Evidence map›Paper›PMID 20051377›Full record

Trial reportCancer prevention research (Philadelphia, Pa.)2010

Sulindac and sulindac metabolites in nipple aspirate fluid and effect on drug targets in a phase I trial.

Patricia A Thompson, Chiu-Hsieh Hsu, Sylvan Green, Alison T Stopeck, Karen Johnson, David S Alberts, H-H Sherry Chow

Open access · bronzeAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Cancer prevention research (Philadelphia, Pa.), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Sulindac, a Nonselective NSAID, Reduces Breast Density in Postmenopausal Women with Breast Cancer Treated with Aromatase Inhibitors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Trial
  2. Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Opportunities and challenges for selected emerging technologies in cancer epidemiology: mitochondrial, epigenomic, metabolomic, and telomerase profiling.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2013
    Review
  8. 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

7 authors at 2 institutions in 1 country.

Patricia A ThompsonArizona Cancer Center, University of Arizona, Tucson, 85724-5024, USA. pthompson@azcc.arizona.edu
Chiu-Hsieh Hsu
Sylvan Green
Alison T Stopeck
Karen Johnson
David S Alberts
H-H Sherry Chow
National Cancer Institute · USUniversity of Arizona · US

Funding

PHASE I AND II CLINICAL TRIALS OF CANCER CHEMOPREVENTIVE AGENTS-261035-261035158N01CN035158 · CN · UNIVERSITY OF ARIZONA · PI ALBERTS, DAVID S · 2004 to 2006
–
NCI NIH HHS N01 CN035158
6 · The paper itself

Abstract

Regular use of nonsteroidal anti-inflammatory drugs (NSAID) has been associated with reduced risk of breast cancer. Sulindac, a nonselective NSAID with both cyclooxygenase-2-dependent and -independent activities, is a candidate for breast chemoprevention. We conducted a phase Ib trial in 30 women at increased risk for breast cancer to evaluate the breast tissue distribution of sulindac at two dose levels (150 mg daily and 150 mg twice daily for 6 weeks), using nipple aspirate fluid (NAF) as a surrogate of breast tissue drug exposure. We also explored the effect of sulindac on drug-induced biomarkers in NAF. We show that sulindac and its metabolites partition to human breast as measured by NAF levels. Sulindac intervention did not decrease 13,14-dihydro-15-keto prostaglandin A(2), a stable derivative of prostaglandin E(2), in NAF, but exposure was associated with a significant trend towards higher levels of growth differentiation factor 15 in NAF in women receiving 150 mg twice daily (P = 0.038). These results are the first to show partitioning of sulindac and metabolites to human breast tissue and the first evidence for a potential dose-dependent effect of sulindac on growth differentiation factor 15 levels in NAF.

Indexed as

Antineoplastic AgentsBiomarkers, TumorBreast NeoplasmsCarcinoma, Ductal, BreastChromatography, High Pressure LiquidC-Reactive ProteinDinoprostoneFemaleGenetic Predisposition to DiseaseGrowth Differentiation Factor 15HumansNipple Aspirate FluidSulindacTissue Distribution15-keto-13,14-dihydroprostaglandin E2Antineoplastic AgentsBiomarkers, TumorC-Reactive ProteinDinoprostoneGDF15 protein, humanGrowth Differentiation Factor 15Sulindac

Identifiers

PMID20051377
PMCPMC3993089
OpenAlexW2131237577

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.