AI Summary & Key Takeaways
AI InsightDisease-freesurvival at 5 and 10 years were 66%; whereas, overall patient survival at 5 and 10 years were 78.1%and 71.0%, respectively.
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Abstract
Objective: The aim of this study was to evaluate the histopathological features of primary extremitymyxoid liposarcoma before and after neoadjuvant radiation therapy, and to evaluate the oncologicaloutcomes of the patients.Methods: The study included 23 patients (16 men and 7 women with a mean age of 43 (24e69) years)with primary myxoid liposarcoma of the extremities, who were treated between January 1998 andDecember 2015. Inclusion criteria were histopathological conŞrmation of the diagnosis with both theinitial biopsy and the resection specimen, and having undergone neoadjuvant radiotherapy. Demographic, clinical and histopathological data were evaluated.Results: Over a mean follow-up time of 55.2 (8e139) months, 5 patients (21.7%) died secondary todisease progression, leaving 18 patients (78.3%) still alive at the time of last follow-up. Only one patient(4%) experienced local recurrence and six (26%) patients developed distant metastases. Disease-freesurvival at 5 and 10 years were 66%; whereas, overall patient survival at 5 and 10 years were 78.1%and 71.0%, respectively. Tumor size (>15 cm) and presence of metastasis were signiŞcantly associatedwith increased overall mortality. On histopathology, necrosis was present in 12/23 resection specimens.Hyalinization/Şbrosis and residual viable tumor was present in all specimens. Adipocytic maturation/cytodifferentiation was seen in 8/23 patients.Conclusion: Neoadjuvant radiotherapy was effective for myxoid liposarcomas histopathologically,although these histopathological features did not affect the patients' oncological outcomes. Favorableoncological outcomes were obtained with neoadjuvant radiotherapy, surgical resection and chemotherapy.Level of evidence: Level IV, therapeutic study.© 2017 Turkish Association of Orthopaedics and Traumatology. Publishing services by Elsevier B.V. This isan open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).