Pleural effusion is a negative prognostic factor for immunotherapy in patients with non-small cell lung cancer (NSCLC): The pluie study.


Journal

Lung cancer (Amsterdam, Netherlands)
ISSN: 1872-8332
Titre abrégé: Lung Cancer
Pays: Ireland
ID NLM: 8800805

Informations de publication

Date de publication:
05 2021
Historique:
received: 27 01 2021
revised: 17 03 2021
accepted: 19 03 2021
pubmed: 3 4 2021
medline: 22 6 2021
entrez: 2 4 2021
Statut: ppublish

Résumé

Pleural effusion (PE) is a common metastatic site of NSCLC, associated with poor outcomes. As very few data are available about immune checkpoint inhibitors (ICI) and PE, we aimed to assess the clinical outcome of PE in NSCLC treated with ICI. Multicenter international retrospective study of patients with metastatic NSCLC treated with ICI, between 2012 and 2019. Stratification according to the presence of PE at ICI baseline or appearance under ICI treatment (PE group) versus no history of PE (non-PE group). Primary endpoints were overall survival (OS) and early death rate (EDR, OS ≤ 3 months). A total of 538 patients were included: 196 in the PE group and 342 in the non-PE group. In the PE group, median age was 64, 31.6 % were female, 77.6 % had non-squamous histology, PD-L1 was ≥50 % in 38.6 % of cases (95 missing). PE was more likely associated with >2 metastatic sites (70.4 % vs. 50 %) and worse performance status (PS ≥ 2, 30.8 % vs 23.1 %). Globally, the overall median OS was 9.7 months [95 %CI: 8.1-11.8]; 6.3 [95 % CI: 4.0-8.6] in PE vs. 11.4 [95 %CI: 9.7-13.8] in the non-PE respectively, P = 0.002. Overall the EDR was 31.4 %; higher in the PE group (38.3 % vs. 27.5 %; OR 1.63, 95 %CI: 1.13-2.37, P = 0.01). In the PE PD-L1≥50 % group, EDR was 33.3 %. In multivariate analysis, after adjustment on PS, liver/intracranial/bone metastasis, ICI line and dNLR, PE remained an independent prognostic factor for OS [HR: 1.38, 95 %CI: 1.09-1.74, P = 0.007]. In the PE group, PE appeared under ICI for 31 patients (16.4 %). We observed lower EDR in this group compared to patients whom PE was already present (29.0 % vs 40.5 %, P = 0.2). PE is associated with worse immunotherapy outcomes in NSCLC treated with ICI, including in patients with ≥50 % PD-L1 tumors. Thus, in these patients, combination strategies should be explored.

Sections du résumé

BACKGROUND
Pleural effusion (PE) is a common metastatic site of NSCLC, associated with poor outcomes. As very few data are available about immune checkpoint inhibitors (ICI) and PE, we aimed to assess the clinical outcome of PE in NSCLC treated with ICI.
METHOD
Multicenter international retrospective study of patients with metastatic NSCLC treated with ICI, between 2012 and 2019. Stratification according to the presence of PE at ICI baseline or appearance under ICI treatment (PE group) versus no history of PE (non-PE group). Primary endpoints were overall survival (OS) and early death rate (EDR, OS ≤ 3 months).
RESULTS
A total of 538 patients were included: 196 in the PE group and 342 in the non-PE group. In the PE group, median age was 64, 31.6 % were female, 77.6 % had non-squamous histology, PD-L1 was ≥50 % in 38.6 % of cases (95 missing). PE was more likely associated with >2 metastatic sites (70.4 % vs. 50 %) and worse performance status (PS ≥ 2, 30.8 % vs 23.1 %). Globally, the overall median OS was 9.7 months [95 %CI: 8.1-11.8]; 6.3 [95 % CI: 4.0-8.6] in PE vs. 11.4 [95 %CI: 9.7-13.8] in the non-PE respectively, P = 0.002. Overall the EDR was 31.4 %; higher in the PE group (38.3 % vs. 27.5 %; OR 1.63, 95 %CI: 1.13-2.37, P = 0.01). In the PE PD-L1≥50 % group, EDR was 33.3 %. In multivariate analysis, after adjustment on PS, liver/intracranial/bone metastasis, ICI line and dNLR, PE remained an independent prognostic factor for OS [HR: 1.38, 95 %CI: 1.09-1.74, P = 0.007]. In the PE group, PE appeared under ICI for 31 patients (16.4 %). We observed lower EDR in this group compared to patients whom PE was already present (29.0 % vs 40.5 %, P = 0.2).
CONCLUSION
PE is associated with worse immunotherapy outcomes in NSCLC treated with ICI, including in patients with ≥50 % PD-L1 tumors. Thus, in these patients, combination strategies should be explored.

Identifiants

pubmed: 33798900
pii: S0169-5002(21)00122-7
doi: 10.1016/j.lungcan.2021.03.015
pii:
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

114-119

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Auteurs

Nicolas Epaillard (N)

Medical and Thoracic Oncology Department, Hôpital Européen Georges Pompidou AP-HP, Université de Paris, France.

Jose Carlos Benitez (JC)

Medical Oncology Department, Institut Gustave Roussy, Villejuif, France.

Teresa Gorria (T)

Medical Oncology Department, Hospital Clinic, Barcelona, Spain.

Elizabeth Fabre (E)

Medical and Thoracic Oncology Department, Hôpital Européen Georges Pompidou AP-HP, Université de Paris, France.

Mariona Riudavets (M)

Medical Oncology Department, Institut Gustave Roussy, Villejuif, France.

Roxana Reyes (R)

Medical Oncology Department, Hospital Clinic, Barcelona, Spain.

David Planchard (D)

Medical Oncology Department, Institut Gustave Roussy, Villejuif, France.

Stéphane Oudard (S)

Medical and Thoracic Oncology Department, Hôpital Européen Georges Pompidou AP-HP, Université de Paris, France.

Nuria Viñolas (N)

Medical Oncology Department, Hospital Clinic, Barcelona, Spain.

Noemi Reguart (N)

Medical Oncology Department, Hospital Clinic, Barcelona, Spain.

Benjamin Besse (B)

Medical Oncology Department, Institut Gustave Roussy, Villejuif, France.

Laura Mezquita (L)

Medical Oncology Department, Hospital Clinic, Barcelona, Spain.

Edouard Auclin (E)

Medical and Thoracic Oncology Department, Hôpital Européen Georges Pompidou AP-HP, Université de Paris, France. Electronic address: edouard.auclin@aphp.fr.

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