Evidence map›Paper›PMID 33827546›Full record

ArticleBMC veterinary research2021

A canine case of malignant melanoma carrying a KIT c.1725_1733del mutation treated with toceranib: a case report and in vitro analysis.

Hiroyuki Tani, Ryo Miyamoto, Syunya Noguchi, Sena Kurita, Tomokazu Nagashima, Masaki Michishita, Naoko Yayoshi, Kyoichi Tamura, Makoto Bonkobara

Open access · goldAbstract readCase Reports
In one paragraph

Article in BMC veterinary research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.5field-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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Review
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 1 institution in 1 country.

Hiroyuki TaniDepartment of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Ryo MiyamotoDepartment of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Syunya NoguchiDepartment of Veterinary Anatomy, Nippon Veterinary and Life Science University, Tokyo, Japan.
Sena KuritaDepartment of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Tomokazu NagashimaDepartment of Veterinary Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Masaki MichishitaDepartment of Veterinary Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Naoko YayoshiVeterinary Medical Teaching Hospital, Nippon Veterinary and Life Science University, Tokyo, Japan.
Kyoichi TamuraDepartment of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan.
Makoto BonkobaraDepartment of Veterinary Clinical Pathology, Nippon Veterinary and Life Science University, Tokyo, Japan. bonkobara@nvlu.ac.jp.ORCID http://orcid.org/0000-0002-0054-7730
Nippon Veterinary and Life Science University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCanine malignant melanoma is highly aggressive and generally chemoresistant. Toceranib is a kinase inhibitor drug that inhibits several tyrosine kinases including the proto-oncogene receptor tyrosine kinase KIT. Although canine malignant melanoma cells often express KIT, a therapeutic effect for toceranib has yet to be reported for this tumor, with only a small number of patients studied to date. This is a case report of a dog with malignant melanoma that experienced a transient response to toceranib. Furthermore, the KIT expressed in the tumor of this case was examined using molecular analysis. CASE PRESENTATION: A Shiba Inu dog presented with a gingival malignant melanoma extending into surrounding structures with metastasis to a submandibular lymph node. The dog was treated with toceranib (Palladia®; 2.6-2.9 mg/kg, orally, every other day) alone. Improvement of tumor-associated clinical signs (e.g., halitosis, tumor hemorrhage, trismus, and facial edema) with reduced size of the metastatic lymph node was observed on Day 15. The gingival tumor and associated masses in the masseter and pterygoid muscles decreased in size by Day 29 of treatment. Toceranib treatment was terminated on Day 43 due to disease progression and the dog died on Day 54. The tumor of this dog had a novel deletion mutation c.1725_1733del within KIT and the mutation caused ligand-independent phosphorylation of KIT, which was suppressed by toceranib. This mutation was considered to be an oncogenic driver mutation in the tumor of this dog, thereby explaining the anti-tumor activity of toceranib.

conclusionsThis is the first report that presents a canine case of malignant melanoma that responded to toceranib therapy. KIT encoded by KIT harboring a mutation c.1725_1733del is a potential therapeutic target for toceranib in canine malignant melanoma. Further investigation of the KIT mutation status and toceranib therapy in canine malignant melanoma will need to be undertaken.

Indexed as

AnimalsAntineoplastic AgentsBase SequenceDog DiseasesDogsGene DeletionGenetic Predisposition to DiseaseGingival NeoplasmsIndolesLymphatic MetastasisMaleMelanomaProtein Kinase InhibitorsProto-Oncogene Proteins c-kitPyrrolesAntineoplastic AgentsIndolesProtein Kinase InhibitorsProto-Oncogene Proteins c-kitPyrrolestoceranib phosphateDogKITMalignant melanomaMutationToceranib

Identifiers

PMID33827546
PMCPMC8028755
OpenAlexW3145953253

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.