4.6 Review

Trial watch: Immune checkpoint blockers for cancer therapy

期刊

ONCOIMMUNOLOGY
卷 6, 期 11, 页码 -

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/2162402X.2017.1373237

关键词

Atezolizumab; avelumab; durvalumab; ipilimumab; nivolumab; pembrolizumab

资金

  1. DOD BCRP [W81XWH-13-1-0012]
  2. Kellen Junior Faculty Fellowship from the Anna-Maria and Stephen Kellen Foundation
  3. Sara Borrell fellowship from Instituto de Salud Carlos III [CD15/00016]
  4. Department of Radiation Oncology of Weill Cornell Medical College (New York, US)
  5. Sotio a.c. (Prague, Czech Republic)
  6. NIH [R01 CA201246, R01 CA198533]
  7. French Ligue contre le Cancer (equipe labellisee)
  8. Agence National de la Recherche (ANR) - Projets blancs
  9. ANR under E-Rare-2
  10. ERA-Net for Research on Rare Diseases
  11. Association pour la recherche sur le cancer (ARC)
  12. Canceropole Ile-de-France
  13. Institut National du Cancer (INCa)
  14. Institut Universitaire de France
  15. Fondation pour la Recherche Medicale (FRM)
  16. European Commission (ArtForce)
  17. European Research Council (ERC)
  18. LeDucq Foundation
  19. LabEx Immuno-Oncology
  20. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  21. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  22. Paris Alliance of Cancer Research Institutes (PACRI)

向作者/读者索取更多资源

Immune checkpoint blockers (ICBs) are literally revolutionizing the clinical management of an ever more diversified panel of oncological indications. Although considerable attention persists around the inhibition of cytotoxic T lymphocyte-associated protein 4 (CTLA4) and programmed cell death 1 (PDCD1, best known as PD-1) signaling, several other co-inhibitory T-cell receptors are being evaluated as potential targets for the development of novel ICBs. Moreover, substantial efforts are being devoted to the identification of biomarkers that reliably predict the likelihood of each patient to obtain clinical benefits from ICBs in the absence of severe toxicity. Tailoring the delivery of specific ICBs or combinations thereof to selected patient populations in the context of precision medicine programs constitutes indeed a major objective of the future of ICB-based immunotherapy. Here, we discuss recent preclinical and clinical advances on the development of ICBs for oncological indications.

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