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@ARTICLE{Kotecha:1052252,
author = {Kotecha, Rupesh and Akdemir, Eyub Y and Kutuk, Tugce and
Ilgın, Can and Ahluwalia, Manmeet S and Bi, Wenya L and
Blakeley, Jaishri and Dixit, Karan S and Dunn, Ian F and
Galanis, Evanthia and Galldiks, Norbert and Huang, Raymond Y
and Johnson, Derek R and Kaley, Thomas J and Kamson, David O
and Kurz, Sylvia C and McDermott, Michael W and Odia, Yazmin
and Preusser, Matthias and Raizer, Jeffrey and Reardon,
David A and Rogers, C Leland and Ruda, Roberta and Schiff,
David and Vogelbaum, Michael A and Weller, Michael and Wen,
Patrick Y and Mehta, Minesh P},
title = {{B}enchmarking the efficacy of salvage systemic therapies
for recurrent meningioma: {A} {RANO} group systematic review
and meta-analysis to guide clinical trial design},
journal = {Neuro-Oncology},
volume = {27},
number = {7},
issn = {1522-8517},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {FZJ-2026-00869},
pages = {1670 - 1685},
year = {2025},
note = {Neuro Oncol . 2025 Sep 8;27(7):1670-1685.Funding: none
declared},
abstract = {Background. Despite advances in our understanding of the
molecular underpinnings of meningioma progressionand
innovations in systemic and local treatments, recurrent
meningiomas remain a substantial therapeutic challenge.The
objective of this systematic review and meta-analysis is to
provide a historical baseline, contemporaryanalysis, and
propose a “rate of probable interest” to inform future
clinical trial design and development on behalfof the
Response Assessment in Neuro-Oncology meningioma
group.Methods. PubMed, ClinicalTrials.gov, and ASCOpubs
databases were screened for clinical trials evaluating
theactivity of systemic therapies for adults with recurrent
meningiomas. The pooled progression-free survival at6-months
and 1-year (PFS-6 and PFS-1 year) values were calculated
using the random effects technique withI2 indices.Results.
The pooled PFS-6 and PFS-1 year rates for recurrent WHO
grade 1 meningiomas were $43.6\%$ $(95\%$ $CI:22.7-67.0\%,$
I2 = $80\%)$ and $21.7\%$ $(95\%$ CI: $6.2-53.9\%,$ I2 =
$76\%),$ and for grades 2-3 meningiomas, the PFS-6 was
$38.0\%(95\%$ CI: $28.3-48.8\%,$ I2 = $68\%).$ In the
targeted therapy group, PFS-6 and PFS-1 year rates stood at
$62.0\%$ (I2 = $58\%)and$ $49.0\%$ (I2 = $63\%)$ for grade
1, while for grades 2-3 tumors, the PFS-6 rates with
targeted therapy and immunotherapywere $42.1\%$ (I² =
$60\%)$ and $46.0\%$ (I² = $0\%),$ respectively. The
benchmarks were set at $67\%$ and $54\%$ for PFS-6and PFS-1
year for grade 1 tumors, and PFS-6 of $49\%$ for grades 2-3
tumors.Conclusions. Several studies have reported outcomes
in patients with recurrent meningiomas testing a variety
ofagents with modest, but variable and progressively
increasing activity. In this context, we recommend new
benchmarksfor future trials to define efficacy of future
investigational therapies.},
cin = {INM-3},
ddc = {610},
cid = {I:(DE-Juel1)INM-3-20090406},
pnm = {5252 - Brain Dysfunction and Plasticity (POF4-525)},
pid = {G:(DE-HGF)POF4-5252},
typ = {PUB:(DE-HGF)16},
doi = {10.1093/neuonc/noaf009},
url = {https://juser.fz-juelich.de/record/1052252},
}