% IMPORTANT: The following is UTF-8 encoded. This means that in the presence
% of non-ASCII characters, it will not work with BibTeX 0.99 or older.
% Instead, you should use an up-to-date BibTeX implementation like “bibtex8” or
% “biber”.
@ARTICLE{Slavc:182306,
author = {I. Slavc and L. Mayr and N. Stepien and J. Gojo and M.
Aliotti Lippolis and A. A. Azizi and M. Chocholous and A.
Baumgartner and C. S. Hedrich and S. Holm and A. Sehested
and P. Leblond and K. Dieckmann and C. Haberler and T. Czech
and M. Kool$^*$ and A. Peyrl},
title = {{I}mproved {L}ong-{T}erm {S}urvival of {P}atients with
{R}ecurrent {M}edulloblastoma {T}reated with a
'{MEMMAT}-like' {M}etronomic {A}ntiangiogenic {A}pproach.},
journal = {Cancers},
volume = {14},
number = {20},
issn = {2072-6694},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2022-02563},
pages = {5128},
year = {2022},
abstract = {Medulloblastoma (MB) recurrence is usually incurable
despite intensive therapy including high-dose chemotherapy.
An evolving alternative approach to conventional
chemotherapy aims at interfering with tumor angiogenesis at
different levels. We report on a novel combinatorial
metronomic antiangiogenic approach. The study is a
retrospective observational study of 29 consecutive patients
with first or multiple recurrences prospectively treated
according to the MEMMAT strategy ('MEMMAT-like') before the
formal protocol (MEMMAT; ClinicalTrials.gov Identifier:
NCT01356290) started. The study period was 11/2006 to
06/2016. Treatment consisted of daily oral thalidomide,
fenofibrate, celecoxib, and alternating 21-day cycles of
low-dose oral etoposide and cyclophosphamide supplemented by
IV bevacizumab and intraventricular therapy consisting of
alternating etoposide and liposomal cytarabine. Median
overall survival (OS) after recurrence for the whole group
was 29.5 months, OS was 48.3 ± $9.3\%$ at three years and
34.5 ± $8.8\%$ at five years, and progression-free survival
was 42.0 ± $9.5\%$ at three years and 29.4 ± $9\%$ at five
years. As of 07/2022, 9/29 patients are alive 86 to 164
months after the recurrence that prompted the 'MEMMAT-like'
therapy. Treatment was primarily out-patient and generally
well-tolerated. Toxicities did occur but were manageable. In
conclusion, antiangiogenic therapy according to the MEMMAT
strategy increased median OS of patients with recurrent MB
and may lead to long-term survival. Adherence to the
protocol, including intraventricular therapy, appears
important.},
keywords = {MEMMAT (Other) / antiangiogenic therapy (Other) /
bevacizumab (Other) / intraventricular therapy (Other) /
low-dose oral therapy (Other) / medulloblastoma recurrence
(Other) / metronomic therapy (Other)},
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:36291912},
doi = {10.3390/cancers14205128},
url = {https://inrepo02.dkfz.de/record/182306},
}