Evidence map›Paper›PMID 34041638›Full record

ArticleInvestigational new drugs2021

Real-world pharmacokinetics and pharmacodynamics of everolimus in metastatic breast cancer.

Masahide Fukudo, Kei Ishibashi, Masahiro Kitada

Abstract read
PubMed Publisher
In one paragraph

Article in Investigational new drugs, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
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  5. Programmed cell death, redox imbalance, and cancer therapeutics.Apoptosis : an international journal on programmed cell death · 2021
    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

3 authors at 2 institutions in 1 country.

Masahide FukudoDepartment of Hospital Pharmacy and Pharmacology, Asahikawa Medical University, Asahikawa, Japan. fukudom@sapmed.ac.jp.ORCID 0000-0002-7703-7827
Kei IshibashiBreast Disease Center, Asahikawa Medical University Hospital, Asahikawa, Japan.
Masahiro KitadaBreast Disease Center, Asahikawa Medical University Hospital, Asahikawa, Japan.
Asahikawa Medical University · JPSapporo Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose This study investigated the relationship between the pharmacokinetics and pharmacodynamics of everolimus in patients with metastatic breast cancer (mBC) in real-world practice.Methods Twenty-two patients with mBC treated with everolimus plus exemestane were enrolled. Blood everolimus concentrations were measured at outpatient visits. The inhibition of the mammalian target of rapamycin (mTOR) activity in peripheral blood mononuclear cells (PBMCs) was examined. The efficacy and safety endpoints were progression-free survival (PFS) and the cumulative incidence of dose-limiting toxicities (DLTs), respectively. Results Blood samples were obtained from 19 consenting patients. Everolimus did not completely inhibit mTOR activity in PBMCs at therapeutic concentrations (~ 56 % maximal inhibition). The most common adverse event was stomatitis (any grade 77 %). The trough concentration (C

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsBreast NeoplasmsDose-Response Relationship, DrugEverolimusFemaleGenotypeHumansMaximum Tolerated DoseMiddle AgedProgression-Free SurvivalProspective StudiesTOR Serine-Threonine KinasesAntineoplastic AgentsEverolimusTOR Serine-Threonine KinasesBreast cancerEverolimusPharmacodynamicsPharmacokineticsTherapeutic drug monitoring

Identifiers

PMID34041638
OpenAlexW3163990765

What OpenQuestion holds

Textmetadata
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.