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Clinical Trials/NCT00371345
NCT00371345
Completed
Phase 2

Phase II Study of Dasatinib (BMS-354825) for Advanced Estrogen/Progesterone Receptor-Positive or Her2/Neu-Positive Breast Cancer

Bristol-Myers Squibb8 sites in 2 countries92 target enrollmentDecember 2006

Overview

Phase
Phase 2
Intervention
Dasatinib
Conditions
Breast Cancer
Sponsor
Bristol-Myers Squibb
Enrollment
92
Locations
8
Primary Endpoint
Number of Participants With Objective Response
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

This study will determine whether the investigational drug dasatinib is effective in treatment of women with progressive advanced ER+/PR+ or Her2/neu+ breast cancer

Registry
clinicaltrials.gov
Start Date
December 2006
End Date
May 2009
Last Updated
15 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • females, 18 or older
  • recurrent, locally advanced, or metastatic breast cancer with expression of ER/PR receptor and/or overexpression of Her2/neu
  • paraffin-embedded tissue block must be available
  • measurable disease
  • prior chemotherapy with an anthracycline and/or a taxane (neoadjuvant, adjuvant, or metastatic setting)
  • 0, 1 or 2 chemotherapies in the metastatic setting
  • adequate organ function

Exclusion Criteria

  • Metastatic disease confined to bone only
  • Symptomatic central nervous system (CNS) metastasis
  • Concurrent medical condition which may increase the risk of toxicity
  • Unable to take oral medication

Arms & Interventions

Dasatinib

Participants with either a Human epidermal growth factor (Her2/neu)-amplified tumor type or ER and/or PgR positive tumor types received oral dasatinib twice daily (BID).

Intervention: Dasatinib

Dasatinib

Participants with either a Human epidermal growth factor (Her2/neu)-amplified tumor type or ER and/or PgR positive tumor types received oral dasatinib twice daily (BID).

Intervention: Dasatinib 100 mg

Outcomes

Primary Outcomes

Number of Participants With Objective Response

Time Frame: From day of first treatment through Week 25 or at time of discontinuation from study treatment.

Tumor response was assessed according RECIST criteria: PR=at least 30% reduction in the sum of the LD of all target lesions in reference to the baseline sum LD, CR=Disappearance of all non-target lesions. Objective tumor response was defined as a PR or CR.

Percentage of Participants With Objective Response

Time Frame: From day of first treatment through Week 25 or at time of discontinuation from study treatment

Tumor response was assessed according RECIST criteria: PR=at least 30% reduction in the sum of the LD of all target lesions in reference to the baseline sum LD, CR=Disappearance of all non-target lesions. Percentage of participants with objective tumor response was determined by the number of participants with PR or CR divided by the total number of response-evaluable participants.

Best Overall Response

Time Frame: From day of first treatment through Week 25 or at time of discontinuation from study treatment

Response assessed using Response Evaluation Criteria In Solid Tumors (RECIST) criteria: Complete Response (CR)=disappearance of all target and non-target lesions; Partial Response (PR)=≥30% decrease in sum of longest diameter (LD) of target lesions; SD=small changes not meeting above criteria; Progressive Disease (PD)=appearance of new lesion(s), ≥ 20% increase in the sum of the LD of target lesions, or progression of existing non-target lesions; Clinical Progression (cPD)=deterioration related to disease requiring treatment without radiographic PD.

Secondary Outcomes

  • Number of Response-evaluable Participants With Disease Control (DCR)(From day of first treatment through Week 25 or at time of discontinuation from study treatment.)
  • Percentage of Response-evaluable Participants With Disease Control (DCR)(From day of first treatment through Week 25 or at time of discontinuation from study treatment.)
  • Number of Participants Who Progressed(From Baseline (Week 0) to time of PD or discontinuation of last participant from study treatment (Week 45))
  • Median Progression Free Survival (PFS)(From Baseline (Week 0) to time of PD or discontinuation of last participant from study treatment (Week 45))
  • Percentage of Participants With Progression-free Survival (PFS) at Weeks 9, 17, and 25(At Weeks 9, 17, and 25)
  • Duration Of Objective Response(the time (in weeks) between the first date that criteria for PR were met and the first date that PD or cPD was observed)
  • Number of Participants With Death, Adverse Events (AEs), and AEs Leading to Discontinuation(Continuous assessment beginning at initiation of study drug until 30 days after the last dose of study drug)
  • Number of Participants With On-study CTCAE Version 3.0 Grade 3-4 Laboratory Abnormalities(Continuous assessment beginning at initiation of study drug until 30 days after the last dose of study drug)
  • Number of Participants With Serious AEs (SAEs), Drug-related AEs, Drug-related SAEs, and Drug-Related Grade 3 AEs(Continuous assessment beginning at initiation of study drug until 30 days after the last dose of study drug)
  • Number Of Participants With Notable Drug-related AEs(Continuous assessment beginning at initiation of study drug until 30 days after the last dose of study drug)
  • Pharmacokinetics (PK): Plasma Concentration of Dasatinib at Week 3(PK assessment was performed at Week 3 visit (Day 15 ±4 days). Blood samples were obtained at Time = 0 hours, and at 1, 3 and 6 hours after each dose, and a trough sample was obtained immediately prior to any dose (~12 hours).)
  • PK: Plasma Concentration of Dasatinib at Week 7 or Week 9(PK assessment was performed at Week 7 or 9 visit. Blood samples were obtained at Time = 0 hours, and at 1, 3 and 6 hours after each dose, and a trough sample was obtained immediately prior to any dose (~12 hours).)
  • Pharmacodynamics: Percent Change From Baseline In Plasma Level of Collagen Type IV at Week 3 in Participants With and Without DCR(At Baseline and Week 3 of treatment (Day 15 ±4 days))
  • Pharmacodynamics: Percent Change From Baseline In Plasma Level of Collagen Type IV at Week 5 in Participants With and Without DCR(Week 5)
  • Pharmacodynamics: Percent Change From Baseline In Plasma Level of VEGFR2 at Week 3 in Participants With and Without DCR(At Baseline and Week 3 of treatment (Day 15 ±4 days))
  • Pharmacodynamics: Percent Change From Baseline In Plasma Level of VEGFR2 at Week 5 in Participants With and Without DCR(At Baseline and Week 5 of treatment)

Study Sites (8)

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