Evidence map›Paper›PMID 38056464›Full record

Trial reportCell reports. Medicine2023

Bexmarilimab-induced macrophage activation leads to treatment benefit in solid tumors: The phase I/II first-in-human MATINS trial.

Jenna H Rannikko, Loic Verlingue, Maria de Miguel, Annika Pasanen, Debbie Robbrecht, Tanja Skytta, Sanna Iivanainen, Shishir Shetty, Yuk Ting Ma, Donna M Graham and 12 more

Open access · goldAbstract readClinical Trial, Phase IIClinical Trial, Phase I
In one paragraph

Trial report in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.1field-weighted citation impact, top 6% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 25 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Macrophage Plasticity in Cancer Therapy: Function, Timing, and Tradeoffs.International journal of molecular sciences · 2026
    Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. CLEVER-1Frontiers in immunology · 2026
    Review
  10. Review
  11. Review
  12. Article
  13. Targeting Myeloid Cells for Cancer Immunotherapy.Cancer immunology research · 2025
    Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article
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

22 authors at 16 institutions in 6 countries.

Jenna H RannikkoMediCity Research Laboratory and InFLAMES Flagship, University of Turku, Turku, Finland; Turku Doctoral Program of Molecular Medicine, University of Turku, Turku, Finland.
Loic VerlingueInstitut Gustave Roussy, Paris and Centre Leon Berard in Lyon, Lyon, France.
Maria de MiguelSTART-CIOCC HM Sanchinarro, Madrid, Spain.
Annika PasanenHelsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland.
Debbie RobbrechtErasmus Medical Center/Cancer Institute, Rotterdam, the Netherlands.
Tanja SkyttaTampere University Hospital, Tampere, Finland.
Sanna IivanainenOulu University Hospital, University of Oulu, Oulu, Finland.
Shishir ShettyUniversity of Birmingham/University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Yuk Ting MaUniversity of Birmingham/University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.
Donna M GrahamThe Christie NHS Foundation Trust, Manchester, UK.
Sukeshi Patel AroraMays Cancer Center, UT Health San Antonio, San Antonio, TX, USA.
Panu JaakkolaDepartment of Oncology, Turku University Hospital and University of Turku, Turku, Finland.
Christina YapClinical Trials and Statistics Unit, The Institute of Cancer Research, London, UK.
Yujuan XiangINDIVIDRUG Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.
Jami MandelinFaron Pharmaceuticals Ltd, Turku, Finland.
Matti K KarvonenFaron Pharmaceuticals Ltd, Turku, Finland.
Juho JalkanenFaron Pharmaceuticals Ltd, Turku, Finland.
Sinem KaramanINDIVIDRUG Research Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland; Wihuri Research Institute, Helsinki, Finland.
Jussi P KoivunenOulu University Hospital, University of Oulu, Oulu, Finland; Faron Pharmaceuticals Ltd, Turku, Finland.
Anna MinchomDrug Development Unit, Royal Marsden Hospital/Institute of Cancer Research, Sutton, UK.
Maija HollménMediCity Research Laboratory and InFLAMES Flagship, University of Turku, Turku, Finland; Faron Pharmaceuticals Ltd, Turku, Finland. Electronic address: maijal@utu.fi.
Petri BonoTerveystalo Finland and University of Helsinki, Helsinki, Finland. Electronic address: petri.bono@terveystalo.com.
Faron Pharmaceutical (Finland) · FIUniversity of Helsinki · FIUniversity of Turku · FICentre Léon Bérard · FRErasmus MC Cancer Institute · NLHelsinki University Hospital · FIHospital Universitario HM Sanchinarro · ESInstitute of Cancer Research · GBMays Cancer Center at UT Health San AntonioRoyal Marsden Hospital · GBTampere University · FIThe Christie NHS Foundation Trust · GBTurku University Hospital · FIUniversity Hospitals Birmingham NHS Foundation Trust · GBUniversity of Birmingham · GBUniversity of Oulu · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Macrophage Clever-1 contributes to impaired antigen presentation and suppression of anti-tumor immunity. This first-in-human trial investigates the safety and tolerability of Clever-1 blockade with bexmarilimab in patients with treatment-refractory solid tumors and assesses preliminary anti-tumor efficacy, pharmacodynamics, and immunologic correlates. Bexmarilimab shows no dose-limiting toxicities in part I (n = 30) and no additional safety signals in part II (n = 108). Disease control (DC) rates of 25%-40% are observed in cutaneous melanoma, gastric, hepatocellular, estrogen receptor-positive breast, and biliary tract cancers. DC associates with improved survival in a landmark analysis and correlates with high pre-treatment intratumoral Clever-1 positivity and increasing on-treatment serum interferon γ (IFNγ) levels. Spatial transcriptomics profiling of DC and non-DC tumors demonstrates bexmarilimab-induced macrophage activation and stimulation of IFNγ and T cell receptor signaling selectively in DC patients. These data suggest that bexmarilimab therapy is well tolerated and show that macrophage targeting can promote immune activation and tumor control in late-stage cancer.

Indexed as

Antibodies, Monoclonal, HumanizedNeoplasmsHumansMacrophage ActivationAntibodies, Monoclonal, HumanizedbexmarilimabcancerClever-1first-in-manGeoMximmune activationStabilin-1

Identifiers

PMID38056464
PMCPMC10772343
OpenAlexW4389334708

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.