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@ARTICLE{Kalish:293613,
author = {J. M. Kalish and K. D. Becktell and G. Bougeard and G. M.
Brodeur and L. R. Diller and A. S. Doria and J. R. Hansford
and S. D. Klein and W. K. Kohlmann and C. P. Kratz and S. P.
MacFarland and K. Pajtler$^*$ and S. P. Rednam and J.
Schienda and L. J. States and A. Villani and R. Weksberg and
K. Zelley and G. E. Tomlinson and J. J. Brzezinski},
title = {{U}pdate on surveillance for {W}ilms tumor and
hepatoblastoma in {B}eckwith-{W}iedemann {S}yndrome and
other predisposition syndromes.},
journal = {Clinical cancer research},
volume = {30},
number = {23},
issn = {1078-0432},
address = {Philadelphia, Pa. [u.a.]},
publisher = {AACR},
reportid = {DKFZ-2024-01929},
pages = {5260-5269},
year = {2024},
note = {2024 Dec 2;30(23):5260-5269},
abstract = {Wilms tumors are commonly associated with predisposition
syndromes many, but not all, of which include overgrowth.
Several of these syndromes also include a risk of other
embryonal malignancies - particularly hepatoblastoma.
Guidelines for surveillance in this population were
published in 2017 and recently members of the AACR Pediatric
Cancer Working Group met to update those guidelines with a
review of more recently published evidence and risk
estimates. This perspective serves to update pediatric
oncologists, geneticists, radiologists, counselors and other
healthcare professionals on revised diagnostic criteria,
review previously published surveillance guidelines and
harmonize updated surveillance recommendations in the North
American and Australian context for patients with overgrowth
syndromes and other syndromes associated with Wilms tumor
predisposition.},
subtyp = {Review Article},
cin = {B062 / HD01},
ddc = {610},
cid = {I:(DE-He78)B062-20160331 / I:(DE-He78)HD01-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39320341},
doi = {10.1158/1078-0432.CCR-24-2100},
url = {https://inrepo02.dkfz.de/record/293613},
}