dc.contributor.author
Kleo, Karsten
dc.contributor.author
Jovanovic, Vladimir M.
dc.contributor.author
Arndold, Alexander
dc.contributor.author
Lehmann, Annika
dc.contributor.author
Lammert, Hedwig
dc.contributor.author
Berg, Erika
dc.contributor.author
Harloff, Hannah
dc.contributor.author
Treese, Christoph
dc.contributor.author
Hummel, Michael
dc.contributor.author
Daum, Severin
dc.date.accessioned
2024-09-23T11:35:43Z
dc.date.available
2024-09-23T11:35:43Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/44988
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-44699
dc.description.abstract
Objectives: Perioperative chemo-(radio-) therapy is the accepted standard in European patients with locally advanced adenocarcinoma of the esophagogastric junction or stomach (AEG/AS). However, 30-85% of patients do not respond to this treatment. The aim of our study was the identification of predictive biomarkers in pre-therapeutic endoscopic tumor biopsies from patients with histopathologic response (Becker-1) versus non-response (Becker-2/3) to preoperative chemotherapy.
Methods: Formalin-fixed paraffin-embedded biopsies from 36 Caucasian patients (Becker-1 n = 11, Becker-2 n = 7, Becker-3 n = 18) with AEG/AS, taken prior to neoadjuvant chemotherapy were selected. For RNA expression analysis, we employed the NanoString nCounter System. To identify genomic alterations like single nucleotide variants (SNV), copy number variation (CNV) and fusion events, we used Illumina TST170 gene panel. For HER2 and FGFR2 protein expression, immunostaining was performed. Furthermore, we analyzed the microsatellite instability (MSI) and Epstein-Barr virus (EBV) infection status by EBER in situ hybridization.
Results: Heat map and principal component analyses showed no clustering by means of gene expression according to regression grade. Concerning two recently proposed predictive markers, our data showed equal distribution for MSI (Becker-1: 2; Becker-2: 1; Becker-3: 3; out of 29 tested) and EBV infection was rare (1/32). We could not reveal discriminating target genes concerning SNV, but found a higher mutational burden in non-responders versus responders and fusion (in 6/14) and CNV events (in 5/14) exclusively in Becker-3.
Conclusions: Although we could not identify discriminating target genes, our data suggest that molecular alterations are in general more prevalent in patients with AEG/AS belonging to the non-responding Becker group 3.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Gastric and esophagogastric adenocarcinoma
en
dc.subject
Perioperative chemotherapy
en
dc.subject
Histopathological response according to Becker score
en
dc.subject
Predictive biomarker in pre-therapeutic biopsies
en
dc.subject
Single nucleotide variants (SNV)
en
dc.subject
copy number variations (CNV)
en
dc.subject
gene expression
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Response prediction in patients with gastric and esophagogastric adenocarcinoma under neoadjuvant chemotherapy using targeted gene expression analysis and next-generation sequencing in pre-therapeutic biopsies
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1007/s00432-022-03944-z
dcterms.bibliographicCitation.journaltitle
Journal of Cancer Research and Clinical Oncology
dcterms.bibliographicCitation.number
3
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.pagestart
1049
dcterms.bibliographicCitation.pageend
1061
dcterms.bibliographicCitation.volume
149
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
35246724
dcterms.isPartOf.issn
0171-5216
dcterms.isPartOf.eissn
1432-1335