanced non-small cell lung cancer (NSCLC) patients for anti-programmed cell death-1 (PD-1) or programmed death ligand 1 (PD-L1) therapy. In this study, we investigate for the first time to the best of our knowledge the prognostic and predictive utility of the LIPI in a multicenter nivolumab monotherapy-based cohort. We retrospectively analyzed the influence of the baseline LIPI on overall survival (OS), progression-free survival (PFS), disease control rate (DCR), and overall response rate (ORR) among 153 patients of a cohort of 188 advanced NSCLC patients treated with nivolumab in the second line of therapy or beyond. Worse LIPI was significantly associated with shorter OS in univariate [hazard ratio (HR) =3.12, 95% confidence interval (CI), 2.12-4.60; P<0.0001] and multivariate (HR =3.67, 95% CI, 1.96-6.86; P<0.0001) analyses. Worse LIPI was associated with shorter PFS (HR =1.45, 95% CI, 1.05-2.03; P=0.03), but this correlation did not reach statistical significance in multivariate analysis (HR =1.49, 95% CI, 0.94-2.38; P=0.09). Worse LIPI was associated with lower DCR in univariate [odds ratio (OR) =0.41, 95% CI, 0.24-0.70; P=0.001] and multivariate (OR =0.44, 95% CI, 0.25-0.78; P=0.005) analyses. This study confirms the utility of the LIPI in prognostication and disease control prediction in advanced NSCLC patients treated with nivolumab in the second line of therapy or beyond.

Keywords: Lung immune prognostic index (LIPI); biomarkers; immunotherapy; lung cancer; nivolumab.

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Conflict of interest statement

Conflicts of Interest: Juan Ruiz-Bañobre - Travel, Accommodations, Expenses: Bristol-Myers Squibb, Merck Sharp & Dohme, Ipsen, PharmaMar. Speakers’ Bureau: Roche. María C. Areses-Manrique - Consulting or Advisory Role: Roche/Genentech, AstraZeneca, Boehringer Ingelheim, Merck Sharp & Dohme, Takeda, Lilly, Bristol-Myers Squibb. Francisco J. Afonso-Afonso - Consulting or Advisory Role: Merck Sharp & Dohme, AstraZeneca, Bristol-Myers Squibb, Pfizer, Novartis, Takeda, Boehringer Ingelheim. Travel, Accommodations, Expenses: Bristol-Myers Squibb, Merck Sharp & Dohme, Pfizer. Margarita Amenedo - Consulting or Advisory Role: Boehringer Ingelheim, Clovis Oncology. Speakers' Bureau: AstraZeneca; PharmaMar, Roche, Pierre Fabre, Lilly. Travel, Accommodations, Expenses: Roche, Lilly. José Luis Fírvida-Pérez - Consulting or Advisory Role: Roche/Genentech, AstraZeneca, Boehringer Ingelheim, MSD Oncology, Takeda, Lilly, Bristol-Myers Squibb. Rosario García-Campelo - Consulting or Advisory Role: Roche/Genentech, MSD Oncology, AstraZeneca, Bristol-Myers Squibb, Pfizer, Novartis, Takeda, Boehringer Ingelheim. Speakers’ Bureau: Roche, AstraZeneca, Bristol-Myers Squibb, Pfizer, Novartis, Takeda, Boehringer Ingelheim, MSD Oncology. Jorge García-González - Consulting or Advisory Role: Bristol-Myers Squibb, MSD Oncology, Roche/Genentech, Lilly, Boehringer Ingelheim, AstraZeneca, Pierre Fabre. Travel, Accommodations, Expenses: Bristol-Myers Squibb, Merck Sharp & Dohme, Roche/Genentech. Sergio Vázquez - Consulting or Advisory Role: Pfizer, Astellas, Janssen, MSD Oncology, Bayer, Roche, Bristol-Myers Squibb, Boehringer Ingelheim, AstraZeneca, Ipsen, Novartis, Eusa Pharma, Eisai and Sanofi. Speakers’ Bureau: Lilly, Astellas, Bayer, Roche, Boehringer Ingelheim, Ipsen, Novartis, AstraZeneca and Sanofi. Travel, Accommodations, Expenses: Pfizer, Roche and AstraZeneca. The other authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
Kaplan-Meier overall survival and progression-free survival curves according to lung immune prognostic index (LIPI).
Figure 2
Figure 2
Nivolumab response distribution by lung immune prognostic index (LIPI) groups. NE, not evaluable; PD, progressive disease; SD, stable disease; PR, partial response; CR, complete response.
Figure S1
Figure S1
Flow diagram of the patient selection process. aNSCLC, advanced non-small cell lung cancer; LDH, lactate dehydrogenase; LIPI, lung immune prognostic index; dNLR, derived neutrophil to lymphocyte ratio. CHUO, Complejo Hospitalario Universitario de Ourense; CHUAC, Complejo Hospitalario Universitario de A Coruña; CHUS, Complejo Hospitalario Universitario de Santiago de Compostela; CHUF, Complejo Hospitalario Universitario de Ferrol; CHUVI, Complejo Hospitalario Universitario de Vigo; HULA, Hospital Universitario Lucus Augusti; CHOP, Complejo Hospitalario de Pontevedra; COG, Centro Oncológico de Galicia; POVISA, Hospital Povisa.

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