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@ARTICLE{Lindsay:180837,
author = {H. B. Lindsay and M. Massimino and S. Avula and S. Stivaros
and R. Grundy and K. Metrock and A. Bhatia and A.
Fernández-Teijeiro and L. Chiapparini and J. Bennett and K.
Wright and L. M. Hoffman and A. Smith and K. Pajtler$^*$ and
T. Y. Poussaint and K. E. Warren and N. K. Foreman and D. M.
Mirsky},
title = {{R}esponse assessment in paediatric intracranial
ependymoma: recommendations from the {R}esponse {A}ssessment
in {P}ediatric {N}euro-{O}ncology ({RAPNO}) working group.},
journal = {The lancet / Oncology},
volume = {23},
number = {8},
issn = {1470-2045},
address = {London},
publisher = {The Lancet Publ. Group},
reportid = {DKFZ-2022-01586},
pages = {e393-e401},
year = {2022},
note = {2022 Aug;23(8):e393-e401},
abstract = {Response criteria for paediatric intracranial ependymoma
vary historically and across different international
cooperative groups. The Response Assessment in the Pediatric
Neuro-Oncology (RAPNO) working group, consisting of an
international panel of paediatric and adult
neuro-oncologists, neuro-radiologists, radiation
oncologists, and neurosurgeons, was established to address
both the issues and the unique challenges in assessing the
response in children with CNS tumours. We established a
subcommittee to develop response assessment criteria for
paediatric ependymoma. Current practice and literature were
reviewed to identify major challenges in assessing the
response of paediatric ependymoma to clinical trial therapy.
For areas in which data were scarce or unavailable,
consensus was reached through an iterative process. RAPNO
response assessment recommendations include assessing
disease response on the basis of changes in tumour volume,
and using event-free survival as a study endpoint for
patients entering clinical trials without bulky disease. Our
recommendations for response assessment include the use of
brain and spine MRI, cerebral spinal fluid cytology,
neurological examination, and steroid use. Baseline
postoperative imaging to assess for residual tumour should
be obtained 24-48 h after surgery. Our consensus
recommendations and response definitions should be
prospectively validated in clinical trials.},
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:35901835},
doi = {10.1016/S1470-2045(22)00222-4},
url = {https://inrepo02.dkfz.de/record/180837},
}