Neoadjuvant chemotherapy for Ewing's sarcoma of bone in patients older than thirty-nine years - Experience of twenty-three cases at the Istituto Ortopedico Rizzoli

Citation
G. Bacci et al., Neoadjuvant chemotherapy for Ewing's sarcoma of bone in patients older than thirty-nine years - Experience of twenty-three cases at the Istituto Ortopedico Rizzoli, ACTA ONCOL, 39(1), 2000, pp. 111-116
Citations number
24
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ACTA ONCOLOGICA
ISSN journal
0284186X → ACNP
Volume
39
Issue
1
Year of publication
2000
Pages
111 - 116
Database
ISI
SICI code
0284-186X(2000)39:1<111:NCFESO>2.0.ZU;2-V
Abstract
The aim of this study was to determine whether the behaviour of Ewing's sar coma of bone in adult patients is the same as that observed in children and adolescents. We reviewed the clinical features and outcomes of 23 patients over the age of 39 (17 males, 6 females) who had been treated with neoadju vant chemotherapy between 1983 and 1995 at our institution. The most common primary sites of tumor were the extremities (16 cases); tumor volume was m ore than 100 ml in 17 patients, and elevated serum LDH levels were found in 6 cases. The local treatment was surgery in 8 cases, surgery plus radiothe rapy in 8, and radiotherapy alone in 7 cases. Chemotherapy comprised a 4-dr ug regimen in 10 patients, while the other 13 patients received 6 drugs. At a follow-up of 5.8 years (3.5-15) 13 patients remained continuously free o f disease and 10 relapsed. The 5-year disease-free survival and overall sur vival rates were 53% and 59%, respectively. Clinical features, dose intensi ty, and toxicity of chemotherapy. as well as the outcome of these 23 patien ts were found to be exactly comparable to the findings observed in 327 pati ents younger than 40 years treated at our institution in the same period, w ith the same therapy. We conclude that Ewing's sarcoma of bone in adults is no different from that occurring in children, and we therefore recommend t he inclusion of all adult patients in multidisciplinary treatment trials of this tumor.