TY - JOUR
T1 - Association Between Lung Immune Prognostic Index and Durvalumab Consolidation Outcomes in Patients With Locally Advanced Non‐Small‐Cell Lung Cancer
AU - Riudavets, Mariona
AU - Auclin, Edouard
AU - Mosteiro, Miguel
AU - Dempsey, Naomi
AU - Majem, Margarita
AU - Prelaj, Arsela
AU - López-Castro, Rafael
AU - Bosch-Barrera, Joaquim
AU - Pilotto, Sara
AU - Escalera, Elena
AU - Tagliamento, Marco
AU - Mosquera, Joaquin
AU - Zalcman, Gérard
AU - Aboubakar Nana, Frank
AU - Ponce, Santiago
AU - Albarrán-Artahona, Víctor
AU - Dal Maso, Alessandro
AU - Spotti, Martina
AU - Mielgo, Xabier
AU - Mussat, Elodie
AU - Reyes, Roxana
AU - Benítez, Jose Carlos
AU - Lupinacci, Lorena
AU - Duchemann, Boris
AU - De Giglio, Andrea
AU - Blaquier, Juan Bautista
AU - Audigier-Valette, Clarisse
AU - Scheffler, Matthias
AU - Nadal, Ernest
AU - Lopes, Gilberto
AU - Signorelli, Diego
AU - Garcia-Campelo, Rosario
AU - Menis, Jessica
AU - Bluthgen, Virginia
AU - Campayo, Marc
AU - Recondo, Gonzalo
AU - Besse, Benjamin
AU - Mezquita, Laura
AU - Planchard, David
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2024/5/1
Y1 - 2024/5/1
N2 - Introduction: The LIPI, based on pretreatment derived neutrophils/[leukocytes-neutrophils] ratio (dNLR) and LDH, is associated with immune checkpoint inhibitors (ICI) outcomes in advanced non–small-cell lung cancer (NSCLC). We aimed to assess baseline LIPI correlation with durvalumab consolidation outcomes in the locally advanced setting. Material and Methods: Multicentre retrospective study (330 patients) with stage III unresectable NSCLC treated with durvalumab after chemo-radiotherapy between April 2015 and December 2020; 65 patients treated with chemo-radiotherapy only. Baseline LIPI characterized 3 groups: good (dNLR≤3+LDH≤ULN), intermediate (dNLR>3/LDH>ULN) and poor (dNLR>3+LDH>ULN). Primary endpoint was overall survival (OS). Results: In the durvalumab cohort, median age was 67 years, 95% smokers, 98% with a performance status of 0-1; 60% had nonsquamous histology and 16% a PD-L1 expression <1%. Radiotherapy was delivered concurrently in 81%. LIPI was evaluable in 216 patients: 66% good, 31% intermediate, 3% poor. LIPI significantly correlated with median OS (median follow-up: 19 months): 18.1 months vs. 47.0 months vs. not reached in poor, intermediate and good LIPI groups, respectively (P = .03). A trend between objective response rate and LIPI groups was observed: 0% vs. 41% vs. 45%, respectively (P = .05). The pooled intermediate/poor LIPI group was associated with shorter OS (HR 1.97; P = .03) and higher risk of progressive disease (OR 2.68; P = .047). Survivals and response were not influenced in the control cohort. Conclusion: Baseline LIPI correlated with outcomes in patients with locally advanced NSCLC treated with durvalumab consolidation, but not in those who only received chemo-radiotherapy, providing further evidence of its prognostic and potential predictive role of ICI benefit in NSCLC.
AB - Introduction: The LIPI, based on pretreatment derived neutrophils/[leukocytes-neutrophils] ratio (dNLR) and LDH, is associated with immune checkpoint inhibitors (ICI) outcomes in advanced non–small-cell lung cancer (NSCLC). We aimed to assess baseline LIPI correlation with durvalumab consolidation outcomes in the locally advanced setting. Material and Methods: Multicentre retrospective study (330 patients) with stage III unresectable NSCLC treated with durvalumab after chemo-radiotherapy between April 2015 and December 2020; 65 patients treated with chemo-radiotherapy only. Baseline LIPI characterized 3 groups: good (dNLR≤3+LDH≤ULN), intermediate (dNLR>3/LDH>ULN) and poor (dNLR>3+LDH>ULN). Primary endpoint was overall survival (OS). Results: In the durvalumab cohort, median age was 67 years, 95% smokers, 98% with a performance status of 0-1; 60% had nonsquamous histology and 16% a PD-L1 expression <1%. Radiotherapy was delivered concurrently in 81%. LIPI was evaluable in 216 patients: 66% good, 31% intermediate, 3% poor. LIPI significantly correlated with median OS (median follow-up: 19 months): 18.1 months vs. 47.0 months vs. not reached in poor, intermediate and good LIPI groups, respectively (P = .03). A trend between objective response rate and LIPI groups was observed: 0% vs. 41% vs. 45%, respectively (P = .05). The pooled intermediate/poor LIPI group was associated with shorter OS (HR 1.97; P = .03) and higher risk of progressive disease (OR 2.68; P = .047). Survivals and response were not influenced in the control cohort. Conclusion: Baseline LIPI correlated with outcomes in patients with locally advanced NSCLC treated with durvalumab consolidation, but not in those who only received chemo-radiotherapy, providing further evidence of its prognostic and potential predictive role of ICI benefit in NSCLC.
KW - Consolidation
KW - Durvalumab
KW - Host-related biomarkers
KW - LIPI
KW - Stage III
UR - http://www.scopus.com/inward/record.url?scp=85180304843&partnerID=8YFLogxK
U2 - 10.1016/j.cllc.2023.11.007
DO - 10.1016/j.cllc.2023.11.007
M3 - Article
AN - SCOPUS:85180304843
SN - 1525-7304
VL - 25
SP - 233-243.e8
JO - Clinical Lung Cancer
JF - Clinical Lung Cancer
IS - 3
ER -