Low-Intensity Chemotherapy and Venetoclax in Treating Patients With Relapsed or Refractory B- or T-Cell Acute Lymphoblastic Leukemia

Recurrent B Acute Lymphoblastic Leukemia Clinical Trial

Official title:

Phase I/II Study of the Combination of Low-Intensity Chemotherapy and Venetoclax (ABT-199) in Patients With Relapsed/Refractory Acute Lymphoblastic Leukemia (ALL)

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03808610
• Other study ID #: 2016-0629
• Secondary ID: NCI-2018-0336020
• Status: Active, not recruiting
• Phase: Phase 1/Phase 2
• Start date: April 3, 2019
• Est. completion date: December 31, 2026

Study information

• Verified date: June 2024
• Source: M.D. Anderson Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase I/II trial studies the side effects and best dose of venetoclax and how well it works in combination with low-intensity chemotherapy in patients with B- or T-cell acute lymphoblastic leukemia that has not responded to treatment or that has come back. Venetoclax may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, including vincristine, cyclophosphamide, dexamethasone, rituximab, methotrexate, and cytarabine, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving venetoclax with low-intensity chemotherapy may work better in treating patient with B- or T-cell acute lymphoblastic leukemia.

Description:

PRIMARY OBJECTIVES: I. Determine the maximum tolerated dose (MTD) and dose-limited toxicities (DLTs) of venetoclax in combination with low-intensity chemotherapy in patients with relapsed/refractory acute lymphoblastic leukemia (ALL) (Phase I). II. Evaluate the overall response rate (complete response [CR] + CR with inadequate count recovery [CRi]) of the regimen after 2 cycles. (Phase II) SECONDARY OBJECTIVES: I. Evaluate other clinical efficacy endpoints (minimal residual disease [MRD] negativity, duration of response [DOR], event-free survival [EFS] and overall survival [OS]). II. Determine the safety of the combination regimen. EXPLORATORY OBJECTIVES: I. To correlate apoptotic protein expression and Bcl-2 dependency on response and resistance to the combination regimen. OUTLINE: This is a phase I, dose-escalation study of venetoclax, followed by a phase II study. CHEMOTHERAPY AND VENETOCLAX: CYCLE 1: Patients receive venetoclax orally (PO) once daily (QD) on days 1-21, vincristine intravenously (IV) over 15 minutes on days 7 and 17, cyclophosphamide IV twice daily (BID) over 3 hours on days 7-9, and dexamethasone IV over 30 minutes or PO QD on days 7-10 and 17-20. Patients may also receive rituximab IV over 4-6 hours on days 7 and 17 per physician discretion. CYCLES 2, 4, 6, and 8: Patients receive venetoclax PO QD on days 1-21, methotrexate IV over 24 hours on day 1, and cytarabine IV BID over 3 hours on days 2 and 3. Patients may also receive rituximab IV over 4-6 hours on days 1 and 8 per physician discretion. CYCLES 3, 5, and 7: Patients receive venetoclax PO QD on days 1-21, cyclophosphamide IV BID over 3 hours on days 1-3, vincristine IV over 15 minutes on days 1 and 11, and dexamethasone IV over 30 minutes or PO QD on days 1-4 and 11-14. Patients may also receive rituximab IV over 4-6 hours on days 1 and 11 per physician discretion. T-CELL ALL: After the first 4 cycles, patients receive nelarabine IV over 2 hours on days 1-5 and pegaspargase IV over 2 hours on day 5. Cycles repeat every 28 days for 2 cycles (after cycle 4 and 5) in the absence of disease progression or unacceptable toxicity. MAINTENANCE THERAPY: Patients may receive prednisone PO QD on days 1-5, vincristine IV over 15 minutes on day 1, and venetoclax, PO QD on days 1-21. Cycles repeat every 28 days for 2 years in the absence of disease progression or unacceptable toxicity. T-CELL ALL (MAINTENANCE THERAPY): After the first 5 cycles of maintenance therapy, patients who received nelarabine and pegaspargase will receive nelarabine IV QD over 2 hours on days 1-5 and pegaspargase IV over 2 hours on day 5 during maintenance cycles 6 and 7 instead of prednisone, vincristine, and venetoclax. After completion of study treatment, patients are followed up for 30 days and then every 3 months thereafter.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 50
• Est. completion date: December 31, 2026
• Est. primary completion date: December 31, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Diagnosis of one of the following

1. Patients = 18 years of age with relapsed/refractory B- or T-cell ALL (for phase II only)

2. Patients = 60 years of age with previously untreated B- or T-cell ALL. Patients <60 years of age may be enrolled if they are considered unfit for intensive chemotherapy

3. Patients = 60 years of age with previously treated B- or T-cell ALL who received 1-2 courses of any frontline chemotherapy. Patients <60 years of age may be enrolled if they are considered unfit for intensive chemotherapy

• If they achieved CR/CRi, they are assessable only for event-free and overall survival
• If they failed to achieve CR/CRi, they are assessable for response, event-free, and overall survival

2. Performance status = 3 (Eastern Cooperative Oncology Group [ECOG] Scale)

3. Adequate liver and renal function as defined by the following criteria:

• Total serum bilirubin = 1.5 x upper limit of normal (ULN)
• Alanine aminotransferase (ALT) = 3 x ULN, unless due to disease involvement of the liver or hemolysis, in which case an ALT = 10 x ULN is acceptable
• Aspartate aminotransferase (AST) = 3 x ULN, unless due to disease involvement of the liver or hemolysis, in which case an ALT = 10 x ULN is acceptable
• Creatinine clearance = 30 mL/min
• INR = 1.5 x ULN and aPTT . 1.5 x ULN

4. For females of childbearing potential, a negative pregnancy test must be documented within 1 week of starting treatment

5. Female and male patients who are fertile must agree to use an effective form of contraception (birth control methods while on study, such as birth control pills or injections, intrauterine devices [IUDs]), or double-barrier methods (for example, a condom in combination with spermicide) with their sexual partners for 4 months after the end of treatment

6. Signed informed consent

Exclusion Criteria:

1. Patients with Philadelphia chromosome-positive ALL or Burkitt leukemia

2. Patients who are willing and eligible to receive intensive chemotherapy (only for patients enrolling in frontline cohort)

3. Active serious infection not controlled by oral or intravenous antibiotics

4. Known CNS leukemia requiring radiation

5. Active GVHD

6. Active secondary malignancy other than skin cancer (e.g., basal cell carcinoma or squamous cell carcinoma) that in the investigator's opinion will shorten survival to less than 1 year

7. Known hepatitis B or C infection, or known seropositivity for human immunodeficiency virus (HIV)

8. Active grade III-V cardiac failure as defined by the New York Heart Association Criteria

9. Patients with a cardiac ejection fraction (as measured by either multigated acquisition [MUGA] or echocardiogram) < 40%

10. Received moderate or strong CYP3A inhibitors or strong CYP3A inducers within 7 days of starting venetoclax

11. Received medication that interferes with coagulation or platelet function within 7 days prior to the first dose of study drug or during the study treatment period

12. Consumed grapefruit, grapefruit products, Seville oranges, or star fruit within 3 days prior to starting venetoclax

13. Prior history of treatment with navitoclax.

14. Treatment with any investigational antileukemic agents or chemotherapy agents in the last 7 days before study entry, unless full recovery from side effects has occurred or patient has rapidly progressive disease judged to be life-threatening by the investigator. Exception: Treatment with hydroxyurea and/or dexamethasone are allowed prior to study treatment, without window of exclusion

15. Pregnant and lactating women will not be eligible; women of childbearing potential should have a negative pregnancy test prior to entering on the study and be willing to practice methods of contraception. Women do not have childbearing potential if they have had a hysterectomy or are postmenopausal without menses for 12 months. In addition, men enrolled on this study should understand the risks to any sexual partner of childbearing potential and should practice an effective method of birth control

16. History of significant bleeding disorder unrelated to cancer, including: diagnosed congenital bleeding disorders (e.g., von Willebrand's disease); diagnosed acquired bleeding disorder within one year (e.g., acquired anti-factor VIII antibodies)

17. Patient with total serum bilirubin > 1.5 x upper limit of normal (ULN).

Related Conditions & MeSH terms

• Leukemia
• Leukemia, Lymphoid
• Precursor Cell Lymphoblastic Leukemia-Lymphoma
• Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
• Recurrence
• Recurrent B Acute Lymphoblastic Leukemia
• Recurrent T Acute Lymphoblastic Leukemia
• Refractory B Acute Lymphoblastic Leukemia
• Refractory T Acute Lymphoblastic Leukemia

Intervention

Drug:
• Cyclophosphamide
Given IV
• Cytarabine
Given IV
• Dexamethasone
Given IV or PO
• Methotrexate
Given IV
• Nelarabine
Given IV
• Pegaspargase
Given IV
• Prednisone
Given PO

Biological:
• Rituximab
Given IV

Drug:
• Venetoclax
Given PO
• Vincristine
Given IV

Locations

Country	Name	City	State
United States	M D Anderson Cancer Center	Houston	Texas

Sponsors (2)

Lead Sponsor	Collaborator
M.D. Anderson Cancer Center	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Apoptotic protein expression and Bcl-2 dependency	Apoptotic protein expression and Bcl-2 dependency will be correlated on response and resistance to the combination regimen.	Up to 4 years
Primary	Maximum tolerated dose (MTD) (Phase I)	The MTD is the highest dose level in which < 2 patients of 6 develop first cycle dose-limiting toxicity (DLT).	Up to 28 days
Primary	DLT (Phase I)	A non-hematologic DLT is defined as a clinically significant (as assessed by treating physician) grade 3 or 4 adverse event or abnormal laboratory value (according to Common Terminology Criteria for Adverse Events [CTCAE] criteria). Toxicity type, severity and attribution will be summarized for each patient using frequency tables.	Up to 28 days
Secondary	Overall response rate (Phase II)	Will be defined as the percentage of patients achieving a complete response (CR) or CR with inadequate count recovery (CRi). Will estimate the overall response (OR) for the combination treatment, along with the 95% credible interval.	Up to 56 days (2 courses)
Secondary	Minimal residual disease (MRD) negativity	Will be summarized using descriptive statistics such as mean, standard deviation, median and range.	Up to 4 years
Secondary	Duration of response (DOR)	Will be summarized using descriptive statistics such as mean, standard deviation, median and range. The association between response and patient's clinical characteristics will be examined by Wilcoxon's rank sum test or Fisher's exact test, as appropriate.	Up to 4 years
Secondary	Event-free survival (EFS)	The association between response and patient's clinical characteristics will be examined by Wilcoxon's rank sum test or Fisher's exact test, as appropriate.	From the first day of treatment until any failure (resistant disease, relapse, or death), assessed up to 4 years
Secondary	Overall survival (OS)	The association between response and patient's clinical characteristics will be examined by Wilcoxon's rank sum test or Fisher's exact test, as appropriate.	From the first day of treatment to time of death from any cause, assessed up to 4 years
Secondary	Incidence of adverse events	Will be summarized using descriptive statistics such as mean, standard deviation, median and range.	Up to 4 years

External Links

•   MD Anderson Cancer Center