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A Phase II Study of Dasatinib in Children and Adolescents With Newly Diagnosed Chronic Phase Chronic Myelogenous Leukemia (CML) or With Ph+ Leukemias Resistant or Intolerant to Imatinib

Phase 2
Completed
Conditions
Leukemia
Interventions
Registration Number
NCT00777036
Lead Sponsor
Bristol-Myers Squibb
Brief Summary

The purpose of this study is to determine whether dasatinib is safe and effective in children and adolescents with newly diagnosed chronic myeloid leukemia (CML), or in children with Ph+ acute lymphoblastic leukemia (ALL), accelerated or blast phases CML who relapse after imatinib or who are resistant or intolerant to imatinib. The side effects of this oral investigational drug in children and adolescents will be evaluated

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
130
Inclusion Criteria
  • CP-CML who prove resistant or intolerant to imatinib (Cohort 1)
  • Ph+ ALL, AP-CML, or BP-CML who are resistant or intolerant to or who relapse after imatinib therapy (Cohort 2)
  • Newly diagnosed, treatment naive CP-CML (Cohort 3)
  • Lansky or Karnofsky scale >50
  • Life expectancy ≥12 weeks
  • Adequate hepatic and renal function
  • Written informed consent
  • Target Population for the PK substudy must obtain written informed consent from subject, or from parents or legal guardians for minor subjects, according to local law and regulation
  • Target Population for the PK substudy subjects must have CP-CML and be taking daily dasatinib (tablets or PFOS) either as part of Cohort 1 or Cohort 3 of this protocol. Patients receiving commercial dasatinib tablets outside of this protocol may be invited to participate in this PK substudy
  • Target Population for the PK substudy subjects with CP-CML who are tolerating dasatinib tablet dose of at least 60 mg/m2 or dasatinib PFOS dose of at least 72 mg/m2
  • Target Population for the PK substudy prior exposure to imatinib or other TKI therapy is permissible
  • Target Population for the PK substudy subjects must meet relevant inclusion criteria
Exclusion Criteria
  • Eligibility for potentially-curative therapy including hematopoietic stem-cell transplantation
  • Symptomatic CNS involvement (other than signs and symptoms caused by leptomeningeal disease)
  • Isolated extramedullary disease
  • Prior therapy with Dasatinib
  • Target Population for the PK substudy subjects participating in the PK substudy must comply with the relevant exclusion criteria
  • Target Population for the PK substudy subjects are not allowed to use proton pump inhibitors, H2 antagonists, CYP3A4 inhibitors and inducers when entering the PK substudy

Other inclusion/exclusion criteria may apply

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Cohort 1: Imatinib-resistant/intolerant CP-CMLDasatinibDasatinib 60 mg/m² tablet every day (QD) \[with a maximum dose of 100 mg QD for subjects with high BSA\] for minimum of 24 months, may continue as long as deriving clinical benefit OR Dasatinib 72 mg/m² powder for oral suspension (PFOS) QD \[with a maximum dose of 120 mg QD for subjects with high BSA\] for minimum of 24 months, may continue as long as deriving clinical benefit
Cohort 3: Newly diagnosed, treatment naïve CP-CMLDasatinibDasatinib 60 mg/m² tablet QD \[with a maximum dose of 100 mg QD for subjects with high BSA\] for minimum of 24 months, may continue as long as deriving clinical benefit OR Dasatinib 72 mg/m² PFOS QD \[with a maximum dose of 120 mg QD for subjects with high BSA\] for minimum of 24 months, may continue as long as deriving clinical benefit
Cohort 2: Ph+ALL or AP- or BP-CMLDasatinibDasatinib 80 mg/m² tablet QD \[with a maximum dose of 140 mg QD for subjects with high BSA\] for minimum of 24 months, may continue as long as deriving clinical benefit OR Dasatinib 96 mg/m² PFOS QD \[with a maximum dose of 170 mg QD for subjects with high BSA\] for minimum of 24 months, may continue as long as deriving clinical benefit
Primary Outcome Measures
NameTimeMethod
Complete Hematologic Response (CHR) RateFrom first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)

Complete Hematologic Response (CHR) rate is defined as the proportion of all treated participants who achieve a confirmed CHR while on-study, expressed as percentage. CHR is defined as including no more than 5% blasts in bone marrow and normal white blood cell count without blasts in peripheral blood, expressed as percentage. The denominator of the CHR response rate consists of all treated participants in Cohort 2, and the numerator is all participants in Cohort 2 achieving CHR. 95% confidence interval was calculated by Clopper-Pearson exact method.

Major Cytogenetic Response (MCyR) RateFrom first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)

Major Cytogenetic Response (MCyR) rate is defined as the proportion of all treated participants who achieved a complete (0%) or partial (1%-35% Ph+ metaphases in at least 20 metaphases in bone marrow) cytogenetic response, expressed as percentage. The denominator of the MCyR response rate consists of all treated participants in Cohort 1, and the numerator is all participants in Cohort 1 achieving MCyR. 95% confidence interval was calculated by Clopper-Pearson exact method.

Complete Cytogenetic Response (CCyR) RateFrom first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)

Complete Cytogenetic Response (CCyR) rate is defined as the proportion of all treated participants who achieve a CCyR while on-study, expressed as a percentage. CCyR rate is defined as 0% Ph+ metaphases in at least 20 metaphases in bone marrow. The denominator of the CCyR response rate consists of all treated participants in Cohort 3, and the numerator is all participants in Cohort 3 achieving CCyR. 95% confidence interval was calculated by Clopper-Pearson exact method.

Secondary Outcome Measures
NameTimeMethod
Major Cytogenetic Response (MCyR) Rate in Cohort 2From first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)

Major Cytogenetic Response (MCyR) rate was defined as the proportion of all treated participants who achieved a complete (0%) or partial (1%-35% Ph+ metaphases in at least 20 metaphases in bone marrow) cytogenetic response. The percentage of treated participants in each arm with MCyR is reported.

Progression-Free Survival (PFS) Rate at 2 Years2 years

PFS is defined as time from the first dosing date until the time PD is first documented by the investigator or death. Participants who die without a reported date of progression will be considered to have progressed on the date of death. Participants who neither progress nor die will be censored on the date of their last cytogenetic or hematologic assessment. The percentages of progression-free participants at 2 years are based on Kaplan-Meier estimation. Disease Progression was defined as any of the following criteria: -For CP-CML, progression to AP-CML or BP-CML while at highest tolerated dose -Increasing WBC -Loss of CHR (defined as any of the following: WBC count rises to \>20.0x10\^9/L; Platelet count rises to \>600x10\^9/L; appearance of extramedullary disease; appearance of \>5% myelocytes+metamyelocytes in blood; appearance of blasts/promyelocytes in peripheral blood) -Loss of MCyR or increase in Ph+ bone marrow cells by \>=30% from nadir -Death from any case during treatment

Major Cytogenetic Response (MCyR) Rate up to 2 Years24 months

Major Cytogenetic Response (MCyR) rate is defined as the proportion of all treated participants who achieved a complete (0%) or partial (1%-35% Ph+ metaphases in at least 20 metaphases in bone marrow) cytogenetic response. The percentage of treated participants with MCyR is reported by arm.

Time to Major Cytogenetic Response (MCyR)From first dose until MCyR criteria are met (assessed up to September 2016, approximately 90 months)

Time to MCyR is defined as the time from first dose of dasatinib until the first day MCyR criteria are met, computed only for participants whose best response is MCyR. (Based on \>=20 Metaphases)

Time to Complete Cytogenetic Response (CCyR)From first dose until CCyR criteria are met, assessed up to September 2016 (approximately 90 months)

Time to CCyR is defined as the time from first dose of dasatinib until the first day CCyR criteria are met, computed only for participants whose best response is CCyR. (Based on \>=20 Metaphases)

Time to Complete Hematologic Response (CHR)From first dose until CHR criteria are met, assessed up to September 2016 (approximately 90 months)

Time to CHR is defined as the time from first dose of dasatinib until the first day CHR criteria are met, provided they are confirmed 4 weeks later, computed only for participants whose best response is CHR.

Major Molecular Response (MMR) RateFrom date of first treatment to date of MMR (assessed up to September 2016, approximately 90 months)

Molecular response was assessed using BCR-ABL transcript levels measurement by real-time quantitative polymerase chain reaction (qPCR). MMR for participants with the p210 BCR-ABL transcript variant was defined as a ratio BCR-ABL/ABL \<= 10-3 or 0.1% on the international scale. In this study, ABL was used as the control-gene. For a participant with the p190 BCR-ABL transcript variant (occurring in Cohort 2 only), on-study assessments were compared to the participant's individual baseline BCR-ABL/ABL ratio and a reduction to \< 0.1% or a 3-log reduction from baseline was considered an MMR.

Complete Hematologic Response (CHR) Rate in Cohorts 1 and 3From first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)

Complete Hematologic Response (CHR) rate defined as the proportion of all treated participants who achieve a confirmed CHR while on-study. CHR is defined as including no more than 5% blasts in bone marrow and normal white blood cell count without blasts in peripheral blood. The percentage of treated participants in each arm with CHR is reported.

Duration of Complete Cytogenetic Response (CCyR)From first day criteria are met for CCyR until the date of progressive disease or death (assessed up to September 2016, approximately 90 months)

Duration of CCyR will be computed from the first day criteria are met for CCyR until the date progressive disease (PD) is reported (or treatment is discontinued for PD) or death. Participants who neither discontinue due to PD nor die will be censored on the date of their last hematologic or cytogenetic assessment, whichever comes last. (Based on \>=20 Metaphases)

Disease-Free Survival Rate at 2 Years2 years

Disease free survival is defined as time from CCyR for participants with newly diagnosed chronic phase CML and for participants with chronic phase CML who are resistant or intolerant to imatinib (cohort 3 and cohort 1), and as time from CHR for participants with advanced phase CML and PH + ALL (cohort 2) until the time progression is first documented by the investigator or death from any cause. The percentages of disease-free participants at 2 years are based on Kaplan-Meier estimation. (CML: Chronic Myeloid Leukemia)

Complete Cytogenetic Response (CCyR) Rate up to 2 Years24 months

Complete Cytogenetic Response (CCyR) rate is defined as the proportion of all treated participants who achieve a CCyR while on-study. CCyR rate is defined as 0% Ph+ metaphases in at least 20 metaphases in bone marrow. The percentage of treated participants with CCyR is reported by arm.

Duration of Major Cytogenetic Response (MCyR)From first day criteria are met for MCyR until the date PD is reported or death (assessed up to September 2016, approximately 90 months)

Duration of MCyR will be computed from the first day criteria are met for MCyR until the date progressive disease (PD) is reported (or treatment is discontinued for PD) or death. Participants who neither discontinue due to PD nor die will be censored on the date of their last hematologic or cytogenetic assessment, whichever comes last. (Based on \>=20 Metaphases)

Overall Survival (OS) Rate at 2 Years2 years

OS is defined as time from the first dosing date until the time of death. All participants will be followed yearly for survival for up to 5 years after treatment discontinuation. Participants who have not died or who are lost to follow-up will be censored on the last date the participant is known to be alive. The percentages of surviving participants at 2 years are based on Kaplan-Meier estimation.

Rate of Best Cytogenetic ResponseFrom first dose of study therapy until 30 days after last dose (Assessed up to September 2016, approximately 90 months)

The number of participants achieving their best on-study cytogenetic response was reported as a percentage of all treated participants in that arm. (Based on \>=20 Metaphases)

Duration of Complete Hemotologic Response (CHR)From first day criteria are met for CHR until date of disease progression or death (assessed up to September 2016, approximately 90 months)

Duration of CHR will be computed from the first day all criteria are met for CHR, provided they are confirmed 4 weeks later, until the date progressive disease (PD) is reported (or treatment is discontinued for PD) or death. Participants who neither discontinue due to PD nor die will be censored on the date of their last hematologic assessment.

Complete Molecular Response (CMR) RateFrom date of first treatment to date of CMR (assessed up to September 2016, approximately 90 months)

Molecular response was assessed using BCR-ABL transcript levels measurement by real-time quantitative polymerase chain reaction (qPCR). (CMR) is defined as absence of BCR-ABL rearrangements by real-time qPCR analysis. The percentage of treated participants with CMR is reported by arm.

Complete Molecular Response (CMR) Rate up to 2 Years24 months

Molecular response will be assessed using BCR-ABL transcript levels measurement by real-time quantitative polymerase chain reaction (qPCR). (CMR) is defined as absence of BCR-ABL rearrangements by real-time qPCR analysis. The percentage of treated participants with CMR is reported by arm.

Major Molecular Response (MMR) Rate up to 2 Years24 months

Molecular response will be assessed using BCR-ABL transcript levels measurement by real-time qPCR. MMR for participants with the p210 BCR-ABL transcript variant is defined according to the recommendations of Hughes et al. as a ratio BCR-ABL/ABL \<= 10-3 or 0.1% on the international scale proposed by the authors. The standardized baseline, as established in the IRIS trial, is taken to represent 100% on the international scale and a 3-log reduction in ratio (BCR-ABL transcripts/ABL or BCR) from the standardized baseline (MMR) is fixed at 0.1%. In this study, ABL or other housekeeping gene, will be used as the control-gene. For a participant with the p190 BCR-ABL transcript variant, on-study assessments will be compared to the participant's individual baseline BCR-ABL/ABL ratio and a reduction to \< 0.1% or a 3-log reduction from baseline will be considered an MMR. The percentage of treated participants with MMR is reported by arm.

Trial Locations

Locations (109)

Local Institution - 0078

🇨🇦

Edmonton, Alberta, Canada

Local Institution - 0028

🇺🇸

Seattle, Washington, United States

Seattle Children'S

🇺🇸

Seattle, Washington, United States

Local Institution - 0043

🇦🇷

Bunos Aires, Buenos Aires, Argentina

Hospital Nacional Profesor Alejandro Posadas

🇦🇷

El Palomar, Buenos Aires, Argentina

Local Institution - 0049

🇦🇷

El Palomar, Buenos Aires, Argentina

Local Institution - 0042

🇦🇷

Cordoba, Argentina

Local Institution - 065

🇦🇺

Randwick, New South Wales, Australia

Local Institution - 069

🇦🇺

Westmead, New South Wales, Australia

Local Institution - 0064

🇦🇺

Sth Brisbane, Queensland, Australia

Local Institution - 067

🇦🇺

North Adelaide, South Australia, Australia

Local Institution - 0066

🇦🇺

Parkville, Victoria, Australia

Local Institution - 0021

🇧🇷

Curitiba, Parana, Brazil

Local Institution - 0022

🇧🇷

Porto Alegre, Rio Grande Do Sul, Brazil

Local Institution - 0019

🇧🇷

São Paulo, SAO Paulo, Brazil

Local Institution - 0020

🇧🇷

Campinas, Brazil

Local Institution - 0039

🇧🇷

Sao Paulo, Brazil

Alberta Children'S Hospital

🇨🇦

Calgary, Alberta, Canada

Local Institution - 0079

🇨🇦

Calgary, Alberta, Canada

Local Institution - 080

🇨🇦

Montreal, Quebec, Canada

Local Institution - 0030

🇫🇷

Lyon, France

Local Institution - 0032

🇫🇷

Nantes, France

Local Institution - 0037

🇫🇷

Paris, France

Local Institution - 0029

🇫🇷

Paris, France

Local Institution - 036

🇫🇷

Poitiers, France

Local Institution - 075

🇩🇪

Frankfurt, Germany

Local Institution - 0074

🇩🇪

Hannover, Germany

Stollery Children'S Hospital

🇨🇦

Edmonton, Alberta, Canada

Bc Children'S Hospital

🇨🇦

Vancouver, British Columbia, Canada

Local Institution

🇬🇧

Birmingham, West Midlands, United Kingdom

Local Institution - 0005

🇺🇸

Phoenix, Arizona, United States

Local Institution - 077

🇨🇦

Vancouver, British Columbia, Canada

Phoenix Children'S Hospital

🇺🇸

Phoenix, Arizona, United States

Jonathan Jaques Children'S Cancer Center

🇺🇸

Long Beach, California, United States

Local Institution - 0001

🇺🇸

Long Beach, California, United States

Children'S Hospital Of Orange County

🇺🇸

Orange, California, United States

Local Institution - 0024

🇺🇸

Orange, California, United States

Children'S Hospital

🇺🇸

Aurora, Colorado, United States

Local Institution - 0004

🇺🇸

Aurora, Colorado, United States

Children's Healthcare Of Atlanta - Egleston

🇺🇸

Atlanta, Georgia, United States

Local Institution - 047

🇺🇸

Atlanta, Georgia, United States

Children's Hospital of Chicago

🇺🇸

Chicago, Illinois, United States

Local Institution - 0072

🇺🇸

Chicago, Illinois, United States

Dana Faber Cancer Institute

🇺🇸

Boston, Massachusetts, United States

Dana Farber Cancer Institute.

🇺🇸

Boston, Massachusetts, United States

Local Institution - 0040

🇺🇸

Boston, Massachusetts, United States

Stephen D. Hassenfeld Children'S Center

🇺🇸

New York, New York, United States

Local Institution - 0061

🇺🇸

New York, New York, United States

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

Memorial Sloan Kettering Nassau

🇺🇸

New York, New York, United States

Oregon Health & Sci Univ

🇺🇸

Portland, Oregon, United States

Local Institution - 0002

🇺🇸

Portland, Oregon, United States

Iwk Health Centre

🇨🇦

Halifax, Nova Scotia, Canada

Local Institution - 073

🇨🇦

Halifax, Nova Scotia, Canada

Children'S Hospital Of Philadelphia

🇺🇸

Philadelphia, Pennsylvania, United States

Local Institution - 0014

🇺🇸

Philadelphia, Pennsylvania, United States

Children'S Hospital Of Pittsburgh

🇺🇸

Pittsburgh, Pennsylvania, United States

Local Institution - 0003

🇺🇸

Pittsburgh, Pennsylvania, United States

Local Institution - 0035

🇺🇸

Houston, Texas, United States

Children'S Hospital Of Eastern Ontario

🇨🇦

Ottawa, Ontario, Canada

Local Institution - 086

🇨🇦

Ottawa, Ontario, Canada

Local Institution - 076

🇨🇦

Toronto, Ontario, Canada

The Hospital For Sick Children

🇨🇦

Toronto, Ontario, Canada

Chu Ste-Justine

🇨🇦

Montreal, Quebec, Canada

MD Anderson Cancer Center

🇺🇸

Houston, Texas, United States

Local Institution - 0048

🇺🇸

Houston, Texas, United States

Texas Children'S Cancer Center

🇺🇸

Houston, Texas, United States

Local Institution - 0089

🇮🇳

Navrangpura, Ahmedabad, Gujarat, India

Local Institution - 0094

🇮🇳

Pune, Maharashtra, India

Local Institution - 0093

🇮🇳

Madurai, Tamil Nadu, India

Local Institution - 0088

🇮🇳

Bangalore, India

Local Institution - 0082

🇮🇳

Kolkatta, India

Local Institution - 0085

🇮🇳

Mumbai, India

Local Institution - 0084

🇮🇳

Trivandrum, India

Local Institution - 038

🇮🇹

Bologna, Italy

Local Institution - 006

🇮🇹

Monza, Italy

Local Institution - 070

🇮🇹

Roma, Italy

Local Institution - 0059

🇮🇹

Roma, Italy

Local Institution - 015

🇮🇹

Torino, Italy

Local Institution - 0092

🇰🇷

Seoul, Korea, Republic of

Local Institution - 0091

🇰🇷

Seoul, Korea, Republic of

Local Institution - 0051

🇲🇽

Cuauhtémoc, Distrito Federal, Mexico

Local Institution - 0052

🇲🇽

Mexico D.f., Distrito Federal, Mexico

Local Institution - 0053

🇲🇽

Mexico, Distrito Federal, Mexico

Hospital Civil De Guadalajara - Nuevo Dr. Juan I. Menchaca

🇲🇽

Guadalajara, Jalisco, Mexico

Local Institution - 0054

🇲🇽

Guadalajara, Jalisco, Mexico

Local Institution - 0060

🇲🇽

Monterrey, N.l., Nuevo Leon, Mexico

Local Institution - 0050

🇲🇽

Monterrey, Nuevo Leon, Mexico

Local Institution - 0007

🇳🇱

Rotterdam, Netherlands

Local Institution - 0099

🇳🇱

Utrecht, Netherlands

Local Institution - 0095

🇷🇴

Bucharest, Romania

Local Institution - 0097

🇷🇴

Sector 2, Romania

Local Institution - 0017

🇷🇺

Moscow, Russian Federation

Local Institution - 0023

🇷🇺

Moscow, Russian Federation

Local Institution - 0018

🇷🇺

Saint-petersburg, Russian Federation

Local Institution - 0071

🇸🇬

Singapore, Singapore

Local Institution - 0055

🇿🇦

Bloemfontein, FREE State, South Africa

Local Institution - 058

🇿🇦

Pretoria, Gauteng, South Africa

Local Institution - 0057

🇿🇦

Cape Town, Western CAPE, South Africa

Local Institution - 062

🇿🇦

Tygerberg, Western CAPE, South Africa

Local Institution - 0013

🇪🇸

Barcelona, Spain

Local Institution - 0012

🇪🇸

Barcelona, Spain

Local Institution - 0011

🇪🇸

Madrid, Spain

Local Institution - 0010

🇪🇸

Madrid, Spain

Local Institution - 0041

🇪🇸

Malaga, Spain

Local Institution - 0033

🇪🇸

Valencia, Spain

Local Institution - 0016

🇬🇧

Glasgow, Central, United Kingdom

Local Institution - 0009

🇬🇧

Sutton, Surrey, United Kingdom

Local Institution - 0008

🇬🇧

Birmingham, West Midlands, United Kingdom

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