POETIC Plerixafor as a Chemosensitizing Agent for Relapsed Acute Leukemia and MDS in Pediatric Patients
In this Phase I study, we will test the safety of the drug plerixafor (MOBOZIL) at different dose levels, used together with other anti-cancer drugs—cytarabine and etoposide. We want to find out what effects, good and /or bad, this combination of drugs has on leukemia. Plerixafor is a drug that blocks a receptor on the leukemia cell, which prevents it from staying in the bone marrow where it can be resistant to chemotherapy. Plerixafor is FDA approved for mobilizing stem cells from the bone marrow in preparation for an autologous stem cell transplant. Cytarabine and etoposide have been used as part of standard chemotherapy for ALL and AML. However, the use of plerixafor with cytarabine and etoposide in pediatric patients with relapsed or refractory ALL, AML and MDS is considered experimental.
Acute Leukemia of Ambiguous Lineage
Drug: Plerixafor Dose Escalation
|Study Design:||Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||A Phase I Study Using Plerixafor as a Chemosensitizing Agent for Relapsed Acute Leukemia and MDS in Pediatric Patients|
- Maximum Tolerated Dose (MTD) of Plerixafor given in combination with chemotherapy [ Time Frame: 6 months post final enrollment ] [ Designated as safety issue: Yes ]To determine the safety and tolerability of plerixafor in combination with reinduction chemotherapy in pediatric and young adult patients with relapsed/refractory acute leukemia (AML/MDS and ALL)
- Response Rate [ Time Frame: 6 months post completion of treatment for final enrollment ] [ Designated as safety issue: No ]To estimate the response rate, within the context of a Phase I study, of Plerixafor given in sequential combination with cytarabine/etoposide (AE) in patients with relapsed or refractory ALL and AML/MDS.
- Pharmacokinetics [ Time Frame: 12 months following last sample collection ] [ Designated as safety issue: No ]To determine the pharmacokinetics of Plerixafor when administered to pediatric and young adult patients with relapsed acute leukemias.
- Leukemic blast mobilization [ Time Frame: 12 months after final sample collection ] [ Designated as safety issue: No ]To measure peripheral blood mobilization of leukemic blasts by flow cytometry by comparing blood samples obtained before and after dose 1 of plerixafor, and to correlate degree of mobilization (expressed as % increase in circulating blasts) with response.
- CXCR4 expression on leukemic blasts [ Time Frame: 12 months after last patient completes therapy ] [ Designated as safety issue: No ]To measure the quantitative expression of CXCR4 on leukemic blasts at baseline and end of first course of treatment using flow cytometry and qRT-PCR, and correlate expression level with response.
|Study Start Date:||March 2011|
|Estimated Study Completion Date:||July 2014|
|Estimated Primary Completion Date:||December 2013 (Final data collection date for primary outcome measure)|
Experimental: Plerixafor, Dose Escalation
Dose escalation of plerixafor administered intravenously in combination with IV cytarabine and IV etoposide in pediatric patients wtih relapsed/refractory AML/ALL.
Drug: Plerixafor Dose Escalation
Plerixafor dose escalation Dose Level -1 = 3 mg/m2/dose Dose Level 1 = 6 mg/m2/dose Dose Level 2 = 9 mg/m2/dose Dose Level 3 = 12 mg/m2/dose Dose Level 4 = 15 mg/m2/dose
Doses administered 4 hours prior to chemotherapy, then at the same approximate time of day on subsequent days, through the end of that cycle of chemotherapy.
Approximately 500 children are diagnosed with AML every year, of whom around 60% are cured with current regimens based on anthracyclines and high dose cytarabine with or without stem cell transplant (SCT). Among the remaining 40% who are refractory or who relapse, outcome is dismal. Additionally, 20-30% of patients with childhood ALL relapse or become refractory to frontline therapies. The prognosis is poor in this patient population, particularly in patients with second or subsequent relapse and those who relapse following SCT. These patients present myriad challenges, as they usually have received a high cumulative anthracycline dose, and in the case of SCT, may have had significant organ toxicities and/or total body irradiation (TBI). Therefore, new therapeutic strategies need to be identified to enhance possible improved outcomes.
Recently, scientists have described a resistant, quiescent population of leukemia cells that have limitless self-renewal potential. The identification of these "leukemia stem cells" (LSCs) provides an additional strategy in treating and preventing relapsed/refractory acute leukemia. One mechanism for resistance to treatment is the protection afforded LSCs via the interaction between stem cell derived growth factor (CXCL-12/SDF-1α) and its receptor, CXCR4. These interactions are implicated in chemotaxis, homing, and survival/apoptosis of hematopoietic stem cells and progenitor cells. All AML and ALL cells express CXCR4 and SDF-1α. AMD3100 (plerixafor, MOBOZIL®) is a bicyclam that blocks CXCL-12 binding to and signaling through CXCR4, thus disrupting tumor-stroma interactions and mobilizing leukemia cells from their protective stromal environment. Plerixafor is currently FDA approved for use in stem cell mobilization for autologous transplantation in hematologic malignancies. Clinical trials in adult patients with relapsed AML have demonstrated promising results when combining plerixafor with cytotoxic chemotherapy.
This Phase I clinical trial will be the first to test the concept of a "chemosensitization" approach in children using Plerixafor. Patients aged 3 to 30 with relapsed/refractory AML, ALL or MDS will receive Plerixafor followed 4 hours later with combination chemotherapy consisting of etoposide and cytarabine daily for five days. We will determine the safety and tolerability of Plerixafor in combination with cytarabine and etoposide in pediatric and young adults with relapsed/refractory acute leukemias. The secondary objectives of this study will quantify the peripheral blood mobilization of blasts in response to Plerixafor using flow cytometry, measure initial CXCR4 expression on leukemic blasts and correlate with response, and determine the change in CXCR4 expression after protocol therapy. Finally, we will determine the pharmacokinetics of Plerixafor when administered with cytotoxic chemotherapy in this patient population.
|Contact: Sindy Midorofirstname.lastname@example.org|
|Contact: Jaclyn Smith, MBAemail@example.com|
|United States, Arizona|
|Phoenix Children's Hospital||Not yet recruiting|
|Phoenix, Arizona, United States, 85016|
|Contact: Brianna McGerty 602-546-5067 firstname.lastname@example.org|
|Contact: Jessica Boklan, MD 602-546-0920 email@example.com|
|Principal Investigator: Jessica Boklan, MD|
|United States, Colorado|
|The Children's Hospital of Denver||Recruiting|
|Denver, Colorado, United States, 80045|
|Contact: Deb Schissel, RN 720-777-2879 firstname.lastname@example.org|
|Contact: Lia Gore, MD 720-777-4159 email@example.com|
|Principal Investigator: Lia Gore, MD|
|United States, Georgia|
|Children's Healthcare of Atlanta/Emory University||Recruiting|
|Atlanta, Georgia, United States, 30322|
|Contact: Sindy Midoro 404-785-1441 firstname.lastname@example.org|
|Contact: Jaclyn Smith, MBA 404-785-0692 email@example.com|
|Principal Investigator: Todd Cooper, DO|
|United States, Maryland|
|Johns Hopkins Medical Center||Recruiting|
|Baltimore, Maryland, United States, 21231|
|Contact: Tammy Scott, RN, BSN 410-614-5990 firstname.lastname@example.org|
|Contact: Robert Arceci, MD, PhD 410-502-7519 email@example.com|
|Principal Investigator: Robert Arceci, MD, PhD|
|United States, Missouri|
|The Children's Mercy Hospital and Clinics||Recruiting|
|Kansas City, Missouri, United States, 64108|
|Contact: Sara Soliman, RN, BSN, CPN 816-855-1977 firstname.lastname@example.org|
|Contact: Kathleen Neville, MD 816-234-3059 email@example.com|
|Principal Investigator: Kathleen Neville, MD|
|United States, New York|
|Memorial Sloan-Kettering Cancer Center||Not yet recruiting|
|New York, New York, United States, 10021|
|Contact: Jennifer DiRenzo 646-888-5714 firstname.lastname@example.org|
|Contact: Tanya Trippett, MD 212-639-8267 email@example.com|
|Principal Investigator: Tanya Trippett, MD|
|United States, Ohio|
|Cincinnati Children's Hospital Medical Center||Recruiting|
|Cincinnati, Ohio, United States, 45229|
|Contact: Kristina Kruskamp, CCRP 513-636-5336 firstname.lastname@example.org|
|Principal Investigator: Michael Absalon, MD, PhD|
|United States, Pennsylvania|
|Penn State Hershey Children's Hospital||Not yet recruiting|
|Hershey, Pennsylvania, United States, 17033|
|Contact: Kathryn Byrnes, BS, CCRP 717-531-3098 email@example.com|
|Principal Investigator: John Kuttesch, PhD, MD|
|Alberta Children's Hospital||Not yet recruiting|
|Calgary, Alberta, Canada, T3B 6A8|
|Contact: Janice Hamilton 403-955-7641 firstname.lastname@example.org|
|Contact: Aru Narendran, MD, PhD 703-210-6418 email@example.com|
|Principal Investigator: Aru Narendran, MD, PhD|
|Principal Investigator:||Todd Cooper, DO||Emory University/Children's Healthcare of Atlanta|