Evidence map›Paper›PMID 36605436›Full record

ArticleFrontiers in oncology2022

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

Joseph Tintelnot, Inka Ristow, Markus Sauer, Donjete Simnica, Christoph Schultheiß, Rebekka Scholz, Eray Goekkurt, Lisa von Wenserski, Edith Willscher, Lisa Paschold and 17 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03174405 (Avelumab and Cetuximab in Combination With FOLFOX in Patients With Previously Untreated Metastatic Colorectal Cancer - The Phase II AVETUX- Colorectal Cancer), which is not on this map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03174405 phase2completednot on this map

Avelumab and Cetuximab in Combination With FOLFOX in Patients With Previously Untreated Metastatic Colorectal Cancer - The Phase II AVETUX- Colorectal Cancer (CRC) Trial.

TypeinterventionalSponsorAIO-Studien-gGmbHRan2017 to 2021Enrolled43ConditionsMetastatic Colorectal CancerArmsAvelumab
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 12 institutions in 1 country.

Joseph TintelnotDepartment of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Inka RistowDepartment of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Markus SauerDepartment of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Donjete SimnicaDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Christoph SchultheißDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Rebekka ScholzDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Eray GoekkurtDepartment of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Lisa von WenserskiDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Edith WillscherDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Lisa PascholdDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Sylvie LorenzenDepartment of Internal Medicine III (Haematology/Medical Oncology), Technical University of Munich Hospital Rechts der Isar, Munchen, Bayern, Germany.
Jorge Riera-KnorrenschildUniversity Hospital of Giessen and Marburg, Marburg, Hessen, Germany.
Reinhard DepenbuschPrivate Practice Onkodoc GmbH Götersloh, Götersloh, Nordrhein-Westfalen, Germany.
Thomas J EttrichDepartment of Internal Medicine I, University Hospital Ulm, Ulm, Baden-Wörttemberg, Germany.
Steffen DörfelPrivate Practice Onkozentrum Dresden, Dresden, Sachsen, Germany.
Salah-Eddin Al-BatranInstitute of Clinical Cancer Research Institut für Klinisch-Onkologische Forschung (IKF) at Northwest Hospital, Frankfurt, Hessen, Germany.
Meinolf KarthausDepartment of Hematology and Oncology, Munich Hospital Neuperlach, Munchen, Bayern, Germany.
Uwe PelzerDepartment of Hematology, Oncology and Tumorimmunology, Charite Universitatsmedizin Berlin, Berlin, Germany.
Axel HinkeClinical Cancer Research Consulting (CCRC), Dösseldorf, Germany.
Marcus BauerInstitute of Pathology, Martin Luther University Halle Wittenberg, Halle, Sachsen-Anhalt, Germany.
Chiara MassaInstitute of Medical Immunology, Martin-Luther-Universität Halle-Wittenberg, Halle, Germany.
Barbara SeligerInstitute of Medical Immunology, Martin-Luther-Universität Halle-Wittenberg, Halle, Germany.
Claudia WickenhauserInstitute of Pathology, University Hospital Halle, Halle, Germany.
Carsten BokemeyerDepartment of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Susanna Hegewisch-BeckerHämatologisch-Onkologische Praxis Eppendorf, Hamburg, Germany.
Mascha BinderDepartment of Internal Medicine IV - Oncology/Hematology, Martin-Luther-Universitat Halle-Wittenberg, Halle, Sachsen-Anhalt, Germany.
Alexander SteinDepartment of Oncology and Hematology, Bone Marrow Transplantation with Section Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Martin Luther University Halle-Wittenberg · DEEppendorf (Germany) · DEUniversity Medical Center Hamburg-Eppendorf · DEBayer (Germany) · DECharité - Universitätsmedizin Berlin · DEInstitute of Clinical Cancer Research · DEKlinikum rechts der Isar · DEOnkozentrum Dresden · DEUniversität Hamburg · DEUniversitätsklinikum Gießen und Marburg · DEUniversity Hospital in Halle · DEUniversity Hospital Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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).

Indexed as

deepness of responseETSimmunotherapyMSS mCRCT cell diversity

Identifiers

PMID36605436
PMCPMC9808039
OpenAlexW4312078688

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.