Treatment of canine mast cell tumors with CCNU (lomustine)

J Vet Intern Med. 1999 Nov-Dec;13(6):601-5. doi: 10.1892/0891-6640(1999)013<0601:tocmct>2.3.co;2.

Abstract

The efficacy and toxicity of CCNU (1-[2-chloroethyl]3-cyclohexyl-1-nitrosourea) were evaluated in 23 dogs with measurable mast cell tumors (MCT). Twenty-two dogs had cutaneous MCT and 1 dog had an intranasal MCT Nineteen (83%) dogs had biopsy of their original mass performed and 4 (17%) had aspiration cytology of masses. Of the 19 tumors histologically graded, 1 (5%) neoplasm was classified as grade I, 10 (53%) were grade II, and the remaining 8 (42%) were grade III. Dogs were treated with CCNU at a dosage of 90 mg/m2 body surface area every 3 weeks. Response could be evaluated in 19 dogs. Eight of the 19 dogs (42%) had a measurable response to CCNU. One dog had a durable complete response for 440 days. Seven dogs (37%) had a partial response for a median and mean duration of 77 days and 109 days, respectively (range, 21-254 days). Treatment with CCNU resulted in stable disease in 6 dogs (32%) for a median and mean duration of 78 days and 122 days, respectively (range, 42-347 days). The acute dose-limiting toxicity was neutropenia 7 days after administration of CCNU. The median and mean neutrophil counts 7 days after CCNU were 1,452 cells/microL and 1,683 cells/microL, respectively (n = 17). Other toxicoses were uncommon. CCNU should be considered an active agent in the treatment of MCT in dogs.

Publication types

  • Clinical Trial

MeSH terms

  • Animals
  • Antineoplastic Agents, Alkylating / adverse effects
  • Antineoplastic Agents, Alkylating / therapeutic use*
  • Dog Diseases / drug therapy*
  • Dogs
  • Lomustine / adverse effects
  • Lomustine / therapeutic use*
  • Mast-Cell Sarcoma / drug therapy
  • Mast-Cell Sarcoma / veterinary*
  • Nasal Cavity*
  • Neutropenia / chemically induced
  • Nose Neoplasms / drug therapy
  • Nose Neoplasms / veterinary*
  • Skin Neoplasms / drug therapy
  • Skin Neoplasms / veterinary*
  • Treatment Outcome

Substances

  • Antineoplastic Agents, Alkylating
  • Lomustine