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@ARTICLE{Thomas:298170,
author = {M. Thomas and P. Christopoulos$^*$ and W. T. Iams and J.
Mazières and A. B. Cortot and N. Peled and G. Minuti and E.
F. Smit and F. Audhuy and K. Berghoff and S. P. Eggleton and
F. Fries and M. Hildenbrand and P. Liu and S. H. Mahmoudpour
and C. Menzel and D. Oksen},
title = {{MOMENT} registry: {P}atients with advanced non-small-cell
lung cancer harboring {MET} exon 14 skipping treated with
systemic therapy.},
journal = {Journal of Comparative Effectiveness Research},
volume = {14},
number = {2},
issn = {2042-6305},
address = {Royston, UK},
publisher = {Becaris Publishing},
reportid = {DKFZ-2025-00189},
pages = {e240127},
year = {2025},
note = {2025 Feb;14(2):e240127},
abstract = {Aim: MET exon 14 (METex14) skipping occurs in $3-4\%$ of
non-small-cell lung cancer (NSCLC) cases. Low frequency of
this alteration necessitated open-label, single-arm trials
to investigate MET inhibitors. Since broad MET biomarker
testing was only recently introduced in many countries,
there is a lack of historical real-world data from patients
with METex14 skipping NSCLC receiving conventional
therapies. Given the rarity of this population and
limitations of existing real-world data sources, the MOMENT
registry aims to prospectively collect uniform,
comprehensive, high-quality data from patients with METex14
skipping advanced NSCLC treated in routine clinical
practice, which can support clinical and regulatory decision
making. Patients $\&$ methods: MOMENT is a multinational,
non-interventional disease registry collecting data on
patients with METex14 skipping advanced NSCLC receiving any
systemic anticancer therapy. Newly diagnosed patients and
those already receiving treatment are eligible. Patients
with previous participation in a clinical trial can be
included if they receive at least one subsequent therapy
line in a routine clinical setting. Eligible systemic
treatment includes all available anticancer therapies
(approved, conditionally approved or provided through Early
Access). Data collection includes biomarker testing results,
demographics, baseline clinical characteristics, treatment
details and effectiveness, safety information and imaging.
Registry site inclusion is dependent on confirmation that
local METex14 skipping detection methods are sufficient to
confirm METex14 skipping status. MOMENT is currently active
at more than 60 sites across Europe and North America and
approximately 700 patients are expected to be enrolled
within the next 4 years. The first patient was enrolled on 4
October 2022. After completion of data collection, MOMENT
data can be shared with external parties to conduct
non-interventional studies. Discussion/conclusion: The
MOMENT registry collects comprehensive, high-quality
real-world data from patients with METex14 skipping advanced
NSCLC receiving systemic anticancer treatment in a routine
clinical setting, to enable future studies informing
regulatory decisions and optimal care for this rare
population. Clinical Trial Registration: NCT05376891
(ClinicalTrials.gov); EUPAS47602 (EU PAS register no.).},
keywords = {METex14 skipping (Other) / NSCLC (Other) / cancer registry
(Other) / real-world data (Other) / targeted therapy
(Other)},
cin = {B063},
ddc = {610},
cid = {I:(DE-He78)B063-20160331},
pnm = {312 - Funktionelle und strukturelle Genomforschung
(POF4-312)},
pid = {G:(DE-HGF)POF4-312},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:39836056},
doi = {DOI:10.57264/cer-2024-0127},
url = {https://inrepo02.dkfz.de/record/298170},
}