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Landscape of Biomarkers and Actionable Gene Alterations in Adenocarcinoma of GEJ and Stomach - A Real World Data Analysis

: Hempel, Louisa; Veloso de Oliveira, Julia; Gaumann, Andreas; Milani, Valeria; Schweneker, Katrin; Schenk, Kristina; Fleischmann, Bastian; Philipp, Patrick; Mederle, Stefanie; Garg, Arun; Piehler, Armin; Gandorfer, Beate; Schick, Cordula; Kleespies, Axel; Sellmann, Ludger; Bartels, Marius; Goetze, Thorsten Oliver; Stein, Alexander; Goekkurt, Eray; Pfitzner, Lucia; Robert, Sebastian; Hempel, Dirk

Volltext urn:nbn:de:0011-n-6402343 (2.0 MByte PDF)
MD5 Fingerprint: 58b4dd18e1cc3beadae60c5669d85b7a
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Erstellt am: 8.9.2021

Cancers 13 (2021), Nr.17, Art. 4453, 12 S.
ISSN: 2072-6694
Zeitschriftenaufsatz, Elektronische Publikation
Fraunhofer IOSB ()
GEJ; GC; next-generation sequencing; Her2neu; PD-L1; personalized medicine; molecular target; checkpoint inhibitor; actionable gene variants

After several years of negative phase III trials in gastric and esophageal cancer, a significant breakthrough in the treatment of metastatic adenocarcinomas of the gastroesophageal junction (GEJ) and stomach (GC) is now becoming evident with the emerging of precision oncology and implementation of molecular targets in tumor treatment. In addition, new generation studies such as umbrella and basket trials are focused on these molecular targets, which makes an early molecular diagnosis based on IHC/ISH and NGS necessary. The required companion diagnostics of Her2neu over amplification or PD-L1 expression is based on immunohistochemistry (IHC) or additionally in situ hybridization (ISH) in case of an IHC Her2neu score of 2+. However, there are investigator-dependent differences in the assessment of Her2neu amplification and different PD-L1 scoring systems obtained by IHC/ISH. The use of high-throughput technologies such as next-generation sequencing (NGS) holds the potential to standardize the analysis and thus make them more comparable. In the presented study, real-world multigene sequencing data of 72 Caucasian patients diagnosed with metastatic adenocarcinomas of GEJ and stomach were analyzed. In the clinical companion diagnostics, we found ESCAT level I molecular targets in one-third of our patients, which directly determined the therapy. In addition, we found potential targets in 14/72 patients (19.4%) who potentially qualify for precision therapies in corresponding molecular studies. The study highlights the importance of comprehensive molecular profiling for precision treatment of GEJ/GC and indicates that a biomarker evaluation should be performed for all patients with metastatic adenocarcinomas before the initiation of first-line treatment and during second-line or subsequent treatment.