Kraemer, Max ORCID: 0009-0006-9275-6121, Wirsik, Naita M. ORCID: 0000-0003-1619-6354, Alakus, Hakan ORCID: 0000-0002-3889-3276, Schloesser, Hans A. ORCID: 0000-0002-1304-7719, Fuchs, Hans ORCID: 0000-0003-4764-8050, Schroeder, Wolfgang ORCID: 0000-0002-8700-069X, Bruns, Christiane J. ORCID: 0000-0001-6590-8181, Lyu, Su Ir ORCID: 0009-0002-4125-6048, Baehr, Friederike, Zander, Thomas ORCID: 0000-0002-4266-6818 and Quaas, Alexander ORCID: 0000-0002-3537-6011 (2025). Adjuvant FLOT provides survival benefit for oesophagogastric junction and gastric adenocarcinoma patients with low tumour regression after neoadjuvant chemotherapy. International Journal of Cancer, 157 (12). pp. 2558-2568. Wiley. ISSN 0020-7136

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Identification Number:10.1002/ijc.70048

Abstract

Oesophagogastric junction and gastric adenocarcinoma (OGA) are associated with high mortality rates, with 5-year survival rates below 50% in the curative setting. This study evaluates the efficacy of adjuvant chemotherapy (a chemotherapy regimen consisting of docetaxel, oxaliplatin, leucovorin and 5-fluorouracil [FLOT]) in patients with low tumour regression grades (TRG) following neoadjuvant FLOT (>10% viable tumour cells in surgical specimen, TRG 2/3 analogue Becker's classification). Data from all patients who had undergone ≥3 cycles of neoadjuvant FLOT with R0 resection and TRG 2/3 in surgical specimen, diagnosed between 2017 and 2020 at the University of Cologne (n = 134), were analyzed. Patients were categorised into three groups based on the administration of postoperative FLOT: ‘FLOT complete’ (four cycles), ‘FLOT incomplete’ (one to three cycles) and ‘no FLOT’ (0 cycles). Progression-free survival (PFS) and overall survival (OS) were compared. There is a statistically significant PFS advantage for the ‘FLOT complete’ group compared to ‘no FLOT’ (p = .028) in the total patient cohort and a tendency for an OS benefit. In the subgroup of patients with lymph node metastasis in surgical specimen (ypN+ cohort, n = 91), the PFS advantage of ‘FLOT complete’ was diminished and statistically no longer significant, and there is no OS benefit for these patients. However, multivariate analysis confirmed a significant PFS benefit for ‘FLOT complete’ both in the total cohort (p = .011) and in ypN+ patients (p = .018). These findings suggest that full adjuvant FLOT is beneficial even for OGA patients with low tumour regression; however, its efficacy appears reduced in those with lymph node metastasis, warranting further investigation into individualising treatment strategies.

Item Type: Article
Creators:
Creators
Email
ORCID
ORCID Put Code
Kraemer, Max
UNSPECIFIED
UNSPECIFIED
Wirsik, Naita M.
UNSPECIFIED
UNSPECIFIED
Alakus, Hakan
UNSPECIFIED
UNSPECIFIED
Schloesser, Hans A.
UNSPECIFIED
UNSPECIFIED
Fuchs, Hans
UNSPECIFIED
UNSPECIFIED
Schroeder, Wolfgang
UNSPECIFIED
UNSPECIFIED
Bruns, Christiane J.
UNSPECIFIED
UNSPECIFIED
Lyu, Su Ir
UNSPECIFIED
UNSPECIFIED
Baehr, Friederike
UNSPECIFIED
UNSPECIFIED
UNSPECIFIED
Zander, Thomas
UNSPECIFIED
UNSPECIFIED
Quaas, Alexander
UNSPECIFIED
UNSPECIFIED
URN: urn:nbn:de:hbz:38-805303
Identification Number: 10.1002/ijc.70048
Journal or Publication Title: International Journal of Cancer
Volume: 157
Number: 12
Page Range: pp. 2558-2568
Number of Pages: 11
Date: 15 December 2025
Publisher: Wiley
ISSN: 0020-7136
Language: English
Faculty: Faculty of Medicine
Divisions: Faculty of Medicine > Chirurgie > Klinik und Poliklinik für Allgemein-, Viszeral-, Thorax- und Transplantationschirurgie
Faculty of Medicine > Innere Medizin > Klinik I für Innere Medizin - Hämatologie und Onkologie
Faculty of Medicine > Pathologie und Neuropathologie > Institut für Pathologie
Faculty of Medicine > Weitere > Centrum für integrierte Onkologie (CIO)
Subjects: Medical sciences Medicine
Uncontrolled Keywords:
Keywords
Language
adjuvant chemotherapy ; FLOT ; gastric adenocarcinoma ; oesophagogastric junction adenocarcinoma ; tumour regression
English
['eprint_fieldname_oa_funders' not defined]: Publikationsfonds UzK
Refereed: Yes
URI: http://kups.ub.uni-koeln.de/id/eprint/80530

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