Venetoclax as Consolidation in CLL Patients Treated With BTK Inhibitor Monotherapy

Official title

Study of the Efficacy and Safety of Venetoclax as Consolidation to Achieve Fix-Duration Treatment in CLL Patients Treated With BTK Inhibitor Monotherapy

Overview

This is an open-label, multicenter, phase 2, non-randomized study aiming to study the efficacy and safety of fixed-duration venetoclax consolidation in CLL patients who are on BTK inhibitor monotherapy. Patients who are on BTK inhibitor monotherapy for ≥ 6 months and still responsive are included. The study includes patients who are treatment-naive before taking BTK inhibitors. Patients will be treated with the BTK inhibitor plus full-dose venetoclax for 12 cycles after a standard 5-week dose ramp-up. Peripheral blood and bone marrow MRD status will be evaluated during and after the treatment. After the completion of combination therapy, patients will stop both BTK inhibitor and venetoclax and be followed.

Interventions

• Drug Venetoclax combined with Ibrutinib
  All Patients will be treated with venetoclax for 12 cycles after a standard 5-week dose ramp-up, as an add-on to the primary using ibrutinib. After the completion of combination therapy, patients will stop both the ibrutinib and venetoclax then be followed. Each cycle is 28 days. At the start of cycle 0, patients will start venetoclax by 20mg-50mg-100mg-200mg daily in a weekly dose escalation way. The combination of full dose venetoclax (400mg) and ibrutinib will continue for an additional 12 c
• Drug Venetoclax combined with Zanubrutinib
  All Patients will be treated with venetoclax for 12 cycles after a standard 5-week dose ramp-up, as an add-on to the primary using zanubrutinib. After the completion of combination therapy, patients will stop both the zanubrutinib and venetoclax then be followed. Each cycle is 28 days. At the start of cycle 0, patients will start venetoclax by 20mg-50mg-100mg-200mg daily in a weekly dose escalation way. The combination of full dose venetoclax (400mg) and zanubrutinib will continue for an additi
• Drug Venetoclax combined with Acalabrutinib
  All Patients will be treated with venetoclax for 12 cycles after a standard 5-week dose ramp-up, as an add-on to the primary using acalabrutinib. After the completion of combination therapy, patients will stop both the acalabrutinib and venetoclax then be followed. Each cycle is 28 days. At the start of cycle 0, patients will start venetoclax by 20mg-50mg-100mg-200mg daily in a weekly dose escalation way. The combination of full dose venetoclax (400mg) and acalabrutinib will continue for an add
• Drug Venetoclax combined with Orelabrutinib
  All Patients will be treated with venetoclax for 12 cycles after a standard 5-week dose ramp-up, as an add-on to the primary using orelabrutinib. After the completion of combination therapy, patients will stop both the orelabrutinib and venetoclax then be followed. Each cycle is 28 days. At the start of cycle 0, patients will start venetoclax by 20mg-50mg-100mg-200mg daily in a weekly dose escalation way. The combination of full dose venetoclax (400mg) and orelabrutinib will continue for an add

Primary outcome measures

• Rate of BM-uMRD after completion of combination therapy (Day 1 of Cycle 16) [Time frame: On Day 1 of Cycle 16 (each cycle is 28 days)]

Secondary outcome measures (6)

• Rate of undetected peripheral blood MRD by flow cytometry [Time frame: On screening, Day 1 of Cycle 4, Day 1 of Cycle 7, Day 1 of Cycle 10, Day 1 of Cycle 16, Day 1 of Cycle 20, Day 1 of Cycle 24, Day 1 of Cycle 28 and Day 1 of Cycle 34 (each cycle is 28 days)]
• Rate of complete response (CR) [Time frame: On Day 1 of Cycle 7, Day 1 of Cycle 16, Day 1 of Cycle 22, and Day 1 of Cycle 28 (each cycle is 28 days)]
• Progression-free survival (PFS) [Time frame: From the first dose of venetoclax until the date of progression or date of death from any cause, whichever came first, assessed up to 112 months]
• Overall survival (OS) [Time frame: From the first dose of venetoclax until the date of death from any cause, assessed up to 112 months]
• Time to next treatment (TTNT) [Time frame: From the first dose of venetoclax to the next CLL-directed therapies due to progression, assessed up to 112 months]
• Adverse Events [Time frame: From screening to 30 days after the end of cycle 12 (each cycle is 28 days)]

Eligibility criteria

Inclusion criteria

• 1\. Age: 18-80 years-old.
• 2\. Patients must have a diagnosis of CLL/SLL.
• 3\. Detectable MRD by flow cytometry (10\^-4 sensitivity) in the peripheral blood.
• 4\. Patients who are on BTK inhibitor monotherapy for more than 6 months. This study includes patients who are taking one of the following BTK inhibitors: ibrutinib, zanubrutinib, orelabrutinib, and acalabrutinib.
• 5\. Patients need to have a response of at least PR (CR/PR) to BTK inhibitor monotherapy.
• 6\. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 2.
• 7\. Patients must have adequate renal and hepatic function:
• Serum bilirubin ≤ 1.5 × upper limit of normal (ULN) or ≤ 3 × ULN for patients with Gilbert's disease;
• Serum creatinine clearance of ≥ 50 ml/min (calculated or measured);
• ALT and AST ≤ 3.0 × ULN, unless clearly due to disease involvement.
• 8\. Adequate bone marrow function:
• Platelet count of greater than 50,000/µl, with no platelet transfusion in prior 2 weeks;
• ANC ≥ 1000/µl in the absence of growth factor support unless due to compromised bone marrow production from CLL, indicated by ≥ 80% CLL in marrow;
• Hemoglobin ≥ 8g/dL.
• 9\. Adequate cardiac function, as assessed by:
• Absence of uncontrolled cardiac arrhythmia;
• Echocardiogram demonstrating LVEF ≥ 35%;
• NYHA functional class ≤ 2.
• 10\. Ability to provide informed consent and adhere to the required follow-up.

Exclusion criteria

• 1\. Richter transformation.
• 2\. Active malignancy requiring systemic therapy, other than CLL, with the exception of: adequately treated in situ carcinoma of the cervix uteri; adequately treated basal cell carcinoma or localized squamous cell carcinoma of the skin; previous malignancy confined and surgically resected (or treated with other modalities) with curative intent.
• 3\. Major surgery, radiotherapy, chemotherapy, biologic therapy, immunotherapy, experimental therapy within 3 weeks prior to the first dose of the study drug.
• 4\. Grade 3 or 4 hemorrhage within the past 3 weeks.
• 5\. Uncontrolled active infections (viral, bacterial, and fungal).
• 6\. Females who are pregnant or lactating.
• 7\. Known HIV positive.
• 8\. Active hepatitis B infection (defined as the presence of detectable HBV DNA or HBe antigen). Patients who are HBsAg positive or HBcAb positive are eligible, provided HBV DNA is negative. These patients must have monthly monitoring of HBV DNA for the duration of the study.
• 9\. Active hepatitis C, defined by the detection of hepatitis C RNA in plasma by PCR.
• 10\. Active, uncontrolled autoimmune phenomenon (autoimmune hemolytic anemia or immune thrombocytopenia) requiring steroid therapy > 20 mg prednisone daily or equivalent, within 7 days of starting venetoclax.
• 11\. Received other therapeutic agents for CLL/SLL during BTK inhibitor treatment prior to enrollment.
• 12\. Concurrent use of warfarin or equivalent vitamin K inhibitor or other oral anticoagulant treatment.
• 13\. Received strong CYP3A inhibitors or strong CYP3A inducers within 7 days of starting venetoclax.
• 14\. Consuming grapefruit, grapefruit products, Seville oranges, or star fruit within 7 days of starting venetoclax.
• 15\. Prior treatment with venetoclax or other Bcl-2 inhibitor.
• 16\. Malabsorption syndrome or other condition that precludes enteral route of administration.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation

Non-randomized

Model

Parallel assignment

Masking

Open label

Primary purpose

Treatment

Study locations

China · 1 center

• Department of Haematology, the First Affiliated Hospital of Nanjing Medical University, Ji — Nanjing

Identifiers

NCT: NCT06958705 · 2024-SR-1147

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗