Background: High-dose chemotherapy (HDT) was added to conventional chemotherapy in Ewing sarcoma family tumor (EFT) patients, poor responders (PRs) to induction chemotherapy in order to improve their survival. Patients and methods: Patients aged ≤40 years with nonmetastatic Ewing sarcoma (ES) received vincristine (V), doxorubicin (A), cyclofosfamide (C), actinomycin (Ac), ifosfamide (I) and etoposide (E) (VACAc-IE regimen) as induction chemotherapy. As maintenance treatment, good responders (GR) received nine cycles of VACAc-IE regimen. PRs received three cycles of VAC-IE, mobilizing cycle with CE and HDT with Busulfan and Melphalan with stem cell support. Results: Three hundred patients [median age 15 years (3–40 years)] entered the study. One patient refused local treatment, 242 (81%) underwent surgery [with radiotherapy (RT) in 80] and 57 (19%) RT alone. No toxic deaths were recorded. Overall GR were 146 (49%). Twenty-eight PR did not receive HDT. At a median follow-up of 64 months (21–116 months), 5-year overall and event-free survival (EFS) were 75% and 69%, respectively. Five-year EFS was 75% for GR, 72% for PR treated with HDT and 33% for PR who did not receive HDT. Conclusions: High-dose therapy added to the VACA-IE regimen in PR patients is feasible and effective. Selected groups of patients with ES can benefit from HDT.

Nonmetastatic Ewing family tumors: high-dose chemotherapy with stem cell rescue in poor responder patients. Results of the Italian Sarcoma Grouo/Scandinavian Sarcoma Group III protocol / S. Ferrari; H.K. Sundby; R. Luksch; A. Tienghi; T. QWiebe.F. Fagioli; TA Alvegard; A. Brach Del Prever; A. Tamburini; M. Alberghini. L. Gendola; M. Mercuri; R. Capanna; S. Mapelli; A. Prete; M. Carli; P. Picci; E. Barbieri; G. Bacci; S. Smeland. - In: ANNALS OF ONCOLOGY. - ISSN 0923-7534. - ELETTRONICO. - 22:5(2011), pp. 1221-1227. [10.1093/annonc/mdq573]

Nonmetastatic Ewing family tumors: high-dose chemotherapy with stem cell rescue in poor responder patients. Results of the Italian Sarcoma Grouo/Scandinavian Sarcoma Group III protocol

MERCURI, MARIO;PICCI, PIERO;BARBIERI, ENZA;BACCI, GAETANO;
2011

Abstract

Background: High-dose chemotherapy (HDT) was added to conventional chemotherapy in Ewing sarcoma family tumor (EFT) patients, poor responders (PRs) to induction chemotherapy in order to improve their survival. Patients and methods: Patients aged ≤40 years with nonmetastatic Ewing sarcoma (ES) received vincristine (V), doxorubicin (A), cyclofosfamide (C), actinomycin (Ac), ifosfamide (I) and etoposide (E) (VACAc-IE regimen) as induction chemotherapy. As maintenance treatment, good responders (GR) received nine cycles of VACAc-IE regimen. PRs received three cycles of VAC-IE, mobilizing cycle with CE and HDT with Busulfan and Melphalan with stem cell support. Results: Three hundred patients [median age 15 years (3–40 years)] entered the study. One patient refused local treatment, 242 (81%) underwent surgery [with radiotherapy (RT) in 80] and 57 (19%) RT alone. No toxic deaths were recorded. Overall GR were 146 (49%). Twenty-eight PR did not receive HDT. At a median follow-up of 64 months (21–116 months), 5-year overall and event-free survival (EFS) were 75% and 69%, respectively. Five-year EFS was 75% for GR, 72% for PR treated with HDT and 33% for PR who did not receive HDT. Conclusions: High-dose therapy added to the VACA-IE regimen in PR patients is feasible and effective. Selected groups of patients with ES can benefit from HDT.
2011
Nonmetastatic Ewing family tumors: high-dose chemotherapy with stem cell rescue in poor responder patients. Results of the Italian Sarcoma Grouo/Scandinavian Sarcoma Group III protocol / S. Ferrari; H.K. Sundby; R. Luksch; A. Tienghi; T. QWiebe.F. Fagioli; TA Alvegard; A. Brach Del Prever; A. Tamburini; M. Alberghini. L. Gendola; M. Mercuri; R. Capanna; S. Mapelli; A. Prete; M. Carli; P. Picci; E. Barbieri; G. Bacci; S. Smeland. - In: ANNALS OF ONCOLOGY. - ISSN 0923-7534. - ELETTRONICO. - 22:5(2011), pp. 1221-1227. [10.1093/annonc/mdq573]
S. Ferrari; H.K. Sundby; R. Luksch; A. Tienghi; T. QWiebe.F. Fagioli; TA Alvegard; A. Brach Del Prever; A. Tamburini; M. Alberghini. L. Gendola; M. Mercuri; R. Capanna; S. Mapelli; A. Prete; M. Carli; P. Picci; E. Barbieri; G. Bacci; S. Smeland
File in questo prodotto:
Eventuali allegati, non sono esposti

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/94901
 Attenzione

Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo

Citazioni
  • ???jsp.display-item.citation.pmc??? 33
  • Scopus 99
  • ???jsp.display-item.citation.isi??? 87
social impact