MedPath

Combination Chemotherapy Plus PSC-833 in Treating Children With Refractory or Relapsed Acute Leukemia

Phase 1
Completed
Conditions
Leukemia
Interventions
Registration Number
NCT00002912
Lead Sponsor
National Cancer Institute (NCI)
Brief Summary

Phase I trial to study the effectiveness of PSC-833 plus etoposide and mitoxantrone in treating children who have refractory or relapsed acute leukemia. Drugs used in chemotherapy use different ways to stop cancer cells from dividing so they stop growing or die. Some cancers become resistant to chemotherapy drugs. Combining PSC-833 with chemotherapy may reduce resistance to the drug and allow more cancer cells to be killed.

Detailed Description

OBJECTIVES:

I. Determine the maximum tolerated dose of PSC-833 in combination with mitoxantrone and etoposide in children with refractory or relapsed acute leukemia.

II. Determine the effects of PSC-833 on mitoxantrone and etoposide pharmacokinetics.

III. Quantify MDR1 gene expression and MDR1 P-glycoprotein expression and function in patient-derived leukemia cells.

OUTLINE: This is a dose escalation study of PSC-833.

Patients undergo induction therapy consisting of etoposide IV and mitoxantrone IV on days 1-5. Patients then receive PSC-833 IV over 124 hours beginning on day 2. A second course is administered no sooner than 21 days from the start of the first course if the marrow is hypocellular after the first course. Patients with persistent disease after 2 induction courses are removed from the study. Patients receive a total of 3 courses of etoposide/mitoxantrone. Patients who achieve complete remission after 1 induction course receive 2 courses of etoposide/mitoxantrone with PSC-833 as consolidation, beginning within 4 weeks of attainment of complete remission. Patients who achieve complete remission after 2 induction courses receive 1 course of etoposide/mitoxantrone with PSC-833 as consolidation. Cohorts of 3-6 patients receive escalating doses of PSC-833 until the maximum tolerated dose is determined. Patients are followed every 6 months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
3
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Arm Imitoxantrone hydrochloridePatients undergo induction therapy consisting of etoposide IV and mitoxantrone IV on days 1-5. Patients then receive PSC-833 IV over 124 hours beginning on day 2. A second course is administered no sooner than 21 days from the start of the first course if the marrow is hypocellular after the first course. Patients with persistent disease after 2 induction courses are removed from the study. Patients receive a total of 3 courses of etoposide/mitoxantrone. Patients who achieve complete remission after 1 induction course receive 2 courses of etoposide/mitoxantrone with PSC-833 as consolidation, beginning within 4 weeks of attainment of complete remission. Patients who achieve complete remission after 2 induction courses receive 1 course of etoposide/mitoxantrone with PSC-833 as consolidation. Cohorts of 3-6 patients receive escalating doses of PSC-833 until the maximum tolerated dose is determined. Patients are followed every 6 months.
Arm IetoposidePatients undergo induction therapy consisting of etoposide IV and mitoxantrone IV on days 1-5. Patients then receive PSC-833 IV over 124 hours beginning on day 2. A second course is administered no sooner than 21 days from the start of the first course if the marrow is hypocellular after the first course. Patients with persistent disease after 2 induction courses are removed from the study. Patients receive a total of 3 courses of etoposide/mitoxantrone. Patients who achieve complete remission after 1 induction course receive 2 courses of etoposide/mitoxantrone with PSC-833 as consolidation, beginning within 4 weeks of attainment of complete remission. Patients who achieve complete remission after 2 induction courses receive 1 course of etoposide/mitoxantrone with PSC-833 as consolidation. Cohorts of 3-6 patients receive escalating doses of PSC-833 until the maximum tolerated dose is determined. Patients are followed every 6 months.
Arm IvalspodarPatients undergo induction therapy consisting of etoposide IV and mitoxantrone IV on days 1-5. Patients then receive PSC-833 IV over 124 hours beginning on day 2. A second course is administered no sooner than 21 days from the start of the first course if the marrow is hypocellular after the first course. Patients with persistent disease after 2 induction courses are removed from the study. Patients receive a total of 3 courses of etoposide/mitoxantrone. Patients who achieve complete remission after 1 induction course receive 2 courses of etoposide/mitoxantrone with PSC-833 as consolidation, beginning within 4 weeks of attainment of complete remission. Patients who achieve complete remission after 2 induction courses receive 1 course of etoposide/mitoxantrone with PSC-833 as consolidation. Cohorts of 3-6 patients receive escalating doses of PSC-833 until the maximum tolerated dose is determined. Patients are followed every 6 months.
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (55)

Cancer Institute of New Jersey

🇺🇸

New Brunswick, New Jersey, United States

Children's Hospital of Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

Simmons Cancer Center - Dallas

🇺🇸

Dallas, Texas, United States

Hospital for Sick Children

🇨🇦

Toronto, Ontario, Canada

Children's Memorial Hospital, Chicago

🇺🇸

Chicago, Illinois, United States

Boston Floating Hospital Infants and Children

🇺🇸

Boston, Massachusetts, United States

Children's Hospital of Pittsburgh

🇺🇸

Pittsburgh, Pennsylvania, United States

Jonsson Comprehensive Cancer Center, UCLA

🇺🇸

Los Angeles, California, United States

City of Hope National Medical Center

🇺🇸

Los Angeles, California, United States

Emory University Hospital - Atlanta

🇺🇸

Atlanta, Georgia, United States

Robert H. Lurie Comprehensive Cancer Center, Northwestern University

🇺🇸

Chicago, Illinois, United States

Washington University School of Medicine

🇺🇸

Saint Louis, Missouri, United States

Memorial Sloan-Kettering Cancer Center

🇺🇸

New York, New York, United States

State University of New York - Upstate Medical University

🇺🇸

Syracuse, New York, United States

Cook Children's Medical Center - Fort Worth

🇺🇸

Fort Worth, Texas, United States

Princess Margaret Hospital for Children

🇦🇺

Perth, Western Australia, Australia

Children's Hospital of Orange County

🇺🇸

Orange, California, United States

University of Mississippi Medical Center

🇺🇸

Jackson, Mississippi, United States

University of Florida Health Science Center

🇺🇸

Gainesville, Florida, United States

Royal Children's Hospital

🇦🇺

Parkville, Victoria, Australia

Montreal Children's Hospital

🇨🇦

Montreal, Quebec, Canada

Johns Hopkins Oncology Center

🇺🇸

Baltimore, Maryland, United States

University of Wisconsin Comprehensive Cancer Center

🇺🇸

Madison, Wisconsin, United States

Children's Hospital Los Angeles

🇺🇸

Los Angeles, California, United States

Dana-Farber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

University of Arkansas for Medical Sciences

🇺🇸

Little Rock, Arkansas, United States

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

Children's National Medical Center

🇺🇸

Washington, District of Columbia, United States

Hackensack University Medical Center

🇺🇸

Hackensack, New Jersey, United States

Hopital Sainte Justine

🇨🇦

Montreal, Quebec, Canada

UCSF Cancer Center and Cancer Research Institute

🇺🇸

San Francisco, California, United States

Children's Hospital of Michigan

🇺🇸

Detroit, Michigan, United States

University of Minnesota Cancer Center

🇺🇸

Minneapolis, Minnesota, United States

Mayo Clinic Cancer Center

🇺🇸

Rochester, Minnesota, United States

Duke Comprehensive Cancer Center

🇺🇸

Durham, North Carolina, United States

Children's Hospital Medical Center - Cincinnati

🇺🇸

Cincinnati, Ohio, United States

University of Oklahoma Health Sciences Center

🇺🇸

Oklahoma City, Oklahoma, United States

Vanderbilt Cancer Center

🇺🇸

Nashville, Tennessee, United States

Texas Children's Cancer Center

🇺🇸

Houston, Texas, United States

University of Texas - MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

University of Texas Health Science Center at San Antonio

🇺🇸

San Antonio, Texas, United States

Primary Children's Medical Center

🇺🇸

Salt Lake City, Utah, United States

Children's Hospital and Regional Medical Center - Seattle

🇺🇸

Seattle, Washington, United States

Midwest Children's Cancer Center

🇺🇸

Milwaukee, Wisconsin, United States

Indiana University Cancer Center

🇺🇸

Indianapolis, Indiana, United States

University of California San Diego Cancer Center

🇺🇸

La Jolla, California, United States

Roswell Park Cancer Institute

🇺🇸

Buffalo, New York, United States

Columbia Presbyterian Hospital

🇺🇸

New York, New York, United States

Children's Mercy Hospital

🇺🇸

Kansas City, Missouri, United States

Cardinal Glennon Children's Hospital

🇺🇸

Saint Louis, Missouri, United States

NYU School of Medicine's Kaplan Comprehensive Cancer Center

🇺🇸

New York, New York, United States

University of Michigan Comprehensive Cancer Center

🇺🇸

Ann Arbor, Michigan, United States

Children's Hospital of Columbus

🇺🇸

Columbus, Ohio, United States

Stanford University Medical Center

🇺🇸

Stanford, California, United States

University of Kansas Medical Center

🇺🇸

Kansas City, Kansas, United States

© Copyright 2025. All Rights Reserved by MedPath