1. Evaluation of mechlorethamine, vinblastine, procarbazine, and prednisone for the treatment of resistant multicentric canine lymphoma.
- Author
-
Zimmerman K, Walsh KA, Ferrari JT, Keuler NS, Atherton MJ, and Lenz JA
- Subjects
- Animals, Dogs, Prednisone therapeutic use, Vinblastine therapeutic use, Mechlorethamine therapeutic use, Mechlorethamine adverse effects, Vincristine, Procarbazine therapeutic use, Antineoplastic Combined Chemotherapy Protocols adverse effects, Doxorubicin therapeutic use, Neoplasm Recurrence, Local drug therapy, Neoplasm Recurrence, Local veterinary, Dog Diseases chemically induced, Lymphoma drug therapy, Lymphoma veterinary, Lymphoma, Non-Hodgkin drug therapy, Lymphoma, Non-Hodgkin veterinary
- Abstract
Multi-agent chemotherapy successfully induces remission in most naïve, high-grade canine lymphoma patients; however, disease recurrence is common. MOPP (mechlorethamine, vincristine, procarbazine, and prednisone) is an effective rescue protocol used to re-induce remission, but is associated with gastrointestinal toxicity and can be a less desirable option for patients that previously failed vincristine-containing protocols. Therefore, alternative members of the vinca alkaloid family, such as vinblastine, could be potentially advantageous as substitutes for vincristine to reduce gastrointestinal toxicity and chemoresistance. The objective of this study was to report the clinical outcomes and toxicity of 36 dogs with relapsed or refractory multicentric lymphoma treated with a modified MOPP protocol whereby vincristine was replaced with vinblastine (MVPP). The overall response rate to MVPP was 25% with a median progression free survival of 15 days and a median overall survival of 45 days. MVPP at the prescribed doses resulted in modest and transient clinical benefit, but was well tolerated with no treatment delays or hospitalizations secondary to side effects. Given the minimal toxicity, dose intensification could be considered to improve clinical responses., (© 2023 John Wiley & Sons Ltd.)
- Published
- 2023
- Full Text
- View/download PDF