Palbociclib in Combination With Chemotherapy in Pediatric Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia (RELPALL2)

NCT ID: NCT04996160

Last Updated: 2025-01-24

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 22 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-07-09
• Study Completion Date: 2025-12-31

Brief Summary

With this research study has following goals

• To confirm the highest tolerable dose of palbociclib in combination with chemotherapy is safe and well-tolerated.
• To learn more about side effects of palbociclib in combination with chemotherapy;
• To learn more about the biological effects of palbociclib on the cells in your body

Detailed Description

Primary objective: To confirm the safety of the previously estimated MTD of 100 mg/m2/daily palbociclib on Days 1 to 5; 11 to 15; and 21 to 30, in combination with chemotherapy, on the basis of observed DLTs for pediatric relapsed ALL patients that do not have Ph+ and Ph like mutations (Cohort 1), and to determine the MTD of palbociclib in combination with chemotherapy and kinase inhibition in pediatric relapsed ALL patients with Ph+ and Ph like subtypes (Cohort 2).

Secondary objective: To estimate the overall response rate (ORR) to the combination of palbociclib and chemotherapy in pediatric subjects with relapsed or refractory ALL that does not carry Ph+ or Ph like mutations (Cohort 2).

Conditions

Acute Lymphoblastic Leukemia, Pediatric; Relapsed Acute Lymphoblastic Leukemia; Refractory Acute Lymphoblastic Leukemia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Cohort 1 -(without Ph+ / Ph like mutation)

Dose expansion phase-10 subjects in Cohort 1, 100 mg/m2/daily palbociclib on Days 1 to 5; 11 to 15; and 21 to 30, in combination with chemotherapy. All subjects will receive palbociclib with dexamethasone, bortezomib, and doxorubicin. dexamethasone of each 30 day cycle for up to 3 cycles for responders which include complete remission, complete remission morphologic, and partial response as defined in section 10.2.1. Bortezomib will be given on Days 7, 10, 17 and 20. Doxorubicin will be given on Days 7 and 17.

Group Type: EXPERIMENTAL

Palbociclib

Intervention Type: DRUG

Oral

Dexamethasone

Intervention Type: DRUG

8 mg/m2/day divided BID, PO, NG, or IV

Bortezomib

Intervention Type: DRUG

1.3 mg/m2/dose, IV (preferred) or SC

Doxorubicin

Intervention Type: DRUG

25 mg/m2/dose IV

Cohort 2-(Ph+ / Ph like ALL subtypes):

Dose escalation phase- 12 subjects in Cohort 2, Palbociclib dose escalation will begin at 75 mg/m2/day, on Days 1 to 5; 11 to 15; and 21 to 30, and escalate or de escalate. All subjects will receive palbociclib with dexamethasone, bortezomib, and doxorubicin. dexamethasone of each 30 day cycle for up to 3 cycles for responders which include complete remission, complete remission morphologic, and partial response as defined in section 10.2.1. Bortezomib will be given on Days 7, 10, 17 and 20. Doxorubicin will be given on Days 7 and 17. Subjects with Ph+ / Ph-like mutation will receive a tyrosine kinase inhibitor (TKI or KI, either dasatinib or ruxolitinib).3 on 3 dose escalation with 2 dose levels.

Group Type: EXPERIMENTAL

Palbociclib

Intervention Type: DRUG

Oral

Dexamethasone

Intervention Type: DRUG

8 mg/m2/day divided BID, PO, NG, or IV

Bortezomib

Intervention Type: DRUG

1.3 mg/m2/dose, IV (preferred) or SC

Doxorubicin

Intervention Type: DRUG

25 mg/m2/dose IV

Interventions

Palbociclib

Oral

Intervention Type: DRUG

Dexamethasone

8 mg/m2/day divided BID, PO, NG, or IV

Intervention Type: DRUG

Bortezomib

1.3 mg/m2/dose, IV (preferred) or SC

Intervention Type: DRUG

Doxorubicin

25 mg/m2/dose IV

Intervention Type: DRUG

Other Intervention Names

Ibrance; PD-0332991; 6-acetyl-8-cyclopentyl-5-methyl-2-((5-(piperazin-1-yl)pyridin-2-yl)amino)pyrido[2,3-d]pyrimidin-7(8H)-one; dexamethasone intensol; doxorubicin.HCl

Eligibility Criteria

Inclusion Criteria

1. Participants must have a diagnosis of acute lymphoblastic leukemia and disease meets at least one of the following criteria:

1. relapsed or refractory to chemotherapy as defined by ≥ 5% leukemic blasts in the bone marrow or flow cytometry confirmed leukemic blasts in the peripheral blood

2. relapsed after hematopoietic stem cell transplantation (HSCT)

3. Subjects must have had histologic, morphologic or flow cytometric verification of the malignancy at relapse

2. Prior Treatment:

1. Subjects who relapse while receiving standard ALL maintenance chemotherapy will not be required to have a waiting period before entry onto this study.

Exclusion Criteria

3. At least 14 days must have elapsed since the completion of cytotoxic therapy, with the exception of standard maintenance therapy and steroids.

4. At least 7 days must have elapsed since completion of therapy with a biologic agent. For agents that have known adverse events occurring beyond 7 days after administration, this period prior to enrollment must be extended beyond the time during which adverse events are known to occur.

6. At least 42 days must have elapsed since CAR T cell therapy.

7. At least 90 days have elapsed since bone marrow transplant and participant is off immune suppression for > 2 weeks, if applicable with no evidence of active GVHD.

8. At least 2 weeks must have elapsed since local XRT (small port); ≥ 3 months must have elapsed if prior cranial or craniospinal XRT was received, if ≥ 50% of the pelvis was irradiated, or if TBI was received; ≥ 6 weeks must have elapsed if other substantial bone marrow irradiation was given.

3. Participants must be < 25 years of age.

4. Karnofsky or Lansky performance score is > 50% (corresponding to ECOG Score of < 2). The Lansky performance score should be used for participants < 16 years and the Karnofsky performance score for participants ≥ 16 years (see Appendix D). Subjects who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.

5. Adequate renal function defined as glomerular filtration rate > 60 mL/min/1.73 m2 or serum creatinine based on age as follows:

Max serum creatine (mg/dL) Age (years) Male Female < 6 months 0.4 0.4 6 months to < 1 year 0.5 0.5 1 to < 2 years 0.6 0.6 2 to < 6 years 0.8 0.8 6 to < 10 years 1 1 10 to < 13 years 1.2 1.2 13 to < 16 years 1.5 1.4 > 16 years 1.7 1.4

6. Adequate hepatic function defined as

1. Total bilirubin ≤ 2 x upper limit of normal (ULN) for age, and

2. ALT < 3 x ULN for age, unless elevation is due to leukemic infiltration

7. Adequate cardiac function defined as shortening fraction of > 27% or ejection fraction > 45%.

8. Adequate pulmonary function defined as

1. No evidence of dyspnea at rest, no exercise intolerance, and a pulse oximetry > 94%.

2. No evidence of acute pulmonary infiltrates on chest radiograph

9. Adequate central nervous system (CNS) function defined as

1. Subjects with seizure disorder may be enrolled if on allowed anti convulsants and well controlled. Benzodiazepines and gabapentin are acceptable.

2. CNS toxicity < Grade 2

10. Adequate peripheral nervous system (PNS) function defined as PNS toxicity < Grade 2

1. Extramedullary disease status: subjects with isolated CNS disease or isolated testicular disease are not eligible.

2. Concurrent chemotherapy or targeted anti cancer agents, other than intrathecal therapy.

3. Subjects who have previously received bortezomib or other proteasome inhibitors that did not have a response while receiving the inhibitor are not eligible. Subjects that responded but had a subsequent relapse are eligible.

4. Subjects who have previously received palbociclib or other CDK4/6 inhibitors are not eligible.

5. Subject with concurrent severe and/or uncontrolled medical conditions that, in the opinion of the investigator, may impair participation in the study or the evaluation of safety and/or efficacy.

6. Subjects that have an active, uncontrolled infection are not eligible.

7. Known HIV infection or active hepatitis B (defined as hepatitis B surface antigen-positive) or C (defined as hepatitis C antibody-positive).

8. Pregnant or lactating (female participant of childbearing potential must have negative serum or urine pregnancy test required within 7 days prior to start of treatment).

9. Male or female participant of reproductive potential must agree to use appropriate methods of contraception for the duration of study treatment and for at least 30 days after last dose of protocol treatment.

10. Cumulative anthracyclines must not be projected to exceed 450 mg/m2 doxorubicin equivalents following completion of treatment on protocol. Therefore, for subjects receiving one course on protocol cumulative anthracyclines cannot exceed 400 mg/m2 doxorubicin equivalents at the time of enrollment (≤ 200 mg/m2 doxorubicin equivalents for subject with prior radiation therapy to the mediastinum).

11. Inability or unwillingness or research participant or legal guardian/representative to give written informed consent.

• Maximum Eligible Age: 25 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Tanja Andrea Gruber

OTHER

Sponsor Role: lead

Responsible Party

Tanja Andrea Gruber

Chambers Family Endowed Professor for Pediatric Cancer University

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Tanja A Gruber, MD

Role: PRINCIPAL_INVESTIGATOR

Stanford Universiy

Locations

Lucile Packard Children's Hospital Stanford

Stanford, California, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Tanja A Gruber

Role: CONTACT

tagruber@stanford.edu

650-725-4318

Other Identifiers

PEDSHEMALL0012

Identifier Type: OTHER

Identifier Source: secondary_id

IRB-60392

Identifier Type: -

Identifier Source: org_study_id