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Brief Title: Acalabrutinib and Rituximab in Elderly Patients With Untreated Mantle Cell Lymphoma
Official Title: Acalabrutinib and Rituximab in Elderly Patients With Untreated Mantle Cell Lymphoma
Study ID: NCT05214183
Brief Summary: This is a phase II trial, with the aim of developing a chemotherapy-free regimen for untreated patients with mantle cell lymphoma (MCL). Acalabrutinib (ACP-196) is a next generation bruton tyrosine kinase (BTK) inhibitor, more selective than ibrutinib, and without in vitro antagonism of anti-CD20 directed immunotherapies, indicating that its combination with rituximab may be more active than the combination of ibrutinib and rituximab. In this trial proposal, we will also assess the activity of this combination in comparison to a historical control of ibrutinib + rituximab, consisting of the experimental arm of ibrutinib + rituximab in the randomized ENRICH trial (EudraCT number 2015-000832-13), and data from our previous trial with R-bendamustine-lenalidomide (NLG-MCL4). The duration of treatment will be a minimum of 12 months. Patients in molecular remission in blood and bone marrow and in complete remission according to CT, will then stop acalabrutinib, but continue on rituximab for a maximum of 36 months. Patients that are minimal residual disease positive (MRD+) will be evaluated again every 6 months and continue on acalabrutinib for a maximum of 36 months. Patients without a molecular marker, that cannot be followed with MRD, will stop treatment if in CR with PET at 12 months, and be followed by PET-CT every 6 months for a maximum of 36 months. Patients who convert back to MRD positive after stopping acalabrutinib are reinstalled on acalabrutinib until progression. Patients with TP53 aberrations and/or blastoid histology, will monitor MRD but continue with treatment until progression regardless of MRD results. A planned interim analysis will be performed when 40 patients have undergone response assessment after 6 months, for futility and efficacy. If less than 16 of 40 patients obtain a CR, the trial will be stopped due to futility.
Detailed Description:
Minimum Age: 60 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Department of Hematology X, Odense University Hospital, Odense, , Denmark
Department of Hematology, Zeeland University Hospital Roskilde, Roskilde, , Denmark
Department of Hematology, Helsinki University Hospital Comprehensive Cancer Center, Helsinki, , Finland
Oulu University Hospital, Oulu, , Finland
Division of Hematology-Oncology Samsung Medical Center Seoul, Seoul, , Korea, Republic of
Department of Oncology, Haukeland University Hospital, Bergen, , Norway
Avd. for Kreftbehandling, Oslo Universitetssykehus, Oslo, , Norway
Avdeling for Blod- og Kreftsykdommer, Stavanger Universitetssykehus, Stavanger, , Norway
Kreftklinikken, St Olavs Hospital, Trondheim, , Norway
Hematological Department, Falu Hospital, Falun, Falun, , Sweden
Department of Hematology and Coagulation, Sahlgrenska University Hospital, Göteborg, , Sweden
Department of Medicine, Halmstad Country Hospital, Halmstad, , Sweden
Department of Internal Medicine, Kalmar County Hospital, Kalmar, , Sweden
Hematologiska Kliniken, Universitetssjukhuset, Linköping, , Sweden
Department of Medicine, Sunderbyn Hospital, Luleå, , Sweden
Mats Jerkeman, Lund, , Sweden
Center of Hematology, Karolinska University Hospital, Stockholm, , Sweden
Uddevalla Hospital, Uddevalla, , Sweden
Cancercentrum, Norrlands Universitetsjukhus, Umeå, , Sweden
Department of Oncology, Uppsala Academic Hospital, Uppsala, , Sweden
Name: Mats Jerkeman
Affiliation: Department of Oncology, Skåne University Hospital
Role: PRINCIPAL_INVESTIGATOR