Long-term Survival with 18-Fluorodeoxyglucose Positron Emission Tomography-directed Therapy in Non-small Cell Lung Cancer with Synchronous Solitary Brain Metastasis.


Journal

Clinical oncology (Royal College of Radiologists (Great Britain))
ISSN: 1433-2981
Titre abrégé: Clin Oncol (R Coll Radiol)
Pays: England
ID NLM: 9002902

Informations de publication

Date de publication:
03 2021
Historique:
received: 27 05 2020
revised: 28 07 2020
accepted: 13 10 2020
pubmed: 2 11 2020
medline: 15 10 2021
entrez: 1 11 2020
Statut: ppublish

Résumé

At diagnosis, <1% of patients with non-small cell lung cancer (NSCLC) have synchronous solitary brain metastasis (SSBM). In prior cohorts without 18-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT) staging, definitive treatment to intracranial and intrathoracic disease showed a 5-year overall survival (OS) of 11-21%. We investigated the long-term survival outcomes for patients with SSBM NSCLC, diagnosed in the FDG-PET/CT era and treated definitively with local therapies to both intracranial and intrathoracic sites of disease. This retrospective study assessed patients staged with FDG-PET/CT who received definitive lung and SSBM treatment from February 1999 to December 2017. A lung-molecular graded prognostic assessment (lung-molGPA) score was assigned for each patient using age, performance status score, and, where carried out, molecular status. Overall survival and progression-free survival (PFS) were calculated using Kaplan-Meier methods. Cox proportional hazard models determined OS and PFS prognostic factors. Forty-nine patients newly diagnosed with NSCLC and SSBM had a median age of 63 years (range 34-76). The median follow-up of all patients was 3.9 years. Thirty-three patients (67%) had ≥T2 disease, 23 (47%) had ≥N2. At 2 years, 45% of first failures were intracranial only (95% confidence interval 30-59). At 3 and 5 years, OS was 45% (95% confidence interval 32-63) and 30% (95% confidence interval 18-51), respectively. In ≥N1 disease, 5-year OS was 34% (95% confidence interval 18-63). The 3- and 5-year PFS was 8% (95% confidence interval 3-22) and 0%, respectively. Higher lung-molGPA was associated with longer OS (hazard ratio 0.26, 95% confidence interval 0.11-0.61, P = 0.002). Higher lung-molGPA (hazard ratio 0.33, 95% confidence interval 0.15-0.71, P = 0.005) and lower N-stage (hazard ratio 1.56, 95% confidence interval 1.13-2.15, P = 0.007) were associated with longer PFS. Definitive treatment of patients with NSCLC and SSBM staged with FDG-PET/CT can result in 5-year survivors, including those with ≥N1 disease.

Identifiants

pubmed: 33129655
pii: S0936-6555(20)30391-5
doi: 10.1016/j.clon.2020.10.010
pii:
doi:

Substances chimiques

Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

163-171

Informations de copyright

Copyright © 2020 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.

Auteurs

S Newman (S)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

N Bucknell (N)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia; Sir Peter MacCallum Department of Oncology, Melbourne University, Parkville, Victoria, Australia.

M Bressel (M)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

P Tran (P)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

B A Campbell (BA)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia; Sir Peter MacCallum Department of Oncology, Melbourne University, Parkville, Victoria, Australia.

S David (S)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

N Haghighi (N)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

G G Hanna (GG)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia; Sir Peter MacCallum Department of Oncology, Melbourne University, Parkville, Victoria, Australia.

D Kok (D)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

M MacManus (M)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia; Sir Peter MacCallum Department of Oncology, Melbourne University, Parkville, Victoria, Australia.

C Phillips (C)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

N Plumridge (N)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

M Shaw (M)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

A Wirth (A)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

G Wheeler (G)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia.

D Ball (D)

Sir Peter MacCallum Department of Oncology, Melbourne University, Parkville, Victoria, Australia.

S Siva (S)

Peter MacCallum Cancer Centre, Radiation Oncology, Parkville, Victoria, Australia; Sir Peter MacCallum Department of Oncology, Melbourne University, Parkville, Victoria, Australia. Electronic address: shankar.siva@petermac.org.

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Classifications MeSH