RecruitingPhase 2NCT06275919

Regorafenib for Recurrent Meningioma (MIRAGE Trial)

Regorafenib for Recurrent Meningioma. A Multicenter, Randomized Phase II Study (MIRAGE Trial)


Sponsor

Istituto Oncologico Veneto IRCCS

Enrollment

104 participants

Start Date

Sep 23, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The focus of this study will be to investigate whether Regorafenib demonstrates antitumor activity against recurrent meningiomas. Small trials and case series suggest clinical relevant activity of several VEGF inhibitors such as sunitinib, bevacizumab and valatinib reporting a 6m-PFS rate of 42-64%. Indeed, VEGF and VEGF receptors (VEGFR) are regularly overexpressed in meningiomas and can correlate with outcome. Regorafenib inhibits angiogenic receptor tyrosine kinases (RTKs) and is highly selective for VEGFR1/2/3; moreover Regorafenib inhibits PDGFRB, FGFR1 and oncogenic intracellular signalling cascades involving c-RAF/RAF1 and BRAF highly expressed in meningiomas. Noteworthy, Regorafenib showed antitumor activity in vitro and in vivo in a recent study; indeed, Regorafenib showed significant inhibition of meningioma cell motility and invasion and in vivo, mice with orthotopic meningioma xenografts showed a reduced volume of signal enhancement in MRI following Regorafenib therapy; this translated in a significantly increased overall survival time (p\<0.05) for Regorafenib treated mice. Moreover, Regorafenib showed good efficacy in different cancer types, such as colorectal cancer, GIST, hepatocellular carcinoma and glioblastoma (REGOMA trial) , maintainingmaintaining a good quality of life.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Local Standard of Care and a drug called Regorafenib 40 MG Oral Tablet for people with meningioma, malignant. The study is currently recruiting participants at 17 locations.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRegorafenib 40 MG Oral Tablet

REGORAFENIB 40 mg tablets once daily (160 mg/die), 3 weeks on, 1 week off, until disease progression or unacceptable toxicity

DRUGLocal Standard of Care

In this setting there are not drugs with indication. Every site will treat patients as per their experience.


Locations(17)

IRST Istituto Romagnolo per lo Studio dei Tumori "Dino Amadori"

Meldola, Forlì-Cesena, Italy

Azienda Ospedaliera Universitaria Gaetano Martino

Messina, Italia/Messina, Italy

Humanitas Cancer Center

Rozzano, Milano, Italy

A.O.U. Policlinico di Bari

Bari, Italy

Ospedale San Paolo

Bari, Italy

Ospedale Bellaria - AUSL Bologna

Bologna, Italy

Azienda Ospedaliero Universitaria Careggi

Florence, Italy

Policlinico San Martino

Genova, Italy

Spedali Riuniti

Livorno, Italy

Fondazione IRCCS Istituto Neurologico Carlo Besta

Milan, Italy

IRCCS Ospedale San Raffaele

Milan, Italy

Ospedale del Mare

Naples, Italy

Istituto Oncologico Veneto

Padova, Italy

Fondazione Policlinico Universitario Agostino Gemelli IRCCS

Roma, Italy

IRCCS Istituto Tumori Regina Elena

Roma, Italy

Policlinico Umberto I - Università Sapienza Roma

Roma, Italy

A.O.U. Città della Salute e della Scienza di Torino

Torino, Italy

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NCT06275919


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