Evidence map›Paper›PMID 38127812›Full record

ArticleJCO oncology practice2024

Use of Peripheral Intravenous Access in Patients Undergoing Chemotherapy for Testicular Cancer.

Brett Wiesen, Michael Atwell, Colton Leavitt, Nathan Clark, Elizabeth Kessler, Elaine Lam, Thomas Flaig, Janet Kukreja, Simon Kim, Paul Maroni and 1 more

Open access · greenAbstract read
In one paragraph

Article in JCO oncology practice, 2024. 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
1.4field-weighted citation impact, top 17% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Brett WiesenThe University of Colorado, Division of Urology, Aurora, CO.ORCID 0009-0008-9914-9388
Michael AtwellThe University of Colorado, Division of Urology, Aurora, CO.ORCID 0009-0005-3073-638X
Colton LeavittThe University of Utah, Department of Urology, Salt Lake City, UT.
Nathan ClarkThe University of Colorado, Division of Urology, Aurora, CO.
Elizabeth KesslerThe University of Colorado, Division of Medical Oncology, Aurora, CO.ORCID 0000-0001-7285-867X
Elaine LamThe University of Colorado, Division of Medical Oncology, Aurora, CO.ORCID 0000-0001-5629-3402
Thomas FlaigThe University of Colorado, Division of Medical Oncology, Aurora, CO.ORCID 0000-0001-6145-9040
Janet KukrejaThe University of Colorado, Division of Urology, Aurora, CO.
Simon KimThe University of Colorado, Division of Urology, Aurora, CO.ORCID 0000-0002-7117-1443
Paul MaroniThe University of Colorado, Division of Urology, Aurora, CO.
Nicholas G CostThe University of Colorado, Division of Urology, Aurora, CO.ORCID 0000-0002-5785-3704
University of Colorado Boulder · USUniversity of Utah · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
NCI NIH HHS P30 CA046934
6 · The paper itself

Abstract

purposeSystemic chemotherapy, depending on the regimen, can be administered through peripheral intravenous (pIV) access or through central venous access devices (CVADs). There is no current best practice regarding optimal access for chemotherapy for patients with testicular cancer (TC). We retrospectively evaluated patients undergoing systemic chemotherapy for TC and compared baseline characteristics and complications of patients using pIV versus CVADs.

methodsWe included patients with TC who underwent first-line systemic chemotherapy at the University of Colorado Hospitals from 2005 to 2020. Data were collected on demographics, cancer characteristics, type, duration of chemotherapy, pIV or CVAD use, and associated complication rates. We then performed univariate and multivariate regression analyses to compare complication rates and risk factors for each group.

resultsOne hundred fifty-four patients met inclusion criteria. Ninety-two (60%) patients used CVADs, and 62 patients (40%) used pIV for their initial treatment. Only six (9.7%) of 62 patients transitioned from pIV to CVADs during therapy. Similarly, 10 of 92 (10.9%) patients with initial CVAD needed to transition to a different type of CVAD or to pIV (

conclusionPeripheral IV use for first-line nonvesicant chemotherapy in patients with TC appears to be well tolerated with high rates of therapy completion and lower rates of complications when compared with CVADs. These data support our preferred treatment approach and provide evidence that pIV access is a safe and effective way to deliver chemotherapy for patients with TC.

Indexed as

Neoplasms, Germ Cell and EmbryonalTesticular NeoplasmsHospitalsHumansMaleRetrospective Studies

Identifiers

PMID38127812
PMCPMC11005905
OpenAlexW4390046846

What OpenQuestion holds

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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.