dc.contributor.author |
Attarbaschi A |
|
dc.contributor.author |
Carraro E |
|
dc.contributor.author |
Abla O |
|
dc.contributor.author |
Barzilai-Birenboim S |
|
dc.contributor.author |
Bomken S |
|
dc.contributor.author |
Brugieres L |
|
dc.contributor.author |
Bubanska E |
|
dc.contributor.author |
Burkhardt B |
|
dc.contributor.author |
Chiang AK |
|
dc.contributor.author |
Csóka, Monika |
|
dc.contributor.author |
Fedorova A |
|
dc.contributor.author |
Jazbec J |
|
dc.contributor.author |
Kabickova E |
|
dc.contributor.author |
Krenova Z |
|
dc.contributor.author |
Lazic J |
|
dc.contributor.author |
Loeffen J |
|
dc.contributor.author |
Mann G |
|
dc.contributor.author |
Niggli F |
|
dc.contributor.author |
Miakova N |
|
dc.contributor.author |
Osumi T |
|
dc.contributor.author |
Ronceray L |
|
dc.contributor.author |
Uyttebroeck A |
|
dc.contributor.author |
Williams D |
|
dc.contributor.author |
Woessmann W |
|
dc.contributor.author |
Wrobel G |
|
dc.contributor.author |
Pillon M |
|
dc.contributor.author |
European Intergroup for Childhood Non-Hodgkin Lymphoma (EICNHL) |
|
dc.contributor.author |
The International Berlin-Frankfur t-Münster (i-BFM) Study Group |
|
dc.contributor.author |
The International Berlin-Frankfur t-Münster (i-BFM) Study Group |
|
dc.contributor.author |
The International Berlin-Frankfur t-Münster (i-BFM) Study Group |
|
dc.date.accessioned |
2017-06-19T08:54:23Z |
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dc.date.available |
2017-06-19T08:54:23Z |
|
dc.date.issued |
2016 |
|
dc.identifier |
85002412781 |
|
dc.identifier.citation |
pagination=1581-1591;
journalVolume=101;
journalIssueNumber=12;
journalTitle=HAEMATOLOGICA; |
|
dc.identifier.uri |
http://repo.lib.semmelweis.hu//handle/123456789/4276 |
|
dc.identifier.uri |
doi:10.3324/haematol.2016.147116 |
|
dc.description.abstract |
Children and adolescents with pre-existing conditions such as DNA repair defects or other primary immunodeficiencies have an increased risk of non-Hodgkin lymphoma. However, large-scale data on patients with non-Hodgkin lymphoma and their entire spectrum of pre-existing conditions are scarce. A retrospective multinational study was conducted by means of questionnaires sent out to the national study groups or centers, by the two largest consortia in childhood non-Hodgkin lymphoma, the European Intergroup for Childhood non-Hodgkin Lymphoma, and the international Berlin-Frankfurt-Munster Study Group. The study identified 213 patients with non-Hodgkin lymphoma and a pre-existing condition. Four subcategories were established: a) cancer predisposition syndromes (n=124, 58%); b) primary immunodeficiencies not further specified (n=27, 13%); c) genetic diseases with no increased cancer risk (n=40, 19%); and d) non-classifiable conditions (n=22, 10%). Seventy-nine of 124 (64%) cancer predispositions were reported in groups with more than 20 patients: ataxia telangiectasia (n=32), Nijmegen breakage syndrome (n=26), constitutional mismatch repair deficiency (n=21). For the 151 patients with a known cancer risk, 5-year event-free survival and overall survival rates were 40%+/-4% and 51%+/-4%, respectively. Five-year cumulative incidences of progression/relapse and treatment-related death as a first event were 22%+/-4% and 24%+/-4%, respectively. Ten-year incidence of second malignancy was 24%+/-5% and 7-year overall survival of the 21 patients with a second malignancy was 41%+/-11%. Patients with non-Hodgkin lymphoma and pre-existing conditions have an inferior survival rate with a large proportion of therapy-related deaths compared to patients with non-Hodgkin lymphoma and no pre-existing conditions. They may require special vigilance when receiving standard or modified/reduced-intensity chemotherapy or when undergoing allogeneic stem cell transplantation. |
|
dc.relation.ispartof |
urn:issn:0390-6078 |
|
dc.title |
Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents |
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dc.type |
Journal Article |
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dc.date.updated |
2017-04-05T12:04:30Z |
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dc.language.rfc3066 |
en |
|
dc.identifier.mtmt |
3161298 |
|
dc.identifier.wos |
000392584400018 |
|
dc.identifier.pubmed |
27515251 |
|
dc.contributor.department |
SE/AOK/K/II. Sz. Gyermekgyógyászati Klinika |
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dc.contributor.institution |
Semmelweis Egyetem |
|
dc.mtmt.swordnote |
Dr. Csóka Monika nyilatkozom, hogy az alábbi közleményben szerzőként szerepelek. A közlemény tudományos együttműködés keretében született (nem study és nem szponzorált vizsgálat) és mind a mintagyűjtésben, mintafeldolgozásban, mind pedig a közleményhez szükséges adatfeldolgozásban és elemzésben aktív szerepem volt. 2017.01.30. |
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