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EGFR and KRAS mutation status in non-small-cell lung cancer occurring in HIV-infected patients

Authors :
Christos Chouaid
Virginie Poulot
Valérie Gounant
T. Vieira
Jacques Cadranel
Marie Wislez
Martine Antoine
Anne-Marie Ruppert
Armelle Lavolé
Perrine Créquit
N. Rozensztajn
CHU Tenon [AP-HP]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Theranoscan
Université Pierre et Marie Curie - Paris 6 (UPMC)
Service de Pneumologie (CRETEIL - Pneumologie)
CHI Créteil
Service de Pneumologie - Oncologie Thoracique - Maladies Pulmonaires Rares [CHU Tenon]
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Service d'anatomie pathologique [CHU Tenon]
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Tenon [AP-HP]
Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)
Source :
Lung Cancer, Lung Cancer, 2015, 96, pp.74-77. ⟨10.1016/j.lungcan.2015.11.021⟩, Lung Cancer, Elsevier, 2015, 96, pp.74-77. ⟨10.1016/j.lungcan.2015.11.021⟩
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

International audience; Non–small-cell lung cancer (NSCLC) is the most common non-acquired immune deficiency syndrome-related malignancy responsible for death. Mutational status is crucial for choosing treatment of advanced NSCLC, yet no data is available on the frequency of epidermal growth factor receptor (EGFR) and Kirsten ras (KRAS) mutations and their impact on NSCLC in human immunodeficiency virus (HIV)-infected patients (HIV-NSCLC).All consecutive HIV-NSCLC patients diagnosed between June 1996 and August 2013 at two Paris university hospitals were reviewed, with tumor samples analyzed for EGFR and KRAS mutational status.Overall, 63 tumor samples were analyzed out of 73HIV-NSCLC cases, with 63% of advanced NSCLC. There were 60 non-squamous and nine squamous cell carcinomas, with EGFR and KRAS mutations identified in two (3.3%) and seven (11.5%) tumors, respectively. The proportion of KRAS mutations was 29% if solely the more sensitive molecular techniques were considered. The two patients with advanced adenocarcinoma harboring EGFR mutations exhibited lasting partial response to EGFR-tyrosine kinase inhibitors. Overall survival for patients with advanced NSCLC were >30 months for those with EGFR mutations

Details

ISSN :
01695002
Volume :
96
Database :
OpenAIRE
Journal :
Lung Cancer
Accession number :
edsair.doi.dedup.....94c2697f1674b738cb8f86fd6d24acd9