Evidence map›Paper›PMID 37874926›Full record

ArticleThe oncologist2024

Real-World Patient Experience of Pexidartinib for Tenosynovial Giant-Cell Tumor.

Feng Lin, Winghan Jacqueline Kwong, Irene Pan, Xin Ye, Dong Dai, William Tap

Open access · goldAbstract read
In one paragraph

Article in The oncologist, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  4. Observational
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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

6 authors at 2 institutions in 1 country.

Feng LinHealth Economics and Outcomes Research, Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.ORCID 0000-0001-8520-0420
Winghan Jacqueline KwongHealth Economics and Outcomes Research, Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.
Irene PanEpidemiology and Real-World Evidence, United BioSource LLC, Blue Bell, PA, USA.
Xin YeHealth Economics and Outcomes Research, Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.ORCID 0000-0002-5929-3798
Dong DaiHealth Economics and Outcomes Research, Daiichi Sankyo, Inc., Basking Ridge, NJ, USA.
William TapSarcoma Medical Oncology Service, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Daiichi Sankyo (United States) · USMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Daiichi-SankyoNCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

backgroundPexidartinib (Turalio) is the only systemic therapy approved by the FDA for the treatment of adult patients with symptomatic tenosynovial giant-cell tumor (TGCT) associated with severe morbidity or functional limitations, and not amenable to improvement with surgery. This study assessed patient-reported treatment experiences and symptom improvement among patients receiving pexidartinib.

methodsA cross-sectional, web-based survey collected data on demographics, disease history, pexidartinib dosing, and symptoms before and after pexidartinib use.

resultsOf 288 patients enrolled in the Turalio REMS program in May 2021, 83 completed the survey: mean age was 44.2 years, 62.7% were female, and most common tumor sites were in knee (61%) and ankle (12%). Mean initial dose was 622 mg/day: 29 patients reported reduction from initial dose and 8 had dose reduction after titrating up to a higher dose. At the time of survey completion, median time on pexidartinib was 6.0 months; 22 (26.5%) patients discontinued pexidartinib due to physician suggestion, abnormal laboratory results, side effect, or symptom improvement. Compared with before pexidartinib initiation, most patients reported improvement in overall TGCT symptom (78.3%) and physical function (77.2%) during pexidartinib treatment. Significant improvement was reported during pexidartinib treatment in worst stiffness numeric rating scale (NRS) (3.0 vs. 6.2, P < .05) and worst pain NRS (2.7 vs. 5.7, P < .05).

conclusionFindings from this cross-sectional survey confirmed the benefit of pexidartinib in improving symptoms and functional outcomes among patients with symptomatic TGCTs from the patients' perspective. Future research is warranted to examine the long-term benefit and risk of pexidartinib.

Indexed as

Giant Cell Tumor of Tendon SheathPyrrolesAdultAminopyridinesCross-Sectional StudiesFemaleHumansMalePatient Outcome AssessmentAminopyridinespexidartinibPyrrolespatient-reported outcomepexidartinibsymptom changetenosynovial giant-cell tumor

Identifiers

PMID37874926
PMCPMC10994266
OpenAlexW4387900753

What OpenQuestion holds

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LicenceCC BY
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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.