LIQUID BIOPSY IN Low-grade Glioma Patients

NCT ID: NCT05133154

Last Updated: 2025-07-11

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-12-15
• Study Completion Date: 2025-07-01

Brief Summary

Diffuse low-grade gliomas (DLGG) (or WHO grade II gliomas) are rare tumors, with an incidence estimated at 1/105 person-year. DLGG are characterized by a continuous growth and an unavoidable anaplastic transformation. DLGG malignant progression is classically characterized by a continuum, from grade II to grade III or IV tumors.

To date, the histomolecular diagnosis of lower grade gliomas (that is, grade II and III gliomas) is achieved on tumor samples obtained from surgical resection or biopsy. Indeed, whereas brain MRI is often suggestive of DLGG, there is a need for a histological confirmation of diagnosis prior to any medical treatment. Moreover, MRI features to not always accurately predict the tumor grade, with grade II tumor presenting with contrast enhancement or non-enhancing authentic grade III tumors.

In this setting, the value of liquid biopsy (in blood or cerebrospinal fluid CSF) as a non-invasive, disease-associated biomarker has gained interest in the past decade, either at tumor diagnosis or to monitor tumor evolution in order to guide patient management and to detect changes of molecular features over time. While extracranial metastasis of glioma rarely occurs, recent reports suggest the possible presence of circulating tumor cells (CTCs) in blood of high-grade glioma patients. Beside CTCs, other circulating biomarkers have been recently investigated in glioma, including circulating tumor DNA, microRNA or tumor-educated platelet (TEP) RNA. Some of these techniques allow genome-wide characterization of RNA/DNA contents.

However, these studies are all small exploratory studies that have mainly included glioblastoma (grade IV glioma) patients rather than lower-grade gliomas, or glioma patients with no precision on tumor grade. Moreover, some of these studies analyzed samples performed after the patient received a medical oncological treatment (chemotherapy or radiation therapy). They advocate for the search of a circulating signature that would not be restricted to biomarkers directly derived from the tumor but include markers induced at a distance by the tumor. Indeed, slow-growing DLGG are likely to induce a systemic reaction to allow, for many years, an immuno-tolerance of the tumor. This reaction could have an impact on peripheral blood cells, including their RNA content.

In this study, the investigators aim at conducting an exploratory study in DLGG patients to explore the value of several blood-based biomarkers for the disease diagnosis and/or monitoring.

Detailed Description

This study is a prospective, exploratory and bi-centric study.

The primary objective is to evaluate the presence of CTCs in a preoperative sample for the 3 following groups : patients with low-grade glioma, patients with high-grade glioma and patients undergoing neurosurgery for a non-tumor disease.

Visits in this study are as follows :

Inclusion Visit (V0) : 2 days (+/- 2 days) before brain surgery

Postoperative visits :

• Visit 1: 2 days (+/- 2 days) following brain surgery
• Visit 2: 3 months (+/- 1 month) following brain surgery

Conditions

Glioma

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Patients with low-grade glioma

Group 1

Group Type: OTHER

Blood samples

Intervention Type: BIOLOGICAL

In total, about 20 ml of blood will be collected on EDTA tubes : collection of CTCs, TEPs and biobanking (V0, V1 and V2)

Patients with high-grade glioma

Group 2

Group Type: OTHER

Blood samples

Intervention Type: BIOLOGICAL

In total, about 20 ml of blood will be collected on EDTA tubes : collection of CTCs, TEPs and biobanking (V0, V1 and V2)

Patients undergoing brain surgery for a non-tumor disease

Group 3

Group Type: OTHER

Blood samples

Intervention Type: BIOLOGICAL

In total, about 20 ml of blood will be collected on EDTA tubes : collection of CTCs, TEPs and biobanking (V0, V1 and V2)

Interventions

Blood samples

In total, about 20 ml of blood will be collected on EDTA tubes : collection of CTCs, TEPs and biobanking (V0, V1 and V2)

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Adult patient aged ≥ 18, no age limit
• A signed informed consent obtained before any study specific procedures
• Patient affiliated to a French social security system
• Patient ability to understand experimental procedures
• Patient able to speak, read and understand French

• Brain surgery for a suspected low-grade tumor, histologically confirmed on tumor sample

• Brain surgery for a suspected high-grade glioma, histologically confirmed on tumor sample

• Brain surgery for a non-tumor disease (cavernoma, arteriovenous malformation)

Exclusion Criteria

• Legal incapacity or physical, psychological social or geographical status interfering with the patient's ability to sign the informed consent or to terminate the study
• Pregnant and/or breastfeeding women (this will be checked in declarative way)
• Patients with medical history of cancer other than the brain tumor, whatever the treatment received

• Previous chemotherapy or radiation therapy for the low-grade glioma (but previous surgery/ies is/are allowed)
• No indication for chemotherapy for 6 month after surgery

• Previous chemotherapy or radiation therapy for the glioma

• Diagnosis or suspicion of primary or secondary brain tumor

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Montpellier

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Catherine PANABIERES, MCU-PH, Ph.D.

Role: STUDY_DIRECTOR

University Hospital, Montpellier

Locations

University Hospital, Montpellier

Montpellier, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Catherine PANABIERES, MCU-PH, Ph.D.

Role: CONTACT

c-panabieres@chu-montpellier.fr

04 11 75 99 31 ext. +33

Hugues DUFFAU, PU-PH

Role: CONTACT

h-duffau@chu-montpellier.fr

04 67 33 66 12 ext. +33

Facility Contacts

Hugues DUFFAU, PU-PH

Role: primary

Other Identifiers

2021-A00584-37

Identifier Type: OTHER

Identifier Source: secondary_id

RECHMPL20_0671

Identifier Type: -

Identifier Source: org_study_id