A Phase 1 Trial of TST of PD 0332991 Followed by Cytarabine and Mitoxantrone for Adults With Relapsed and Refractory Acute Leukemias and High-Risk Myelodysplasia

Phase 1

Terminated

• Conditions: Relapsed Acute Leukemia; Refractory Acute Leukemia; High-Risk Myelodysplasia
• Interventions: Drug: PD 0332991

• Registration Number: NCT01701375
• Lead Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Brief Summary

1.1 Primary Objectives

* To determine the feasibility, tolerability, and toxicities of administering the selective CDK 4/6 inhibitor PD 0332991 prior to the combination of ara-C and Mitoxantrone for adults with relapsed and refractory acute leukemias and high risk myelodysplasias (MDS), including primary refractory disease

* To determine the direct cytotoxic effects of single agent PD 0332991 on malignant blasts

* To determine the maximal tolerated dose (MTD) of PD 0332991 in timed sequential combination with ara-C and Mitoxantrone

* To determine if the timed sequential combination of PD 0332991 with ara-C and mitoxantrone can induce clinical responses in adults with relapsed or refractory acute leukemias and high-risk MDS

1.2 Secondary Objectives:

* To determine the ability of PD 0332991 to directly induce apoptosis in malignant cell populations in vivo

* To obtain pharmacodynamic (PD) data regarding the ability of PD 0332991 to arrest malignant cells in the G 1 phase of cell cycle, followed by synchronized release of those cells into S phase upon discontinuation of PD 0332991 and resultant enhanced ara-C cytotoxicity

Detailed Description

Not available

Study Timeline

• Study Start: 2012-09
• Study First Submitted: 2012-09-11
• Study First Submitted QC: 2012-10-03
• Study First Posted: 2012-10-05
• Primary Completion: 2013-04
• Study Completion: 2013-04
• Results First Submitted: 2013-06-14
• Status Verified: 2013-08
• Results First Submitted QC: 2013-08-30
• Last Update Submitted: 2013-08-30
• Results First Posted: 2013-09-09
• Last Update Posted: 2013-09-09

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 2

Inclusion Criteria

• Adults age ≥ 18 years

  • Multilineage bone marrow failure
  • Serum creatinine ≤ 2.0 mg/dl
  • Hepatic enzymes (AST, ALT) ≤ 3x upper limit of normal (ULN)
  • Bilirubin ≤ 2.0 mg/dl, unless due to Gilbert's disease, hemolysis or leukemic infiltration
  • Left ventricular ejection fraction ≥ 45%
  • QTc ≤ 470 msec
  • RB expression is required for the action of PD 0332991. Because rb deletions and mutations are rare in acute leukemias and MDS, screening for RB expression will not be required before enrollment. Pretreatment biopsies will be stored and analyzed for RB expression if needed subsequently.

Exclusion Criteria

• • No more than 5 cytotoxic regimens

  • Previous allogeneic or autologous stem cell transplantation permitted
  • ≥ 3 weeks delay from prior cytotoxic chemotherapy or radiation therapy
  • ≥ 2 week delay from prior biologic therapies including hematopoietic growth factors and vidaza or decitabine
  • If using Hydroxyurea, steroids, tyrosine kinase/src kinase inhibitors, arsenic, interferon for count control, must be off therapy for ≥ 48 hours prior to beginning PD 0332991
  • No concomitant use of potent CYP450 3A4 inhibitors (e.g. triazole antifungal agents) or inducers (e.g. omperazole, dilantin, dexamethasone) within 7 days prior to beginning PD 0332991

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Arm 1	PD 0332991	* PD 0332991 will be given orally days 1,2,3 * Cytarabine (ara-C) will be given by continuous 72 hour intravenous infusion beginning on day 6 * Mitoxantrone will be given over 2 hour infusion day 9, 12 hours after the completion of the ara-C infusion. The mitoxantrone dose may be reduced by 25-50% for patients who have received previous anthracyclines as determined by total previous anthracycline dose

Primary Outcome Measures

Name	Time	Method
The Toxicities of Administration of PD 0332991 in Combination With Cytarabine and Mitoxantrone.	42 days	The number of participants experiencing toxicities of administration of PD 0332991 in combination with cytarabine and mitoxantrone will be measured according to NCI-Common Terminology Criteria for Adverse Events (CTCAE) version 4.0

Secondary Outcome Measures

Name	Time	Method
To Determine the Maximal Tolerated Dose (MTD) of PD 0332991 in Timed Sequential Combination With Ara-C and Mitoxantrone	42 days	Dose escalation decisions will be based on nonhematologic toxicities in Cycle 1 (28 days) and hematologic toxicities, in the case of an aplastic marrow through Day 56, For cytopenias including ANC \< 500/mm3 or platelets \< 50, 000/mm3 a bone marrow will be performed between days 42 and 49.. Dose limiting toxicity (DLT) will be measured according to NCI-Common Terminology Criteria for Adverse Events (CTCAE) version 4.0

Trial Locations

Locations (2)

Weill Cornell Medical Center; 🇺🇸 New York, New York, United States

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins; 🇺🇸 Baltimore, Maryland, United States