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Peer-reviewed veterinary case report

Canine splenic hemangiosarcoma treatment with PSP and doxorubicin

By Gedney, Allison et al.·Published in Veterinary and comparative oncology·2022·Department of Clinical Sciences and Advanced Medicine, United States·View original on PubMed

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Original publication title: Evaluation of the anti-tumour activity of Coriolus versicolor polysaccharopeptide (I'm-Yunity) alone or in combination with doxorubicin for canine splenic hemangiosarcoma.

Species:
dog

Plain-English summary

A group of dogs with splenic hemangiosarcoma, an aggressive type of cancer, were treated after surgery to remove their spleens. Some received a polysaccharopeptide supplement called I'm-Yunity (PSP), while others received the standard chemotherapy drug doxorubicin, or a placebo. The study found that female dogs treated with PSP alone had shorter survival times compared to those who received doxorubicin, while the addition of PSP to doxorubicin did not improve survival rates overall. Unfortunately, the findings suggest that PSP alone may not be effective for improving outcomes in these dogs.

People also search for: dog splenic hemangiosarcoma treatment · I'm-Yunity for dogs cancer · doxorubicin side effects in dogs

Abstract

Canine splenic hemangiosarcoma (HSA) is an aggressive tumour of vascular endothelium that carries a grave prognosis following standard of care treatment with surgery and doxorubicin. A previous pilot study revealed potential anti-tumour activity of I'm-Yunity polysaccharopeptide (PSP) for canine HSA. The aim of this prospective study was to assess patient outcome when treated with PSP alone or in combination with doxorubicin post-splenectomy compared to patients treated with surgery and doxorubicin that received a placebo in place of PSP. Dogs undergoing splenectomy for splenic HSA were eligible. Following splenectomy, owners were offered treatment with PSP alone or adjuvant doxorubicin chemotherapy (unblinded). Patients with owners that selected to proceed with doxorubicin chemotherapy were blindly randomized to receive placebo or PSP. Dogs were evaluated weekly for 15&#x2009;weeks, then scheduled for monthly visits until death. One hundred and one dogs were included in the final analysis: 51 PSP alone, 25 doxorubicin/placebo, and 25 combination PSP/doxorubicin. On multivariate analysis, dogs treated with single agent PSP, female dogs, decreased haematocrit at diagnosis, and stage III disease were negatively significantly associated with outcome; however, an interaction between treatment group and sex was documented. Gender-specific outcomes revealed no significant difference in survival between treatment groups for male dogs, but female dogs treated with PSP alone had significantly reduced survival compared to females receiving doxorubicin/placebo (HR 0.21; p&#xa0;=&#xa0;.004). Anaemia (HR 5.28; p&#x2009;<&#x2009;.001) and stage III disease (HR 2.9; p&#xa0;=&#xa0;.014) remained negatively associated with survival when controlling for sex and treatment group. The addition of PSP to doxorubicin post-splenectomy did not improve survival in dogs with splenic HSA.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/35442554/