Long-term outcome for patients with non-metastatic Ewing's sarcoma treated with adjuvant and neoadjuvant chemotherapies. 402 patients treated at Rizzoli between 1972 and 1992
Adult
Male
0301 basic medicine
Adolescent
Infant, Newborn
Infant
Bone Neoplasms
Middle Aged
Disease-Free Survival
3. Good health
03 medical and health sciences
Chemotherapy, Adjuvant
Child, Preschool
Antineoplastic Combined Chemotherapy Protocols
Multivariate Analysis
Humans
Female
Neoplasm Metastasis
Neoplasm Recurrence, Local
Child
Adjuvant chemotherapy; Ewing's sarcoma; Follow-up; Late relapse; Neodjuvant chemotherapy; Outcome; Oncology; Cancer Research
Aged
Follow-Up Studies
Retrospective Studies
DOI:
10.1016/j.ejca.2003.08.022
Publication Date:
2003-10-21T11:16:40Z
AUTHORS (10)
ABSTRACT
We evaluated the long-term results obtained in 402 patients with non-metastatic Ewing's sarcoma (ES) of the bone treated in a single institution with adjuvant and neoadjuvant chemotherapies between 1972 and 1992. Multivariate analyses showed male gender, age older than 14 years, high serum lactate dehydrogenase (LDH) level, axial location of the tumour, use of radiotherapy alone as a local treatment, and poor histological response to chemotherapy, to be independent, adverse prognostic factors for event-free survival (EFS). At a mean follow-up of about 18 years (10-30 years), 177 patients (44.0%) remained continuously free of disease, 2 died of doxorubicin-induced cardiotoxicity and 8 developed a second neoplasm (5 died, and 3 are alive and free of disease). 215 patients relapsed with metastases and/or local recurrence: 14 are alive and free of disease, 1 is alive with uncontrolled disease, and 200 died. The overall survival (OS) at real follow-ups of 5-, 10-, 15- and 20-years was 57.2, 49.3, 44.9 and 38.4%, respectively. We conclude that since local or systemic relapses, treatment-complications and second malignancies are more common after 5 years or more from the beginning of treatment; a long-term follow-up is mandatory for patients with ES.
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