A Prospective, Multicenter, Phase-II Trial of Ibrutinib Plus Venetoclax in Patients With Creatinine Clearance >= 30 ml/Min Who Have Relapsed or Refractory Chronic Lymphocytic Leukemia (RR-CLL) With or Without TP53 Aberrations

• Status: Active, not recruiting
• Trial end date: 2026-01-01
• Target enrollment: 0
• Participant gender: All

Summary

The aim of the current trial is to evaluate if combination treatment with venetoclax + ibrutinib in patients with relapsed or refractory chronic lymphocytic leukemia (RR CLL) can lead to MRD negativity, which may induce long lasting remissions for MRD-negative patients randomized to stopping treatment after 15 induction cycles.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Stichting Hemato-Oncologie voor Volwassenen Nederland
• Collaborator: Nordic CLL Study Group
• Treatments: Venetoclax

Criteria

Inclusion Criteria:

• Documented CLL or SLL requiring treatment according to IWCLL criteria after either being refractory to first line therapy or relapse after initial therapy.

• Age at least 18 years.

• Adequate bone marrow function defined as:

• Absolute neutrophil count (ANC) >0.75 x 109/L

• Platelet count >30,000 /μL 30 x 109/L.

• Hemoglobin >8.0 g/dL (5 mmol/L) Unless directly attributable to CLL infiltration of the bone marrow, proven by bone marrow biopsy

• Creatinine clearance (CrCL) ≥ 30ml/min calculated according to the modified formula of Cockcroft and Gault or directly measured with 24hr urine collection.

• Adequate liver function as indicated

• Serum aspartate transaminase (AST) or alanine transaminase (ALT) ≤ 3.0 x upper limit of normal (ULN)

• Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of nonhepatic origin)

• Prothrombin time (PT)/International normal ratio (INR) <1.5 x ULN and PTT (activated partial thromboplastin time [aPTT]) <1.5 x ULN (unless abnormalities are related to coagulopathy or bleeding disorder).

• Negative serological testing for hepatitis B (HBsAg negative and anti-HBc negative; patients positive for anti-HBc may be included if PCR for HBV DNA is negative and HBV-DNA PCR is performed every month until 12 months after last dose), negative testing for hepatitis C RNA within 42 days prior to registration.

• WHO/ECOG performance status 0-3 (appendix C), stage 3 only if attributable to CLL.

• Negative pregnancy test at study entry (for women of childbearing potential).

• Male and female subjects of reproductive potential must agree to use both a highly effective method of birth control (e.g. implants, injectables, combined oral contraceptives, some intrauterine devices [IUDs], complete abstinence , or sterilized partner) and a barrier method (e.g., condoms, cervical ring, sponge, etc.) during the period of therapy and for 90 days after the last dose of study drug.

• Ability and willingness to provide written informed consent and to adhere to the study visit schedule and other protocol requirements.

• Written informed consent.

Exclusion Criteria:

• Any prior therapy with ibrutinib and/or venetoclax.

• Transformation of CLL (Richter's transformation).

• Patients with a history of confirmed progressive multifocal leukoencephalopathy (PML).

• Malignancies other than CLL currently requiring systemic therapies or not being treated in curative intention before or showing signs of progression after curative treatment.

• Known allergy to xanthine oxidase inhibitors and/or rasburicase.

• Known bleeding disorders (e.g., von Willebrand's disease or hemophilia).

• Uncontrolled or active infection.

• Patients requiring treatment with a strong cytochrome P450 (CYP) 3A inhibitor (see appendix K). or anticoagulant therapy with warfarin or phenoprocoumon or other vitamin K antagonists. Please note: Patients being treated with NOACs can be included, but must be properly informed about the potential risk of bleeding under treatment with ibrutinib.

• History of stroke or intracranial hemorrhage within 6 months prior to registration.

• Major surgery within 28 days prior to registration.

• Use of investigational agents which might interfere with the study drug within 28 days prior to registration.

• Vaccination with live vaccines within 28 days prior to registration

• Steroid therapy within 7 days prior to registration, with the exception of inhaled steroids for asthma, topical steroids, steroids up to 25 mg of prednisolone daily to control autoimmune phenomenon's, or replacement/stress corticosteroids.

• Pregnant women and nursing mothers.

• Any psychological, familial, sociological and geographical condition potentially hampering compliance with the study protocol and follow-up schedule.