Evidence map›Paper›PMID 42383807›Full record

ArticleCancer reports (Hoboken, N.J.)2026

Development of a Tumor-Bearing Animal Model to Evaluate Chemotherapy Efficacy and Toxicity.

Ifeoma J Dikeocha, Emma Bateman, Hannah R Wardill, Joanne M Bowen

Abstract read
In one paragraph

Article in Cancer reports (Hoboken, N.J.), 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

4 authors.

Ifeoma J DikeochaDiscipline of Physiology, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, South Australia, Australia.ORCID 0000-0003-1700-828X
Emma BatemanDiscipline of Physiology, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, South Australia, Australia.ORCID 0000-0003-1665-102X
Hannah R WardillDiscipline of Physiology, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, South Australia, Australia.ORCID 0000-0002-6613-3661
Joanne M BowenDiscipline of Physiology, School of Pharmacy and Biomedical Sciences, Adelaide University, Adelaide, South Australia, Australia.ORCID 0000-0003-0876-0031

Funding

Danone Nutricia ResearchHospital Research Foundation GroupNHMRC
6 · The paper itself

Abstract

backgroundThe value of cancer therapies lies in enhancing anti-tumor efficacy while minimizing toxicity. However, these aspects are rarely studied together, often due to the challenges of modelling both within the same framework. In preclinical settings, rat models like the Dark Agouti Mammary Adenocarcinoma (DAMA) model are used to evaluate both efficacy and toxicity concurrently but are limited in duration, relying on a single dose to evaluate efficacy and toxicity outcomes.

aimThis study aimed to develop a cyclical chemotherapy model using the DAMA model to better mimic multi-cycle clinical scenarios.

methodsMethotrexate (MTX) was administered in various dosing schedules to assess tumor control and animal welfare.

resultsA dose of 2 mg/kg administered once weekly provided sufficient tumor control and the longest survival (14.25 ± 2.87 days), while maintaining animal welfare and yielding an acceptable efficacy-to-toxicity ratio. Dosing frequency, rather than cumulative dose, had a greater impact on welfare, as 2 mg/kg MTX once weekly substantially affected animal welfare, whereas the total cumulative dose of 4 mg/kg MTX did not.

conclusionThese findings will be utilized in future studies testing interventions designed for preventing chemotherapy toxicity whilst maintaining tumor efficacy.

Indexed as

AdenocarcinomaAntimetabolites, AntineoplasticDisease Models, AnimalMammary Neoplasms, ExperimentalMethotrexateAnimalsDose-Response Relationship, DrugDrug Administration ScheduleFemaleHumansRatsAntimetabolites, AntineoplasticMethotrexate

Identifiers

PMID42383807
PMCPMC13321817

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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.