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

      1 , 2 , 2 , 3 , 4 , 5 , 3 , 6 , 3 , 7 , 3 , 8 , 3 , 9 , 3 , 6 , 2 , 2 , 2 , 3 , 10 , 10 , 3 , 2 , 11 , 4 , 12 , 2
      Clinical cancer research : an official journal of the American Association for Cancer Research
      American Association for Cancer Research (AACR)
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          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), including EGFR/MET/KRAS/PI3K/PTEN mutations and EGFR/MET/KRAS amplifications. 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. Clin Cancer Res; 24(5); 1082-9. ©2017 AACR.

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          Author and article information

          Journal
          Clin. Cancer Res.
          Clinical cancer research : an official journal of the American Association for Cancer Research
          American Association for Cancer Research (AACR)
          1078-0432
          1078-0432
          Mar 01 2018
          : 24
          : 5
          Affiliations
          [1 ] Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. filippo.pietrantonio@istitutotumori.mi.it.
          [2 ] Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
          [3 ] Department of Pathology and Laboratory Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
          [4 ] University of Torino, Department of Oncology and Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Italy.
          [5 ] Department of Oncology, ULSS8 Berica, San Bortolo General Hospital, Vicenza, Italy.
          [6 ] Division of Medical Oncology, Department of Clinical and Experimental Medicine and Surgery, University of Campania 'Luigi Vanvitelli', School of Medicine, Naples, Italy.
          [7 ] Department of Oncology, ASST Ospedale di Cremona, Cremona, Italy.
          [8 ] Department of Oncology, University and General Hospital, Udine, Italy.
          [9 ] Medical Oncology Unit, Azienda Ospedaliero-Universitaria Careggi, Florence, Italy.
          [10 ] Molecular Targeting Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
          [11 ] Oncology and Haemato-Oncology Department, University of Milan, Università degli Studi di Milano, Milan, Italy.
          [12 ] Unit of Medical Oncology 2, Azienda Ospedaliera-Universitaria Pisana, Pisa, Italy.
          Article
          1078-0432.CCR-17-2781
          10.1158/1078-0432.CCR-17-2781
          29208673
          50968f70-5be3-433b-804a-4a2110d28d71
          History

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