Evidence map›Paper›PMID 26062540›Full record

ArticleBMC veterinary research2015

Maintenance therapy with toceranib following doxorubicin-based chemotherapy for canine splenic hemangiosarcoma.

Heather L Gardner, Cheryl A London, Roberta A Portela, Sandra Nguyen, Mona P Rosenberg, Mary K Klein, Craig Clifford, Douglas H Thamm, David M Vail, Phil Bergman and 4 more

Open access · goldAbstract read
In one paragraph

Article in BMC veterinary research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-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

19 citing papers in PubMed, 48 citations in OpenAlex.

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  14. Canine visceral hemangiosarcoma treated with surgery alone or surgery and doxorubicin: 37 cases (2005-2014).The Canadian veterinary journal = La revue veterinaire canadienne · 2018
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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

14 authors at 8 institutions in 1 country.

Heather L GardnerDepartments of Veterinary Biosciences and Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, 454 VMAB, 1925 Coffey Rd, 43210, Columbus, OH, USA.
Cheryl A LondonDepartments of Veterinary Biosciences and Veterinary Clinical Sciences, College of Veterinary Medicine, The Ohio State University, 454 VMAB, 1925 Coffey Rd, 43210, Columbus, OH, USA. london.20@osu.edu.
Roberta A PortelaDepartment of Veterinary Clinical Medicine, University of Illinois at Urbana-Champaign, College of Veterinary Medicine, Champaign, IL, USA.
Sandra NguyenAnimal Referral Hospital, Sydney, Australia.
Mona P RosenbergVeterinary Cancer Group, Tustin, CA, USA.
Mary K KleinSouthwest Veterinary Oncology, Tucson, AZ, USA.
Craig CliffordHope Veterinary Specialists, Malvern, PA, USA.
Douglas H ThammDepartment of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.
David M VailDepartment of Medical Sciences, School of Veterinary Medicine, University of Wisconsin, Madison, WI, USA.
Phil BergmanVCA Katonah Bedford Veterinary Center, Bedford Hill, NY, USA.
Martin Crawford-JakubiakSage Centers for Veterinary Specialty and Emergency Care, Concord, CA, USA.
Carolyn HenryDepartment of Veterinary Medicine and Surgery, College of Veterinary Medicine, University of Missouri, Columbia, MO, USA.
Jennifer LockeSoutheast Veterinary Oncology and Medicine, Orange Park, FL, USA.
Laura D GarrettDepartment of Veterinary Clinical Medicine, University of Illinois at Urbana-Champaign, College of Veterinary Medicine, Champaign, IL, USA.
The Ohio State University · USUniversity of Illinois Urbana-Champaign · USArchaeology Southwest · USBedford VA Research Corporation · USChildren's Oncology Group · USColorado State University · USMissouri College · USUniversity of Wisconsin–Madison · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
University of Iowa Clinical and Translational Science Program (TL1)UL1RR025755 · NCRR · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2008 to 2011
$26.3M
The Ohio State University Center for clinical and Translational ScienceUL1TR001070 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2013 to 2017
$22.6M
The Ohio State University Center for Clinical and Translational Science (UL1)UL1TR000090 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2012 to 2013
$7.9M
NCATS NIH HHS UL1 TR000090NCATS NIH HHS UL1 TR001070NCATS NIH HHS UL1TR001070NCI NIH HHS P30 CA016058NCI NIH HHS P30CA016058NCRR NIH HHS UL1 RR025755
6 · The paper itself

Abstract

backgroundSpenic hemangiosarcoma (HSA) in dogs treated with surgery alone is associated with short survival times, and the addition of doxorubicin (DOX) chemotherapy only modestly improves outcome. The purpose of this study was to evaluate the impact of toceranib administration on progression free survival in dogs with stage I or II HSA following splenectomy and single agent DOX chemotherapy. We hypothesized that dogs with splenic HSA treated with adjuvant DOX followed by toceranib would have prolonged disease-free interval (DFI) and overall survival time (OS) when compared to historical dogs treated with DOX-based chemotherapy alone.

resultsDogs with stage I or II splenic HSA were administered 5 cycles of single-agent DOX every 2 weeks beginning within 14 days of splenectomy. Dogs were restaged 2 weeks after completing DOX, and those without evidence of metastatic disease began toceranib therapy at 3.25 mg/kg every other day. Forty-three dogs were enrolled in this clinical trial. Seven dogs had evidence of metastatic disease either before or at re-staging, and an additional 3 dogs were found to have metastatic disease within 1 week of toceranib administration. Therefore 31 dogs went on to receive toceranib following completion of doxorubicin treatment. Twenty-five dogs that received toceranib developed metastatic disease. The median disease free interval for all dogs enrolled in this study (n = 43) was 138 days, and the median disease free interval for those dogs that went on to receive toceranib (n = 31) was 161 days. The median survival time for all dogs enrolled in this study was 169 days, and the median survival time for those dogs that went on to receive toceranib was 172 days.

conclusionsThe use of toceranib following DOX chemotherapy does not improve either disease free interval or overall survival in dogs with stage I or II HSA.

Indexed as

AnimalsAntineoplastic AgentsDog DiseasesDogsDoxorubicinFemaleHemangiosarcomaIndolesMalePyrrolesSplenic NeoplasmsAntineoplastic AgentsDoxorubicinIndolesPyrrolestoceranib phosphate

Identifiers

PMID26062540
PMCPMC4464614
OpenAlexW1560608058

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.