Abstract
The ImbruVeRCHOP trial is an investigator-initiated, multicenter, single-arm, open label Phase I/II study for patients 61-80 years of age with newly diagnosed CD20+ diffuse large B-cell lymphoma and a higher risk profile (International Prognostic Index ≥2). Patients receive standard chemotherapy (CHOP) plus immunotherapy (Rituximab), a biological agent (the proteasome inhibitor Bortezomib) and a signaling inhibitor (the Bruton's Tyrosine Kinase-targeting therapeutic Ibrutinib). Using an all-comers approach, but subjecting patients to another lymphoma biopsy acutely under first-cycle immune-chemo drug exposure, ImbruVeRCHOP seeks to identify an unbiased molecular responder signature that marks diffuse large B-cell lymphoma patients at risk and likely to benefit from this regimen as a double, proximal and distal B-cell receptor/NF-κB-co-targeting extension of the current R-CHOP standard of care. EudraCT-Number: 2015-003429-32; ClinicalTrials.gov identifier: NCT03129828.
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CITATION STYLE
Denker, S., Bittner, A., Na, I.-K., Kase, J., Frick, M., Anagnostopoulos, I., … Schmitt, C. A. (2019). A Phase I/II First-Line Study of R-Chop Plus B-Cell Receptor/NF-κB-Double-Targeting to Molecularly Assess Therapy Response. International Journal of Hematologic Oncology, 8(4). https://doi.org/10.2217/ijh-2019-0010
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