Evidence map›Paper›PMID 24951267›Full record

ArticleBreast cancer research and treatment2014

Duration of tamoxifen use and the risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers.

Jacek Gronwald, Andre Robidoux, Charmaine Kim-Sing, Nadine Tung, Henry T Lynch, William D Foulkes, Siranoush Manoukian, Peter Ainsworth, Susan L Neuhausen, Rochelle Demsky and 15 more

Open access · greenAbstract read
In one paragraph

Article in Breast cancer research and treatment, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 4 pooled it
3.7field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 4 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Review
  8. Article
  9. Article
  10. Prognostic Impact ofBiology · 2021
    Article
  11. Article
  12. Cancers · 2018
    Review
  13. Article
  14. BRCA1 and BRCA2 mutations and treatment strategies for breast cancer.Integrative cancer science and therapeutics · 2017
    Article
  15. Review
  16. Article
  17. 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

25 authors at 20 institutions in 6 countries.

Jacek GronwaldHereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland.
Andre Robidoux
Charmaine Kim-Sing
Nadine Tung
Henry T Lynch
William D Foulkes
Siranoush Manoukian
Peter Ainsworth
Susan L Neuhausen
Rochelle Demsky
Andrea Eisen
Christian F Singer
Howard Saal
Leigha Senter
Charis Eng
Jeffrey Weitzel
Pal Moller
Dawna M Gilchrist
Olufunmilayo Olopade
Ophira Ginsburg
Ping Sun
Tomasz Huzarski
Jan Lubinski
Steven A Narod
Hereditary Breast Cancer Clinical Study Group
Pomeranian Medical University · PLWomen's College Hospital · CABC Cancer Agency · CABeth Israel Deaconess Hospital · USCancer Care Ontario · CACincinnati Children's Hospital Medical Center · USCity of Hope · USCity Of Hope National Medical Center · USCleveland Clinic · USCreighton University · USFondazione IRCCS Istituto Nazionale dei Tumori · ITMcGill University · CAMedical University of Vienna · ATNorwegian Cancer Society · NOSunnybrook Health Science Centre · CAThe Ohio State University · USUniversité de Montréal · CAUniversity of Alberta · CAUniversity of Illinois Chicago · USUniversity of Toronto · CA

Funding

GENETIC EPIDEMIOLOGY OF BREAST CANCER--BRCA1 AND BRCA2R01CA074415 · NCI · UNIVERSITY OF UTAH · PI NEUHAUSEN, SUSAN L. · 1998 to 2007
$3.9M
NCI NIH HHS R01 CA074415NCI NIH HHS R01 CA74415
6 · The paper itself

Abstract

Women with a mutation in BRCA1 or BRCA2 face a lifetime risk of breast cancer of approximately 80 %. Tamoxifen treatment of the first cancer has been associated with a reduction in the risk of a subsequent contralateral cancer. We studied 1,504 women with a known BRCA1 or BRCA2 mutation, 411 women with bilateral breast cancer (cases) and 1,093 women with unilateral breast cancer (controls) in a matched case-control study. Control women were of similar age and had a similar age of diagnosis of first breast cancer as the cases. For each woman who used tamoxifen, the starting and stopping dates were abstracted and the duration of tamoxifen use was calculated. Three hundred and thirty-one women had used tamoxifen (22 %); of these 84 (25 %) had completed four or more years of tamoxifen, the remainder stopped prematurely or were current users. For women with up to 1 year of tamoxifen use, the odds ratio for contralateral breast cancer was 0.37 (95 % CI 0.20-0.69; p = 0.001) compared to women with no tamoxifen use. Among women with 1-4 years of tamoxifen use the odds ratio was 0.53 (95 % CI 0.32-0.87; p = 0.01). Among women with four or more years of tamoxifen use the odds ratio was 0.83 (95 % CI 0.44-1.55; p = 0.55). Short-term use of tamoxifen for chemoprevention in BRCA1 and BRCA2 mutation carriers may be as effective as a conventional 5-year course of treatment.

Indexed as

Genes, BRCA1Genes, BRCA2HeterozygoteMutationAdultAgedAntineoplastic Agents, HormonalBreast NeoplasmsCase-Control StudiesFemaleHumansMiddle AgedNeoplasms, Second PrimaryOdds RatioRisk FactorsTamoxifenAntineoplastic Agents, HormonalTamoxifen

Identifiers

PMID24951267
PMCPMC4131437
OpenAlexW1994262858

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.