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Translational analysis and final efficacy of the AVETUX trial – Avelumab, cetuximab and FOLFOX in metastatic colorectal cancer

Authors :
Joseph Tintelnot
Inka Ristow
Markus Sauer
Donjete Simnica
Christoph Schultheiß
Rebekka Scholz
Eray Goekkurt
Lisa von Wenserski
Edith Willscher
Lisa Paschold
Sylvie Lorenzen
Jorge Riera-Knorrenschild
Reinhard Depenbusch
Thomas J. Ettrich
Steffen Dörfel
Salah-Eddin Al-Batran
Meinolf Karthaus
Uwe Pelzer
Axel Hinke
Marcus Bauer
Chiara Massa
Barbara Seliger
Claudia Wickenhauser
Carsten Bokemeyer
Susanna Hegewisch-Becker
Mascha Binder
Alexander Stein
Source :
Frontiers in Oncology, Vol 12 (2022)
Publication Year :
2022
Publisher :
Frontiers Media S.A., 2022.

Abstract

IntroductionIn metastatic colorectal cancer (mCRC), the efficacy of immune checkpoint blockade (ICB) has so far been limited to patients with microsatellite instability high tumors (MSI-H). Unfortunately, most mCRC patients suffer from non-immunogenic microsatellite stable (MSS) tumors. Therefore, new combinatorial strategies are urgently needed to enhance the immunogenicity of MSS tumors to finally increase the number of patients benefiting from ICB.MethodsThe AVETUX trial aimed to combine the PD-L1 antibody avelumab with the standard of care chemotherapy combination FOLFOX and the anti-EGFR antibody cetuximab. Furthermore, we performed a central radiological review of the pre- and on-treatment computed tomography scans to better define the individual response to treatment.Results and DiscussionIn total, 43 patients were treated of which 39 patients were confirmed as RAS/BRAF wildtype in central tissue review and finally response evaluated. A final progression-free survival (PFS) of 11.1 (range: 0.8 to 22.3 months) and a herein updated final overall survival (OS) of 32.9 months (range: 0.8 to 47.1 months) was reached. We observed a strong median depth of response of 67.5% tumor shrinkage and deepness of response correlated significantly with survival. On the other hand, early tumor shrinkage was not an indicator of better outcome at a cut-off of 20% (median values). In a next step, we correlated the individual best radiological response with potential ICB response biomarkers and found that the clonality and diversity, but not frequency of tumor infiltrating lymphocytes (TiLs) and peripheral blood mononuclear cells (PBMCs), strongly correlated with response. In summary, we report the final overall survival of the AVETUX trial and propose T cell clonality and diversity as a potential marker to predict response to chemo-immunotherapy combinations in MSS mCRC by performing a central radiological review.Clinical Trial RegistrationClinicalTrials.gov, identifier (NCT03174405).

Details

Language :
English
ISSN :
2234943X
Volume :
12
Database :
Directory of Open Access Journals
Journal :
Frontiers in Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.795ba3985b7d4bf2aa05f0aac74d61e4
Document Type :
article
Full Text :
https://doi.org/10.3389/fonc.2022.993611