Evidence map›Paper›PMID 19010927›Full record

Trial reportCancer research2008

Effect of fenretinide and low-dose tamoxifen on insulin sensitivity in premenopausal women at high risk for breast cancer.

Harriet Johansson, Sara Gandini, Aliana Guerrieri-Gonzaga, Simona Iodice, Massimiliano Ruscica, Bernardo Bonanni, Marcella Gulisano, Paolo Magni, Franca Formelli, Andrea Decensi

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Cancer research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Article
  5. Review
  6. Prognostic Value ofCancers · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Emerging Roles of Ceramides in Breast Cancer Biology and Therapy.International journal of molecular sciences · 2022
    Review
  12. Review
  13. Fenretinide in Cancer and Neurological Disease: A Two-Face Janus Molecule.International journal of molecular sciences · 2022
    Review
  14. Drug Repurposing by Tumor Tissue Editing.Frontiers in oncology · 2022
    Review
  15. Article
  16. Review
  17. Review
  18. Targeting Sphingolipids for Cancer Therapy.Frontiers in oncology · 2021
    Review
  19. Review
  20. The mitochondrial PKCδ/retinol signal complex exerts real-time control on energy homeostasis.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2020
    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

10 authors at 6 institutions in 3 countries.

Harriet JohanssonDivision of Cancer Prevention and Genetics, European Institute of Oncology, University of Milan, Italy. harriet.johansson@ieo.it
Sara Gandini
Aliana Guerrieri-Gonzaga
Simona Iodice
Massimiliano Ruscica
Bernardo Bonanni
Marcella Gulisano
Paolo Magni
Franca Formelli
Andrea Decensi
Cancer Genetics (United States) · USEuropean Institute of Oncology · ITUniversity of Milan · ITEnte Ospedaliero Ospedali Galliera · ITFondazione IRCCS Istituto Nazionale dei Tumori · ITOspedale San Bortolo · IT

Funding

LOW DOSE TAMOXIFEN AND 4HPR IN EARLY BREAST CANCERU01CA077188 · NCI · ISTITUTO EUROPEO DI ONCOLOGIA · PI DECENSI, ANDREA U · 1997 to 2000
$354k
NCI NIH HHS CA-77188NCI NIH HHS U01 CA077188
6 · The paper itself

Abstract

The prevalence of metabolic syndrome is increasing along with breast cancer incidence worldwide. Because fenretinide improves insulin action and glucose tolerance in insulin-resistant obese mice and because tamoxifen has shown to regulate several markers involved in metabolic syndrome, we sought to investigate the effect of fenretinide or tamoxifen at low dose on features linked to insulin resistance in premenopausal women at risk for breast cancer. We randomized 235 women to low-dose tamoxifen (5 mg/daily), fenretinide (200 mg/daily), or their combination or placebo for 2 years. We used the homeostasis model assessment (HOMA; fasting insulin x glucose/22.5) to estimate insulin sensitivity. Women were considered to improve insulin sensitivity when they shifted from a HOMA >/=2.8 to <2.8. There was no effect of fenretinide or tamoxifen on HOMA overall, but overweight women (body mass index, >or=25 kg/m(2)) had a 7-fold greater probability to normalize HOMA after 2 years of fenretinide treatment [odds ratio (OR), 7.0; 95% confidence interval (95% CI), 1.2-40.5], with 25% of women improving their insulin sensitivity, whereas tamoxifen decreased insulin sensitivity by almost 7 times compared with subjects not taking tamoxifen (OR, 0.15; 95% CI, 0.03-0.88). In this group only, 5% improved their insulin sensitivity. Interestingly, women with intraepithelial or microinvasive neoplasia had higher HOMA (3.0) than unaffected subjects (2.8; P = 0.07). Fenretinide can positively balance the metabolic profile in overweight premenopausal women and this may favorably affect breast cancer risk. Furthermore, features of the metabolic syndrome should be taken into consideration before proposing tamoxifen for breast cancer prevention. The clinical implications of these results require further investigations.

Indexed as

Insulin ResistanceAntineoplastic AgentsBody Mass IndexBreast NeoplasmsCholesterol, HDLDouble-Blind MethodFemaleFenretinideHumansInsulin-Like Growth Factor ILeptinPremenopauseRetinol-Binding Proteins, PlasmaTamoxifenAntineoplastic AgentsCholesterol, HDLFenretinideInsulin-Like Growth Factor ILeptinRBP4 protein, humanRetinol-Binding Proteins, PlasmaTamoxifen

Identifiers

PMID19010927
PMCPMC2599903
OpenAlexW2123383121

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.