Evidence map›Paper›PMID 35083783›Full record

ArticleBritish journal of clinical pharmacology2022

Muscle mass affects paclitaxel systemic exposure and may inform personalized paclitaxel dosing.

Daniel L Hertz, Li Chen, N Lynn Henry, Jennifer J Griggs, Daniel F Hayes, Brian A Derstine, Grace L Su, Stewart C Wang, Manjunath P Pai

Open access · bronzeAbstract read
In one paragraph

Article in British journal of clinical pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Impact of sarcopenia on paclitaxel-induced peripheral neuropathy in early-stage breast cancer: a prospective observational study (the neuro-sarc study).Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2025
    Observational
  8. Article
  9. Review
  10. Observational
  11. Article
  12. Using maximum plasma concentration (CCancer chemotherapy and pharmacology · 2024
    Review
  13. Evolution of predictive risk factor analysis for chemotherapy-related toxicity.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2023
    Review
  14. 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

9 authors at 2 institutions in 1 country.

Daniel L HertzDepartment of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, MI, USA.ORCID 0000-0003-0501-1035
Li ChenDepartment of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, MI, USA.
N Lynn HenryDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0002-4771-5930
Jennifer J GriggsDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Medical School, Ann Arbor, MI, USA.
Daniel F HayesDepartment of Internal Medicine, Division of Hematology/Oncology, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0003-3620-7575
Brian A DerstineMorphomic Analysis Group, University of Michigan Medical School, Ann Arbor, MI, USA.
Grace L SuMorphomic Analysis Group, University of Michigan Medical School, Ann Arbor, MI, USA.
Stewart C WangMorphomic Analysis Group, University of Michigan Medical School, Ann Arbor, MI, USA.ORCID 0000-0001-7780-7687
Manjunath P PaiDepartment of Clinical Pharmacy, University of Michigan College of Pharmacy, Ann Arbor, MI, USA.ORCID 0000-0001-7119-5034
University of Michigan · USMorpho (United States) · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Michigan Institute for Clinical and Health Research (MCHR)UL1TR000433 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$49.9M
Training Program in Gastrointestinal EpidemiologyT32DK062708 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Peter D.R. Higgins, Elliot Tapper · 2003 to 2026
$3.9M
NOVEL STRATEGIES TO IMPROVE LIVER CANCER SURVEILLANCE UPTAKE AND EARLY DETECTIONU01CA230669 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LOK, ANNA S.F., SU, GRACE L. · 2018 to 2022
$3.3M
Precision Prophylaxis of Surgical Site Infection Utilizing PharmacomorphomicsR01HS027183 · AHRQ · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, STEWART C · 2019 to 2023
$2.4M
Michigan Institute for Clinical and Health Research (MCHR)KL2TR000434 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MASHOUR, GEORGE ALEXANDER · 2012 to 2016
$1.7M
AHRQ HHS R01 HS027183NCATS NIH HHS KL2 TR000434NCATS NIH HHS UL1 TR000433NCI NIH HHS P30 CA046592NCI NIH HHS U01 CA230669NIDDK NIH HHS T32 DK062708
6 · The paper itself

Abstract

aimsPatients with low muscle mass have increased risk of paclitaxel-induced peripheral neuropathy, which is dependent on systemic paclitaxel exposure. Dose optimization may be feasible through the secondary use of radiologic data for body composition. The objective of this study was to interrogate morphomic parameters as predictors of paclitaxel pharmacokinetics to identify alternative dosing strategies that may improve treatment outcomes.

methodsThis was a secondary analysis of female patients with breast cancer scheduled to receive 80 mg/m

resultsThirty-nine patients were included in the analysis. The optimal model was a two-compartment pharmacokinetic model with T11 skeletal muscle area as a covariate of paclitaxel volume of distribution (Vd). Simulations suggest that extending infusion of the standard paclitaxel dose from 1 hour to 2 and 3 hours in patients who have skeletal muscle area 4907-7080 mm

conclusionExtending paclitaxel infusion duration in ~25% of patients who have low skeletal muscle area is predicted to reduce peripheral neuropathy while maintaining systemic exposure, suggesting that personalizing paclitaxel dosing based on body composition may improve treatment outcomes.

Indexed as

Antineoplastic Agents, PhytogenicBreast NeoplasmsPeripheral Nervous System DiseasesFemaleHumansImmunotherapyMusclesPaclitaxelAntineoplastic Agents, PhytogenicPaclitaxelmodelling and simulationmorphomicsmuscle masspaclitaxelperipheral neuropathypharmacokineticssarcopeniatherapeutic drug monitoring

Identifiers

PMID35083783
PMCPMC9197985
OpenAlexW4210498024

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.