Retinoblastoma mutation predicts poor outcomes in advanced non small cell lung cancer.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
04 2019
Historique:
received: 09 10 2018
revised: 07 01 2019
accepted: 16 01 2019
pubmed: 19 2 2019
medline: 8 5 2020
entrez: 19 2 2019
Statut: ppublish

Résumé

The retinoblastoma gene (RB1) encodes the retinoblastoma (RB) pocket protein that plays an important role in cell cycle progression. Here we determine the frequency and prognostic significance of RB1 mutation in non small cell lung cancer (NSCLC), restricting inclusion to Stage III and IV patients with linked genomic and clinical data. The primary outcome was median overall survival (OS). We identified RB1 mutation in 8.2% of NSCLC patients. The median OS for wild-type (wt) RB1 was 28.3 months vs 8.3 months for mutant RB1 (Hazard Ratio = 2.59, P = 0.002). Of special interest, RB1 mutation also correlated with lack of response to immunotherapy. Our study focused on RB1 mutation in locally advanced and advanced non small cell lung cancer to better facilitate comparisons with small cell lung cancer (SCLC). In our SCLC cohort, RB1 mutation was identified in 75% of patients and wt RB1 was associated with significantly shorter OS (P = 0.002). The different outcomes of RB1 mutation observed among lung cancer subtypes suggest a more complicated mechanism than simple regulation of cell cycle or response to chemotherapy.

Identifiants

pubmed: 30773851
doi: 10.1002/cam4.2023
pmc: PMC6488103
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
RB1 protein, human 0
Retinoblastoma Binding Proteins 0
Ubiquitin-Protein Ligases EC 2.3.2.27

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1459-1466

Informations de copyright

© 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Priyanka Bhateja (P)

Department of Hematology and Oncology, Case Western Reserve University, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Michelle Chiu (M)

School of Medicine, Case Western Reserve University, Cleveland, Ohio.

Gary Wildey (G)

School of Medicine, Case Western Reserve University, Cleveland, Ohio.

Mary Beth Lipka (MB)

Department of Hematology and Oncology, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

Pingfu Fu (P)

Department of Population and Quantitative Health Sciences, Case Western Reserve University, Cleveland, Ohio.

Michael Chiu Lee Yang (MCL)

Department of Pathology, University Hospitals Cleveland Medical Center, Cleveland, Ohio.

Fatemeh Ardeshir-Larijani (F)

Department of Internal Medicine, University Hospitals Cleveland Medical Center, Cleveland, Ohio.

Neelesh Sharma (N)

Department of Biomedical Research, Novartis Pharmaceuticals Corporation, East Hanover, New Jersey.

Afshin Dowlati (A)

Department of Hematology and Oncology, Case Western Reserve University, University Hospitals Seidman Cancer Center, Cleveland, Ohio.

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Classifications MeSH