Evidence map›Paper›PMID 42584460›Full record

ArticleJournal of clinical pharmacology2026

Tamoxifen Therapy Is Associated With Altered Intestinal P-Glycoprotein Activity In Vivo.

Álef Machado Gomes Pego, Fernanda de Lima Moreira, Ana Flavia Mendes Batista, Adriana Rocha, Maria Paula Marques Pereira, Eduardo Barbosa Coelho, Jurandyr Moreira de Andrade, Geraldo Duarte, Vera Lucia Lanchote, João Paulo Bianchi Ximenez

Abstract read
In one paragraph

Article in Journal of clinical pharmacology, 2026. 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

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.

Álef Machado Gomes PegoSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Fernanda de Lima MoreiraFaculty of Pharmacy, Federal University of Rio de Janeiro, Rio de Janeiro, Rio de Janeiro, Brazil.
Ana Flavia Mendes BatistaSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.ORCID https://orcid.org/0009-0004-0764-4228
Adriana RochaSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Maria Paula Marques PereiraSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Eduardo Barbosa CoelhoRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Jurandyr Moreira de AndradeRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Geraldo DuarteRibeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
Vera Lucia LanchoteSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.
João Paulo Bianchi XimenezSchool of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Ribeirão Preto, São Paulo, Brazil.

Funding

Brazilian National Council for Scientific and Technological Development (CNPq)São Paulo Research Foundation 2024/05744-2São Paulo Research Foundation FAPESP numbers: 2014/16360-9 2018/05616-3
6 · The paper itself

Abstract

Preclinical studies suggest that tamoxifen (TAM) may interact with the efflux transporter P-glycoprotein (P-gp); however, its effect on intestinal P-gp activity in vivo remains poorly characterized. This study evaluated intestinal P-gp activity in women receiving tamoxifen therapy using fexofenadine (FEXO) as a probe substrate. Sixteen women receiving tamoxifen (20 mg/day for ≥80 days) and 12 healthy women were enrolled. All participants received a single oral dose of fexofenadine (120 mg), and serial plasma samples were collected over 12 h. Pharmacokinetic parameters were determined by noncompartmental analysis, and plasma fexofenadine concentrations were quantified by LC-MS/MS. Systemic exposure to fexofenadine was lower in women receiving tamoxifen than in healthy women. Geometric mean (95% confidence interval [CI]) AUC

Indexed as

Antineoplastic Agents, HormonalATP Binding Cassette Transporter, Subfamily B, Member 1Intestinal MucosaTamoxifenTerfenadineAdministration, OralAdultArea Under CurveFemaleHumansMiddle AgedYoung AdultAntineoplastic Agents, HormonalATP Binding Cassette Transporter, Subfamily B, Member 1fexofenadineTamoxifenTerfenadinedrug transportersfexofenadinep‐glycoproteinpharmacokineticstamoxifen

Identifiers

PMID42584460
PMCPMC13464512

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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.