Mast Cell Tumors in Dogs
Quick Facts at a Glance
- 20-25% of all skin/subcutaneous tumors in dogs
are mast cell tumors (MCT)
- 10-15% of canine MCT are clinically indistinguishable
from subcutaneous lipomas (fatty tumors)
- Definitive diagnosis of MCT cannot be made without
cytologic (aspirate) or histologic (biopsy) evaluation of the
lesion
- Behavior of individual MCTs is difficult to predict
but should always be considered aggressive until proven otherwise
- MCT of the perineal and inguinal regions tend
to behave more aggressively than their tumor grade would predict
- Most dogs with MCT have a normal CBC(complete
blood count)
- 20% of dogs with MCT will have multiple primary
tumors in their lifetime
- Aggressive surgical resection remains the cornerstone
of treatment
What are the clinical features?
Mast cell tumors in dogs occur primarily as either a skin or subcutaneous
mass. It is important to remember that mast cell tumors are extremely
variable in their clinical presentation. They can resemble any
other type of skin or subcutaneous tumor, both benign (i.e. lipoma)
and malignant. Most canine MCT are solitary although multiple primary
tumors develop in 20% of patients. Approximately 50% of canine
MCT are located on the trunk and perineum, 40% on the extremities
and 10% on the head and neck.
Regional lymphadenopathy (lymph node enlargement) may occur when
high-grade mast cell tumors metastasize (spread) to draining lymph
nodes. Hepatomegaly (liver enlargement) and splenomegaly (spleen
enlargement) are features of advanced stage, metastatic MCT. Malignant
mast cells may be detected in the blood and bone marrow of dogs
with advanced stage disease.
Cytology vs. histopathology?
The diagnosis of MCT is often made simply with cytologic evaluation
of a fine needle aspirate of the mass. Although cytology may allow
us to confirm the diagnosis, it provides little prognostic information.
Histopathology (biopsy) allows us to grade the tumor so we can
predict biologic behavior and make appropriate treatment recommendations.
Survival Times of Dogs After Surgery Based on Histologic
Grade
| Grade |
#of Dogs |
Alive 6 Months Post-Surgery |
| I |
39 |
77 |
| II |
30 |
45 |
| III |
45 |
13 |
Surgery: 3cm margins!!!
The most frustrating feature of MCT is how aggressively they can
behave, regardless of their gross appearance and histologic grade.
MCT are notorious for their invasive nature and tendency to extend
far beyond visible margins. If 2-3 cm surgical margins, both lateral
and deep, are not obtained then chances are good that the tumor
will not be adequately excised. While it may be difficult to remove
2-3 cm deep margins in a patient without much body fat, removing
a layer of muscle below the tumor is advised. A surgical margin
of a couple of millimeters is not adequate. When surgical margins
are very close, a second surgery should be recommended as soon
as possible. It is impossible to comment on completeness of surgical
excision and predict biologic behavior of mast cell tumors without
histopathologic evaluation of the entire tumor.
Depending on where the tumor is located, it may not be possible
to obtain 3 cm surgical margins (i.e. leg). In those cases, it
is appropriate to perform a “debulking” surgery followed
immediately by radiation therapy. Radiation therapy in this setting
can be highly effective at achieving long-term local control. Depending
on the situation, chemotherapy may be recommended in conjunction
with or in lieu of radiation therapy. Administration of prednisone
alone (1mg/kg every 24 hours) for 5-7 days prior to surgery may
result in sufficient reduction of the tumor mass and associated
inflammation thereby increasing success of surgery.
What about lymph nodes?
Whenever possible, the draining lymph nodes (lymph nodes in close
proximity) should be biopsied or excised for histopathologic analysis,
regardless of gross appearance and tumor grade. The presence of
lymph node metastasis worsens the prognosis and necessitates treatment
with chemotherapy.
When is it essential to stage the patient with mast cell
tumor?
Diagnostic tests performed in the staging of MCTs include cytology
or biopsy of the draining lymph node, abdominal ultrasound with
ultrasound guided aspirate and cytology of the spleen and liver,
bone marrow aspirate and cytology, complete blood count (CBC) and
chest radiographs. Although the staging process can provide us
with essential information, we are very limited by the low sensitivity
of these diagnostic tests. In the case of a grade I or low grade
II MCT that has been completely excised with wide surgical margins,
it is unlikely that metastasis has occurred. Early metastasis would
not likely be detected during the staging process.
Staging is essential prior to undergoing an extensive or expensive
treatment procedure (i.e. amputation or radiation therapy). Staging
is also recommended for any grade III or high-grade II MCT, even
if completely excised with wide margins. Histologic evaluation
of draining lymph nodes is preferred over cytology in this situation.
Radiation therapy
Mast cell tumors are generally very sensitive to radiation. Radiation
is most effective at achieving long-term (greater than 5 years)
tumor control when it is delivered to microscopic disease, grade
2 intermediate or lower and in a well-defined radiation field.
Radiation therapy can be used to control local disease after incomplete
resection of high-grade 2 or grade 3 MCT. The size of the tumor
prior to surgical resection has great impact on the effectiveness
of radiation.
Chemotherapy: When to treat?
As with any cancer, chemotherapy for the treatment of MCT is most
effective when combined with other treatment modalities or used
early in the course of the disease. Chemotherapy will not be helpful
in the treatment of a large mast cell tumor that cannot be excised
and has become resistant to prednisone therapy. Chemotherapy is
appropriate when tumor cells extend to surgical margins and a second
surgery and radiation therapy are not feasible treatment options.
Chemotherapy is recommended in all cases with lymph node involvement.
Chemotherapy is recommended for all patients with high-grade II
or grade III MCT, even when the tumor is excised with wide margins.
Prednisone, vinblastine and lomustine are used in combination
to obtain the best results with minimal side effects. Adjuvant
chemotherapy results in survival times of greater than 2 years
in patients with high-grade II MCT with metastasis to regional
lymph nodes, that have been treated with aggressive surgical resection
resulting in complete resection and are negative for visceral (organ,
i.e. spleen) metastasis. Chemotherapy is not of much benefit when
staging confirms systemic metastasis.

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