Evidence map›Paper›PMID 27887709›Full record

ArticleFertility and sterility2017

Impact of tamoxifen therapy on fertility in breast cancer survivors.

Lisa M Shandley, Jessica B Spencer, Amy Fothergill, Ann C Mertens, Amita Manatunga, Elisavet Paplomata, Penelope P Howards

Open access · greenAbstract read
In one paragraph

Article in Fertility and sterility, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 3 pooled it
2.4field-weighted citation impact, top 10% 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

44 citing papers in PubMed, 3 syntheses or guidelines pooled it, 73 citations in OpenAlex.

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  12. A life put on hold? Navigating fertility-related considerations after cancer in adolescence and young adulthood (AYA).Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
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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 4 institutions in 1 country.

Lisa M ShandleySchool of Medicine, Atlanta, Georgia. Electronic address: Lisa.Shandley@emory.edu.
Jessica B SpencerDepartment of Gynecology and Obstetrics, School of Medicine, Atlanta, Georgia.
Amy FothergillDepartment of Epidemiology, Rollins School of Public Health, Atlanta, Georgia.
Ann C MertensAflac Cancer Center, Department of Pediatrics, School of Medicine, Atlanta, Georgia.
Amita ManatungaDepartment of Biostatistics, Rollins School of Public Health, Atlanta, Georgia.
Elisavet PaplomataWinship Cancer Institute, Department of Hematology and Medical Oncology, School of Medicine, Emory University, Atlanta, Georgia.
Penelope P HowardsDepartment of Epidemiology, Rollins School of Public Health, Atlanta, Georgia.
Georgia Department of Public Health · USUniversity of Atlanta · USAflac (United States) · USEmory University · US

Funding

Atlanta Clinical and Translational Science Institute (ACTSI) RenewalUL1TR000454 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$25.8M
A Population-Based Study of Fertility in Female Survivors of Young Adult CancerR01HD066059 · NICHD · EMORY UNIVERSITY · PI HOWARDS, PENELOPE P. · 2010 to 2014
$3.1M
Atlanta Clinical and Translational Science Institute (ACTSI) RenewalTL1TR000456 · NCATS · EMORY UNIVERSITY · PI STEPHENS, DAVID S · 2012 to 2016
$1.2M
NCATS NIH HHS TL1 TR000456NCATS NIH HHS UL1 TR000454NICHD NIH HHS R01 HD066059
6 · The paper itself

Abstract

objectiveTo determine whether tamoxifen use is associated with decreased ovarian reserve and decreased likelihood of having a child after a breast cancer diagnosis, using data from the Furthering Understanding of Cancer, Health, and Survivorship in Adult (FUCHSIA) Women Study.

designPopulation-based cohort study.

settingNot applicable. PATIENT(S): Three hundred ninety-seven female breast cancer survivors aged 22-45 years whose cancer was diagnosed between ages 20 and 35 years and who were at least 2 years after diagnosis; 108 survivors also participated in a clinic visit. INTERVENTION(S): None. MAIN OUTCOME MEASURE(S): Time to first child after cancer diagnosis, clinical measures of ovarian reserve (antimüllerian hormone [AMH] and antral follicle count [AFC]) after cancer. RESULT(S): Women who had ever used tamoxifen were substantially less likely to have a child after the breast cancer diagnosis (hazard ratio [HR] 0.29; 95% confidence interval [CI], 0.16, 0.54) than women who had never used tamoxifen. After adjusting for age at diagnosis, exposure to an alkylating agent, and race, the HR was 0.25 (95% CI, 0.14, 0.47). However, after adjusting for potential confounders, women who had used tamoxifen had an estimated geometric mean AMH level 2.47 times higher (95% CI, 1.08, 5.65) than women who had never taken tamoxifen. Antral follicle count was also higher in the tamoxifen group compared with the tamoxifen nonusers when adjusted for the same variables (risk ratio 1.21; 95% CI, 0.84, 1.73). CONCLUSION(S): Breast cancer survivors who had used tamoxifen were less likely to have a child after breast cancer diagnosis compared with survivors who never used tamoxifen. However, tamoxifen users did not have decreased ovarian reserve compared with the tamoxifen nonusers.

Indexed as

SurvivorsAdultAnti-Mullerian HormoneAntineoplastic Agents, HormonalBiomarkersBreast NeoplasmsFemaleFertilityGeorgiaHumansInfertility, FemaleKaplan-Meier EstimateMiddle AgedOvarian FollicleOvarian ReserveParityAnti-Mullerian HormoneAntineoplastic Agents, HormonalBiomarkersSelective Estrogen Receptor ModulatorsTamoxifenBreast cancercancer survivorshipinfertilityovarian reservetamoxifen

Identifiers

PMID27887709
PMCPMC5203952
OpenAlexW2549736137

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.