Ewing Sarcoma of the Hand or Foot
Overview
Affiliations
Purpose: Ewing Sarcoma (ES) of the hand or foot is a rare clinical condition. Due to the critical site, it is of major importance to choose an optimal procedure for local control in terms of outcome and function. Local therapeutic options for these patients range from: surgery (OP), surgery followed by radiotherapy (OP & RT), or radiotherapy (RT) alone.
Patients And Methods: Data from 80 patients with ES of the hand or foot were analyzed. All patients received chemotherapy according to the protocols of the Cooperative Ewing Sarcoma Study Group (CESS) from 1991 to 2009 (EICESS-92 and EURO-E.W.I.N.G.99). Local therapy consisted of: OP in 39%, OP & RT in 44%, and RT in 12%. In 5% of the patients no local therapy (noL) was performed. Primary endpoint of our study was the event-free-survival (EFS).
Results: The 3-year overall EFS was 62% (95%CI 0.50-0.72). Patients with localized disease had a significantly better outcome with an EFS of 77% (95%CI 0.63-0.86), compared to patients with primary disseminated disease with an EFS of 30% (95%CI 0.14-0.49; p<0.001). In comparing local treatment modalities, no significant difference was observed. The 3-year EFS for OP was 61% (95% CI 0.40-0.76), for OP & RT 66% (95%CI 0.47-0.79) and for RT only 70% (95%CI 0.32-0.89) (p=0.253). Patients who did not receive local treatment had an unfavourable prognosis (3-year EFS=0.25; 95%CI 0.01-0.67; p=0.024). A multivariate analysis which included local treatment modality and known prognosticators, showed that primary dissemination was the only significant prognostic factor.Ewing sarcoma of the hand or foot is associated with a favourable outcome.
Conclusion: Our data analysed a limited group of patients and thus did not provide a clear indication for a preferred local treatment modality.
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Neder Filho A, da Costa A, Barros R, Nakachima L, Rodrigues M, Souza S Rev Assoc Med Bras (1992). 2024; 70(suppl 1):e2024S108.
PMID: 38865528 PMC: 11164264. DOI: 10.1590/1806-9282.2024S108.
Malignant Bone and Soft Tissue Lesions of the Foot.
Angelini A, Biz C, Cerchiaro M, Longhi V, Ruggieri P J Clin Med. 2023; 12(8).
PMID: 37109375 PMC: 10146676. DOI: 10.3390/jcm12083038.
Survival of children treated for Ewing sarcoma in Lithuania: a single centre experience.
Jakutis G, Rageliene L, Rascon J Acta Med Litu. 2018; 24(4):199-208.
PMID: 29487483 PMC: 5818255. DOI: 10.6001/actamedica.v24i4.3615.
Peinemann F, Enk H, Smith L Cochrane Database Syst Rev. 2017; 4:CD008216.
PMID: 28407197 PMC: 6478255. DOI: 10.1002/14651858.CD008216.pub5.