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Mast Cell Tumors

Description- Mast cell tumors (MCTs) or mastocytomas are the most common cutaneous tumor found in dogs. It accounts for 16-21% of all cutaneous tumors. Older dogs of mixed breeds have a high propensity for the disease. It has been reported in breeds like Boxers, Boston Terriers, Labrador Retrievers, Beagles and Schnauzers. Boxers, however, have the highest incidence. But the disease develops in histologically low or intermediate grade forms in them. No gender predilection has been reported. Mast cells are cells that occur in the skin and other tissues, like the intestines and respiratory tract. They are also an integral part of the immune system. They consist of large amounts of histamine, heparin, and proteolytic enzymes (enzymes which break down protein). These have a toxic effect on foreign invaders, like parasites, and are released when the mast cell is triggered by the immune system. A mast cell tumor results from these mast cells. When histamine, heparin, and enzymes are damaged by some external invasion, they pose health hazards. Large amounts of these substances are released into the body that usually have adverse effects on heart rate, blood pressure, and other body functions. Sites where the tumors are removed can sometimes refuse to heal and can become unmanageable. Normal mast cells are found in plenty in the lung and gastrointestinal tract. But tumors generally don’t originate in these sites. They rather develop in the dermis and sub-cutaneous tissues. They are most frequently found on trunks. The limbs account for generally ¼ the of the sites of these lesions. Mast cell tumors have been reported to develop infrequently in other sites like head, neck, conjunctiva, salivary gland, nasopharynx, larynx, oral cavity, gastrointestinal tract, ureter and spine.

Classification of Mast Cell Tumors

Mast cell tumors have been classified according to their degree of proliferativeness. The higher the grade, the more aggressive the tumor.

  • Grade I: Occur in the skin and are considered non-malignant. Although they may be large and difficult to remove, they do not spread to other areas of the body. Most mast cell tumors belong to Grade I.
  • Grade II: Found below the skin into the subcutaneous tissues. Their cells show some characteristics of malignancy and their response to treatment can be unpredictable.
  • Grade III: Originate in areas deep below the skin, are very aggressive, and require extensive treatment.

Staging Mast Cell Tumors

Mast cell tumors should be staged because it gives us an idea abou how they have metatasized in the body. A tumor is staged after it is surgically excised and examined, along with the surrounding lymph nodes. The factors on which staging depends include the number of tumors present and lymph node involvement.

  • Stage 0: One tumor in the skin incompletely removed, with no lymph node involvement.
  • Stage I: One tumor in the skin, with no lymph node involvement.
  • Stage II: One tumor in the skin with lymph node involvement
  • Stage III: Multiple large, deep skin tumors, with or without lymph node involvement
  • Stage IV: One or more tumors with metastasis in the skin with lymph node involvement. This stage is further divided into those that have no other signs (substage a) and those that have some other clinical symptoms (substage b).

Causes- Like most of the cancers, the etiology of mast cell tumors is also not known. On rare occasions, they have been associated with chronic inflammation or the application of skin irritants. Studies have indicated that chromosomal fragile site expression (unstable genomic loci susceptible to breakage, rearrangement), a phenomenon that is thought to genetically predispose humans to the development of certain tumors, have been found to be increased in Boxer dogs with MCTs. However, this study was conducted on young, non-tumor bearing boxers. So it was believed that the increased expression was likely due to the age difference. The genetic alterations that increase the likelihood of tumors in humans are not absolutely understood in dogs. Changes in the pathway of p53 tumor suppressor have been indicated in some canines Disturbances in the expression of proteins like p21 and p27, cyclin dependent kinase (A protein kinase inhibitor is a type of enzyme inhibitor that specifically blocks the action of one or more protein kinases) inhibitors that regulate the cell cycle, have been identified in several dogs. Recently an expression of c-Kit, a tyrosine kinase receptor for the growth of hematopoietic stem cells (multipotent stem cells that give rise to all types of blood cells) have been identified in canine MCTs. Several studies have also suggested the presence of mutations in the juxtamemebrane (adjacent to a membrane on one side of it) region of c-Kit leading to constitutive activation (synthesis of a protein or an enzyme at a constant rate) in the absence of hematopoietic growth stem cell factor. Although it is not clearly understood, but studies indicate that estrogen and progesterone may also influence mast cell tumors.

Symptoms-The clinical signs may vary greatly. Most tumors are solitary, but 11-14% of tumors have multiple lesions. Well differentiated tumors are generally solitary with 1-4cm in diameter. They usually grow slowly and are rubbery in appearance. They are normally present for at least 6 months. They are not ulcerative, but the hair on the skin may be lost. Undifferentiated mast cell tumors are generally ulcerating and they can cause extreme discomfiture. They grow faster in size. Surrounding tissues may become inflamed and edematous, and small satellite nodules may develop in the surrounding tissues. Intermediate tumors are somewhere between these two extremes. Gastrointestinal ulceration may occur with related signs of vomiting, anorexia, melena (black, tarry feces that are associated with gastrointestinal hemorrhage).

Although very uncommon, visceral MCT can occur in dogs. It is generally preceded by an undifferenciated primary cutaneous lesion. Consistent abnormalities include lymphadenopathy (enlarged lymph nodes), splenomegaly (enlarged spleen) and hepatomegaly (enlarged liver). Bone marrow and peripheral blood involvement are common in cancerous mast cell tumors. Pleural and peritoneal effusions (excess fluid in the pleural cavity and peritoneum) comprising neoplastic cells have been observed.

Treatment- Fine needle aspiration and cytology (FNAC) is first step in the diagnosis of mast cell tumors. Occasional MCTs (predominantly undifferentiated MCTs) must be diagnosed by other means like histopathology, special stains, etc. From the diagnosis it can found if the MCT is in a location that is amenable to wide surgical excision. If that is so, then the surgery should be performed right away. The excised tissue is given for assessment of histologic grade. FNAC is not adequate for grading, therefore histologic assessment is strongly recommended. Further diagnosis is performed only if the lesion is found to be undifferentiated with incomplete surgical margins. If it is found that the location of the lesion is not suitable for surgery, further diagnosis is performed for staging the disease. Complete staging includes cytologic assessment of regional lymph nodes, a complete blood count and buffy coat smear to establish peripheral mastocytosis, abdominal ultrasound with cytologic assessment of the spleen, or liver, thoracic radiographs and bone marrow aspiration. An incisional biopsy is performed to determine the histologic grade. The steps that comprise pre-surgical staging include standard geriatric preanesthetic blood work, needle aspiration cytology, of the regional node and abdominal ultrasound. Thoracic radiographs are not adequate in determining metastasis. But they are very useful in ruling out unrelated disease processes or occult cardio pulmonary disease that can complicate anesthesia.

With regard to lymph node cytology, an occasional solitary lymph node cell is not alarming. But if they are found in clusters there is cause for worry. However, buffy coat smears, bone marrow aspiration and aspiration of structurally normal abdominal organs is generally not indicated. In these cases, surgical extirpation of a cytologically suspicious node for histological assessment is recommended.

The extent of metastasis before surgery is determined by digital palpation. It can be improved by using diagnostic ultrasound, or computed tomography.

Surgical excision and radiation therapy are the two most successful treatment options available. In tumors, which are localized and are favorable for wide excision, surgery is the treatment of choice.Pretreatment with an antihistamine is recommended before the excision. Surgery that includes a 3cm margin of surrounding normal tissue has been suggested for MCTs. A more recent study has indicated that 2 cm lateral margins may be adequate for complete excision of most MCTs. Deep margins hold the same significance as lateral margins and one fascial plane deep to the lesion may be removed. If required muscle layers deep to the tumor should also be removed. All surgical margins should be investigated histologically. Inoperable tumors should be evaluated by incisional biopsy for histologic grade.

There are three therapeutic options for a low grade or intermediate grade distal extremity MCT. The most aggressive option is amputation. In this case, surgical margins are wide, but the prognosis is very poor. The next option is external beam radiotherapy alone. Results indicated that dosages of 40-50 Gray results in a 1 year control rate in approximately 50% of cases. More aggressive doses of 48-57 Gray might show improved results. The combination of surgery and radiotherapy is believed to be ideal for MCTs where wide surgical excision is not feasible. Veterinary literature has established that complementary use of surgery to achieve clinical stage 0 disease (ie, microscopically incomplete margins), followed by external beam radiation therapy has proved successful in controlling the disease up to 2 years in 85% to 95% of cases. Many oncologists suggest prophylactic nodal irradiation (PNI) for cytologically negative regional lymph nodes. In MCTs with minimal chance of metastasis, PNI has not proven successful. But for MCTs with high incidence for metastasis, PNI may have a positive outcome. However, dogs with low or intermediate grade tumors need to be monitored regularly. When planned curative surgery proves unsuccessful, a second local therapy is needed in the form of a second excision with additional wide margins for the surgical scar or adjuvant radiotherapy. In these cases, vets also take recourse to adjuvant chemotherapy, but with little success. It has been reported that dogs with incompletely resected MCTs show decreased survival rates.

Alternative therapies include hyperthermia (It is referred to as heat stroke or sunstroke. This condition is created artificially with the help of drugs) with radiotherapy, intralesional brachytherapy (a radioactive source is placed inside or next to the area requiring treatment), photodynamic therapy, intralesional corticosteroids, cryotherapy (cryotherapy is the local or general use of low temperatures in medical therapy or the removal of heat from a body part) and intralesional deiodized water. However, none of these therapies have been thoroughly investigated.

Treatment of intermediate MCTs with only regional node involvement have a better outcome than high grade ones. But vets believe that till proper investigations are carried out, treatment of the intermediate grade tumors should be attached highest priority. These lesions are treated with local surgery or radiotherapy only if thorough staging fails to reveal dissemination. The outcome is not very gratifying due to distant and regional metastasis. Since the prognosis is guarded for high grade tumors, a less expensive, coarse fraction radiation therapy protocol can be considered. For several years the use of prednisone has been found to be highly beneficial.

Recent studies have found adjuvant chemotherapy effective in a vast majority of cases. In this setting, vinblastine (2 mg/m2 given intravenously) is administered weekly for 4 treatments, followed by 4 additional treatments given every 2 weeks. Corticocosteroid like Prednisone is given with VBL initially at a dosage of 2 mg/kg given orally for 1 week then 1 mg/kg given orally daily for 2 weeks, followed by 1 mg/kg given orally every other day. Prednisone is stopped once VBL treatment is over.

Intermediate grade tumors that are clearly excised, post operative treatment remains a source of controversy for them. Studies reveal that these type of tumors show good prognosis. Therefore, vets generally do not recommend any therapy for these patients. Only regular follow-up is advised.

Ancillary therapy for the systemic effects of MCTs related to degranulation is sometimes suggested. The effects of histamine release can be blocked by giving H1 blocker diphenhydramine (2 to 4 mg/kg given orally twice daily) and the H2 blockers cimetidine (4 mg/kg given orally thrice daily) or rantidine (2 mg/kg given once daily orally). Another drug called Omeprazole (0.5 to 1 mg/kg given once daily orally) has proved effective in controlling clinical symptoms of gastrointestinal ulceration associated with gastrinoma.

In cases where there is enough evidence to substantiate the presence of gastro intestinal and duodenal ulceration, sucralfate (0.5 to 1 g given orally thrice daily and rarely misoprostol to histamine blockers is advisable.

Prognosis- The outcome sorely depends upon histologic grade. Dogs with well differentiated tumors live longer after complete surgical excision. Dogs with undifferentiated lesions die within 1 year after surgery due to metastasis. Studies have suggested that patients with a single MCT and those with multiple cutaneous MCTs have similar prognosis. Symptoms like anorexia, vomiting, melena, widespread erythema and edema associated with visceral forms of MCT have poor prognosis.

Therefore we can say that more aggressive treatment at the time of the first appearance of the disease rather than at the time of recurrence may improve the chances of prognosis.

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Reference

Withrow and MacEwen’s Small Animal Clinical Oncology- Stephen J. Withrow, DVM, DACVIM (Oncology), Director, Animal Cancer Center Stuart Chair In Oncology, University Distinguished Professor, Colorado State University Fort Collins, Colorado; David M. Vail, DVM, DACVIM (Oncology), Professor of Oncology, Director of Clinical Research, School of Veterinary Medicine University of Wisconsin-Madison Madison, Wisconsin

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