Q: Why was the T-STAT model developed when it is known that the probability of hemangiosarcoma in dogs with splenic
masses is approximately 70%?
A: The T-STAT calculator estimates the probability of malignancy using a variety of data from the individual patient
rather than broad probabilities that pertain to the general population of dogs with splenic masses. This is particularly valuable given
that dogs with benign and malignant splenic masses may present with virtually indistinguishable histories and physical exam findings.
Q: Does T-STAT differentiate between splenic hemangiosarcoma and other malignant splenic masses?
A: No - approximately 28% of the malignant masses included in the study were tumors
other than hemangiosarcoma. Nevertheless, almost all of these tumor types were either
multicentric in nature or highly metastatic, and like hemangiosarcoma are unlikely to be
cured by splenectomy alone.
Q: Can T-STAT be used if all of the data requested is not available for a particular
patient?
A: No - missing data invalidates the calculation.
Q: How should I weight the probability of malignancy produced by the calculator
against other data pertaining to my patient?
A: While the accuracy of T-STAT is very good, it should not take the place of your own
clinical judgment; at most, T-STAT should provide an objective adjunct to your decision-
making process.
Q: Does the model apply to all breeds and ages of dogs?
A: The T-STAT model was developed using data from a cohort of dogs undergoing
splenectomy for a splenic mass at our institution. The vast majority of our population
consisted of middle sized and larger breed dogs. Additionally there were relatively few
dogs less than 5 or greater than 12 years of age. Consequently our model may have
limited applicability to small breed dogs and to very young and very old dogs.
Q: Some of the variables request a yes or no response. How were the categories
determined?
A: Severity of abdominal effusion and splenic mass inhomogeneity were initially
assigned to one of four categories (none, mild, moderate and marked). However, our
analysis indicated that for both variables, the selection of categories could be simplified
by combining the none and mild categories and the moderate and marked categories,
without losing predictive value. For both variables, if you are uncertain which category
best fits your patient, selection of the none/mild category will result in a more
conservative estimate of the probability of malignancy.
Q: How do I best determine the severity of abdominal effusion and inhomogeneity
within the splenic mass?
A: A limitation of the calculator is that quantification of these variables based on
ultrasound is inherently subjective. Consequently, tutorials for making these assessments
are available on the calculator page.
Q: Why were advanced imaging techniques not considered for the model?
A: The predictive model is based on clinical tests that are commonly performed in
general and referral practice. CT and MRI are rarely used in the evaluation of splenic
masses, and while they may eventually prove less subjective and more informative than
abdominal ultrasound, as of yet there is little data regarding their relative utility in this
application.
Q: Why would the presence of nRBC’s be associated with splenic malignancy?
A: It is likely that elevated nRBC levels in dogs with splenic masses is related to active
erythropoiesis secondary to acute blood loss.
Q: Historically the presence of acanthocytes and/or schistocytes has been associated
with splenic malignancy, in particular hemangiosarcoma. Why was this not the case
in this population of dogs?
Although both acanthocytes and schistocytes can be observed in dogs with
hemangiosarcoma, they are also frequently present in dogs with non-neoplastic diseases
that may cause RBC fragmentation, and therefore have limited value in documenting the
presence of hemangiosarcoma.
Q: In the T-STAT scoring system, multiple splenic masses or nodules are associated
with increased probability for malignancy. In the study used to develop the
calculator, were all of these nodules sampled and confirmed to be metastatic?
In the population of dogs used to develop the predictive model, dogs with multiple
splenic masses or nodules had a higher probability of having malignant disease than dogs
with solitary lesions. It can be intuited that many of these nodules represented intra-
splenic metastatic disease; however, histopathology was generally confined to the largest
mass.