Evidence map›Paper›PMID 28370378›Full record

Trial reportJournal of veterinary internal medicine2017

Alternating Rabacfosadine/Doxorubicin: Efficacy and Tolerability in Naïve Canine Multicentric Lymphoma.

D H Thamm, D M Vail, G S Post, T M Fan, B S Phillips, S Axiak-Bechtel, R S Elmslie, M K Klein, D A Ruslander

Open access · goldAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Journal of veterinary internal medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
  2. Development of a First-in-Class Click Chemistry-Based Cancer Therapeutic, from Preclinical Evaluation to a First-in-Human Dose Escalation Clinical Trial.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
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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

9 authors at 9 institutions in 1 country.

D H ThammDepartment of Clinical Sciences, Flint Animal Cancer Center, Colorado State University, Fort Collins, CO.ORCID http://orcid.org/0000-0002-8914-7767
D M VailSchool of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI.
G S PostThe Veterinary Cancer Center, Norwalk, CT.
T M FanCollege of Veterinary Medicine, University of Illinois at Urbana-Champaign, Urbana, IL.
B S PhillipsVeterinary Specialty Hospital of San Diego, San Diego, CA.
S Axiak-BechtelCollege of Veterinary Medicine, University of Missouri, Columbia, MO.
R S ElmslieVeterinary Referral Center of Colorado, Englewood, CO.
M K KleinSouthern Arizona Veterinary Specialty and Emergency Center, Tucson, AZ.
D A RuslanderVeterinary Specialty Hospital of the Carolinas, Cary, NC.
Carolina Veterinary Specialists · USColorado Neurological Institute · USMissouri College · USNorwalk Hospital · USOrthopedic Specialty Hospital · USSouthern Arizona VA Health Care System · USUniversity of Colorado Cancer Center · USUniversity of Illinois Urbana-Champaign · USUniversity of Wisconsin–Madison · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStandard of care treatment for multicentric lymphoma in dogs remains doxorubicin (DOX)-based combination chemotherapy, but owners may hesitate to commit the time and financial resources to complete such a protocol, typically requiring 12-16 visits. Rabacfosadine (RAB), a double prodrug of the nucleotide analog 9-(2-phosphonylmethoxyethyl) guanine, has substantial single-agent activity in dogs with lymphoma, and a different mechanism of action than DOX. HYPOTHESIS/

objectivesOur objective was to evaluate the efficacy and adverse effect (AE) profile of alternating doses of RAB and DOX in dogs with naïve multicentric lymphoma. ANIMALS: Fifty-four dogs with previously untreated lymphoma.

methodsOpen-label, multicenter prospective clinical trial. Dogs received alternating RAB (1.0 mg/kg IV weeks 0, 6, 12) and DOX (30 mg/m

resultsThe overall response rate was 84% (68%; CR; 16%; partial response [PR)]. The overall median progression-free interval (PFI) was 194 days (216 for CR and 63 for PR). Most AEs were mild and self-limiting: gastrointestinal and hematologic AEs were most common. Thirteen dogs experienced dermatologic AEs, and 2 dogs developed grade 5 pulmonary fibrosis. CONCLUSIONS AND CLINICAL IMPORTANCE: Alternating RAB/DOX generally was well tolerated and resulted in PFIs comparable to standard DOX-based multi-agent protocols, with fewer treatment visits. Most adverse events were mild or moderate and self-limiting. Further studies are warranted to explore long-term outcome and other RAB chemotherapy combinations.

Indexed as

AlanineAntineoplastic AgentsDog DiseasesDoxorubicinLymphomaProdrugsPurinesAnimalsDogsDrug Administration ScheduleFemaleMaleTreatment OutcomeAlanineAntineoplastic AgentsDoxorubicinProdrugsPurinesrabacfosadineChemotherapyDogGuanineLymphosarcoma

Identifiers

PMID28370378
PMCPMC5435064
OpenAlexW2604157923

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.