Evidence map›Paper›PMID 12838293›Full record

ReviewBritish journal of cancer2003

Surrogate markers in antiangiogenesis clinical trials.

D W Davis, D J McConkey, J L Abbruzzese, R S Herbst

Open access · hybridAbstract readReview
In one paragraph

Review in British journal of cancer, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
  2. Therapeutic Potential of Curcumin for the Treatment of Brain Tumors.Oxidative medicine and cellular longevity · 2016
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Bevacizumab for the treatment of recurrent glioblastoma.Clinical Medicine Insights. Oncology · 2011
    Article
  8. Medical imaging in new drug clinical development.Journal of thoracic disease · 2010
    Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. 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

4 authors at 1 institution in 1 country.

D W Davis1Department of Cancer Biology, Unit 173, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA. dardavis@mdanderson.org
D J McConkey
J L Abbruzzese
R S Herbst
The University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Novel antiangiogenic agents currently being developed may ultimately be more effective against solid tumours and less toxic than cytotoxic chemotherapy. As a result of the early clinical trials of angiogenesis inhibitors, investigators are beginning to appreciate the complexity of targeting angiogenesis and the realisation that developing clinically useful antiangiogenic therapy will be more challenging than originally thought. It is now apparent that new methods and surrogate markers to assess these agents' biological activity are crucial for their successful development. This review summarises the currently available clinical data on the development of surrogate markers of angiogenesis inhibitors.

Indexed as

Angiogenesis InhibitorsBiomarkers, TumorBiopsyClinical Trials as TopicHumansMicroscopy, ConfocalNeoplasmsTreatment OutcomeAngiogenesis InhibitorsBiomarkers, Tumor

Identifiers

PMID12838293
PMCPMC2394225
OpenAlexW2028070840

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.