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Spots Global Cancer Trial Database for Acalabrutinib and Rituximab in Elderly Patients With Untreated Mantle Cell Lymphoma

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Trial Identification

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

Study Description

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:

Keywords

Eligibility

Minimum Age: 60 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Name: Mats Jerkeman

Affiliation: Department of Oncology, Skåne University Hospital

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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