4.4 Review

Antagonists of PD-1 and PD-L1 in Cancer Treatment

Journal

SEMINARS IN ONCOLOGY
Volume 42, Issue 4, Pages 587-600

Publisher

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1053/j.seminoncol.2015.05.013

Keywords

-

Categories

Funding

  1. AstraZeneca
  2. Genentech
  3. Bristol-Myers Squibb
  4. GlaxoSmithKline
  5. Pfizer
  6. SFJ Pharmaceuticals Group
  7. Roche
  8. NATIONAL CANCER INSTITUTE [R01CA142779] Funding Source: NIH RePORTER

Ask authors/readers for more resources

The PD-1 pathway, comprising the immune cell co-receptor Programmed Death 1 (PD-1) and its ligands, PD-L1 (B7-H1) and PD-L2 (B7-DC), mediates local immunosuppression in the tumor microenvironment. Drugs designed to block PD-1 or PD-L1 release the brakes on anti-tumor immunity and have demonstrated clinical activity in several types of advanced cancers, validating this pathway as a target for cancer therapy. Two such drugs have recently been approved to treat melanoma and lung cancers, and regulatory approvals in first- and second-line settings for additional cancer types are anticipated. The manageable safety profile of PD-1/PD-L1 blocking drugs identifies them as suitable for outpatient administration and the development of combinatorial therapies. Ongoing studies aim to identify biomarkers to guide patient selection, which would further improve the risk:benefit ratio for these drugs. (C) 2015 Elsevier Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available