OncRef

Clinical Trial: NCT04626791

Modified VR-CAP and Acalabrutinib as First Line Therapy for the Treatment of Transplant-Eligible Patients With Mantle Cell Lymphoma

Status:

ACTIVE NOT RECRUITING

Phase:

Phase 2

Lead Sponsor:Academic and Community Cancer Research United
Information Provided By:Academic and Community Cancer Research United
Last Update Posted:2026-08-25

Study Overview

Brief Summary

This phase II trial investigates how well modified VR-CAP (bortezomib, rituximab, cyclophosphamide, doxorubicin hydrochloride, prednisone, and cytarabine hydrochloride) and acalabrutinib as first line therapy work in treating transplant-eligible patients with mantle cell lymphoma. Modified VR-CAP is a combination of drugs used as standard first line treatment for mantle cell lymphoma. Chemotherapy drugs, such as bortezomib, cyclophosphamide, doxorubicin hydrochloride, and cytarabine hydrochloride, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Rituximab is a monoclonal antibody that binds and depletes malignant B cells, by inducing immune responses and direct toxicity. Acalabrutinib blocks a key enzyme which is needed for malignant cell growth in mantle cell lymphoma. Combining modified VR-CAP and acalabrutinib as first line therapy may be more useful against mantle cell lymphoma compared to the usual treatment.

Official Title

A Phase II Study of Modified VR-CAP and Acalabrutinib as First Line Therapy for Transplant-Eligible Patients With Mantle Cell Lymphoma

Conditions

Mantle Cell Lymphoma

Intervention / Treatment

  • Drug: Acalabrutinib
  • Drug: Bortezomib
  • Drug: Cyclophosphamide
  • Drug: Cytarabine
  • Drug: Doxorubicin Hydrochloride
  • Drug: Prednisone
  • Biological: Rituximab
  • Biological: Rituximab and Hyaluronidase Human

Other Study ID Numbers

  • ACCRU-LY-1804
  • NCI-2020-04428
  • ACCRU-LY-1804
  • P30CA015083

Start Date (Actual)

2021-08-03

Primary Completion Date (Actual)

2025-08-03

Study Completion Date (Estimated)

2028-08-03

Enrollment (Actual)

41

Study Type

Interventional

Phase

Phase 2