Evidence map›Paper›PMID 24880938›Full record

ReviewLung cancer (Amsterdam, Netherlands)2014

Immunotherapy in the treatment of non-small cell lung cancer.

Raghav Sundar, Richie Soong, Byoung-Chul Cho, Julie R Brahmer, Ross A Soo

Open access · greenAbstract readReview
In one paragraph

Review in Lung cancer (Amsterdam, Netherlands), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

53 citing papers in PubMed, 113 citations in OpenAlex.

  1. Trial
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  9. The role of PD-1/PD-L1 checkpoint in arsenic lung tumorigenesis.Toxicology and applied pharmacology · 2021
    Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Immunohistochemical detection of PD-L1 among diverse human neoplasms in a reference laboratory: observations based upon 62,896 cases.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2019
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. ZWINT is the next potential target for lung cancer therapy.Journal of cancer research and clinical oncology · 2019
    Article
  20. 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

5 authors at 4 institutions in 4 countries.

Raghav SundarDepartment of Haematology-Oncology, National University Cancer Institute, National University Health System, Singapore.
Richie SoongCancer Science Institute of Singapore, National University of Singapore, Singapore; Department of Pathology, National University Health System, Singapore.
Byoung-Chul ChoDivision of Medical Oncology, Yonsei Cancer Center, Seoul, South Korea.
Julie R BrahmerDepartment of Oncology, The Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins, Baltimore, MD, United States.
Ross A SooDepartment of Haematology-Oncology, National University Cancer Institute, National University Health System, Singapore; Cancer Science Institute of Singapore, National University of Singapore, Singapore; Department of Surgery, University of Western Australia, Australia. Electronic address: ross_soo@nuhs.edu.sg.
National University Cancer Institute, Singapore · SGNational University Health System · SGSidney Kimmel Comprehensive Cancer Center · USYonsei University · KR

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

Advances in the understanding of the role of the immune system in tumor immunosurveillance have resulted in the recognition that tumors can evade immune destruction via the dysregulation of co-inhibitory or checkpoint signals. This has led to the development of a generation immunotherapeutic agents targeting the immune checkpoint pathway. Recent early phase studies of immune checkpoint modulators, such as CTLA-4, PD-1 and PD-L1 inhibitors in NSCLC have reported promising results with prolonged clinical responses and tolerable toxicity. This article provides an overview of co-stimulatory and inhibitory molecules that regulate the immune response to tumors, recent therapies that have been developed to exploit these interactions and the role of predictive biomarkers in treatment selection.

Indexed as

ImmunotherapyAnimalsAntibodies, MonoclonalCarcinoma, Non-Small-Cell LungCarrier ProteinsCostimulatory and Inhibitory T-Cell ReceptorsHumansLung NeoplasmsProtein BindingAntibodies, MonoclonalCarrier ProteinsCostimulatory and Inhibitory T-Cell ReceptorsCTLA-4ImmunotherapyIpilimumabNivolumabNon-small cell lung cancerPD-L1

Identifiers

PMID24880938
PMCPMC4332778
OpenAlexW2088877484

What OpenQuestion holds

Textmetadata
LicenceTDM
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.