Imaging characteristics of BRAF-mutant non-small cell lung cancer by functional class.


Journal

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

Informations de publication

Date de publication:
03 2019
Historique:
received: 02 12 2018
revised: 12 01 2019
accepted: 16 01 2019
entrez: 25 2 2019
pubmed: 25 2 2019
medline: 1 1 2020
Statut: ppublish

Résumé

Mutations in the BRAF gene have emerged as a validated molecular target in the treatment of non-small cell lung cancer (NSCLC). These mutations can be classified into three functional classes based on their mechanisms of oncogenesis. The relationship between these functional classes and their imaging features has not been systematically investigated. The goal of this work is to determine if imaging features of the primary tumor and the pattern of metastasis correlate with the functional class of BRAF mutation. We reviewed pre-treatment computed tomography (CT) images of patients with BRAF-mutated NSCLC with known functional class. We assessed and recorded the features of the primary tumor and the patterns of lymphadenopathy and distant metastasis. Wilcoxon rank-sum test and Kruskal-Wallis test were performed to compare continuous characteristics, and Fisher's exact test was used to compare categorical features between groups. 105 patients with BRAF-mutant NSCLC had pre-treatment imaging available for review (n = 43 class I, n = 40 class II, and n = 22 class III). Approximately half of the primary tumors were considered masses (n = 54/105, 51%) and most were solid (n = 81/105, 77%). There were no statistically significant differences in imaging features of the primary tumor among the three functional classes. Intrathoracic metastases occurred more frequently in class I tumors compared to tumors with class II and III mutations (p = 0.03). The odds of class I mutation were higher among tumors involving the pleural space (OR: 4.39, 95% CI: 1.11-17.4) and lower among tumors disseminating to the abdomen (OR: 0.25, 95% CI: 0.07-0.92). Our findings suggest that class I (V600) mutated NSCLC may be more likely to have intrathoracic metastases, while classes II and III (non-V600) mutated NSCLC may be more likely to have intra-abdominal metastases at the time of presentation.

Identifiants

pubmed: 30797497
pii: S0169-5002(19)30023-6
doi: 10.1016/j.lungcan.2019.01.007
pii:
doi:

Substances chimiques

BRAF protein, human EC 2.7.11.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

80-84

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Dexter P Mendoza (DP)

Department of Radiology, Massachusetts General Hospital, United States.

Ibiayi Dagogo-Jack (I)

Massachusetts General Hospital Cancer Center and Department of Medicine, Massachusetts General Hospital, United States.

Tianqi Chen (T)

Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Harvard Medical School, United States.

Atul Padole (A)

Department of Radiology, Massachusetts General Hospital, United States.

Jo-Anne O Shepard (JO)

Department of Radiology, Massachusetts General Hospital, United States.

Alice T Shaw (AT)

Massachusetts General Hospital Cancer Center and Department of Medicine, Massachusetts General Hospital, United States.

Subba Rao Digumarthy (SR)

Department of Radiology, Massachusetts General Hospital, United States. Electronic address: sdigumarthy@mgh.harvard.edu.

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Classifications MeSH