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Prognostic factors in canine appendicular osteosarcoma – a meta-analysisKeywords: Bone tumor, Dog, Survival, Disease-free interval, Prognostic factors Abstract: A literature review was performed on selected studies and eligible data were extracted. Meta-analyses were done for two of the three selected possible prognostic factors (SALP and location), looking at both survival time (ST) and disease free interval (DFI). The third factor (age) was studied in a qualitative manner. Both elevated SALP level and the (proximal) humerus as location of the primary tumor are significant negative prognostic factors for both ST and DFI in dogs with appendicular osteosarcoma. Increasing age was associated with shorter ST and DFI, however, was not statistically significant because information of this factor was available in only a limited number of papers.Elevated SALP and proximal humeral location are significant negative prognosticators for canine osteosarcoma.Osteosarcoma (OS) is a malignant tumor of mesenchymal origin that produces osteoid. OS accounts for approximately 85?% of all primary canine bone tumors and is almost exclusively observed in large or giant breeds [1-5]. There is anecdotal evidence suggesting that males are more predisposed. The median age of onset of clinical signs ranges from 8 to 10?years [5,6], although it also occurs in younger dogs [7].Dogs are often presented with a history of lameness or in some cases with a pathologic fracture of the affected bone. Predilection sites are the weight-bearing regions of the long bones (humerus, femur, radius, tibia and ulna) [8] with approximately 25?% of tumors arising in the axial skeleton including the flat bones of the skull, ribs, vertebrae, sternum, and pelvis [9,10]. OS is an aggressive and invasive neoplasm that causes local skeletal destruction and resulting in radiographic evidence of both osteoproductive and osteolytic lesions. They are highly metastatic, predominantly to the lungs with a lower frequency of spread to distant bones, regional lymph nodes [11] and other soft tissues [12,13]. A clinical diagnosis is made following assessment of case signalment and histor
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