LIBERTY: Liquid Biopsy to Diagnose and Monitor Central Nervous System (CNS) Involvement in High-risk B Cell Non-Hodgkin Lymphoma

Status: Recruiting
Location: See all (14) locations...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Prevention and treatment of CNS relapse remains a great unmet clinical need in the management of aggressive B-NHL. Hence, investigating novel diagnostic tests is of paramount importance to improve risk-stratification of lymphoma patients at diagnosis, as is the evaluation of novel therapeutic approaches that may prevent and / or treat CNS recurrence. Based on the highlighted evidence, the investigators hypothesize that ctDNA detected within the CSF could potentially improve the detection rate of CNS involvement and consequently improve patients' stratification and better discriminate those in need of consolidative CNS prophylaxis on a molecular basis. Similarly, the investigators postulate that CSF ctDNA could be used as a monitoring tool to assess treatment response and guide therapeutic management.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Informed consent as documented by signature before registration and prior to any trial specific procedures, according to Swiss law and ICH E6 regulations Swiss law and ICH GCP E6(R2) regulations before registration.

• Histologically and/or cytologically confirmed newly diagnosed lymphomas including the following:

• Diffuse large B-cell lymphoma (DLBCL) with at least one of the following characteristics:

‣ CNS IPI \> 4

⁃ Non-GC/ABC subtype with IPI \> 3

⁃ Testicular involvement

⁃ Breast involvement

⁃ Kidney involvement

⁃ Adrenal involvement

⁃ Paranasal sinus / orbit involvement

⁃ Involvement of ≥ 3 extranodal sites

⁃ HIV-positive

⁃ Radiological or histological CNS involvement

• High-grade B-cell lymphoma with MYC translocation with BCL2 and / or BCL6 (HGBL)

• Burkitt lymphoma

• Mantle cell lymphoma (blastoid variant or Ki67 \>30% or TP53 mutated)

• Primary CNS lymphoma

∙ Note:

• Aggressive transformation from indolent lymphomas (pretreated or not) are allowed

• Patients enrolled in other clinical trials may be included

‣ Patients must be willing to undergo a lumbar puncture at screening

⁃ Age ≥ 18 years

Locations
Other Locations
Switzerland
Kantonspital Aarau
NOT_YET_RECRUITING
Aarau
Universitätsspital Basel
RECRUITING
Basel
Istituto Oncologico della Svizzera Italiana (IOSI)
WITHDRAWN
Bellinzona
Inselspital Bern - Universitätsklinik für Medizinische Onkologie
RECRUITING
Bern
Kantonsspital Graubünden
RECRUITING
Chur
Hôpital Fribourgeois - Hôpital Cantonal
RECRUITING
Fribourg
Hopitaux Universitaire de Genève (HUG)
RECRUITING
Geneva
CHUV - Départment d'oncologie
TERMINATED
Lausanne
Kantonsspital Baselland
RECRUITING
Liestal
Kantonsspital Münsterlingen
RECRUITING
Münsterlingen
Kantonsspital St. Gallen
RECRUITING
Sankt Gallen
Hôpital du Valais, Hôpital de Sion
RECRUITING
Sion
Klinik für Hämatologie und Onkologie Hirslanden Zürich
WITHDRAWN
Zurich
Stadtspital Triemli Zürich
RECRUITING
Zurich
Contact Information
Primary
Sabrina Chiquet
trials@swisscancerinstitute.ch
+41 31 389 91 91
Backup
Noémie Lang, MD
noemie.lang@hcuge.ch
+41 022 372 33 11
Time Frame
Start Date: 2024-03-12
Estimated Completion Date: 2026-12
Participants
Target number of participants: 64
Treatments
Experimental: experimental diagnostic test
Lumbar punction at diagnosis. CSF and blood samples will be assessed by the two diagnostic tests (CSF ctDNA and conventional test (CC/FC))
Related Therapeutic Areas
Sponsors
Leads: Swiss Cancer Institute

This content was sourced from clinicaltrials.gov

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