A Phase I Clinical Trial Evaluating the Combination of Volasertib (BI-6727) With Vincristine Sulfate Liposomal Injections (VSLI) in Adult Patients With Relapsed/Refractory Acute Lymphoblastic Leukemia
Overview
- Phase
- Phase 1
- Intervention
- Laboratory Biomarker Analysis
- Conditions
- Recurrent Adult Acute Lymphoblastic Leukemia
- Sponsor
- Northwestern University
- Locations
- 2
- Primary Endpoint
- Maximum Tolerated Dose (MTD)
- Status
- Withdrawn
- Last Updated
- 9 years ago
Overview
Brief Summary
The main purpose of this investigational research study is to determine how safe and tolerable the study drug volasertib is in combination with liposomal vincristine (Marqibo; an FDA-approved drug) in patients with relapsed/refractory acute lymphoblastic leukemia. While VSLI demonstrated an overall response rate of 35% in Acute Lymphoblastic Leukemia (ALL) patients that had failed to respond to or relapsed after chemotherapy, combining it with other agents may increase clinical benefit.
Volasertib inhibits proteins involved in the cell cycle that are increased in ALL. When volasertib inhibits these proteins ALL cells die. In the laboratory, volasertib has been shown to increase activity of vincristine against ALL cells. Therefore, we think the combination of volasertib and VSLI will be more effective against your leukemia than either drug used alone. This study will try to find out what effects, good and/or bad, this drug combination has on the patient and their cancer, and to find a dose that may be used in future studies.
Detailed Description
PRIMARY OBJECTIVES: I. To determine the maximum tolerated dose (MTD) of the combination of volasertib and vincristine sulfate liposomal injection (VSLI) in relapsed/refractory (RR) acute lymphoblastic leukemia (ALL). SECONDARY OBJECTIVES: I. To determine the toxicity profile of volasertib and VSLI, rate of complete remission (with or without complete hematologic recovery; complete response \[CR\]/CR with incomplete hematologic recovery \[CRi\]), duration of remission (DOR), rate of minimal residual disease (MRD)-negativity, progression free survival (PFS), overall survival (OS), 30-day mortality rate. TERTIARY OBJECTIVES: I. To determine if volasertib and polo-like kinase (plk)-inhibition down-regulates the mammalian target of rapamycin (mTOR) pathway. II. Whether plk and mTOR inhibition correlates with clinical response to treatment. III. to determine if volasertib acts synergistically to potentiate the bioavailability and distribution of VSLI. OUTLINE: This is a dose-escalation study of volasertib. Patients receive volasertib intravenously (IV) over 1 hour on day 1 and vincristine sulfate liposome IV over 1 hour on days 1, 8, 15, and 22. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression, development of an inter-current illness that prevents further administration of treatment, unacceptable toxicity, patient decides to withdraw or treating investigator determines that the patient should be taken off treatment for any reason. After completion of study, patients are followed up every 28 days for up to 1 year.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients must have histologically confirmed diagnosis of Philadelphia-negative ALL by bone marrow biopsy or aspirate
- •Patients must have \>= 5% blasts in the bone marrow
- •Patients must have refractory disease, disease relapse or progression after at least two prior systemic chemotherapy or immunotherapy regimens
- •Note: Exceptions may be made if a patient is deemed unfit for first-line salvage therapy by the treating physician; such cases should be clearly documented
- •Patients with a history of CNS (central nervous system) leukemia are eligible if they are not symptomatic from current CNS involvement; if there is CNS involvement that is known prior to enrollment or identified subsequently, it will be treated accordingly with intrathecal chemotherapy per the treating physician
- •Patients must exhibit an Eastern Cooperative Oncology Group (ECOG) performance status of =\< 2
- •Patients must have adequate organ function within 14 days prior to registration, as defined below:
- •Total bilirubin =\< 2 x institutional upper limit of normal (ULN)
- •Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \[SGOT\])/aspartate aminotransferase (ALT) (serum glutamic pyruvic transaminase \[SPGT\]) =\< 3 x ULN
- •Creatinine =\< 2 X ULN
Exclusion Criteria
- •Patients who have had chemotherapy, immunotherapy, or radiotherapy within 2 weeks prior to entering the study or those who have not recovered from adverse events (=\< grade 1 or patient's baseline) due to agents administered more than 2 weeks earlier are not eligible
- •Patients may not be receiving any other investigational agents within 7 days of registration
- •Patients may not be receiving any medications that are known to prolong QT interval unless reviewed and approved by the principal investigator (PI)
- •Patients who have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to volasertib or VSLI are not eligible
- •Subject may not have had hematopoietic stem cell transplant (HSCT) meeting any of the following:
- •Is within 2 months of transplant from cycle 1 day 1 (C1D1)
- •Has clinically significant graft-versus-host disease requiring treatment
- •Has \>= grade 2 persistent non-hematological toxicity related to the transplant
- •Donor lymphocyte infusion (DLI) is not permitted \< 30 days prior to study registration
- •Patients with \>= grade 2 sensory or motor neuropathy are not eligible
Arms & Interventions
Treatment (volasertib, vincristine sulfate liposome)
Patients receive volasertib IV over 1 hour on day 1 and vincristine sulfate liposome IV over 1 hour on days 1, 8, 15, and 22. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression, development of an inter-current illness that prevents further administration of treatment, unacceptable toxicity, patient decides to withdraw or treating investigator determines that the patient should be taken off treatment for any reason.
Intervention: Laboratory Biomarker Analysis
Treatment (volasertib, vincristine sulfate liposome)
Patients receive volasertib IV over 1 hour on day 1 and vincristine sulfate liposome IV over 1 hour on days 1, 8, 15, and 22. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression, development of an inter-current illness that prevents further administration of treatment, unacceptable toxicity, patient decides to withdraw or treating investigator determines that the patient should be taken off treatment for any reason.
Intervention: Pharmacological Study
Treatment (volasertib, vincristine sulfate liposome)
Patients receive volasertib IV over 1 hour on day 1 and vincristine sulfate liposome IV over 1 hour on days 1, 8, 15, and 22. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression, development of an inter-current illness that prevents further administration of treatment, unacceptable toxicity, patient decides to withdraw or treating investigator determines that the patient should be taken off treatment for any reason.
Intervention: Vincristine Sulfate Liposome
Treatment (volasertib, vincristine sulfate liposome)
Patients receive volasertib IV over 1 hour on day 1 and vincristine sulfate liposome IV over 1 hour on days 1, 8, 15, and 22. Treatment repeats every 28 days for up to 12 courses in the absence of disease progression, development of an inter-current illness that prevents further administration of treatment, unacceptable toxicity, patient decides to withdraw or treating investigator determines that the patient should be taken off treatment for any reason.
Intervention: Volasertib
Outcomes
Primary Outcomes
Maximum Tolerated Dose (MTD)
Time Frame: Up to day 1 of cycle 2
Determine the MTD of volasertib and VSLI in RR ALL, the MTD will be defined as the highest dose level at which ≤ 1 Dose-Limiting Toxicity (DLT) occurs in 6 patients and will be assessed by the Common Terminology Criteria for Adverse Events (CTCAE) version 4.03.
Secondary Outcomes
- 30-day mortality rate(Up to 30 days from the first dose of treatment)
- Rate of complete remission (CR/Cri)(After every 2 even number cycles during treatment then every 28 days up to 1 year during follow-up)
- Duration of Remission (DOR)(Up to 1 year from end of treatment)
- Minimal Residual Disease (MRD-negativity) rate(Up to 1 year)
- Progression Free Survival (PFS)(Up to 1 year from end of treatment)
- Overall Survival (OS)(Up to 1 year from end of treatment)