| Literature DB >> 33859051 |
Sabine Visser1,2,3, Stijn Koolen4,5, Nadine van Donk6, Nico van Walree2, Cor van der Leest2, Robin Cornelissen1, Ron van Schaik6, Ron Mathijssen4, Joachim Aerts1, Bruno H Stricker7,8.
Abstract
Patients with advanced non-small-cell lung cancer who are treated with pemetrexed display a wide variation in clinical response and toxicity. In this prospective, multicentre cohort study, we investigated the association with treatment effectiveness and toxicity of 10 polymorphisms in nine candidate genes, covering the folate pathway (MTHFR), cell transport (SLC19A1/ABCC2/ABCC4), intracellular metabolism (FPGS/GGH) and target enzymes (TYMS/DHFR/ATIC) of pemetrexed. Adjusted for sex, ECOG performance score and disease stage, the association between ATIC (rs12995526) and overall survival (HR 1.59, 95% CI 1.06 to 2.39) was significant. Regarding toxicity, this ATIC polymorphism was significantly associated with severe laboratory (p=0.014) and clinical (p=0.016) chemotherapy-related adverse events, severe neutropenia (p=0.007) and all-grade diarrhoea (p=0.034) in multivariable analyses. © Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: clinical epidemiology; lung cancer; lung cancer chemotherapy; non-small cell lung cancer
Mesh:
Substances:
Year: 2021 PMID: 33859051 DOI: 10.1136/thoraxjnl-2020-216504
Source DB: PubMed Journal: Thorax ISSN: 0040-6376 Impact factor: 9.139