“…MLS is relatively sensitive to radiotherapy (RT) [ 12 , 17 , 18 ] and chemotherapy [ 19 , 20 ], in comparison to other STSs. Local control is achieved in 60–98% of patients [ 4 , 7 , 8 , 11 – 14 , 18 , 21 – 23 ], resulting in favorable 5-year overall survival (OS) rates of 67–90% [ 5 , 9 , 11 – 13 , 21 , 23 – 25 ].Although sample sizes in most of the previous studies are small due to the rarity of the disease, several prognostic factors in MLS have been identified. Age at diagnosis >45years, tumor size >10 cm, presence of >5% round cell component, and positive resection margins are associated with worse (disease-specific) survival [ 5 , 7 , 8 , 11 , 13 , 21 , 23 – 25 ].…”