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   <subfield code="a">10.1245/s10434-010-1400-x</subfield>
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   <subfield code="a">Radiotherapy for Soft Tissue Sarcomas after Isolated Limb Perfusion and Surgical Resection: Essential for Local Control in All Patients?</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Jan Deroose, Jacobus Burger, Albertus van Geel, Michael den Bakker, Johannes de Jong, Alexander Eggermont, Cornelis Verhoef]</subfield>
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   <subfield code="a">Background: Standard treatment for localized soft tissue sarcoma (STS) is resection plus adjuvant radiotherapy (RTx). In approximately 10% of cases, resection would cause severe loss of function or even require amputation because of the extent of disease. Isolated limb perfusion (ILP) with tumor necrosis factor alpha (TNF-α) and melphalan can achieve regression of the tumor, facilitating limb-saving resection. RTx improves local control but may lead to increased morbidity. Methods: In our database of over 500 ILPs, 122 patients with unifocal STS were treated by ILP followed by limb-sparing surgery. All included patients were candidates for amputation. Results: Surgery resulted in 69 R0 resections (57%), and in 53 specimens (43%) resection margins contained microscopic evidence of tumor (R1). Histopathological examination revealed&gt;50% ILP-induced tumor necrosis in 59 cases (48%). RTx was administered in 73 patients (60%). Local recurrence rate was 21% after median follow-up of 31months (2-182months). Recurrence was significantly less in patients with&gt;50% ILP-induced necrosis versus≤50% necrosis (7% vs. 33%, P=0.001). A similar significant correlation was observed for R0 versus R1 resections (15% vs. 28%, P=0.04). In 36 patients with R0 resection and&gt;50% necrosis, of whom 21 were spared RTx, no recurrences were observed during follow-up. Conclusions: In patients with locally advanced primary STS, treated with ILP followed by R0 resection, and with&gt;50% ILP-induced necrosis in the resected specimen, RTx is of no further benefit.</subfield>
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   <subfield code="a">The Author(s), 2010</subfield>
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   <subfield code="a">Deroose</subfield>
   <subfield code="D">Jan</subfield>
   <subfield code="u">Division of Surgical Oncology, Erasmus MC-Daniel den Hoed Cancer Center, Rotterdam, The Netherlands</subfield>
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   <subfield code="a">Burger</subfield>
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   <subfield code="a">van Geel</subfield>
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   <subfield code="a">Eggermont</subfield>
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   <subfield code="t">Annals of Surgical Oncology</subfield>
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