Literature DB >> 10430250

Italian Cooperative Study for the treatment of children and young adults with localized Ewing sarcoma of bone: a preliminary report of 6 years of experience.

P Rosito1, A F Mancini, R Rondelli, M E Abate, A Pession, L Bedei, G Bacci, P Picci, M Mercuri, P Ruggieri, G Frezza, M Campanacci, G Paolucci.   

Abstract

BACKGROUND: In 1991, the Italian Association for Pediatric Hematology-Oncology and the National Council of Research (CNR) initiated an Italian Cooperative Study (SE 91-CNR Protocol) with the main objective of improving the overall survival (SUR) and the event free survival (EFS) of children and young adults with localized Ewing sarcoma and primitive neuroectodermal tumors of bone compared with a previous study (IOR/Ew2 Protocol).
METHODS: Between November 1991 and November 1997, 165 patients were enrolled in this study, 160 of whom were evaluable. The patients were treated with a multimodal approach characterized by intensified chemotherapy, hyperfractionated and accelerated radiation therapy, and the addition of ifosfamide and etoposide to standard chemotherapy with vincristine, actinomycin-D, doxorubicin, and cyclophosphamide.
RESULTS: After a median follow-up of 37 months, 126 of the 160 evaluable patients remained free of disease recurrence. Thirty-one patients developed a disease recurrence (20 with disseminated disease).
CONCLUSIONS: The 3-year SUR and EFS rates found in the current study (83.6% and 77.8%, respectively) may be considered satisfactory. Only age at diagnosis < or =14 years and a good histologic response appeared to affect the outcome of patients with localized Ewing sarcoma positively. These results appear to demonstrate the efficacy of the addition of ifosfamide in induction chemotherapy to four-drug standard combination chemotherapy, as confirmed by the improved outcome in terms of 3-year EFS reported in the SE 91-CNR Protocol compared with the IOR/Ew2 Protocol (77.8% vs. 60.7%). In addition, the better outcome also could be explained by the change in treatment strategy with a trend toward the use of more surgery than radiation therapy compared with the authors' previous protocol.

Entities:  

Mesh:

Year:  1999        PMID: 10430250     DOI: 10.1002/(sici)1097-0142(19990801)86:3<421::aid-cncr10>3.0.co;2-o

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  27 in total

1.  Long-lasting multiagent chemotherapy in adult high-risk Ewing's sarcoma of bone.

Authors:  Selmin Ataergin; Ahmet Ozet; Luis Solchaga; Mustafa Turan; Murat Beyzadeoglu; Kaan Oysul; Fikret Arpaci; Seref Komurcu; Serdar Surenkok; Mustafa Ozturk
Journal:  Med Oncol       Date:  2008-11-07       Impact factor: 3.064

2.  Role of radiation therapy in the multidisciplinary management of Ewing's Sarcoma of bone in pediatric patients: An effective treatment for local control.

Authors:  Jose Luis Lopez; Patricia Cabrera; Rafael Ordoñez; Catalina Marquez; Gema Lucia Ramirez; Juan Manuel Praena-Fernandez; Maria Jose Ortiz
Journal:  Rep Pract Oncol Radiother       Date:  2011-03-12

3.  Ewing's sarcoma and primitive neuroectodermal tumour (ES/PNET) presenting as a breast mass.

Authors:  Suebwong Chuthapisith; Wilairat Prasert; Malee Warnnissorn; Kanapon Pradniwat; Vichien Srimuninnimit; Tamnit Angsusinha
Journal:  Oncol Lett       Date:  2012-04-27       Impact factor: 2.967

4.  High-dose chemotherapy and autologous peripheral blood stem cell transplantation in adult patients with high-risk or advanced Ewing and soft tissue sarcoma.

Authors:  M Engelhardt; R Zeiser; G Ihorst; J Finke; C I Müller
Journal:  J Cancer Res Clin Oncol       Date:  2006-07-12       Impact factor: 4.553

5.  Clinical features and outcomes in patients with extraskeletal Ewing sarcoma.

Authors:  Mark A Applebaum; Jennifer Worch; Katherine K Matthay; Robert Goldsby; John Neuhaus; Daniel C West; Steven G Dubois
Journal:  Cancer       Date:  2011-01-10       Impact factor: 6.860

6.  Treatment of adult patients with Ewing's sarcoma: compliance with chemotherapy protocols & toxicity.

Authors:  Orit Kaidar-Person; Nissim Haim; Gil Bar-Sela
Journal:  Med Oncol       Date:  2010-11-24       Impact factor: 3.064

Review 7.  Ewing tumour: incidence, prognosis and treatment options.

Authors:  M Paulussen; B Fröhlich; H Jürgens
Journal:  Paediatr Drugs       Date:  2001       Impact factor: 3.022

8.  Prognostic factors and patterns of relapse in ewing sarcoma patients treated with chemotherapy and r0 resection.

Authors:  Hubert Y Pan; Ajaykumar Morani; Wei-Lien Wang; Kenneth R Hess; Arnold C Paulino; Joseph A Ludwig; Patrick P Lin; Najat C Daw; Anita Mahajan
Journal:  Int J Radiat Oncol Biol Phys       Date:  2015-03-12       Impact factor: 7.038

Review 9.  The treatment outcome for adult patients with Ewing's sarcoma.

Authors:  Kristen N Ganjoo; Shreyaskumar Patel
Journal:  Curr Oncol Rep       Date:  2013-08       Impact factor: 5.075

10.  Diagnosis of osteosarcoma in a patient previously treated for Ewing sarcoma.

Authors:  Manabu Hoshi; Makoto Ieguchi; Kazumi Yamato; Sadao Tokimasa; Hiroaki Nakamura
Journal:  Skeletal Radiol       Date:  2014-04-11       Impact factor: 2.199

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.