Frequency of Certain Established Risk Factors in Soft Tissue Sarcomas in Adults: A Prospective Descriptive Study of 658 Cases
Identifieur interne : 000423 ( France/Analysis ); précédent : 000422; suivant : 000424Frequency of Certain Established Risk Factors in Soft Tissue Sarcomas in Adults: A Prospective Descriptive Study of 658 Cases
Auteurs : Nicolas Penel [France] ; Jessica Grosjean [France] ; Yves Marie Robin [France] ; Luc Vanseymortier ; Stéphanie Clisant [France] ; Antoine Adenis [France]Source :
- Sarcoma [ 1357-714X ] ; 2008.
Abstract
Soft tissue sarcomas are rare tumours with infrequent identified aetiological factors. Several genetic syndromes as well as previous radiation therapy and/or chronic lymphoedema have been suspected to predispose to some soft tissue sarcomas. Between January 1997 and September 2005, we carried out a prospective descriptive study to estimate the frequency of some particular etiological factors among 658 patients with soft tissue sarcomas. Sarcomas associated with a clinically identified genetic disease represent 2.8% out of all cases (95%CI: 1.5–3.8%). Most of these cases (14/19) are related to Recklinghausen neurofibromatosis. Radiation-induced sarcomas represent 3.3% out of all cases (95%CI: 1.7–5.1%). Most of these cases (9/22) are related to prior breast cancer treatment. We had observed only 1 case of Stewart-Treves syndrome. Liposarcoma, the most frequent histological subtype observed, is not associated with any particular aetiological entity. Finally, most of the adult soft tissue sarcomas are not related to any classical clinically identified genetic disease or previous radiation therapy and/or chronic lymphoedema risk factors. Frequency of underlying genetic syndrome which may predispose to soft tissue sarcomas could be higher than previously reported.
Url:
DOI: 10.1155/2008/459386
PubMed: 18497869
PubMed Central: 2386887
Affiliations:
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type="old region" nuts="2">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></affiliation></author><author><name sortKey="Grosjean, Jessica" sort="Grosjean, Jessica" uniqKey="Grosjean J" first="Jessica" last="Grosjean">Jessica Grosjean</name><affiliation wicri:level="3"><nlm:aff id="I1">Département de Cancérologie Générale, Centre Oscar Lambret, 59020 Lille, France</nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Département de Cancérologie Générale, Centre Oscar Lambret, 59020 Lille</wicri:regionArea><placeName><region type="region" nuts="2">Hauts-de-France</region><region type="old region" nuts="2">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></affiliation></author><author><name sortKey="Robin, Yves Marie" sort="Robin, Yves Marie" uniqKey="Robin Y" first="Yves Marie" last="Robin">Yves Marie Robin</name><affiliation wicri:level="3"><nlm:aff id="I2">Laboratoire d'Anatomopathologie, Centre Oscar Lambret, 59020 Lille, France</nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Laboratoire d'Anatomopathologie, Centre Oscar Lambret, 59020 Lille</wicri:regionArea><placeName><region type="region" nuts="2">Hauts-de-France</region><region type="old region" nuts="2">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></affiliation></author><author><name sortKey="Vanseymortier, Luc" sort="Vanseymortier, Luc" uniqKey="Vanseymortier L" first="Luc" last="Vanseymortier">Luc Vanseymortier</name><affiliation><nlm:aff>NONE</nlm:aff></affiliation><affiliation><nlm:aff>NONE</nlm:aff></affiliation></author><author><name sortKey="Clisant, Stephanie" sort="Clisant, Stephanie" uniqKey="Clisant S" first="Stéphanie" last="Clisant">Stéphanie Clisant</name><affiliation wicri:level="3"><nlm:aff id="I4">Unité de Recherche Clinique, Centre Oscar Lambret, 59020 Lille, France</nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Unité de Recherche Clinique, Centre Oscar Lambret, 59020 Lille</wicri:regionArea><placeName><region type="region" nuts="2">Hauts-de-France</region><region type="old region" nuts="2">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></affiliation></author><author><name sortKey="Adenis, Antoine" sort="Adenis, Antoine" uniqKey="Adenis A" first="Antoine" last="Adenis">Antoine Adenis</name><affiliation wicri:level="3"><nlm:aff id="I3">Département de Cancérologie Digestive et Urologique, Centre Oscar Lambret, 59020 Lille, France</nlm:aff><country xml:lang="fr">France</country><wicri:regionArea>Département de Cancérologie Digestive et Urologique, Centre Oscar Lambret, 59020 Lille</wicri:regionArea><placeName><region type="region" nuts="2">Hauts-de-France</region><region type="old region" nuts="2">Nord-Pas-de-Calais</region><settlement type="city">Lille</settlement></placeName></affiliation></author></analytic><series><title level="j">Sarcoma</title><idno type="ISSN">1357-714X</idno><idno type="eISSN">1369-1643</idno><imprint><date when="2008">2008</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>Soft tissue sarcomas are rare tumours with infrequent identified aetiological factors. Several genetic syndromes as well as previous radiation therapy and/or chronic lymphoedema have been suspected to predispose to some soft tissue sarcomas.
Between January 1997 and September 2005, we carried out a prospective descriptive study to estimate the frequency of some particular etiological factors among 658 patients with soft tissue sarcomas.
Sarcomas associated with a clinically identified genetic disease represent 2.8% out of all cases (95%CI: 1.5–3.8%). Most of these cases (14/19) are related to Recklinghausen neurofibromatosis. Radiation-induced sarcomas represent 3.3% out of all cases (95%CI: 1.7–5.1%). Most of these cases (9/22) are related to prior breast cancer treatment. We had observed only 1 case of Stewart-Treves syndrome. Liposarcoma, the most frequent histological subtype observed, is not associated with any particular aetiological entity.
Finally, most of the adult soft tissue sarcomas are not related to any classical clinically identified genetic disease or previous radiation therapy and/or chronic lymphoedema risk factors. Frequency of underlying genetic syndrome which may predispose to soft tissue sarcomas could be higher than previously reported.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Zahm, Sh" uniqKey="Zahm S">SH Zahm</name></author><author><name sortKey="Fraumeni, Jf" uniqKey="Fraumeni J">JF Fraumeni</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Levi, F" uniqKey="Levi F">F Levi</name></author><author><name sortKey="La Vecchia, C" uniqKey="La Vecchia C">C La Vecchia</name></author><author><name sortKey="Randimbison, L" uniqKey="Randimbison L">L Randimbison</name></author><author><name sortKey="Te, V C" uniqKey="Te V">V-C Te</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Coindre, J M" uniqKey="Coindre J">J-M Coindre</name></author><author><name sortKey="Terrier, P" uniqKey="Terrier P">P Terrier</name></author><author><name sortKey="Guillou, L" uniqKey="Guillou L">L 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first="Stéphanie" last="Clisant">Stéphanie Clisant</name><name sortKey="Grosjean, Jessica" sort="Grosjean, Jessica" uniqKey="Grosjean J" first="Jessica" last="Grosjean">Jessica Grosjean</name><name sortKey="Robin, Yves Marie" sort="Robin, Yves Marie" uniqKey="Robin Y" first="Yves Marie" last="Robin">Yves Marie Robin</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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|étape= Analysis
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|texte= Frequency of Certain Established Risk Factors in Soft Tissue Sarcomas in Adults: A Prospective Descriptive Study of 658 Cases
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