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1.
Vet Comp Oncol ; 15(3): 996-1013, 2017 Sep.
Article in English | MEDLINE | ID: mdl-27146852

ABSTRACT

Reported post-surgery 1-year survival rate for oral canine malignant melanoma (cMM) is around 30%; novel treatments are needed as the role of adjuvant chemotherapy is unclear. This prospective study regards adjuvant electrovaccination with human chondroitin sulfate proteoglycan-4 (hCSPG4)-encoded plasmid in 23 dogs with resected II/III-staged CSPG4-positive oral cMM compared with 19 dogs with resected only II/III-staged CSPG4-positive oral cMM. Vaccination resulted in 6-, 12-, 18- and 24-month survival rate of 95.6, 73.9, 47.8 and 30.4%, respectively [median survival time (MST) 684 days, range 78-1694, 8 of 23 dogs alive] and 6-, 12-, 18- and 24-month disease-free interval (DFI) rate of 82.6, 47.8, 26.1 and 17.4%, respectively (DFI 477 days, range 50-1694). Non-vaccinated dogs showed 6-, 12-, 18- and 24-month survival rate of 63.2, 26.3, 15.8 and 5.3%, respectively (MST 200 days, range 75-1507, 1 of 19 dogs alive) and 6-, 12-, 18- and 24-month DFI rate of 52.6, 26.3, 10.5 and 5.3%, respectively (DFI 180 days, range 38-1250). Overall survival and DFI of vaccinated dogs was longer in those <20 kg. In vaccinated and non-vaccinated dogs local recurrence rate was 34.8 and 42%, respectively while lung metastatic rate was 39 and 79%, respectively.


Subject(s)
Chondroitin Sulfate Proteoglycans/immunology , Dog Diseases/therapy , Melanoma/veterinary , Mouth Neoplasms/veterinary , Adjuvants, Immunologic/therapeutic use , Animals , Cancer Vaccines/therapeutic use , Combined Modality Therapy , Dog Diseases/mortality , Dogs , Female , Male , Melanoma/mortality , Melanoma/therapy , Mouth Neoplasms/mortality , Mouth Neoplasms/therapy
2.
Vet Comp Oncol ; 14(2): 170-80, 2016 Jun.
Article in English | MEDLINE | ID: mdl-24428588

ABSTRACT

Insulin-like growth factor type II (IGF-II) is the main cause of non-islet cell tumour hypoglycaemia (NICTH) and insulin is thought to be the only factor causing hypoglycaemia in insulinomas. However, two case reports of pancreatic neuroendocrine tumours (PNETs) producing IGF-II have been previously published: a human and a canine patient. In this study, we investigated clinical, histopathological, immunohistochemical and ultrastructural features, and biological behaviour of canine pancreatic IGF-II-omas, a subgroup of PNETs that has not been previously characterized. Case records of 58 dogs with confirmed PNETs and hypoglycaemia were reviewed: six patients were affected by IGF-II-omas. Surgery was performed in all cases and two dogs had metastases. Four patients remained alive and in remission at 370, 440, 560 and 890 days post-diagnosis; two died of non-tumour-related causes. IGF-II-omas can be differentiated from insulinomas through hypoinsulinaemia, IGF-II positive and insulin negative immunostaining. The prevalence of this neoplasia is low, accounting for just 6% of PNETs.


Subject(s)
Adenoma, Islet Cell/veterinary , Dog Diseases/metabolism , Insulin-Like Growth Factor II/metabolism , Pancreatic Neoplasms/veterinary , Adenoma, Islet Cell/genetics , Adenoma, Islet Cell/metabolism , Animals , Dog Diseases/genetics , Dogs , Female , Gene Expression Regulation, Neoplastic/physiology , Insulin-Like Growth Factor II/genetics , Male , Pancreatic Neoplasms/genetics , Pancreatic Neoplasms/metabolism , Retrospective Studies
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