Publication: Association of PALB2 Messenger RNA Expression with Platinum-Docetaxel Efficacy in Advanced Non-Small Cell Lung Cancer.
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Identifiers
Date
2018-11-22
Authors
Karachaliou, Niki
Bracht, Jillian Wilhelmina Paulina
Fernandez Bruno, Manuel
Drozdowskyj, Ana
Gimenez-Capitan, Ana
Moran, Teresa
Carcereny, Enric
Cobo, Manuel
Domine, Manuel
Chaib, Imane
Advisors
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Abstract
Partner and localizer of BRCA2 (PALB2) is essential for homologous recombination repair. We examined mRNA levels of DNA repair genes, including partner and localizer of BRCA2 gene (PALB2), ring finger protein 8 gene (RNF8), replication timing regulatory factor 1 gene (RIF1), ATM serine/threonine kinase gene (ATM), and tumor protein p53 binding protein 1 gene (53BP1) as predictive biomarkers for cisplatin-docetaxel in the European phase III BRCA1, DNA repair associated (BRCA1)-receptor-associated protein 80 (RAP80) expression customization (BREC) phase III clinical trial (ClinicalTrials.gov identifier NCT00617656). The study was a prespecified secondary objective of the BREC trial. We assessed mRNA levels of PALB2 and four more DNA repair genes (RNF8, RIF1, ATM and 53BP1) as biomarkers in tissue from 177 patients with cisplatin-docetaxel-treated NSCLC. We examined the relationship of gene expression levels with progression-free survival, overall survival, and response. In 177 patients with NSCLC (who had a median age of 62 years and included 140 men and 91 patients with adenocarcinoma), only high PALB2 mRNA expression was predictive in the progression-free survival Cox regression analysis (hazard ratio = 0.63, 95% confidence interval: 0.42-0.83, p = 0.0080). PALB2 was also predictive of overall survival (hazard ratio = 0.68, 95% confidence interval: 0.42-0.90, p = 0.0266). Among the 158 patients evaluable for response, high PALB2 mRNA expression was predictive of response to cisplatin-docetaxel. Specifically, an objective response rate of 77% to cisplatin-docetaxel was observed for patients with high PALB2 mRNA expression compared with a rate of only 23 % for those with low PALB2 mRNA expression (p = 0.0448). High PALB2 mRNA expression identified patients with NSCLC who significantly benefited from cisplatin-docetaxel chemotherapy in the European BREC phase III clinical trial. The combination of chemotherapy with immunotherapy will become the standard of care, and a predictive marker of response to chemotherapy may accurately guide therapeutic decision making.
Description
MeSH Terms
Antineoplastic Combined Chemotherapy Protocols
Ataxia Telangiectasia Mutated Proteins
Biomarkers
Carcinoma, Non-Small-Cell Lung
Cisplatin
DNA-Binding Proteins
Docetaxel
Fanconi Anemia Complementation Group N Protein
Female
Gene Expression
Humans
Lung Neoplasms
Male
Middle Aged
Progression-Free Survival
Proportional Hazards Models
RNA, Messenger
Survival Rate
Telomere-Binding Proteins
Treatment Outcome
Tumor Suppressor p53-Binding Protein 1
Ubiquitin-Protein Ligases
Ataxia Telangiectasia Mutated Proteins
Biomarkers
Carcinoma, Non-Small-Cell Lung
Cisplatin
DNA-Binding Proteins
Docetaxel
Fanconi Anemia Complementation Group N Protein
Female
Gene Expression
Humans
Lung Neoplasms
Male
Middle Aged
Progression-Free Survival
Proportional Hazards Models
RNA, Messenger
Survival Rate
Telomere-Binding Proteins
Treatment Outcome
Tumor Suppressor p53-Binding Protein 1
Ubiquitin-Protein Ligases
DeCS Terms
ARN mensajero
Cisplatino
Reparación del ADN
Quimioterapia
Intervalos de confianza
Supervivencia sin progresión
Cisplatino
Reparación del ADN
Quimioterapia
Intervalos de confianza
Supervivencia sin progresión
CIE Terms
Keywords
Docetaxel, Non–small cell lung cancer, PALB2, RNA expression
Citation
Karachaliou N, Bracht JWP, Fernandez Bruno M, Drozdowskyj A, Gimenez Capitan A, Moran T, et al. Association of PALB2 Messenger RNA Expression with Platinum-Docetaxel Efficacy in Advanced Non-Small Cell Lung Cancer. J Thorac Oncol. 2019 Feb;14(2):304-310