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1304   PART XII   Oncology


            again on a modified maintenance protocol. If at the end of   (e.g., Poodle, Bichon Frise); cats (and some dogs) may also
            the induction phase the patient is not in a CR, the author   shed their tactile hairs during treatment.
  VetBooks.ir  recommends that intensification with L-asparaginase be done   pet’s appetite and activity level, measure their lymph nodes
                                                                   During this phase, owners are instructed to monitor their
            before the maintenance phase is initiated. In addition to the
            chemotherapeutic approach discussed in this section, a
                                                                 take their pet’s rectal temperature if they are unwell (pyrexia
            variety of protocols have been used successfully in the treat-  (if peripheral lymphadenopathy was present initially), and
            ment of cats and dogs with lymphoma. (See Suggested Read-  is usually secondary to neutropenia and bacteremia or
            ings for additional information.)                    sepsis). If pyrexia develops, owners are instructed to contact
              Induction of remission                             their veterinarian immediately so that their pet can undergo
              As previously discussed, one author’s (GC) protocol of   a complete physical examination and CBC (for additional
            choice for the induction of remission is COP. The agents in   information, see Chapter 77). Treatment with COP results in
            this protocol consist of cyclophosphamide, vincristine, and   CR within 1 to 14 days of the start of therapy in most animals
            prednisone; these drugs are currently available as generic   (>85% in dogs, >70% in cats) (Figs. 79.9 and 79.10, A and
            products and are relatively inexpensive. The dosages are   B). This remission is usually maintained throughout the
            specified in Box 79.1. These drugs belong to three different   induction phase.
            categories, have different mechanisms of action, and do not   In dogs with diffuse large-cell alimentary lymphoma, the
            have superimposed toxicities. In dogs or cats with CNS or   authors both use a CHOP-based protocol (see  Box 79.1)
            ocular involvement, cytosine arabinoside can be added by   because, on the basis of experience, the response rate to
            the subcutaneous (SC) route or as a continuous rate infusion   COP is low. This protocol is more expensive and slightly
            for 6 to 8 hours (COAP protocol); given its short half-life   more likely to cause adverse effects than the COP protocol.
            and S-phase–specific mechanism of action, an IV bolus
            injection results in minimal cell kill. SC administration of
            this drug is painful in cats (and in some dogs). The induction
            phase lasts 6 to 8 weeks, and weekly chemotherapy visits are
            necessary during this time.
              During the induction phase, toxicity is minimal (<15%)
            and client compliance is high because most of the toxic signs
            are hematologic (i.e., cytopenias) and usually do not result
            in  clinical  signs that  can  be  detected  by the owners.  The
            dose-limiting toxicity of this induction protocol is hemato-
            logic (i.e., myelosuppression leading to neutropenia), and it
            occurs in less than 10% of the patients; the neutrophil nadir
            usually occurs around day 7 or 8 because two myelosuppres-
            sive agents (i.e., cyclophosphamide and cytosine arabino-
            side) are given during the initial 2 to 4 days of treatment in
            the COAP protocol. In most cases, the neutropenia is mild   A
            (2000-3500 cells/µL). The neutropenia can be severe if the
            animals have neoplastic bone marrow infiltration before the
            initiation of treatment, have FeLV- or FIV-associated myelo-
            dysplasia or other retrovirus-associated bone marrow disor-
            ders, or receive the cytosine arabinoside by constant-rate IV
            infusion rather than by the SC route. Also, anecdotally, neu-
            tropenia appears to be common in Cocker Spaniels and West
            Highland White Terriers receiving this protocol. Dosage
            adjustments in cats and dogs that develop neutropenia are
            described in Chapter 77. Gastrointestinal toxicity is minimal
            to nonexistent; however, cats receiving cyclophosphamide
            can occasionally become anorectic. Consequently, this drug
            should be administered once every 3 weeks  in cats  (as
            opposed to every other day as in dogs; see  Box 79.1). If
            anorexia develops, treatment with cyproheptadine, an anti-  B
            serotonin drug, at a dosage of 1 to 2 mg per cat PO every
            12 h or mirtazapine at a dosage of 1.875 to 3.75 mg per cat   FIG 79.10
            PO every 1 to 3 days is indicated. Capromorelin, is a novel   Mixed-breed dog with multicentric lymphoma before (A)
            appetite stimulant (Entyce, Aratana Therapeutics, Leawood,   and 7 days after initiating chemotherapy (B). Note
            KS) given at a dosage of 3 mg/kg PO every 24 h. Hair loss is   complete disappearance of mandibular lymphadenopathy
            also minimal, and it occurs primarily in woolly-haired dogs   and ventral facial edema.
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