Evidence map›Paper›PMID 41694118›Full record

ArticleFrontiers in pain research (Lausanne, Switzerland)2026

Time-course based assessment of patient factors and their relationship to chemotherapy induced peripheral neuropathy.

Carla Bou Dargham, Ken B Johnson, Alper Sen, Bihua Bie, Emily E Rhoades, Jacob Steenblik, Courtney Hershberger, Mei Wei, N Lynn Henry, Anukriti Sharma and 3 more

Abstract read
In one paragraph

Article in Frontiers in pain research (Lausanne, Switzerland), 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

13 authors.

Carla Bou DarghamDepartment of Quantitative Health Sciences, Cleveland Clinic Research, Cleveland Clinic, Cleveland, OH, United States.
Ken B JohnsonDepartment of Anesthesiology, University of Utah, Salt Lake City, UT, United States.
Alper SenDepartment of Anesthesiology, University of Utah, Salt Lake City, UT, United States.
Bihua BieDepartment of Anesthesiology, Cleveland Clinic, Cleveland, OH, United States.
Emily E RhoadesTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.
Jacob SteenblikDepartment of Anesthesiology, University of Utah, Salt Lake City, UT, United States.
Courtney HershbergerDepartment of Quantitative Health Sciences, Cleveland Clinic Research, Cleveland Clinic, Cleveland, OH, United States.
Mei WeiHuntsman Cancer Institute, University of Utah, Salt Lake City, UT, United States.
N Lynn HenryUniversity of Michigan Medical School, Ann Arbor, MI, United States.
Anukriti SharmaDepartment of Quantitative Health Sciences, Cleveland Clinic Research, Cleveland Clinic, Cleveland, OH, United States.
G Thomas BuddDepartment of Anesthesiology, Cleveland Clinic, Cleveland, OH, United States.
Joseph FossDepartment of Anesthesiology, Cleveland Clinic, Cleveland, OH, United States.
Daniel M RotroffDepartment of Quantitative Health Sciences, Cleveland Clinic Research, Cleveland Clinic, Cleveland, OH, United States.

Funding

Multi-Omic Biomarkers for Neuropathic Pain Secondary to ChemotherapyR61NS113258 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI FOSS, JOSEPH F, JOHNSON, KENWARD B · 2020 to 2020
$4.8M
Multi-Omic Biomarkers for Neuropathic Pain Secondary to ChemotherapyR33NS113258 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI FOSS, JOSEPH F, JOHNSON, KENWARD B · 2023 to 2024
$2.6M
NINDS NIH HHS R33 NS113258NINDS NIH HHS R61 NS113258
6 · The paper itself

Abstract

Background: Patients commonly experience chemotherapy-induced peripheral neuropathy (CIPN) as an adverse effect from chemotherapies, such as taxanes. In some patients, CIPN symptoms are severe and significantly impact their quality of life. Gaining a deeper understanding of how patient factors change over time, and identifying predisposing patient factors for CIPN susceptibility, could provide opportunities to mitigate the risk of CIPN and improve patient outcomes. Methods: A total of 229 patients with breast cancer receiving taxane chemotherapy completed study visits over 12 months. Data from patient reported outcomes (PROs) were collected from validated questionnaires to assess CIPN, anxiety, depression, weight, physical function, and sleep disturbance. Wilcoxon signed-rank tests were conducted to evaluate changes in PROs between timepoints (pre-treatment, on-treatment, post-treatment). Logistic regression was used to compare PROs between CIPN and non-CIPN groups at each time point, after adjustment for age, race, and pre-treatment CIPN score. Results were adjusted for multiple comparisons using a false discovery rate (FDR) procedure (FDR Results: Out of 229 patients, 75% developed CIPN. Higher depression scores were associated with CIPN development across the three time periods: pre-treatment (OR = 1.20, FDR Conclusion: These findings indicate that those experiencing CIPN were more likely to report reduced physical functioning, increased anxiety and depression, and have higher BMIs. As new multi-modal approaches are developed for CIPN, pre-treatment physical functioning, BMI and other patient reported measures may provide predictive ability.

Indexed as

anxietycancerchemotherapydepressionneuropathypatient reported clinical outcomesphysical functioning

Identifiers

PMID41694118
PMCPMC12901485

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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.