RecruitingNot ApplicableNCT04109131

A Brain Metastases Research Platform to Tackle the Challenge of CNS Metastases in Solid Tumours

A Brain Metastases Research Platform to Tackle the Challenge of CNS Metastases in Solid Tumours - BrainStorm Program


Sponsor

Jules Bordet Institute

Enrollment

600 participants

Start Date

Jul 1, 2020

Study Type

INTERVENTIONAL

Conditions

Summary

Despite some encouraging data, systemic treatment of CNS metastases from solid tumors remains experimental. Better knowledge on the evolving epidemiology and biology of BM are key elements for the development of new treatment strategies and identification of promising therapeutic targets for new compounds. Further biological findings may help to better understand the heterogeneity between the primary tumor and the CNS metastases and to identify new targets for therapy thus improving patients' outcome. In this context, the Oncodistinct network and the Jules Bordet institute propose to build a multidisciplinary Brain Metastases Clinical Research Platform called BrainStorm. The BrainStorm program will focus on patients with newly diagnosed non-CNS metastatic solid tumors with high risk of developing CNS metastases and will allow building a large clinico pathological database for CNS metastases including ctDNA analyzes from CSF samples. Substudies will be proposed at each time-period with the final objective to develop innovative treatment approaches and strategies.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is building a research platform to better understand how cancers spread to the brain (called brain metastases) in people with breast cancer, lung cancer, melanoma, and other solid tumours. It tracks patients over time using scans, fluid samples, and tumour tissue to guide future treatments. **You may be eligible if...** - You are 18 years old or older - You have one of these cancers: triple-negative breast cancer, HER2-positive breast cancer, non-small cell lung cancer, small cell lung cancer, melanoma, another solid tumour, or confirmed cancer spread to the brain lining (leptomeningeal disease) - You have tumour tissue available for testing - Your expected survival is more than 3 months **You may NOT be eligible if...** - You do not have tumour tissue available for research testing - You are pregnant (without a negative test result) Talk to your doctor to see if this trial is right for you.

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

OTHERSamples collection: Plasma

At baseline Part A: * TNBC/ HER2+ BC: once a year * NSCLC/SCLC: every 4 months * Melanoma: every 6 months Part B: o As close as possible to the diagnosis of CNS metastases and no later than 6 weeks after diagnosis Part C: o Every 3 months (+/- 1 month)

OTHERSamples collection: CSF

Part B: Mandatory CSF sampling at CNS diagnosis when clinically possible unless medically contra-indicated - As close as possible to the diagnosis of CNS metastases and no later than 6 weeks after diagnosis Part C: Additional CSF sampling in case CSF sampling is performed for routine clinical practice

OTHERSamples collection: Non-CNS Metastatic Tumour Tissue

Part B: Highly recommended non-CNS metastatic tumour tissue collection (1FFPE and 1 FT) at CNS metastases diagnosis (Part B) (NB: Bone lesions are excluded) - As close as possible to the diagnosis of CNS metastases and no later than 6 weeks after diagnosis

OTHERBrain MRI

Part A: * Brain MRI at inclusion is allowed within 45 days before enrolment * Brain MRI pre-CNS diagnosis (Part A) : HER2 BC/TNBC: once a year; NSCLC/SCLC: every 4 months; Melanoma: every 6 months (+/- 1 month) Part B: o As close as possible to the diagnosis of CNS metastases and no later than 6 weeks after diagnosis Part C: o Brain MRI post-CNS diagnosis (Part C): every 3 months (+/- 1 month window)

OTHERSamples collection: Serum

At baseline Part A: * TNBC/ HER2+ BC: once a year * NSCLC/SCLC: every 4 months * Melanoma: every 6 months Part B: o As close as possible to the diagnosis of CNS metastases and no later than 6 weeks after diagnosis for cohorts 1-5.


Locations(17)

Institut Jules Bordet

Anderlecht, Belgium

Hôpital Erasme

Brussels, Belgium

Cliniques Universitaires St Luc

Brussels, Belgium

Grand Hôpital de Charleroi

Charleroi, Belgium

Universitair Ziekenhuis Gent

Ghent, Belgium

UZ Brussel

Jette, Belgium

UZ Leuven

Leuven, Belgium

CHU Ambroise Paré

Mons, Belgium

CHU UCL Namur - Site de Sainte-Elisabeth

Namur, Belgium

Centre Oscar Lambret

Lille, France

Institut Paoli-Calmettes

Marseille, France

Institut Universitaire de Cancérologie AP-HP Sorbonne Université, Hopital Tenon

Paris, France

Institut Curie

Paris, France

Centre Henri Becquerel

Rouen, France

Hopitaux Universitaires de Strasbourg

Strasbourg, France

Institut Universitaire du Cancer - Oncopole

Toulouse, France

Centre Hospitalier de Luxembourg

Luxembourg, Luxembourg

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NCT04109131


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