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Translational analysis and final efficacy of the AVETUX trial - Avelumab, cetuximab and FOLFOX in metastatic colorectal cancer.
Tintelnot, Joseph; Ristow, Inka; Sauer, Markus; Simnica, Donjete; Schultheiß, Christoph; Scholz, Rebekka; Goekkurt, Eray; von Wenserski, Lisa; Willscher, Edith; Paschold, Lisa; Lorenzen, Sylvie; Riera-Knorrenschild, Jorge; Depenbusch, Reinhard; Ettrich, Thomas J; Dörfel, Steffen; Al-Batran, Salah-Eddin; Karthaus, Meinolf; Pelzer, Uwe; Hinke, Axel; Bauer, Marcus; Massa, Chiara; Seliger, Barbara; Wickenhauser, Claudia; Bokemeyer, Carsten; Hegewisch-Becker, Susanna; Binder, Mascha; Stein, Alexander.
Afiliação
  • Tintelnot J; Department of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Ristow I; Department of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Sauer M; Department of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Simnica D; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Schultheiß C; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Scholz R; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Goekkurt E; Department of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • von Wenserski L; Hämatologisch-Onkologische Praxis Eppendorf, Hamburg, Germany.
  • Willscher E; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Paschold L; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Lorenzen S; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Riera-Knorrenschild J; Department of Internal Medicine III (Haematology/Medical Oncology), Technical University of Munich Hospital Rechts der Isar, Munchen, Bayern, Germany.
  • Depenbusch R; University Hospital of Giessen and Marburg, Marburg, Hessen, Germany.
  • Ettrich TJ; Private Practice Onkodoc GmbH Götersloh, Götersloh, Nordrhein-Westfalen, Germany.
  • Dörfel S; Department of Internal Medicine I, University Hospital Ulm, Ulm, Baden-Wörttemberg, Germany.
  • Al-Batran SE; Private Practice Onkozentrum Dresden, Dresden, Sachsen, Germany.
  • Karthaus M; Institute of Clinical Cancer Research Institut für Klinisch-Onkologische Forschung (IKF) at Northwest Hospital, Frankfurt, Hessen, Germany.
  • Pelzer U; Department of Hematology and Oncology, Munich Hospital Neuperlach, Munchen, Bayern, Germany.
  • Hinke A; Department of Hematology, Oncology and Tumorimmunology, Charite Universitatsmedizin Berlin, Berlin, Germany.
  • Bauer M; Clinical Cancer Research Consulting (CCRC), Dösseldorf, Germany.
  • Massa C; Institute of Pathology, Martin Luther University Halle Wittenberg, Halle, Sachsen-Anhalt, Germany.
  • Seliger B; Institute of Medical Immunology, Martin-Luther-Universität Halle-Wittenberg, Halle, Germany.
  • Wickenhauser C; Institute of Medical Immunology, Martin-Luther-Universität Halle-Wittenberg, Halle, Germany.
  • Bokemeyer C; Institute of Pathology, University Hospital Halle, Halle, Germany.
  • Hegewisch-Becker S; Department of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Binder M; Hämatologisch-Onkologische Praxis Eppendorf, Hamburg, Germany.
  • Stein A; Department of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Front Oncol ; 12: 993611, 2022.
Article em En | MEDLINE | ID: mdl-36605436
Introduction: In 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. Methods: The 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 Discussion: In 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 Registration: ClinicalTrials.gov, identifier (NCT03174405).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Revista: Front Oncol Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Alemanha