Evidence map›Paper›PMID 39848945›Full record

ArticleScientific reports2025

Characterizing safety, toxicity, and breast cancer risk reduction using a long-term fulvestrant eluting implant.

Scott Thomas, Elysia Roche, Pujan Desai, Nela Pawlowska, Diana Bauer, David Gingrich, Emily Hsu, Amelia N Deitchman, Fran Aweeka, Pamela N Munster

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Scott ThomasDivision of Hematology and Oncology, University of California, 1450 3rd Street, San Francisco, CA, 94143, USA.
Elysia RocheDivision of Hematology and Oncology, University of California, 1450 3rd Street, San Francisco, CA, 94143, USA.
Pujan DesaiDivision of Hematology and Oncology, University of California, 1450 3rd Street, San Francisco, CA, 94143, USA.
Nela PawlowskaDivision of Hematology and Oncology, University of California, 1450 3rd Street, San Francisco, CA, 94143, USA.
Diana BauerLaboratory Animal Resource Center, University of California, San Francisco, USA.
David GingrichDrug Research Unit, Department of Clinical Pharmacy, University of California, San Francisco, USA.
Emily HsuDrug Research Unit, Department of Clinical Pharmacy, University of California, San Francisco, USA.
Amelia N DeitchmanDrug Research Unit, Department of Clinical Pharmacy, University of California, San Francisco, USA.
Fran AweekaDrug Research Unit, Department of Clinical Pharmacy, University of California, San Francisco, USA.
Pamela N MunsterDivision of Hematology and Oncology, University of California, 1450 3rd Street, San Francisco, CA, 94143, USA. Pamela.Munster@ucsf.edu.

Funding

Developing silastic-silicone for the local delivery of hormonal therapy to prevent and treat breast cancerR01CA220131 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MUNSTER, PAMELA N. · 2017 to 2021
$1.8M
NCI NIH HHS R01 CA220131NIH HHS R01 CA220131
6 · The paper itself

Abstract

For individuals at high risk of developing breast cancer, interventions to mitigate this risk include surgical removal of their breasts and ovaries or five years treatment with the anti-estrogen tamoxifen or aromatase inhibitors. We hypothesized that a silicone based anti-estrogen-eluting implant placed within the breast would provide the risk reduction benefit of hormonal therapy, but without the adverse effects that limit compliance. To this end, we demonstrate that when placed adjacent to mammary tissue in the 7,12-dimethylbenz[a]anthracene-induced rat breast cancer model a fulvestrant-eluting implant delays breast cancer with minimal systemic exposure. Using adult female sheep, surgical placement of fulvestrant-eluting implants was safe and did not elicit significant breast tissue pathology when placed at the base of the udder for directed elution into the mammary tissue. At 30 days of elution, fulvestrant was found to penetrate mammary tissue forming a concentration gradient beyond 15 mm from the implant. Consistent with the small animal rat study, minimal systemic fulvestrant biodistribution was found. Together, these studies provide the proof of principle that a breast indwelling fulvestrant-eluting implant can reduce the risk of breast cancer and limit systemic exposure, while penetrating and distributing through breast tissue.

Indexed as

Breast NeoplasmsFulvestrantMammary Neoplasms, ExperimentalAnimalsBreast ImplantsDrug ImplantsFemaleRatsSheepTissue DistributionDrug ImplantsFulvestrant

Identifiers

PMID39848945
PMCPMC11758070

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Registered trials

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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.