Patterns of Failure in Metastatic NSCLC Treated With First Line Pembrolizumab and Use of Local Therapy in Patients With Oligoprogression.

LCT NSCLC Oligoprogression Pembrolizumab SBRT

Journal

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

Informations de publication

Date de publication:
17 Sep 2023
Historique:
received: 05 06 2023
revised: 14 08 2023
accepted: 13 09 2023
medline: 10 10 2023
pubmed: 10 10 2023
entrez: 9 10 2023
Statut: aheadofprint

Résumé

The patterns of failure (POF) for metastatic non-small-cell lung cancer (mNSCLC) treated with immunotherapy are not well established. We conducted a retrospective cohort study of mNSCLC that received first-line pembrolizumab with or without chemotherapy at a single academic center from 2015 to 2021. We defined POF with 2 classifications: 1) local, regional, or distant failure, or 2) failure in existing lesions, new lesions, or a combination. Oligoprogression was defined as disease progression (PD) in ≤3 sites of failure. Overall survival (OS) was measured via Kaplan-Meier and modelled with Cox regression. Of 298 patients identified, 198 had PD. Using POF classification 1, most failures were distant (43.9%) or a combination of locoregional and distant (34.4%). For POF classification 2, failures occurred in a combination of new and existing lesions (45.0%), existing lesions alone (33.3%), or in new lesions only (21.7%). Oligoprogression occurred in 39.9% (n = 79) cases. Median OS was higher in the following: PD in existing lesions vs. new or new + existing lesions (28.7 vs. 20.2 vs. 13.9 months, P < .001) and oligoprogression vs. polyprogression (35.1 vs. 12.2 months, P < .001). In oligoprogression, median OS was better for those who received radiation to all sites of PD (62.2 months) than for those who changed systemic therapy (22.9 months, P = .007). On multivariable analysis, radiation for oligoprogression (HR 0.35, 95% CI: 0.20-0.62, P < .001) was associated with improved OS. In mNSCLC treated with pembrolizumab, oligoprogression is relatively common. Randomized data are needed to define the benefits of radiation in oligoprogressive mNSCLC.

Identifiants

pubmed: 37813713
pii: S1525-7304(23)00184-5
doi: 10.1016/j.cllc.2023.09.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure LLS: Consulting or Advisory Role: Regeneron, GenMab, Seagen, Baye, Research funding: Blueprint Research, Seagen Research, IO Biotech. CA: Consulting or Advisory Role: AstraZeneca Pharmaceuticals, Merck & Co, Janssen Pharmaceuticals (J&J), Sanofi Genzyme, Pfizer Inc. MEM: Consulting or Advisory Role: AstraZeneca, Blueprint Pharmaceuticals, Boehringer Ingelheim, Bristol Myers Squibb (BMS), Ikena, Janssen, Novocure, TakedaResearch, funding: Eli Lilly, Trizell, AstraZeneca, Stock: Gilead Sciences, Portola Pharmaceuticals, Merck, Bluebird Bio, Johnson & Johnson, Pfizer. RBC: Consulting or Advisory Role: AstraZeneca Pharmaceuticals, CantargiaResearch, Funding: Fstar, Cantargia. CJL: Consulting or Advisory Role: Amgen, AstraZeneca Pharmaceuticals, Takeda Pharmaceuticals, Genentech, Novocure, Regeneron Pharmaceuticals, Pfizer Inc., Sanofi Genzyme Research Funding: Merck & Co, Janssen Pharmaceuticals (J&J), Incyte Corporation.

Auteurs

Cole Friedes (C)

Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA. Electronic address: cole.friedes@pennmedicine.upenn.edu.

Nikhil Yegya-Raman (N)

Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Siqi Zhang (S)

Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania, Philadelphia, PA.

Michelle Iocolano (M)

Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Roger B Cohen (RB)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Charu Aggarwal (C)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Jeffrey C Thompson (JC)

Division of Pulmonary, Allergy, and Critical Care, University of Pennsylvania Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.

Melina E Marmarelis (ME)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

William P Levin (WP)

Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Keith A Cengel (KA)

Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Christine A Ciunci (CA)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Aditi P Singh (AP)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Christopher D'Avella (C)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Christiana W Davis (CW)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Corey J Langer (CJ)

Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Steven J Feigenberg (SJ)

Department of Radiation Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.

Classifications MeSH