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Phase 2 Completed N=29 Treatment

Lapatinib in Treating Patients With Prostate Cancer That Did Not Respond to Hormone Therapy

Source: ClinicalTrials.gov NCT00246753 ↗
Enrolled (actual)
29
Serious AEs
13.8%
Results posted
Jun 2017
Primary outcomePrimary: Number of Patients Experiencing Decline in Prostate-specific Antigen — 2 Participants

Summary

RATIONALE: Lapatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase II trial is studying how well lapatinib works in treating patients with prostate cancer that did not respond to hormone therapy.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Patients Experiencing Decline in Prostate-specific Antigen
2
SECONDARY
Time to Prostate-Specific Antigen (PSA) Progression
29
SECONDARY
Predictive Molecular Markers of Response to Treatment With Lapatinib (GW572016)

Eligibility Criteria

Inclusion Criteria

  • Patients must have histologically confirmed diagnosis of adenocarcinoma of the prostate.
  • On androgen deprivation therapy for prostate cancer (either bilateral orchiectomy or medical castration with the testosterone level of 18 years.
  • Life expectancy greater than 12 weeks
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  • Cardiac ejection fraction within the institutional range of normal as measured by echocardiogram or multigated acquisition scan (MUGA) scan.
  • Men must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for the duration of study participation since the effects of GW572016 on the developing human fetus at the recommended therapeutic dose are unknown.
  • Ability to swallow and retain oral medication.
  • Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria

  • Patients who have had prior treatment with ErbB family targeting therapies.
  • Patients who have not recovered from adverse events due to agents administered more than 4 weeks earlier.
  • Prior chemotherapy for prostate cancer
  • Patients with known brain metastases
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to GW572016.
  • Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
  • A history of a positive HIV test in the past.
  • Patients with GI tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for IV alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis).
  • Concomitant requirement for medication classified as CYP3A4 inducers or inhibitors (please refer to section 3.2.2 for a list of medications).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00246753). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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