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NCT03526822Recruiting

Prospective Cohort of Patients With Newly Diagnosed Glioblastoma: Analysis of MMP2 and MMP9 Expression and Correlation to Neuro-imaging Features.

Source: ClinicalTrials.gov · Last updated 28 Jan 2026

Brief summary (registry, in English)

Glioblastoma is the most frequent and aggressive primary brain tumor in adults. A team recently showed that baseline plasma levels of matrix metalloproteinase-2 (MMP2) and matrix metalloproteinase-9 (MMP9) were correlated to bevacizumab activity in patients with recurrent glioblastoma. To date, the biological rationale of this results remains unknown but MMP2 could be involved in classical angiogenesis while MMP9 could promote vasculogenesis. The objectives are to correlate the plasma levels of MMP2 and MMP9 to their Ribonucleic acid (RNA) and protein tissue expression, activity and to patient neuro-imaging features. To analyze the changes of MMP2 and MMP9 plasma levels during peri-operative period and after radio-chemotherapy. Methods: Plasmatic levels of MMP2, MMP9, vascular endothelial growth factor-A (VEGFA), vascular endothelial growth factor-R2 (VEGFR2), stromal cell-derived factor 1 (SDF1) and chemokine receptor-4 (CXCR4) will be analyzed by enzyme-linked immunosorbent assay (ELISA) in pre-, post-operative period, before radiotherapy, before adjuvant temozolomide and at relapse in newly diagnosed glioblastoma. RNA expression of these factors will be analyzed by reverse transcription-Polymerase chain reaction (RT-qPCR) on frozen tumor samples, whereas protein expression will be analyzed by ELISA and immunohistochemistry. Enzymatic activity of MMP2 and MMP9 will be analyzed by zymography. Tumor volume, infiltration and perfusion degrees will be analyzed on Magnetic Resonance Imaging (MRI) performed before and after surgery and before adjuvant temozolomide. Neuro-imaging characteristics will be correlated to plasma and tissue expressions of these factors. The expected results are to better define the expression profile of MMP2, MMP9 and the change in their plasma level during treatment, a prerequisite for their clinical use.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
100 (estimated)
First submitted
4 May 2018
Start date
2 Jul 2018
Primary completion date
1 Jan 2028
Lead sponsor
Assistance Publique Hopitaux De Marseille
Diseases
Glioblastoma
NCT number
NCT03526822

What you commit to

  • Study type: Interventional
  • Planned participants: 100
  • From 2 Jul 2018 to the primary completion date, 1 Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of radiotherapy and / or chemotherapy for this lesion

Age

  • Person in emergency situation, a legal person of legal age (guardianship, guardianship or legal guardianship), or unable to express his or her consent

Other

  • Existence of a contraindication to the MRI
  • Nonoperable lesion
  • Scalability of a low grade lesion
  • No affiliation to a social security scheme (beneficiary or beneficiary)
  • Pregnant or lactating woman

Who the study is looking for

  • Patient, male or female, aged 18 years or over
  • Imaging suggestive of glioblastoma
  • Patient eligible for excision surgery (partial, subtotal or macroscopically complete)
  • Candidate for concomitant and adjuvant radiotherapy chemotherapy (Stupp protocol)
  • Patient having signed an informed consent
  • Patient having undergone a preoperative MRI

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Assistance Publique Hôpitaux de Marseille
Coordinator of this site? Confirm its status
MarseilleFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.