[PNET/Ewing tumours: current treatments and future perspectives].

Abstract:

:Ewing tumours are characterised as tumours consisting of small, blue, round malignant cells that may exhibit varying degrees of neural differentiation. Most of them arise in bony sites, and they represent the second commonest primary osseous malignancy in and adolescence and young adults. During the past 30 years, chemotherapy has increased survival from less than 5% to 65-70% in localized tumours and to 25-30% in primary metastatic tumours. Surgery is a major tool, whereas advances in imaging techniques have improved treatment indication and optimization. Radiotherapy remains useful, either alone or in addition to surgery, and new techniques (conformational RT and IMRT) will reduce short-term toxic effects. However, long-term toxic effects are also of major concern. Clinical and biological prognostic factors has been clearly identified and should guide the therapeutic choice for these patients. The metastatic Ewing tumours are of extremely poor prognosis, and impose the development of new therapeutic agents. This article is a review of the data available in 2009 concerning Ewing's sarcoma either as biologic aspects or as therapeutic aspects.

journal_name

Bull Cancer

journal_title

Bulletin du cancer

authors

Marec-Bérard P,Chotel F,Claude L

doi

10.1684/bdc.2010.1120

subject

Has Abstract

pub_date

2010-06-01 00:00:00

pages

707-13

issue

6

eissn

0007-4551

issn

1769-6917

pii

S0007-4551(15)30834-1

journal_volume

97

pub_type

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  • [What's new in the treatment of cancer pain?].

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  • [The value of MRI in the diagnosis of joint involvement in malignant primitive tumors of the knee].

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