Metronomic chemotherapy entails the chronic administration of low-dosages of chemotherapy, so theoretically the inhibitory impact on the tumor blood vessel growth is maintained, but the dose is insufficient to cause damage to healthy cells. “Your dog has cancer” might be the four scariest words a pet parent can hear. Unable to load your collection due to an error Elsevier Science But we don’t want you to put your dog in a bubble. These appointments are similar to a typical vet visit, she said, and are designed to minimize stress for both dog and pet parent.Side effects for dogs are milder and generally last for a shorter period of time than for humans receiving chemotherapy because dogs are given less-aggressive treatment, Intile said. I use this approach for some patients with metastatic disease — such as spread of the tumor to the lungs — in an attempt to slow progression of the metastatic disease. However, metronomic regimens have 3 types of clinical indications: In fact, 75 to 80 percent of dogs have no side effects, she said. After you get that diagnosis, chances are you scarcely hear your vet lay out the treatment options, which likely include chemotherapy. thank you so much. In fact my preferred metronomic approach combines Palladia with low dose CYC.Personally, when I start these protocols I re-check every two weeks for four to six weeks. Pathologic findings in both the spleen and globe were consistent with hemangiosarcoma with a low mitotic count. Sue Ettinger, DVM. This cancer is common in dogs, but rare in people. The white blood cells are the first line of defense against infection,” and a low white blood cell count can put dogs at risk for infections, she said.Unlike people, dogs typically do not go bald from chemotherapy, although they might lose their whiskers, Intile said. Tumour resistance to cytotoxic drugs is a complex and probably multifactorial challenge, mediated by genetic and biochemical alterations that allow cancer population to survive during therapy.Thanks to its characteristics, MC has gradually become a popular treatment option in companion animals.• MC well tolerated and, at least, as effective as MTD chemotherapy;• Lower dose of CYC resulted in lower frequency of SHC;• EOD dosing better tolerated than daily dosing for some dogs, despite unknown consequences for the treatment effectiveness.• No AEs were reported, but the study period was short.• Metronomic delivery of lomustine well tolerated in short‐term;• Drug‐induced thrombocytopenia as the most likely long‐term consequence, after a median of 432 d of therapy;• The non‐alteration of dosage during treatment resulted in absent of determination of OBD and drug discontinuation for 22 dogs.• Metronomic chlorambucil well tolerated as a single‐agent;• No significant differences between use and non‐use of NSAIDs;• Great response by dogs with HSA who had failed pior CT.• Impossible to determinate if CYC accentuated that decline;• Inverse correlation between the Treg and IFN‐γ levels, suggesting eventual improvement of Treg immunosuppressive effects.• OCB of dogs receiving MC and alkalinization over twice the OCB of dogs receiving MC alone (40%);• No significant differences demonstrated between the 2 groups in terms of clinical response;• Combination of MC with carboplatin and doxorubicin significantly less likely related to high‐grade toxicity (• No significant differences (on DFI, OST and 1‐year survival• More frequent treatment‐related toxicities in toceranib group.• Clinical stage was significantly determinant for the prognosis;• Adjuvant chemotherapy seemed to prolong ST of dogs post‐splenectomy, but no significant difference was found (• Longer OST in dogs treated with the combination DOX and CYC suggests a possible additive or synergetic effect between the 2 drugs, but no significant differences were reported among treatment groups.• Both treatment groups associated with a significant depletion of circulating lymphocytes, but without apparent selectivity for Tregs;• DOX may have been the responsible for this indiscriminant decline;• No DLTs associated with the combination protocol.Surgery and RT with 5 × 6 Gy protocol, twice per week (Thalidomide (1‐2 mg/kg/die, PO) and piroxicam (0.3 mg/kg/die, PO)• Addition of MC significantly improved OST of dogs (• Tumour location and number of surgeries significantly affected PFI, whereas treatment type did not.MTDC‐related toxicity equivalent between dogs on MTDC protocol (• Adjuvant maintenance MC after completion of MTDC significantly improved TTM (• The authors suggested that thalidomide plays an important role in controlling metastization.The first clinical trial documenting the use of MC to treat dogs with cancer was published in 2007 by Lana et al,Altogether, despite their small number, these 15 clinical trials give an idea of the antineoplastic spectrum of this schedule, at least for solid tumours, which include soft tissue sarcomas, hemangiosarcomas, osteosarcomas and transitional cell carcinomas. 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