Multicenter case-control study of risk factors associated with development of vaccine-associated sarcomas in cats

Philip H. Kass Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Philip H. Kass in
Current site
Google Scholar
PubMed
Close
 DVM, PhD, DACVPM
,
William L. Spangler IDEXX-VS, 2825 KOVR Dr, Sacramento, CA 95605.

Search for other papers by William L. Spangler in
Current site
Google Scholar
PubMed
Close
 DVM, PhD, DACVP
,
Mattie J. Hendrick Department of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104.

Search for other papers by Mattie J. Hendrick in
Current site
Google Scholar
PubMed
Close
 VMD, DACVP
,
Lawrence D. McGill ARUP Inc, 500 Chipeta Way, Salt Lake City, UT 84108.

Search for other papers by Lawrence D. McGill in
Current site
Google Scholar
PubMed
Close
 DVM, PhD, DACVP
,
D. Glen Esplin ARUP Inc, 500 Chipeta Way, Salt Lake City, UT 84108.

Search for other papers by D. Glen Esplin in
Current site
Google Scholar
PubMed
Close
 DVM, PhD, DACVP
,
Sally Lester Central Laboratory for Veterinarians, 5645-199th St, Langley, BC, Canada V3A 1H9.

Search for other papers by Sally Lester in
Current site
Google Scholar
PubMed
Close
 DVM, MVSc, DACVP
,
Margaret Slater Department of Veterinary Anatomy and Public Health, College of Veterinary Medicine, Texas A&M University, College Station, TX 77843.

Search for other papers by Margaret Slater in
Current site
Google Scholar
PubMed
Close
 DVM, PhD
,
E. Kathryn Meyer Veterinary Behavior Clinic, 9039 Gaither Rd, Gaithersburg, MD 20877.

Search for other papers by E. Kathryn Meyer in
Current site
Google Scholar
PubMed
Close
 VMD
,
Faith Boucher Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Faith Boucher in
Current site
Google Scholar
PubMed
Close
 PhD
,
Erika M. Peters Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Erika M. Peters in
Current site
Google Scholar
PubMed
Close
 BS
,
Glenna G. Gobar Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Glenna G. Gobar in
Current site
Google Scholar
PubMed
Close
 DVM, MPVM, MS
,
Thurein Htoo Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Thurein Htoo in
Current site
Google Scholar
PubMed
Close
 MS
, and
Kendra Decile Department of Population Health and Reproduction, School of Veterinary Medicine, University of California, Davis, CA 95616.

Search for other papers by Kendra Decile in
Current site
Google Scholar
PubMed
Close
 DVM

Abstract

Objective—To determine whether particular vaccine brands, other injectable medications, customary vaccination practices, or various host factors were associated with the formation of vaccine-associated sarcomas in cats.

Design—Prospective multicenter case-control study.

Animals—Cats in the United States and Canada with soft tissue sarcomas or basal cell tumors.

Procedure—Veterinarians submitting biopsy specimens from cats with a confirmed diagnosis of soft tissue sarcoma or basal cell tumor were contacted for patient medical history. Time window statistical analyses were used in conjunction with various assumptions about case definitions.

Results—No single vaccine brand or manufacturer within antigen class was found to be associated with sarcoma formation. Factors related to vaccine administration were also not associated with sarcoma development, with the possible exception of vaccine temperature prior to injection. Two injectable medications (long-acting penicillin and methyl prednisolone acetate) were administered to case cats more frequently than to control cats.

Conclusions and Clinical Relevance—Findings do not support the hypotheses that specific brands or types of vaccine within antigen class, vaccine practices such as reuse of syringes, concomitant viral infection, history of trauma, or residence either increase or decrease the risk of vaccineassociated sarcoma formation in cats. There was evidence to suggest that certain long-acting injectable medications may also be associated with sarcoma formation. (J Am Vet Med Assoc 2003;223:1283–1292)

Abstract

Objective—To determine whether particular vaccine brands, other injectable medications, customary vaccination practices, or various host factors were associated with the formation of vaccine-associated sarcomas in cats.

Design—Prospective multicenter case-control study.

Animals—Cats in the United States and Canada with soft tissue sarcomas or basal cell tumors.

Procedure—Veterinarians submitting biopsy specimens from cats with a confirmed diagnosis of soft tissue sarcoma or basal cell tumor were contacted for patient medical history. Time window statistical analyses were used in conjunction with various assumptions about case definitions.

Results—No single vaccine brand or manufacturer within antigen class was found to be associated with sarcoma formation. Factors related to vaccine administration were also not associated with sarcoma development, with the possible exception of vaccine temperature prior to injection. Two injectable medications (long-acting penicillin and methyl prednisolone acetate) were administered to case cats more frequently than to control cats.

Conclusions and Clinical Relevance—Findings do not support the hypotheses that specific brands or types of vaccine within antigen class, vaccine practices such as reuse of syringes, concomitant viral infection, history of trauma, or residence either increase or decrease the risk of vaccineassociated sarcoma formation in cats. There was evidence to suggest that certain long-acting injectable medications may also be associated with sarcoma formation. (J Am Vet Med Assoc 2003;223:1283–1292)

Advertisement