Purpose: Refining the selection of HER2-positive metastatic gastric cancer patient candidates for trastuzumab is a challenge of precision oncology. Preclinical studies have suggested several genomic mechanisms of primary resistance, leading to activation of tyrosine kinase receptors other than HER2 or downstream signaling pathways.Experimental Design:We carried out this multicenter, prospective, case-control study to demonstrate the negative predictive impact of a panel of candidate genomic alterations (AMNESIA panel), includingEGFR/MET/KRAS/PI3K/PTENmutations andEGFR/MET/KRASamplifications. Hypothesizing a prevalence of candidate alterations of 30% and 0% in resistant and sensitive HER2-positive patients, respectively, 20 patients per group were needed.Results:AMNESIA panel alterations were significantly more frequent in resistant (11 of 20, 55%) as compared with sensitive (0% of 17) patients (P< 0.001), and in HER2 IHC 2+(7 of 13, 53.8%) than 3+(4 of 24, 16.7%) tumors (P= 0.028). Patients with tumors bearing no candidate alterations had a significantly longer median progression-free [5.2 vs. 2.6 months; HR, 0.34; 95% confidence interval (CI), 0.07-0.48;P= 0.001] and overall survival (16.1 vs. 7.6 months; HR, 0.38; 95% CI, 0.09-0.75;P= 0.015). The predictive accuracy of the AMNESIA panel and HER2 IHC was 76% and 65%, respectively. The predictive accuracy of the combined evaluation of the AMNESIA panel and HER2 IHC was 84%.Conclusions:Our panel of candidate genomic alterations may be clinically useful to predict primary resistance to trastuzumab in patients with HER2-positive metastatic gastric cancer and should be further validated with the aim of molecularly stratifying HER2-addicted cancers for the development of novel treatment strategies.

Biomarkers of Primary Resistance to Trastuzumab in HER2-Positive Metastatic Gastric Cancer Patients: the AMNESIA Case-Control Study

Corso, Simona;Aprile, Giuseppe;Corallo, Salvatore;Giordano, Silvia;
2018-01-01

Abstract

Purpose: Refining the selection of HER2-positive metastatic gastric cancer patient candidates for trastuzumab is a challenge of precision oncology. Preclinical studies have suggested several genomic mechanisms of primary resistance, leading to activation of tyrosine kinase receptors other than HER2 or downstream signaling pathways.Experimental Design:We carried out this multicenter, prospective, case-control study to demonstrate the negative predictive impact of a panel of candidate genomic alterations (AMNESIA panel), includingEGFR/MET/KRAS/PI3K/PTENmutations andEGFR/MET/KRASamplifications. Hypothesizing a prevalence of candidate alterations of 30% and 0% in resistant and sensitive HER2-positive patients, respectively, 20 patients per group were needed.Results:AMNESIA panel alterations were significantly more frequent in resistant (11 of 20, 55%) as compared with sensitive (0% of 17) patients (P< 0.001), and in HER2 IHC 2+(7 of 13, 53.8%) than 3+(4 of 24, 16.7%) tumors (P= 0.028). Patients with tumors bearing no candidate alterations had a significantly longer median progression-free [5.2 vs. 2.6 months; HR, 0.34; 95% confidence interval (CI), 0.07-0.48;P= 0.001] and overall survival (16.1 vs. 7.6 months; HR, 0.38; 95% CI, 0.09-0.75;P= 0.015). The predictive accuracy of the AMNESIA panel and HER2 IHC was 76% and 65%, respectively. The predictive accuracy of the combined evaluation of the AMNESIA panel and HER2 IHC was 84%.Conclusions:Our panel of candidate genomic alterations may be clinically useful to predict primary resistance to trastuzumab in patients with HER2-positive metastatic gastric cancer and should be further validated with the aim of molecularly stratifying HER2-addicted cancers for the development of novel treatment strategies.
2018
Inglese
Esperti anonimi
24
5
1082
1089
8
http://clincancerres.aacrjournals.org/content/early/2018/01/24/1078-0432.CCR-17-2781.long
gastric cancer, primary resistance, trastuzumab
no
1 – prodotto con file in versione Open Access (allegherò il file al passo 6 - Carica)
262
27
Pietrantonio, Filippo; Fucà, Giovanni; Morano, Federica; Gloghini, Annunziata; Corso, Simona; Aprile, Giuseppe; Perrone, Federica; De Vita, Ferdinando...espandi
info:eu-repo/semantics/article
partially_open
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1660557
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