Sequential Regimen of Bendamustine-Debulking Followed by ABT-199 and GA101-Induction and -Maintenance in CLL (CLL2-BAG)
Study Details
Study Description
Brief Summary
The CLL2-BAG-trial is a prospective, open-label, multicenter phase-II trial to evaluate the efficacy and safety of a sequential regimen of a debulking with Bendamustine followed by an induction with GA101 (obinutuzumab) and ABT-199 (venetoclax, GDC-0199) followed by ABT-199 and GA101-maintenance in CLL patients
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Detailed Description
In the CLL2-BAG-trial, a total of 62 patients of an allcomer CLL population (irrespective of physical fitness, previous therapies and prognostic factors) with an indication for treatment will be included. Patient will receive 2 cycles of debulking treatment with Bendamustine unless contraindications (e.g. refractoriness) are present or a debulking is not indicated due to a low tumor load. Afterwards, 6 cycles of induction treatment with GA101 (obinutuzumab, 3 doses in the first cycle and monthly in cycles 2-6) and ABT-199 (venetoclax, continuously starting in cycle 2 with a low dose escalation) will be applied. The primary endpoint overall response rate will be assessed at final restaging (2 months after end of induction treatment). Patients benefitting from treatment receive further therapy with GA101 (3 monthly) and ABT-199 (continuously) in a maintenance phase for up to 24 months. Maintenance treatment will be stopped in case of achievement of a complete remission and confirmation of MRD (minimal residual disease) negativity in peripheral blood or if unacceptable toxicity or progression occurs.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Bendamustine + GA101 + ABT-199 Bendamustine: 70mg/m² i.v. GA101: 1000 mg i.v. ABT-199: 20 - 400 mg p.o. |
Drug: Bendamustine
Debulking: Cycles 1-2, d1 & 2: 70mg/m² i.v.
Drug: GA101
Induction: Cycle 1: d1: 100mg, d1(or 2): 900mg, d8 & 15: 1000mg; Cycle 2-6: d1: 1000mg Maintenance: Cycles 1-8 (Duration 12 weeks): d1: 1000mg
Other Names:
Drug: ABT-199
Induction: Cycle 2: d1-7: 20mg, d8-14: 50mg, d15-21: 100mg, d22-28: 200mg; Cycle 3-6: d1-28: 400mg Maintenance: Cycles 1-8 (Duration 12 weeks): d1-84: 400mg
Other Names:
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Outcome Measures
Primary Outcome Measures
- Overall response rate (ORR) [84 days after start of the last cycle of induction therapy]
Proportion of patients responding according to international working Group on chronic lymphocytic leukemia criteria
Secondary Outcome Measures
- Adverse Events (AEs) and adverse events of special interest (AESI) [up to 40 months after first dose of study drug]
Type, frequency and severity of adverse events (AEs) and adverse events of special interest (AESI) and their relationship to study treatment
- Rate of minimal residual disease (MRD) [up to 40 months]
Rate of MRD responses in peripheral blood measured by immunophenotyping
Eligibility Criteria
Criteria
Inclusion Criteria:
-
documented chronic lymphocytic leukemia (CLL) requiring treatment according to International Working Group on CLL (iwCLL) criteria
-
adequate renal function: a creatinine clearance ≥30ml/min calculated according to the modified formula of Cockcroft and Gault or directly measured with 24 hr. urine collection
-
adequate hematologic function: platelets ≥ 25.000/µl, neutrophils ≥ 1.000/µl and hemoglobin ≥8.0 g/dL, unless directly attributable to the patient´s CLL (e.g. bone marrow infiltration)
-
adequate liver function: total bilirubin ≤2x, aspartate aminotransferase (AST) / alanin aminotransferase (ALT) ≤2.5x the institutional upper Limit of normal (ULN) value, unless directly attributable to the patient's CLL or to Gilbert's Syndrome
-
negative serological testing for hepatitis B, negative testing for hepatitis-C RNA and negative HIV test within 6 weeks prior to registration
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age ≥ 18 years
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Eastern Cooperative Oncology Group (ECOG) Performance Status 0 to 2, ECOG 3 is only permitted if related to CLL
-
life expectancy ≥ 6 months
-
ability and willingness to provide written informed consent and to adhere to the study visit schedule and other protocol requirements
Exclusion Criteria:
-
transformation of CLL (i.e. Richter's transformation, prolymphocytic leukemia)
-
known central nervous system (CNS) involvement
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confirmed progressive multifocal leukoencephalopathy (PML)
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malignancies other than CLL currently requiring systemic therapies
-
uncontrolled infection requiring systemic treatment
-
any comorbidity or organ system impairment rated with a cumulative illness rating scale (CIRS) score of 4, excluding the eyes/ears/nose/throat/larynx organ system or any other life-threatening illness, medical condition or organ system dysfunction that
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in the investigator´s opinion - could compromise the patients safety or interfere with the absorption or metabolism of the study drugs (e.g, inability to swallow tablets or impaired resorption in the gastrointestinal tract)
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requirement of therapy with strong cytochrome P450 isoenzyme 3A4 (CYP3A4) inhibitors/inducers or anticoagulant with warfarin, phenprocoumon (marcumar) or other vitamin K-antagonists
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use of investigational agents within 28 days prior to registration
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known hypersensitivity to GA101 (obinutuzumab), ABT-199 (venetoclax, GDC-0199) or any of the excipients
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pregnant women and nursing mothers
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fertile men or women of childbearing potential unless surgically sterile or ≥ 2 years after the onset of menopause, or willing to use two methods of reliable contraception including one highly effective (Pearl Index <1) and one additional effective (barrier) method during study treatment and for 18 months after end of study treatment
-
vaccination with a live vaccine ≤28 days prior to registration
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legal incapacity
-
prisoners or subjects who are institutionalized by regulatory or court order
-
persons who are in dependence to the sponsor or an investigator
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | German CLL Study Group | Cologne | Germany | 50935 |
Sponsors and Collaborators
- German CLL Study Group
- Hoffmann-La Roche
- AbbVie
Investigators
- Principal Investigator: Paula Cramer, Dr. med., German CLL Study Group
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- CLL2-BAG
- 2014-000580-40