CalPeg for Newly Diagnosed Acute Lymphoblastic Leukemia (ALL)

Acute Lymphoblastic Leukemia Clinical Trial

Official title:

A Single-Arm, Open-Label Phase 1b Study of Hyper-CVAD + Calaspargase Pegol in Young Adults With Newly Diagnosed Acute Lymphoblastic Leukemia

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05581030
• Other study ID #: MCC-21213
• Status: Recruiting
• Phase: Phase 1
• Start date: May 1, 2023
• Est. completion date: November 2027

Study information

• Verified date: February 2024
• Source: H. Lee Moffitt Cancer Center and Research Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to evaluate the safety and tolerability of the study drug, calaspargase pegol, when given with multi-agent chemotherapy.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 20
• Est. completion date: November 2027
• Est. primary completion date: November 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Pathologically confirmed Philadelphia negative B- or T-cell acute lymphoblastic leukemia, with >10% peripheral blood or bone marrow lymphoblasts at diagnosis.

• Treatment and full recovery from arm 1A of the Hyper-CVAD regimen.

• Be willing and able to provide written informed consent/assent for the trial.

• Able to adhere to the study visit schedule and other protocol requirements.

• Eastern Cooperative Oncology Group (ECOG) performance status 0-1.

• Cardiac ejection fraction = 50% by echocardiography or MUGA, as measured prior to arm 1A of Hyper-CVAD.

• Serum bilirubin and creatinine < 1.5x upper limit of normal (ULN). AST and ALT must be <3x ULN.

• Females of childbearing potential (FCBP) must have a negative serum pregnancy test at screening. A FCBP is considered when a sexually mature female: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 12 consecutive months.

• A FCBP must agree to use of two methods of highly effective non-hormonal contraception, be surgically sterile, or abstain from heterosexual activity for the course of the study through 3 monthsafter the last dose of study treatment.

• Male subjects must agree to use an adequate method of contraception starting with the first dose of study therapy through 30 days after the last dose of study therapy. Men must agree to not donate sperm during and after the study for 3 months

Exclusion Criteria:

• Induction therapy with any regimen other than Hyper-CVAD 1A.

• Diagnosis of L3 type Burkitt's lymphoma

• Clinical evidence of active central nervous system (CNS) leukemia.

• Any major surgery or radiation therapy within four weeks.

• Diagnosis of Down Syndrome.

• Any active infection requiring systemic therapy, including HIV, Hepatitis B, and/or Hepatitis C.

• Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator (including but not limited to unstable angina, pre-existing liver disease, recurrent pancreatitis, uncontrolled diabetes, hypertriglyceridemia, pulmonary hypertension, or severeheart failure (New York Heart Association Class III-IV).

• Recurrent thrombosis, or non-central venous catheter associated thrombosis within 3 months prior to enrollment.

• Severe comorbid conditions for which life expectancy would be <6 months.

• Patients with active (uncontrolled, metastatic) second malignancies are excluded.

• Is pregnant, breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 3 months after the last dose of trial treatment.

Related Conditions & MeSH terms

• Acute Lymphoblastic Leukemia
• Leukemia
• Leukemia, Lymphoid
• Precursor Cell Lymphoblastic Leukemia-Lymphoma

Intervention

Drug:
• Hyper CVAD Protocol (Standard of Care Multi-Agent Chemotherapy)
Hyper-CVAD consists of two combinations of drugs (courses A and B) given in an alternating fashion. The term "hyper" refers to the hyperfractionated nature of the chemotherapy, which is given in small doses, more frequently, to minimize side effects. CVAD is the acronym of the drugs in course a: cyclophosphamide, vincristine, doxorubicin and dexamethasone. Course A: Cyclophosphamide days 1, 2 and 3. Vincristine days 4 and 11, Doxorubicin day 4, dexamethasone days 1-4 and 11-14, Cytarabine day 7. Mesna is also given orally with cyclophosphamide, to reduce the incidence of haemorrhagic cystitis, a common side effect of cyclophosphamide. Methotrexate, an antimetabolite, may be given when necessary to get chemotherapy past the blood brain barrier. Course B: Methotrexate Day 1 and Cytarabine Days 2 and 3. Dosage is individualized to the patient.
• Calaspargase Pegol
Calaspargase pegol 2000 IU/m^2 (capped at 3750 IU) will be administered beginning in cycle 1B of Hyper-CVAD, and will continue at this dose for the duration of the trial.
• Rituximab
Rituximab 375mg/m^2 will be administered once per cycle for patients with CD20+ ALL.

Locations

Country	Name	City	State
United States	Moffitt Cancer Center	Tampa	Florida

Sponsors (2)

Lead Sponsor	Collaborator
H. Lee Moffitt Cancer Center and Research Institute	Servier

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Mortality Rate of Hyper-CVAD after first infusion of calaspargase pegol	Mortality rate is hypothesized to be less than 10% when combining calaspargase pegol with Hyper-CVAD.	Up to 12 months
Secondary	Minimal Residual Disease Remission Rate	Minimal Residual Disease (MRD) will be studied as a dichotomous endpoint using a cutoff of 1x10^4 cells/transcripts as the lower limit for residual leukemia and presented as the percentage of patients reaching this landmark as their best response. MRD assessment will be obtained with each bone marrow biopsy assessment, every 3 months in the first year following their last cycle of therapy and every 6 months in the subsequent 2 years following their last cycle.	Up to 3 years
Secondary	Progression Free Survival	Progression Free Survival defined as the time from start of treatment to the time of progression or death.	Up to 42 months
Secondary	Overall Survival	Overall Survival (OS) will be measured from the initial date of treatment to the recorded date of death.	Up to 42 months

External Links

•   Moffitt Cancer Center Clinical Trials website