Prognostic and predictive effects of TP53 co-mutation in patients with EGFR-mutated non-small cell lung cancer (NSCLC). (September 2017)

• Record Type: Journal Article
• Authors: Labbé, Catherine; Cabanero, Michael; Korpanty, Grzegorz J.; Tomasini, Pascale; Doherty, Mark K.; Mascaux, Céline; Jao, Kevin; Pitcher, Bethany; Wang, Rick; Pintilie, Melania; Leighl, Natasha B.; Feld, Ronald; Liu, Geoffrey; Bradbury, Penelope Ann; Kamel-Reid, Suzanne; Tsao, Ming-Sound; Shepherd, Frances A.
• Is Part Of: Lung cancer. Volume 111(2017)
• Page Start: 23
• Page End: 29
• Publication Date: 2017-09
• Subjects: TP53 -- EGFR -- Non-small cell lung cancer -- Survival -- Tyrosine kinase inhibitors; Lungs -- Cancer -- Periodicals; Lung Neoplasms -- Abstracts; Lung Neoplasms -- Periodicals; Poumons -- Cancer -- Périodiques; Lungs -- Cancer; Periodicals; Electronic journals; Electronic journals; 616.99424
• DOI: 10.1016/j.lungcan.2017.06.014
• Languages: English
• ISSNs: 0169-5002

Abstract

Highlights: In EGFR -mutated NSCLC, TP53 co-mutation is not a strong prognostic marker. TP53 missense mutations might be predictive of lower ORR and shorter PFS on TKIs. Larger datasets are required to validate these observations. Abstract: Introduction: TP53 mutations are common in non-small cell lung cancer (NSCLC) and have been reported as prognostic of poor outcome. The impact of TP53 co-mutations in epidermal growth factor receptor ( EGFR )-mutated NSCLC is unclear. Materials and methods: Tissue from 105 patients with EGFR -mutated NSCLC at Princess Margaret Cancer Centre was analyzed by next-generation or Sanger sequencing to determine TP53 mutational status. Associations between TP53 status and baseline patient and tumor characteristics, treatments and outcomes (relapse-free survival [RFS] after surgical resection, overall survival [OS], overall response rate [ORR] and progression-free survival [PFS] on EGFR tyrosine kinase inhibitors [TKIs]), were investigated. Results: Dual TP53/EGFR mutations were found in 43/105 patients (41%). Among 76 patients who underwent surgical resection, neither RFS (HR 0.99, CI 0.56–1.75, p = 0.96) nor OS (HR 1.39, CI 0.70–2.77; p = 0.35) was associated with TP53 status. Sixty patients (24 TP53 MUT; 36 TP53 WT) received first-generation EGFR TKIs for advanced disease. ORR was not significantly different ( TP53 MUT 54%, WT 66%, p = 0.42). There was a non-significant trend towards shorter PFS on EGFR TKIs with TP53 mutation (HR 1.74, CI 0.98–3.10, p = 0.06). When limited to TP53 missense mutations (n = 17), PFS was significantly shorter (HR 1.91, CI 1.01–3.60, p = 0.04). Among 11 evaluable patients treated with T790M inhibitors, ORR was not significantly different ( TP53 MUT 3/3 [100%], WT 7/8 [88%]). Conclusions: Patients with dual TP53/EGFR mutations, especially missense mutations, had marginally lower response rates and shorter PFS when treated with EGFR TKI therapy. Larger datasets are required to validate these observations.