Page 379 - ONLINE PROCEEDING BOOK WSAVA 2017
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WSVA7-0320
MEDICAL ONCOLOGY
CANINE LYMPHOMA
S. Ettinger1
1DR SUE CANCER VET PLLC, Oncology, TARRYTOWN, USA
Canine Lymphoma
Sue Ettinger, DVM, DACVIM (Oncology)
Dr Sue Cancer Vet PLLC and Animal Specialty & Emergency Center Wappinger Falls, NY, USA
drsuecancervet@gmail.com Key Points
• Lymphoma is a common canine cancer and is a systemic disease that requires chemotherapy in almost all cases.
• The majority of dogs achieve a complete remission with chemotherapy (approximately 80%). Higher remission rates are typical with CHOP multi-agent chemotherapy protocols.
• Early accurate diagnostics and careful staging are keys to proper clinical decision-making.
• To determine the best protocol for a patient and owners, it is important to understand ef cacy of the various protocols, the potential toxicities, and prognostic factors.
• Dogs treated with chemotherapy live signi cantly longer than untreated dogs, and chemotherapy is generally well-tolerated in most dogs. Only a minority develops signi cant toxicity.
• The diagnostic and treatment choices can be confusing and overwhelming. In this talk, we will take “My 3 P’s” approach – prognostic, practical and pertinent.
Biology of lymphoma
Lymphoma is a collection of cancers arising from the malignant transformation of lymphocytes. Even though lymphoma is clinically a diverse group of neoplasms, the common origin is the lymphorecticular cells. Lymphoma is one of the most common canine cancers, accounting for 7-24% of all canine tumors and 85% of hematopoietic tumors. Dogs of any age, gender, and breed can be affected with lymphoma. Affected dogs are typically middle aged to older dog.
Anatomic Classi cation
Multicentric (PLN) is the most common form, accounting for 80% of lymphomas. Most dogs are typically asymptomatic, and 20-40% are clinical (substage b) with anorexia, lethargy, fever, V/D, weight loss, melena.
Clinical Appearance
Historic  ndings: The most common complaint is generalized lymphadenomegaly. Owners commonly report that lymph node size is rapidly increasing – over days to 1 to 3 weeks. In the early stages, dogs appear healthy and are not showing clinical signs. When present, clinical signs tend to be nonspeci c and include vomiting, diarrhea, melena, anorexia, fever, and weight loss (substage b).
Common examination  ndings: Lymphoma can
be indolent or aggressive, solitary or multicentric, or node-based or associated with any organ. Non-painful generalized lymphadenomegaly is most common physical exam  nding. Multicentric lymphoma involving the peripheral lymph nodes is most common, accounting for 80% of patients.
Most dogs are “healthy” substage a. T-cell dogs tend to be sick (b). In dogs, multicentric LSA is generally the NHL (non-Hodgkin’s LSA) form. Hepatosplenomegaly is common. Diffuse pulmonary in ltration has been reported in 27-34% based on CXR but on BAL, lung involvement may be higher. The lack of generalized lymphadenomegaly does not eliminate the possibility of lymphoma, as some dogs will have internal involvement only (i.e. hepatosplenic form, GI). Another scenario that can lead to confusion is hypercalcemia, often without peripheral lymphadenomegaly so lymphoma is not suspected.
Preliminary Diagnosis
Cytology Con rmation of lymphoma starts with  ne needle aspirate of an affected lymph node. Cytology
is minimally invasive, less expensive than biopsy, and typically provides rapid results, in 1 to 2 days. Cytology reveals monomorphic abnormal lymphocyte populations. Cytology does not provide complete classi cation, grading, or phenotype. Avoid reactive LN, such as the mandibular LN.
Diagnostic Work Up
The minimum tests required for treatment are cytological con rmation (lymph node or affected organ), CBC, chemistry panel and urinalysis. The next diagnostic
I encourage owners to submit is phenotyping to determine B vs T-cell subtype. Phenotyping is typically determined with immunocytochemistry from aspirates, immunohistochemistry from biopsy, or  ow cytometry
or PARR from aspirates. If there is a peripheral lymphocytosis on CBC (stage V),  ow cytometry can be submitted on a whole blood sample to determine phenotype. Phenotype is the best independent prognostic factor; prognosis is worse with T-cell than B-cell.
An Urban Experience
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