Stereotactic Body Radiation Therapy for Oligoprogressive and Oligorecurrent Non-Small-Cell Lung Cancer.


Journal

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

Informations de publication

Date de publication:
11 2023
Historique:
received: 02 06 2023
revised: 06 08 2023
accepted: 20 08 2023
medline: 3 11 2023
pubmed: 16 9 2023
entrez: 15 9 2023
Statut: ppublish

Résumé

The role of stereotactic body radiation therapy (SBRT) in oligoprogressive non-small-cell lung cancer (NSCLC) is controversial. We evaluated whether SBRT in a subset of patients with oligoprogressive or oligorecurrent NSCLC offers a durable response, obviating the need to change systemic therapy. A retrospective analysis of 168 NSCLC patients who underwent SBRT for oligoprogressive or oligorecurrent disease was performed. Oligoprogression was defined as progression in ≤5 lesions during or after systemic therapy following an initial complete or partial response. Oligorecurrence was defined as progression while off systemic therapy. Progression-free survival (PFS), overall survival (OS) and time to next treatment or death (TNT-D) were estimated. Median age was 68 years. Sixty-seven percent of patients were on systemic therapy at the time of progression. Progression at the primary site was present in 31% of the patients. The number of sites of metastatic progression was 0 to 2 in 76% and 3 to 5 in 24% of the patients. Two-year OS and PFS were 56% (95%CI 46%-64%) and 14% (95%CI 8%-21%), respectively. Median TNT-D was 9 months (95%CI 6-11). No grade 4 or 5 toxicity was seen. In multivariable analysis, patients with 3 to 5 sites of metastatic progression had worse OS (HR 2.6, 95%CI 1.5-4.3, P < .001) and shorter TNT-D (HR 1.7, 95%CI 1.1-2.5, P = .01) than those with 0 to 2 sites. SBRT is a safe and viable treatment option for oligoprogressive and oligorecurrent NSCLC. Patients with 0 to 2 sites had better OS and longer TNT-D compared to those with 3 to 5 lesions.

Sections du résumé

BACKGROUND AND PURPOSE
The role of stereotactic body radiation therapy (SBRT) in oligoprogressive non-small-cell lung cancer (NSCLC) is controversial. We evaluated whether SBRT in a subset of patients with oligoprogressive or oligorecurrent NSCLC offers a durable response, obviating the need to change systemic therapy.
METHODS
A retrospective analysis of 168 NSCLC patients who underwent SBRT for oligoprogressive or oligorecurrent disease was performed. Oligoprogression was defined as progression in ≤5 lesions during or after systemic therapy following an initial complete or partial response. Oligorecurrence was defined as progression while off systemic therapy. Progression-free survival (PFS), overall survival (OS) and time to next treatment or death (TNT-D) were estimated.
RESULTS
Median age was 68 years. Sixty-seven percent of patients were on systemic therapy at the time of progression. Progression at the primary site was present in 31% of the patients. The number of sites of metastatic progression was 0 to 2 in 76% and 3 to 5 in 24% of the patients. Two-year OS and PFS were 56% (95%CI 46%-64%) and 14% (95%CI 8%-21%), respectively. Median TNT-D was 9 months (95%CI 6-11). No grade 4 or 5 toxicity was seen. In multivariable analysis, patients with 3 to 5 sites of metastatic progression had worse OS (HR 2.6, 95%CI 1.5-4.3, P < .001) and shorter TNT-D (HR 1.7, 95%CI 1.1-2.5, P = .01) than those with 0 to 2 sites.
CONCLUSION
SBRT is a safe and viable treatment option for oligoprogressive and oligorecurrent NSCLC. Patients with 0 to 2 sites had better OS and longer TNT-D compared to those with 3 to 5 lesions.

Identifiants

pubmed: 37714807
pii: S1525-7304(23)00180-8
doi: 10.1016/j.cllc.2023.08.015
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

651-659

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure The authors have no conflicts of interest.

Auteurs

Maryam Ebadi (M)

Department of Radiation Oncology, University of Washington, Seattle, WA.

Colton Ladbury (C)

Department of Radiation Oncology, City of Hope National Cancer Center, Duarte, CA.

Jason Liu (J)

Department of Radiation Oncology, City of Hope National Cancer Center, Duarte, CA.

Adam Rock (A)

Department of Medical Oncology & Therapeutics Research, City of Hope National Cancer Center, Duarte, CA.

Mykola Onyshchenko (M)

Department of Medical Oncology & Therapeutics Research, City of Hope National Cancer Center, Duarte, CA.

Victoria Villaflor (V)

Department of Medical Oncology & Therapeutics Research, City of Hope National Cancer Center, Duarte, CA.

Miguel Villalona-Calero (M)

Department of Medical Oncology & Therapeutics Research, City of Hope National Cancer Center, Duarte, CA.

Ravi Salgia (R)

Department of Medical Oncology & Therapeutics Research, City of Hope National Cancer Center, Duarte, CA.

Erminia Massarelli (E)

Department of Medical Oncology & Therapeutics Research, City of Hope National Cancer Center, Duarte, CA.

Percy Lee (P)

Department of Radiation Oncology, City of Hope National Cancer Center, Duarte, CA.

Terence Williams (T)

Department of Radiation Oncology, City of Hope National Cancer Center, Duarte, CA.

Arya Amini (A)

Department of Radiation Oncology, City of Hope National Cancer Center, Duarte, CA. Electronic address: aamini@coh.org.

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Classifications MeSH