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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01460160
Other study ID # CA180-372
Secondary ID 2011-001123-20AA
Status Completed
Phase Phase 2
First received
Last updated
Start date April 13, 2012
Est. completion date June 1, 2021

Study information

Verified date November 2021
Source Bristol-Myers Squibb
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether Dasatinib when added to standard chemotherapy is effective and safe in the treatment of pediatric philadelphia chromosome positive acute lymphoblastic leukemia


Recruitment information / eligibility

Status Completed
Enrollment 106
Est. completion date June 1, 2021
Est. primary completion date May 28, 2017
Accepts healthy volunteers No
Gender All
Age group 1 Year to 17 Years
Eligibility For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com. Inclusion Criteria: - Newly diagnosed Philadelphia chromosome positive Acute Lymphoblastic Leukemia (ALL) - Age >1 year and < less than 18 years old - Induction chemotherapy = 14 days according to institutional standard of care - Adequate liver, renal and cardiac function Exclusion Criteria: - Prior treatment with a Oncogene fusion protein (BCR-ABL) inhibitor - Extramedullary involvement of the testicles - Active systemic bacterial, fungal or viral infection - Down syndrome

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Dasatinib
Tablets, Oral, 60 mg/m2, Once daily, 2 years or until unacceptable toxicity

Locations

Country Name City State
Australia Local Institution Nedlands Western Australia
Australia Local Institution Parkville Victoria
Australia Local Institution Sth Brisbane Queensland
Canada Alberta Children'S Hospital Calgary Alberta
Canada Stollery Children'S Hospital Edmonton Alberta
Canada Local Institution London Ontario
Canada Chu Ste-Justine Montreal Quebec
Canada The Montreal Children's Hospital of the MUHC Montreal Quebec
Canada Children'S Hospital Of Eastern Ontario Ottawa Ontario
Canada Local Institution Saskatoon Saskatchewan
Italy Local Institution Bologna
Italy Local Institution Cagliari
Italy Local Institution Catania
Italy Local Institution Firenze
Italy Local Institution Genova
Italy Local Institution Monza
Italy Local Institution Napoli
Italy Local Institution Palermo
Italy Local Institution Roma
Italy Local Institution Roma
Italy Local Institution Torino
Italy Local Institution Trieste
Puerto Rico Local Institution San Juan
United Kingdom Local Institution Aberdeen Grampian
United Kingdom Local Institution Birmingham West Midlands
United Kingdom Local Institution Bristol Avon
United Kingdom Local Institution Cambridge
United Kingdom Local Institution Cardiff Glamorgan
United Kingdom Local Institution Edinburgh Lothian
United Kingdom Local Institution Glasgow Lanarkshire
United Kingdom Local Institution Leeds North Yorkshire
United Kingdom Local Institution Liverpool Merseyside
United Kingdom Local Institution London Greater London
United Kingdom Local Institution Manchester Greater Manchester
United Kingdom Local Institution Newcastle-upon-tyne Tyne And Wear
United Kingdom Local Institution Nottingham Nottinghamshire
United Kingdom Local Institution Oxford Oxfordshire
United Kingdom Local Institution Sheffield South Yorkshire
United Kingdom Local Institution Southampton Hampshire
United Kingdom Local Institution Sutton Surrey
United States University Of New Mexico Albuquerque New Mexico
United States Children's Healthcare Of Atlanta Atlanta Georgia
United States Children'S Hospital Colorado Aurora Colorado
United States Dell Children'S Medical Center Of Central Texas Austin Texas
United States Johns Hopkins University Baltimore Maryland
United States Sinai Hospital Of Baltimore Baltimore Maryland
United States University Of Alabama At Birmingham Birmingham Alabama
United States Mountain States Tumor Institute Boise Idaho
United States Dana Farber Cancer Institute Boston Massachusetts
United States Levine Children's Hospital Charlotte North Carolina
United States Ann & Robert H Lurie Children's Hospital Of Chicago Chicago Illinois
United States Cincinnati Children'S Hospital Medical Center Cincinnati Ohio
United States University Of Missouri Health Care Columbia Missouri
United States Nationwide Children'S Hospital Columbus Ohio
United States Driscoll Children'S Hospital Corpus Christi Texas
United States Ut Southwestern Dallas Texas
United States Geisinger Medical Center Danville Pennsylvania
United States The Children'S Medical Center Of Dayton Dayton Ohio
United States Children'S Hospital Of Michigan Detroit Michigan
United States Inova Pediatric Specialty Center Ii Fairfax Virginia
United States Lee Memorial Health System Fort Myers Florida
United States Cook Children'S Hem/Onc Center Fort Worth Texas
United States University Of Florida Gainesville Florida
United States Helen Devos Children'S Hospital Grand Rapids Michigan
United States St Vincent Hospital Green Bay Wisconsin
United States Hackensack University Medical Center Hackensack New Jersey
United States Connecticut Children's Medical Center Hartford Connecticut
United States Penn State Hershey Medical Center Hershey Pennsylvania
United States Kapiolani Medical Center For Women & Children Honolulu Hawaii
United States Texas Children'S Cancer Center Houston Texas
United States Children'S Center For Cancer And Blood Diseases Indianapolis Indiana
United States James Whitcomb Riley Hospital For Children Indianapolis Indiana
United States Univ Of Mississippi Med Ctr Jackson Mississippi
United States Nemours Children'S Clinic Jacksonville Florida
United States Children'S Mercy Hospital And Clinics Kansas City Missouri
United States East Tennessee Children'S Hosp Knoxville Tennessee
United States Michigan State University Lansing Michigan
United States Children'S Specialty Center Of Nevada Las Vegas Nevada
United States University Of Kentucky Lexington Kentucky
United States University Of Arkansas For Medical Sciences Little Rock Arkansas
United States Antranik Agop Bedros Loma Linda California
United States Miller Children's and Women Hospital Long Beach California
United States Children'S Hospital Of L.A. Los Angeles California
United States Southern California Permanente Medical Group Los Angeles California
United States Norton Children's Hospital Louisville Kentucky
United States Valley Children's Hospital Madera California
United States Kenneth Desantes, Md Madison Wisconsin
United States Loyola University Medical Center Maywood Illinois
United States Medical College of Wisconsin Milwaukee Wisconsin
United States Childrens Hospitals And Clinics Of Minnesota Minneapolis Minnesota
United States Goryeb Children'S Hospital Morristown New Jersey
United States Vanderbilt University Nashville Tennessee
United States The Cancer Institute Of New Jersey New Brunswick New Jersey
United States New York Presbyterian/Weill Cornell New York New York
United States New York University New York New York
United States The Herbert Irving Pavilion New York New York
United States Newark Beth Israel Medical Center Newark New Jersey
United States Children'S Hosp-Kings Daughter Norfolk Virginia
United States University Of Oklahoma Health Sciences Center Oklahoma City Oklahoma
United States Children's Hospital of Orange County Orange California
United States Md Anderson Cancer Center Orlando Orlando Florida
United States Nemours Childrens Hospital Orlando Florida
United States Lpch & Sumc Palo Alto California
United States St. Joseph's Regional Medical Center Paterson New Jersey
United States Children'S Hospital Of Philadelphia Philadelphia Pennsylvania
United States Phoenix Children'S Hospital/Ctr. For Cancer & Blood Ctr. Phoenix Arizona
United States Children's Hospital Of Pittsburgh Of UPMC Pittsburgh Pennsylvania
United States Legacy Emanuel Hospital & Health Center Portland Oregon
United States Oregon Health & Sci Univ Portland Oregon
United States Rhode Island Hospital Providence Rhode Island
United States Kaiser Medical Center Roseville California
United States Washington University Medical Center Saint Louis Missouri
United States All Children'S Hospital Saint Petersburg Florida
United States Primary Children's Medical Center Salt Lake City Utah
United States Ucsf - Hematology/Oncology San Francisco California
United States Seattle Children'S Seattle Washington
United States Southern Illinois University School Of Medicine Springfield Illinois
United States SUNY Upstate Medical University Syracuse New York
United States St. Joseph's Children's Hospital Tampa Florida
United States Scott & White - McLane Children's Specialty Clinic Temple Texas
United States Mercy Children's Hospital Toledo Ohio
United States The Toledo Children'S Hospital Toledo Ohio
United States New York Medical College Valhalla New York
United States Children'S National Medical Center Washington District of Columbia
United States St. Mary'S West Palm Beach Florida
United States A. I. Dupont Hospital For Children Wilmington Delaware
United States Wake Forest University Winston-Salem North Carolina
United States UMass Memorial Medical Center Worcester Massachusetts

Sponsors (3)

Lead Sponsor Collaborator
Bristol-Myers Squibb Children's Oncology Group, EsPhALL

Countries where clinical trial is conducted

United States,  Australia,  Canada,  Italy,  Puerto Rico,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary 3-year Event-free Survival (EFS) Rate 3-year EFS rate is defined as the percentage of participants without event after 3 years since the start of study treatment.
Events for EFS are defined as ANY first one of the following:
Lack of complete response in bone marrow
Relapse at any site
Development of second malignant neoplasm
Death from any cause
From first dose to 3 years following first dose
Secondary Number of Participants Experiencing Adverse Events Number of participants experiencing different types of all causality all grade adverse events From first dose to 100 days following last dose (up to approximately 23 months)
Secondary Event-Free Survival (EFS) Rate (Kaplan-Meier Estimates) Overall estimation of the EFS of dasatinib plus chemotherapy was performed utilizing the Kaplan-Meier (KM) Product Limit method. The 3-year and 5-year EFS rates were computed with the corresponding 95% CI's using Greenwood's formula. Analyses of EFS included KM plots with number of patients at risk. Participants who neither relapse nor die or who are lost to follow-up were censored on the date of their last bone marrow, CSF assessment or physical exam, whichever occurred last. From first dose to 3 years or 5 years following first dose
Secondary Complete Remission Rate Complete Remission rate is defined as the percentage of participants achieving a complete remission, i.e. < 5% lymphoblasts in bone marrow and in CSF, with no evidence of other extramedullary disease. Complete remission will be assessed at the end of Induction IA, end of induction IB and end of the consolidation period for all treated participants. From first dose to End of Induction Period Ia (up to 5 weeks) or Ib (up to 9 weeks) or End of Consolidation Period (up to 22 weeks)
Secondary Percentage of Participants Negative for Minimal Residual Disease (MRD) MRD was by real-time qPCR for clone-specific immunoglobulin and T-cell receptor gene rearrangements (IG/TCR). Participants were declared as MRD negative if the MRD level is undetectable providing the assay lower limit of quantification is at least 0.1% From first dose to End of Induction Period Ia (up to 5 weeks) or Ib (up to 9 weeks) or End of Consolidation Period (up to 22 weeks)
Secondary Percentage of Participants With BCR-ABL Mutations at Baseline and at Time of Disease Progression or Relapse A BCR-ABL mutation is defined as the presence of a detectable amino acid substitution in the ABL kinase domain, assessed by Real-time quantitative PCR. At baseline (prior to start of study treatment) and at disease progression or relapse (up to approximately 3 years)