Author/Authors :
Omidvari، Shapour نويسنده Department of Radiation Oncology,Shiraz University of
Medical Sciences,Shiraz,Iran , , Nasrolahi، Hamid نويسنده Department of Radiation Oncology,Shiraz University of
Medical Sciences,Shiraz,Iran , , Kadkhodaei، Behnam نويسنده Department of Pathology,Shiraz University of Medical
Sciences,Shiraz,Iran , , Hamedi، Hasan نويسنده Department of Radiation Oncology,Shiraz University of
Medical Sciences,Shiraz,Iran , , Ahmadloo، Niloofar نويسنده Department of Radiation Oncology,Shiraz University of
Medical Sciences,Shiraz,Iran , , Ansari، Mansour نويسنده Department of Radiation Oncology,Shiraz University of
Medical Sciences,Shiraz,Iran , , Mohammadianpanah، Mohammad نويسنده Colorectal Research Center,Shiraz University of Medical
Sciences,Shiraz,Iran , , Mosalaei، Ahmad نويسنده Shiraz Institute for Cancer Research,Shiraz University of
Medical Sciences,Shiraz,Iran ,
Abstract :
Context: Sarcoma is a rare human cancer and pancreatic sarcoma is even rarer. Its treatment and clinical history and prognosis are not well described. Evidence Acquisition: In this review,wecollected all articles in the English language found inPubMedthat were publishedbetween January 2000 to August 2015 to draw conclusions. We found 170 articles in total and 124 articles were excluded. The remaining 46 reports and information of 55 patients were collected and analyzed. Results: Mean age was 57.1 _ 16.7 years and male/female ratio was 27/28. The most common presenting symptom was pain. In 31 cases no adjuvant treatment was prescribed. Others received different chemotherapy agents and only two cases received radiotherapy. Mean tumor size was 9.0_6.8 cm (1 - 27 cm) and the most common type was leiomyosarcoma (16 patients). Nine patients had carcinosarcoma and six cases had MFH. The most common site of metastasis was liver, 14 patients had liver metastasis at presentation. Median survival was 14 months. One, three and five year overall survival were 78.4, 48.5 and 48.5 percent, respectively.We found no effective clinical factor in survival. Conclusions: Pancreatic sarcoma is a rare disease and an optimal treatment, such as surgery, chemotherapy or radiotherapy is not well defined.
