A dramatic lung cancer course in a patient with a rare EGFR germline mutation exon 21 V843I: Is EGFR TKI resistance predictable?


Autoria(s): Demierre N.; Zoete V.; Michielin O.; Stauffer E.; Zimmermann D.R.; Betticher D.C.; Peters S.
Data(s)

2013

Resumo

We report on the medical history of a Caucasian smoker woman diagnosed with a stage IV NSCLC adenocarcinoma, characterized by a rare epidermal growth factor receptor (EGFR) point mutation in exon 21 codon 843 (p.V843I/c.2527G>A/COSMIC ID 85894). This genetic alteration revealed to be germline, after its presence was demonstrated in chondroblasts from the bone biopsy. While it is the first description of germline V843I mutation without concomitant additional known EGFR activating mutation, we modeled the EGFR ATP catalytic domain in complex with ATP, gefitinib and erlotinib using computer-aided approaches to estimate possible changes in affinity upon the V843I mutation.

Identificador

http://serval.unil.ch/?id=serval:BIB_5082D60AB0F2

isbn:1872-8332 (Electronic)

pmid:23380224

doi:10.1016/j.lungcan.2012.11.013

isiid:000316590600014

Idioma(s)

en

Fonte

Lung Cancer, vol. 80, no. 1, pp. 81-84

Tipo

info:eu-repo/semantics/article

article