Evidence map›Paper›PMID 39083809›Full record

ArticleCancer discovery2024

Botensilimab, an Fc-Enhanced Anti-CTLA-4 Antibody, Is Effective against Tumors Poorly Responsive to Conventional Immunotherapy.

Dhan Chand, David A Savitsky, Shanmugarajan Krishnan, Gabriel Mednick, Chloe Delepine, Pilar Garcia-Broncano, Kah Teong Soh, Wei Wu, Margaret K Wilkens, Olga Udartseva and 33 more

Abstract read
In one paragraph

Article in Cancer discovery, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
–field-weighted citation impact
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

37 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Tailored FcγR blockade enhances immune checkpoint therapy and overcomes resistance.Journal of experimental & clinical cancer research : CR · 2026
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. T-Cell Immunity and Lung Cancer.Respirology (Carlton, Vic.) · 2026
    Review
  17. Review
  18. Review
  19. Review
  20. Navigating second-line therapy after immunotherapy in advanced HCC☆.JHEP reports : innovation in hepatology · 2026
    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

43 authors.

Dhan ChandAgenus Inc, Lexington, Massachusetts.ORCID 0009-0003-8124-4399
David A SavitskyAgenus Inc, Lexington, Massachusetts.ORCID 0009-0006-3191-3146
Shanmugarajan KrishnanAgenus Inc, Lexington, Massachusetts.ORCID 0009-0001-1013-6134
Gabriel MednickAgenus Inc, Lexington, Massachusetts.ORCID 0009-0006-5889-2824
Chloe DelepineAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-1856-9583
Pilar Garcia-BroncanoAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-3413-2189
Kah Teong SohAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-0146-0485
Wei WuAgenus Inc, Lexington, Massachusetts.ORCID 0009-0002-7782-4780
Margaret K WilkensAgenus Inc, Lexington, Massachusetts.ORCID 0009-0000-0169-5279
Olga UdartsevaAgenus Inc, Lexington, Massachusetts.ORCID 0000-0003-2896-2300
Sylvia VincentAgenus Inc, Lexington, Massachusetts.ORCID 0009-0004-3308-8499
Bishnu JoshiAgenus Inc, Lexington, Massachusetts.ORCID 0000-0001-8829-5306
Justin G KeithAgenus Inc, Lexington, Massachusetts.ORCID 0009-0008-2130-2186
Mariana ManriqueAgenus Inc, Lexington, Massachusetts.ORCID 0009-0006-2943-1439
Marilyn MarquesAgenus Inc, Lexington, Massachusetts.ORCID 0009-0007-5387-3787
Antoine TanneAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-0164-775X
Daniel L LeveyAgenus Inc, Lexington, Massachusetts.ORCID 0009-0000-6237-6730
Haiyong HanThe Translational Genomics Research Institute, Phoenix, Arizona.ORCID 0000-0001-9031-9880
Serina NgThe Translational Genomics Research Institute, Phoenix, Arizona.ORCID 0000-0001-5019-5828
Jackson RidpathAgenus Inc, Lexington, Massachusetts.ORCID 0009-0003-8320-0269
Olivia HuberAgenus Inc, Lexington, Massachusetts.ORCID 0000-0003-2185-7575
Benjamin MorinAgenus Inc, Lexington, Massachusetts.ORCID 0000-0001-6632-0320
Claire GalandAgenus Inc, Lexington, Massachusetts.ORCID 0000-0001-8005-4831
Sean BourdelaisAgenus Inc, Lexington, Massachusetts.ORCID 0009-0008-5811-1930
Randi B GombosAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-9338-4490
Rebecca WardAgenus Inc, Lexington, Massachusetts.ORCID 0009-0002-0939-167X
Yu QinAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-7280-7108
Jeremy D WaightAgenus Inc, Lexington, Massachusetts.ORCID 0009-0000-5448-9778
Matthew R CostaAgenus Inc, Lexington, Massachusetts.ORCID 0009-0006-4951-4186
Alvaro Sebastian-YagueAgenus Inc, Lexington, Massachusetts.ORCID 0000-0003-2642-1359
Nils-Petter RudqvistAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-9720-3124
Malgorzata Pupecka-SwiderAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-0230-8282
Vignesh VenkatramanAgenus Inc, Lexington, Massachusetts.ORCID 0009-0003-4525-4565
Andrew SleeAgenus Inc, Lexington, Massachusetts.ORCID 0009-0003-0074-4106
Jaymin M PatelAgenus Inc, Lexington, Massachusetts.ORCID 0000-0001-9945-5555
Joseph E GrossmanAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-2130-2783
Nicholas S WilsonAgenus Inc, Lexington, Massachusetts.ORCID 0000-0002-8888-7034
Daniel D Von HoffThe Translational Genomics Research Institute, Phoenix, Arizona.ORCID 0000-0003-4723-7681
Justin StebbingAnglia Ruskin University, Cambridge, United Kingdom.ORCID 0000-0002-1117-6947
Tyler J CurielAgenus Inc, Lexington, Massachusetts.ORCID 0000-0001-6962-9411
Jennifer S BuellAgenus Inc, Lexington, Massachusetts.ORCID 0000-0001-7405-0076
Steven J O'DayAgenus Inc, Lexington, Massachusetts.ORCID 0009-0005-5345-5417
Robert B SteinAgenus Inc, Lexington, Massachusetts.ORCID 0009-0007-9133-168X

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
NCI NIH HHS P30 CA023108
6 · The paper itself

Abstract

significanceThis study reveals that Fc-enhanced anti-CTLA-4 harnesses novel mechanisms to overcome the limitations of conventional anti-CTLA-4, effectively treating poorly immunogenic and treatment-refractory cancers. Our findings support the development of a new class of immuno-oncology agents, capable of extending clinical benefit to patients with cancers resistant to current immunotherapies.

Indexed as

CTLA-4 AntigenImmunotherapyAnimalsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCell Line, TumorHumansImmunoglobulin Fc FragmentsMiceNeoplasmsAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCTLA-4 AntigenCTLA4 protein, humanImmunoglobulin Fc Fragments

Identifiers

PMID39083809
PMCPMC11609826

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.