Evidence map›Paper›PMID 26567614›Full record

ReviewImmunotherapy2015

Emerging targets in cancer immunotherapy: beyond CTLA-4 and PD-1.

Amer Assal, Justin Kaner, Gopichand Pendurti, Xingxing Zang

Open access · greenAbstract readReview
In one paragraph

Review in Immunotherapy, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. AnCancer informatics · 2022
    Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. NK Cell-Based Immune Checkpoint Inhibition.Frontiers in immunology · 2020
    Review
  15. Review
  16. Article
  17. Article
  18. Review
  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

4 authors at 4 institutions in 1 country.

Amer AssalDepartment of Medicine, Adult Bone Marrow Transplant Service, Memorial Sloan Kettering Cancer Center, New York, NY 10065, USA.
Justin KanerDepartment of Medicine, Montefiore Medical Center, Bronx, NY 10467, USA.
Gopichand PendurtiDivision of Hematology/Oncology, Department of Medicine, Jacobi Medical Center, Bronx, NY 10461, USA.
Xingxing ZangDepartment of Medicine, Montefiore Medical Center, Bronx, NY 10467, USA.
Albert Einstein College of Medicine · USJacobi Medical Center · USMemorial Sloan Kettering Cancer Center · USMontefiore Medical Center · US

Funding

Tumor-expressed immune checkpoint B7x-mediated resistance to anti-CTLA-4 therapy.R01CA175495 · NCI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2014 to 2025
$5.1M
Mechanisms and Therapies of B7x and B7-H3 in T1DR01DK100525 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI ZANG, XINGXING · 2015 to 2019
$1.9M
NCI NIH HHS R01 CA175495NCI NIH HHS R01CA175495NIDDK NIH HHS R01 DK100525
6 · The paper itself

Abstract

Manipulation of co-stimulatory or co-inhibitory checkpoint proteins allows for the reversal of tumor-induced T-cell anergy observed in cancer. The field has gained credence given success with CTLA-4 and PD-1 inhibitors. These molecules include immunoglobulin family members and the B7 subfamily as well as the TNF receptor family members. PD-L1 inhibitors and LAG-3 inhibitors have progressed through clinical trials. Other B7 family members have shown promise in preclinical models. TNFR superfamily members have shown variable success in preclinical and clinical studies. As clinical investigation in tumor immunology gains momentum, the next stage becomes learning how to combine checkpoint inhibitors and agonists with each other as well as with traditional chemotherapeutic agents.

Indexed as

ImmunotherapyAnimalsAntigens, CDAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenClinical Trials as TopicCTLA-4 AntigenHumansLymphocyte Activation Gene 3 ProteinMolecular Targeted TherapyNeoplasmsProgrammed Cell Death 1 ReceptorTumor EscapeTumor Necrosis Factor-alphaAntigens, CDB7-H1 AntigenCD274 protein, humanCTLA-4 AntigenLag3 protein, humanLymphocyte Activation Gene 3 ProteinProgrammed Cell Death 1 ReceptorTumor Necrosis Factor-alphaB7 familycheckpoint proteinsimmunotherapyTNFR superfamilytranslational medicine

Identifiers

PMID26567614
PMCPMC4976877
OpenAlexW2176186813

What OpenQuestion holds

Textmetadata
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.