Evidence map›Paper›PMID 42521839›Full record

ArticleBreast cancer research and treatment2026

Antacid co-treatment and pregnane X receptor genetic polymorphisms are survival determinants in patients treated with palbociclib.

Fanny Leenhardt, William Jacot, Lionel Lellouche, Severine Guiu, Marie Viala, Nelly Firmin, Alexandre Payen, Litaty C Mbatchi, Frederic Fiteni, Alexandre Evrard

Registry-linked trialAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04025541 (Analysis of Circulating Tumor Markers in Blood), which is not on this map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

NCT04025541 narecruitingnot on this map

Analysis of Circulating Tumor Markers in Blood

TypeinterventionalSponsorInstitut du Cancer de Montpellier - Val d'AurelleRan2018 to 2029Enrolled992ConditionsCancer, Breast Cancer, Sarcoma, Lung CancersArmsBlood sampling, Blood sampling C3, Blood sampling C4/7/10/13, Blood sampling C5, Blood sampling C6
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

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5 · Who and what money

Authors and funding

10 authors.

Fanny LeenhardtInstitut du Cancer de Montpellier, INSERM U1194, Univ Montpellier, Montpellier, France. fanny.leenhardt@icm.unicancer.fr.ORCID https://orcid.org/0000-0002-9404-5044
William JacotInstitut du Cancer de Montpellier, INSERM U1194, Univ Montpellier, Montpellier, France.
Lionel LelloucheInstitut du Cancer de Montpellier, INSERM U1194, Univ Montpellier, Montpellier, France.
Severine GuiuInstitut du Cancer de Montpellier, INSERM U1194, Univ Montpellier, Montpellier, France.
Marie VialaInstitut du Cancer de Montpellier, INSERM U1194, Univ Montpellier, Montpellier, France.
Nelly FirminInstitut du Cancer de Montpellier, INSERM U1194, Univ Montpellier, Montpellier, France.
Alexandre PayenLaboratory of Molecular Oncology, Nimes University Hospital, Univ Montpellier, Montpellier, France.
Litaty C MbatchiIRCM, Univ Montpellier, INSERM, Montpellier, France.
Frederic FiteniIRCM, Univ Montpellier, INSERM, Montpellier, France.
Alexandre EvrardIRCM, Univ Montpellier, INSERM, Montpellier, France.

Funding

INCa-Cancéropôle No. 2018-E13
6 · The paper itself

Abstract

backgroundPalbociclib is the more extensively evaluated CDK4-6 inhibitor in term of safety, efficacy and sources of pharmacokinetic variability. However, real-life data on the correlation between palbociclib plasma concentration, drug-drug interactions, gene polymorphisms and efficacy remain scarce. We previously characterized the effects of co-medications (CYP3A4 and P-glycoprotein inhibitors and antacid drugs) on palbociclib plasma concentration, and here we wanted to identify factors that influence progression-free survival in the same cohort of patients.

methodsThis multicentric prospective clinical trial included patients with metastatic breast cancer treated with first-line palbociclib and an aromatase inhibitor. Efficacy (progression-free survival) and safety (high-grade neutropenia during the first two cycles) were reported, and the influence of covariates, such as drug-drug interactions, palbociclib plasma concentration and specific gene variants, were analyzed.

resultsIn the 58 included patients, drug-drug interactions (antacid drugs) and pregnane X receptor (NR1I2) single nucleotide polymorphisms (SNP) were identified as survival prognostic factors, but not palbociclib concentration and high-grade neutropenia (p = 0.4 and p = 0.5). Concomitant antacid treatment reduced progression-free survival (26.2 vs. 32.6 months, p = 0.059) and the NR1I2 rs10934498 and rs2276707 SNPs affected survival (p = 0.002 and 0.004).

conclusionThis study consolidated the data on palbociclib as first-line metastatic breast cancer treatment and identified factors that negatively influence survival (co-treatment with antacid drugs and NR1I2 SNPs).

trial registrationNCT04025541, Registration Date 2019-07-16.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsPiperazinesPolymorphism, Single NucleotidePregnane X ReceptorPyridinesAdultAgedAromatase InhibitorsDrug InteractionsFemaleHumansMiddle AgedPrognosisProgression-Free SurvivalProspective StudiesAromatase InhibitorsNR1I2 protein, humanpalbociclibPiperazinesPregnane X ReceptorPyridinesBreast cancer treatmentPharmacogeneticsPharmacokineticsPregnane X receptor

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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.