4.8 Review

The hallmarks of successful anticancer immunotherapy

Journal

SCIENCE TRANSLATIONAL MEDICINE
Volume 10, Issue 459, Pages -

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/scitranslmed.aat7807

Keywords

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Funding

  1. Department of Radiation Oncology at Weill Cornell Medicine (New York)
  2. Luke Heller TECPR2 Foundation (Boston)
  3. Sotio a.s. (Prague, Czech Republic)
  4. Ludwig Institute for Cancer Research
  5. Parker Institute for Cancer Immunotherapy
  6. Swim Across America
  7. National Cancer Institute [P30CA008748]
  8. Ono Pharmaceuticals
  9. Ligue contre le Cancer (equipe labellisee)
  10. Agence National de la Recherche (ANR)-Projets blancs
  11. ANR
  12. ERA-Net for Research on Rare Diseases
  13. Association pour la recherche sur le cancer (ARC)
  14. Canceropole Ile-de-France
  15. Chancelerie des universites de Paris (Legs Poix)
  16. Fondation pour la Recherche Medicale (FRM)
  17. European Commission (ArtForce)
  18. ERA Network on Cardiovascular Diseases (ERA-CVD, MINOTAUR)
  19. European Research Council (ERC)
  20. Fondation Carrefour
  21. Institut National du Cancer (INCa)
  22. INSERM (HTE)
  23. Institut Universitaire de France
  24. LeDucq Foundation
  25. LabEx Immuno-Oncology
  26. RHU Torino Lumiere
  27. Seerave Foundation
  28. SIRIC Stratified Oncology Cell DNA Repair and Tumor Immune Elimination (SOCRATE)
  29. SIRIC Cancer Research and Personalized Medicine (CARPEM)
  30. Paris Alliance of Cancer Research Institutes (PACRI)
  31. Elior
  32. Phosplatin (New York)
  33. NATIONAL CANCER INSTITUTE [P30CA008748] Funding Source: NIH RePORTER

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Immunotherapy is revolutionizing the clinical management of multiple tumors. However, only a fraction of patients with cancer responds to immunotherapy, and currently available immunotherapeutic agents are expensive and generally associated with considerable toxicity, calling for the identification of robust predictive biomarkers. The overall genomic configuration of malignant cells, potentially favoring the emergence of immunogenic tumor neoantigens, as well as specific mutations that compromise the ability of the immune system to recognize or eradicate the disease have been associated with differential sensitivity to immunotherapy in preclinical and clinical settings. Along similar lines, the type, density, localization, and functional orientation of the immune infiltrate have a prominent impact on anticancer immunity, as do features of the tumor microenvironment linked to the vasculature and stroma, and systemic factors including the composition of the gut microbiota. On the basis of these considerations, we outline the hallmarks of successful anticancer immunotherapy.

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