Research Article

Methodologic Approaches to Histologically Distinguishing Vaccine versus Nonvaccine-Associated Sarcomas Using Validated Time and Location Vaccination Histories in Cats

Table 2

Multivariate exact logistic regression analyses of associations between histologic characteristics of vaccine-associated sarcomas occurring within one (case Group 1), two (case Group 2), and three (case Group 3) years of vaccination and occurring at sites typically used for vaccination regardless of vaccine history (case Group 4) and four comparison sarcoma groups varying by location and vaccine history. All models were adjusted for age.

variables*Case Group 1a ( 𝑛 = 1 5 )variablesCase Group 2b ( 𝑛 = 2 7 )variablesCase Group 3c ( 𝑛 = 3 4 )variablesCase Group 4d ( 𝑛 = 8 7 )
OR95% CIP value OR95% CIP value OR95% CIP valueOR95% CIP value

Control A1
( 𝑛 = 1 8 )
Mitotic index0.50.2, 1.00.053
Demarcated borders0.10.0, 1.70.179
Differentiation0.30.0, 1.40.150

Control B2
( 𝑛 = 8 )
Mitotic index0.40.1, 1.10.090Mitotic index0.30.1, 0.90.026
Nuclear pleomorphism0.10.0, 1.50.148Nuclear pleomorphism0.20.0, 1.30.089
Neutrophils0.10.0, 1.20.069

Control C3
( 𝑛 = 1 5 )
Nuclear pleomorphism2.50.7, 10.10.167

Control D4
( 𝑛 = 3 5 )
Inflammation4.20.9, 42.60.081Location in dermis0.040.0, 0.3<0.001Inflammation 2.80.9, 10.90.088Inflammation3.91.3, 13.70.013
Multinucleated giant cells5.70.7, 77.10.112Myxomatous stromal components23.32.3, 1322.00.002Location in dermis0.040.0, 0.3<0.0001Location in dermis0.10.0, 0.4<0.0001
Location in dermis0.030.0, 0.2<0.0001Myxomatous stromal component12.91.0.0, 816.60.047Myxomatous stromal component6.91.5, 46.90.010
Multinucleated giant cells2.60.7, 10.70.172
Neutrophils0.30.1, 1.10.066

Control E5
( 𝑛 = 3 7 )
Inflammation4.51.0, 45.90.056Inflammation2.50.7, 10.5 0.187Inflammation3.11.0, 12.00.052Inflammation3.01.1, 8.6 0.023
Multinucleated giant cells6.10.8, 82.90.094Location in dermis0.10.0, 0.4<0.001Location in dermis0.040.0, 0.3<0.0001Location in dermis0.10.0, 0.4<0.0001
Location in dermis0.030.0, 0.2<0.0001Myxomatous stromal Component12.91.1, 784.10.041Myxomatous stromal component12.51.0, 785.50.051Myxomatous stromal component6.61.5, 40.70.009
Multinucleated giant cells2.40.7, 9.40.187

*Variables listed are those found to have a P value ≤ 0.20 after a backward variable selection process starting with a multivariate model containing all predictors exhibiting a P value ≤ 0.20 in the univariate analyses and patient age.
aCase Group 1: cats with a documented history of vaccination time no less than 30 days to no greater than one year (365 days) injected within one grid on any side of tumor site.
bCase Group 2: cats with a documented history of vaccination time no less than 30 days to no greater than two years (730 days) injected within one grid on any side of tumor site.
cCase Group 3: cats with a documented history of vaccination time no less than 30 days to no greater than three years (1095 days) injected within one grid on any side of tumor site.
dCase Group 4: cats with a documented history of vaccination at sites commonly used for vaccination regardless of vaccine history at tumor site.
1Control Group A: cats with a documented history of vaccination no less than 365 days injected within one grid on any side of the tumor site.
2Control Group B: cats with a documented history of vaccination no less than 730 days injected within one grid on any side of the tumor site.
3Control Group C: cats whose tumors arose at sites typically used for vaccination and with no history of vaccination at tumor site within the previous three years.
4Control Group D: cats whose tumors arose at sites not typically used for vaccination and with verification that they were not previous vaccination sites.
5Control Group E: cats whose tumors arose at sites not typically used for vaccination even if no vaccine history was available.