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Plasma Extracellular Vesicles in Meningioma Patients

Plasma Extracellular Vesicles in Meningioma Patients Following Radiotherapy as Liquid Biopsy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06104930
Acronym
MOLI
Enrollment
60
Registered
2023-10-27
Start date
2023-11-01
Completion date
2028-02-01
Last updated
2026-03-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Meningioma

Brief summary

While surgical resection remains the primary treatment approach for symptomatic or growing meningiomas, radiotherapy represents an auspicious alternative in patients with meningiomas not safely amenable to surgery. Biopsies are often omitted in light of potential postoperative neurological deficits, resulting in a lack of histological grading and (molecular) risk stratification. In this prospective explorative biomarker study, extracellular vesicles in the bloodstream will be investigated in patients with macroscopic meningiomas to identify a biomarker for molecular risk stratification and disease monitoring.

Detailed description

In total, 60 patients with meningiomas and an indication of radiotherapy (RT) and macroscopic tumor on the planning MRI will be enrolled. Blood samples will be obtained before the start, during, and after radiotherapy, as well as during clinical follow-up every 6 months. Extracellular vesicles will be isolated from the blood samples, quantified and correlated with the clinical treatment response or progression. Further, nanopore sequencing-based DNA methylation profiles of plasma EV-DNA will be generated for methylation-based meningioma classification. This study will explore the dynamic of plasma EVs in meningioma patients under/after radiotherapy, with the objective of identifying potential biomarkers of (early) tumor progression. DNA methylation profiling of plasma EVs in meningioma patients may enable molecular risk stratification, facilitating a molecularly-guided clinical management in meningioma patients in the future.

Interventions

OTHERExplorative biomarker study

Analysis of blood biomarker

Sponsors

University Hospital Heidelberg
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Prospective Explorative Biomarker Study / Investigator-Initiated Trial

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* confirmed meningioma (histologically or MRI/DOTATOC-PET CT) * macroscopic tumor in MRI (either as definitive RT, or following subtotal resection or relapse) * indication for radiotherapy * completed wound healing after surgical intervention) * Alter ≥ 18 Jahre * Karnofsky Performance Score ≥ 60% * written informed consent * ability of subject to understand character and individual consequences of the trial * adequate contraception for women of childbearing potential

Exclusion criteria

* previous or known tumor diseases \< 5 years ago * previous (cerebral) radiotherapy * simultaneous chemo/immunotherapy * evidence that the patient cannot adhere to the study protocol (e.g., non-compliance) * the refusal of patients to participate in the study * participation in another clinical study or observation period in a competing trial

Design outcomes

Primary

MeasureTime frameDescription
dynamic of plasma EVsuntil 2 years follwoing radiotherapyChange of amount of plasma EVs in meningioma patients compared to sample taken before radiotherapy

Secondary

MeasureTime frameDescription
progession-fee survivaluntil 2 years follwoing radiotherapynumber of patients without tumor progress
overall survivaluntil 2 years follwoing radiotherapynumber of alive patients

Countries

Germany

Contacts

CONTACTMax Deng, MD
maximilian.deng@med.uni-heidelberg.de+496221 56
CONTACTAdriane Lentz-Hommertgen, PhD
adriane.lentz-hommertgen@med.uni-heidelberg.de+496221 56

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026