Use of carboplatin for treatment of dogs with malignant melanoma: 27 cases (1989–2000)

Kenneth M. Rassnick Harrington Oncology Program, School of Veterinary Medicine, Tufts University, North Grafton, MA 01536.
Present address is Comparative Cancer Program, Department of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853.

Search for other papers by Kenneth M. Rassnick in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM
,
David M. Ruslander Harrington Oncology Program, School of Veterinary Medicine, Tufts University, North Grafton, MA 01536.

Search for other papers by David M. Ruslander in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM, DACVR
,
Susan M. Cotter Harrington Oncology Program, School of Veterinary Medicine, Tufts University, North Grafton, MA 01536.

Search for other papers by Susan M. Cotter in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM
,
Renee Al-Sarraf Veterinary Referral Centre, 48 Notch Rd, Little Falls, NJ 07424.

Search for other papers by Renee Al-Sarraf in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM
,
David S. Bruyette Department of Clinical Sciences, College of Veterinary Medicine, Kansas State University, Manhattan, KS 66506.
Present address is VCA West Los Angeles Animal Hospital, 1818 S Sepulveda Blvd, Los Angeles, CA 90025.

Search for other papers by David S. Bruyette in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM
,
Rance M. Gamblin Akron Veterinary Referral and Emergency Center, PO Box 4369, 1321 Centerview Cir, Akron, OH 44321.
Present address is Metropolitan Veterinary Hospital, 1053 S Cleveland-Massillon Rd, Akron, OH 44321.

Search for other papers by Rance M. Gamblin in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM
,
Karelle A. Meleo Veterinary Oncology Services, 22226 Highway 99, Edmonds, WA 98020.

Search for other papers by Karelle A. Meleo in
Current site
Google Scholar
PubMed
Close
 DVM, DACVIM, DACVR
, and
Antony S. Moore Harrington Oncology Program, School of Veterinary Medicine, Tufts University, North Grafton, MA 01536.

Search for other papers by Antony S. Moore in
Current site
Google Scholar
PubMed
Close
 MVSc, DACVIM

Abstract

Objective—To evaluate response rate and duration of malignant melanomas in dogs treated with carboplatin.

Design—Retrospective study.

Animals—27 client-owned dogs with spontaneously occurring measurable malignant melanomas.

Procedure—Records of dogs with melanomas treated with carboplatin from October 1989 to June 2000 were reviewed. Carboplatin was administered IV at doses of 300 or 350 mg/m2 of body surface area. Response to treatment and evidence of drug toxicity were determined.

Result—Response to treatment could be evaluated in 25 dogs. Of those, overall response rate was 28%. One dog had a complete response, 6 (24%) dogs had a partial response (> 50% reduction in tumor burden). Median duration of partial response was 165 days. Eighteen dogs had stable disease (n = 9; 36%) or progressive disease (9; 36%). Response to treatment was significantly associated with carboplatin dose on a milligram per kilogram basis (15.1 mg/kg [6.9 mg/lb] of body weight vs 12.6 mg/kg [5.7 mg/lb]). Evidence of gastrointestinal toxicosis could be assessed in 27 dogs. Mean body weight of 5 dogs that developed gastrointestinal toxicosis was significantly less than that of 22 dogs without gastrointestinal toxicosis (9.9 kg [21.8 lb] vs 19.3 kg [42.5 lb]).

Conclusions and Clinical Relevance—Carboplatin had activity against macroscopic spontaneously occurring malignant melanomas in dogs and should be considered as an adjunctive treatment for microscopic local or metastatic tumors. Gastrointestinal toxicosis was associated with body weight. Because small dogs are more likely to have adverse gastrointestinal effects, gastrointestinal protectants should be considered for these patients. (J Am Vet Med Assoc 2001;218:1444–1448)

Abstract

Objective—To evaluate response rate and duration of malignant melanomas in dogs treated with carboplatin.

Design—Retrospective study.

Animals—27 client-owned dogs with spontaneously occurring measurable malignant melanomas.

Procedure—Records of dogs with melanomas treated with carboplatin from October 1989 to June 2000 were reviewed. Carboplatin was administered IV at doses of 300 or 350 mg/m2 of body surface area. Response to treatment and evidence of drug toxicity were determined.

Result—Response to treatment could be evaluated in 25 dogs. Of those, overall response rate was 28%. One dog had a complete response, 6 (24%) dogs had a partial response (> 50% reduction in tumor burden). Median duration of partial response was 165 days. Eighteen dogs had stable disease (n = 9; 36%) or progressive disease (9; 36%). Response to treatment was significantly associated with carboplatin dose on a milligram per kilogram basis (15.1 mg/kg [6.9 mg/lb] of body weight vs 12.6 mg/kg [5.7 mg/lb]). Evidence of gastrointestinal toxicosis could be assessed in 27 dogs. Mean body weight of 5 dogs that developed gastrointestinal toxicosis was significantly less than that of 22 dogs without gastrointestinal toxicosis (9.9 kg [21.8 lb] vs 19.3 kg [42.5 lb]).

Conclusions and Clinical Relevance—Carboplatin had activity against macroscopic spontaneously occurring malignant melanomas in dogs and should be considered as an adjunctive treatment for microscopic local or metastatic tumors. Gastrointestinal toxicosis was associated with body weight. Because small dogs are more likely to have adverse gastrointestinal effects, gastrointestinal protectants should be considered for these patients. (J Am Vet Med Assoc 2001;218:1444–1448)

All Time Past Year Past 30 Days
Abstract Views 468 0 0
Full Text Views 1468 1084 35
PDF Downloads 1005 508 54
Advertisement