Steroid Use Independently Predicts for Poor Outcomes in Patients With Advanced NSCLC and High PD-L1 Expression Receiving First-Line Pembrolizumab Monotherapy.


Journal

Clinical lung cancer
ISSN: 1938-0690
Titre abrégé: Clin Lung Cancer
Pays: United States
ID NLM: 100893225

Informations de publication

Date de publication:
03 2021
Historique:
received: 25 04 2020
revised: 15 09 2020
accepted: 21 09 2020
pubmed: 10 11 2020
medline: 22 12 2021
entrez: 9 11 2020
Statut: ppublish

Résumé

Real-world data have suggested a detrimental effect of steroid use in patients with advanced non-small-cell lung cancer (NSCLC) receiving immunotherapy. However, previous studies included heterogeneous cohorts of patients receiving different lines of treatment with several immuno-oncology agents and various combinations of chemotherapy and immuno-oncology agents. A comprehensive clinicopathologic database of patients with NSCLC and programmed cell death ligand 1 >50% treated with frontline pembrolizumab monotherapy was constructed in 14 centers in Italy, Spain, Greece, and Switzerland. A multivariate analysis adjusting for the established prognostic factors was performed using a Cox regression model. For the 265 eligible patients, the median age at diagnosis was 67 years, 66% were male, 90% were current or former smokers, 18% had had an Eastern Cooperative Oncology Group performance status of 2 or 3. Of the NSCLC subtypes, 64% were adenocarcinoma and 25% were squamous cell. Of the patients, 18% had had brain metastases at diagnosis and 24% had received steroids before or during pembrolizumab treatment. The median time to progression was 4.4 months with and 13.7 months without steroid use (hazard ratio [HR], 2.55; 95% confidence interval [CI], 1.69-3.85; log-rank P < .001). The median survival was 22.5 months for the whole cohort, 7.7 months for the steroid group, and not reached for the non-steroid group (HR, 3.64; 95% CI, 2.34-5.68; log-rank P < .001). On multivariate analysis accounting for all established prognostic variables, steroid use was still independently associated with a high risk of progression (HR, 1.864; 95% CI, 1.179-2.949; P = .008) and death (HR, 2.292; 95% CI, 1.441-3.644; P < .001) CONCLUSIONS: In patients with advanced NSCLC and programmed cell death ligand 1 expression > 50% receiving frontline pembrolizumab monotherapy, any use of steroids before or during treatment was associated with an 86% increase in the risk of progression and a 2.3-fold increase in the risk of death, even accounting for palliative indication-related bias, including the presence of central nervous system metastasis. The use of steroids for palliative indications should be restricted to absolutely necessary for patients receiving immuno-oncology monotherapy.

Sections du résumé

BACKGROUND
Real-world data have suggested a detrimental effect of steroid use in patients with advanced non-small-cell lung cancer (NSCLC) receiving immunotherapy. However, previous studies included heterogeneous cohorts of patients receiving different lines of treatment with several immuno-oncology agents and various combinations of chemotherapy and immuno-oncology agents.
PATIENTS AND METHODS
A comprehensive clinicopathologic database of patients with NSCLC and programmed cell death ligand 1 >50% treated with frontline pembrolizumab monotherapy was constructed in 14 centers in Italy, Spain, Greece, and Switzerland. A multivariate analysis adjusting for the established prognostic factors was performed using a Cox regression model.
RESULTS
For the 265 eligible patients, the median age at diagnosis was 67 years, 66% were male, 90% were current or former smokers, 18% had had an Eastern Cooperative Oncology Group performance status of 2 or 3. Of the NSCLC subtypes, 64% were adenocarcinoma and 25% were squamous cell. Of the patients, 18% had had brain metastases at diagnosis and 24% had received steroids before or during pembrolizumab treatment. The median time to progression was 4.4 months with and 13.7 months without steroid use (hazard ratio [HR], 2.55; 95% confidence interval [CI], 1.69-3.85; log-rank P < .001). The median survival was 22.5 months for the whole cohort, 7.7 months for the steroid group, and not reached for the non-steroid group (HR, 3.64; 95% CI, 2.34-5.68; log-rank P < .001). On multivariate analysis accounting for all established prognostic variables, steroid use was still independently associated with a high risk of progression (HR, 1.864; 95% CI, 1.179-2.949; P = .008) and death (HR, 2.292; 95% CI, 1.441-3.644; P < .001) CONCLUSIONS: In patients with advanced NSCLC and programmed cell death ligand 1 expression > 50% receiving frontline pembrolizumab monotherapy, any use of steroids before or during treatment was associated with an 86% increase in the risk of progression and a 2.3-fold increase in the risk of death, even accounting for palliative indication-related bias, including the presence of central nervous system metastasis. The use of steroids for palliative indications should be restricted to absolutely necessary for patients receiving immuno-oncology monotherapy.

Identifiants

pubmed: 33162330
pii: S1525-7304(20)30297-7
doi: 10.1016/j.cllc.2020.09.017
pii:
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
B7-H1 Antigen 0
CD274 protein, human 0
Steroids 0
pembrolizumab DPT0O3T46P

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

e180-e192

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Giannis Mountzios (G)

Second Department of Medical Oncology and Clinical trials Unit, Henry Dunant Hospital Center, Athens, Greece. Electronic address: gmountzios@gmail.com.

Alessandro de Toma (A)

Fondazione IRCCS, Istituto Nazionale Tumori di Milano, Milan, Italy.

Panagiota Economopoulou (P)

Section of Medical Oncology, Second Department of Internal Medicine, Attikon University Hospital, Athens, Greece.

Alex Friedlaender (A)

Oncology Department, Geneva University Hospital, Geneva, Switzerland.

Marco Banini (M)

S.C. Oncologia, Ospedale Santa Maria della Misericordia, Azienda Ospedaliera di Perugia, Perugia, Italy.

Giuseppe Lo Russo (G)

Fondazione IRCCS, Istituto Nazionale Tumori di Milano, Milan, Italy.

Panagiotis Baxevanos (P)

Second Department of Medical Oncology, Saint Savvas Anti-Cancer Hospital, Athens, Greece.

Fausto Roila (F)

S.C. Oncologia, Ospedale Santa Maria della Misericordia, Azienda Ospedaliera di Perugia, Perugia, Italy.

Giuseppe Luigi Banna (GL)

Department of Haematology/Oncology, Queen Alexandra Hospital, Portsmouth, United Kingdom.

Athina Christopoulou (A)

Medical Oncology, Agios Andreas General Hospital of Patras, Patras, Greece.

Beatriz Jimenez (B)

Department of Medical Oncology, Hospital HM Sanchinarro, Madrid, Spain.

Ana Collazo-Lorduy (A)

Department of Medical Oncology, Hospital HM Sanchinarro, Madrid, Spain.

Helena Linardou (H)

Fourth Oncology Department, Metropolitan Hospital, Athens, Greece.

Antonio Calles (A)

Division of Medical Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain.

Domenico Galetta (D)

Medical Thoracic Oncology Unit, IRCCS Istituto Tumori "Giovanni Paolo II," Bari, Italy.

Alfredo Addeo (A)

Oncology Department, Geneva University Hospital, Geneva, Switzerland.

Andrea Camerini (A)

U.O.C. Oncologia, Ospedale Versilia, Lido di Camaiore, Italy.

Pamela Pizzutilo (P)

Medical Thoracic Oncology Unit, IRCCS Istituto Tumori "Giovanni Paolo II," Bari, Italy.

Paris Kosmidis (P)

Second Department of Medical Oncology, Hygeia Hospital, Athens, Greece.

Marina Chiara Garassino (MC)

Fondazione IRCCS, Istituto Nazionale Tumori di Milano, Milan, Italy.

Claudia Proto (C)

Fondazione IRCCS, Istituto Nazionale Tumori di Milano, Milan, Italy.

Diego Signorelli (D)

Fondazione IRCCS, Istituto Nazionale Tumori di Milano, Milan, Italy.

Giulio Metro (G)

S.C. Oncologia, Ospedale Santa Maria della Misericordia, Azienda Ospedaliera di Perugia, Perugia, Italy.

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Classifications MeSH