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Peer-reviewed veterinary case report

Rescue chemo with L-asparaginase and lomustine for relapsed dog

By Saba, C F et al.·Published in Journal of veterinary internal medicine·2009·Department of Medical Sciences, United States·View original on PubMed

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Original publication title: Combination chemotherapy with continuous L-asparaginase, lomustine, and prednisone for relapsed canine lymphoma.

Species:
dog

Plain-English summary

A group of 48 dogs with relapsed lymphoma (a type of cancer) were treated with a combination of lomustine, L-asparaginase, and prednisone to see if it could help them go into remission again. The treatment was well tolerated, and about 77% of the dogs responded positively, with 65% achieving complete remission. However, the time until the cancer progressed again was around 70 days, and the study suggested that using L-asparaginase with each dose of lomustine didn't significantly extend remission time. Overall, this combination therapy remains a viable option for dogs with relapsed lymphoma.

People also search for: dog lymphoma treatment · canine cancer remission · lomustine for dogs lymphoma

Abstract

BACKGROUND: The combination of lomustine, L-asparaginase, and prednisone (LAP) is an effective rescue treatment for canine lymphoma (LSA). In a previous study, we reported that remission was typically lost around the time L-asparaginase was discontinued. HYPOTHESIS: Use of L-asparaginase with each lomustine treatment will be well tolerated and efficacious as a rescue therapy for canine LSA. ANIMALS: Forty-eight client-owned dogs with cytologically confirmed multicentric LSA whose disease had relapsed after a cyclophosphamide, doxorubicin, vincristine, and prednisone-based chemotherapy protocol were included. METHODS: Lomustine was administered orally at 3-week intervals, concurrently with subcutaneous or intramuscular L-asparaginase for a total of 5 doses or until disease progression. Prednisone was administered at a tapering dose for the duration of the protocol. RESULTS: The overall response rate (ORR) for dogs treated with this protocol was 77%, with 65% achieving a complete response (CR). The median time to progression (TTP) was 70 days. Based on loose comparison, these findings are not significantly different from our previously reported historical control. The actual CCNU dosage administered did not affect response rate or remission duration. CONCLUSIONS/CLINICAL IMPORTANCE: These findings support previous data concluding that the LAP protocol is a viable rescue treatment option for dogs with LSA. However, results from this study suggest that continued use of L-asparaginase with each lomustine treatment does not significantly increase remission duration and toxicity appears greater.

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Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/19678892/