Peer-reviewed veterinary case report
Samarium treatment for dogs with skull bone tumors
By Vancil, Jarrod M et al.·Published in Journal of the American Veterinary Medical Association·2012·Department of Veterinary Medicine and Surgery, United States·View original on PubMed →
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Original publication title: Use of samarium Sm 153 lexidronam for the treatment of dogs with primary tumors of the skull: 20 cases (1986-2006).
- Species:
- dog
Plain-English summary
A group of dogs with bony tumors in the skull, specifically multilobular osteochondrosarcoma or osteosarcoma, were treated with a radioactive drug called samarium Sm 153 lexidronam. After treatment, 4 out of 20 dogs showed some improvement in their condition, while 13 continued to have worsening disease. There were no significant side effects noted from the treatment. This option may be helpful for dogs with these types of tumors when other treatments haven't worked or surgery isn't an option.
People also search for: dog skull tumor treatment · osteosarcoma in dogs · samarium treatment for dog cancer
Abstract
OBJECTIVE: To evaluate samarium Sm 153 lexidronam ((153)Sm-EDTMP) as a treatment option for dogs with bony tumors of the skull. DESIGN: Retrospective case series. ANIMALS: Dogs with multilobular osteochondrosarcoma (MLO) or osteosarcoma (OSA) of the skull. PROCEDURES: Veterinary Medical Teaching Hospital records from the Universities of Missouri and Florida from 1986 to 2006 were searched for dogs with primary skull tumors treated with (153)Sm-EDTMP. RESULTS: 25 dogs were initially evaluated, with 5 dogs subsequently excluded because of inadequate follow-up or unrelated death. Seven OSAs and 13 MLOs were diagnosed. Tumors involved the occipital and frontal bones (n = 10), zygomatic arch and maxilla region (6), palate (3), and mandible (1). No clinically important adverse effects related to (153)Sm-EDTMP treatment were documented. Of the 20 dogs evaluated 21 days after injection with (153)Sm-EDTMP, 4 had subjective improvement, 13 had progressive disease, and 3 had insufficient follow-up. On the basis of radiographic findings, metastasis was suspected in 1 dog; 16 dogs had no metastasis evident, and medical records were insufficient for 3 dogs. Survival time, defined as the (153)Sm-EDTMP injection date to the date of death, ranged from 3 to 1,314 days (median, 144 days). CONCLUSIONS AND CLINICAL RELEVANCE: The subjective improvement in 4 patients and lack of clinical evidence of adverse effects suggested that (153)Sm-EDTMP injection may be an option for the treatment of dogs with MLO or OSA of the skull when other treatments have failed or surgery is not possible.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/22607597/