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Phase 2 N=29 Treatment

Single Agent Erlotinib in Chemotherapy-naive Androgen Independent Prostate Cancer

Prostate Cancer

Enrolled (actual)
29
Serious AEs
41.4%
Results posted
Oct 2013
Primary outcome: Primary: Overall Clinical Benefit of Tarceva in CRPC. — 36 percentage of pts w/clinical benefit

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Tarceva (Drug)
Age
Pediatric, Adult, Older Adult
Sex
Male
Sponsor
Oncology Specialists, S.C.
Primary completion
Oct 2010

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Clinical Benefit of Tarceva in CRPC.
36
SECONDARY
Overall Survival
58
SECONDARY
Time to Disease Progression
2

Summary

Objectives to evaluate the activity of Erlotinib in prostate cancer patients who are hormone refractory and androgen independent and have not been exposed to chemotherapy.

Eligibility Criteria

Inclusion Criteria

  • Documented prostate cancer regardless of Gleason score
  • Patients should be considered hormone refractory and androgen independent. They must fail LHRH analogues, and anti-androgen withdrawal trial.
  • Failure is confirmed by an increase in PSA value of 10% or more than the value immediately before, and confirmed by another assessment 2 weeks later.
  • Patients have to have measurable disease either biochemically using rising PSA or/and with metastatic disease to the bone or visceral organs.
  • Performance status of 2 or less using ECOG scale.· Adequate liver function tests with ALT/AST being < 3x normal, total bilirubin of 1.5 or less, and adequate renal function measured by a creatinine of 2.0 mg/dl or less. Alkaline phosphatase values are never exclusion criteria if it is deemed related to bone metastases.
  • Patients need to have adequate bone marrow function. ANC of 1000 or above, Hgb of 9.0 g/dl or above, and platelets of 100,000 or above. If other causes are affecting plts counts such as autoimmune disorders, patients are allowed on study.
  • Patients with inadequate bone marrow function that is deemed related to bone marrow involvement with prostate cancer are allowed at the investigator's discretion.
  • Patients with other malignancies are allowed as long as there is no evidence of the other malignancy present at entry time, and it has been 3 years or more since the treatment for the other disorder was completed.
  • Patients with prior exposure to investigational therapies including vaccines are allowed on this study as long as their last exposure was 4 weeks prior to study entry.Patients with known bone metastases are allowed to receive intravenous bisphosphonates such as aredia or zometa.
  • Patients on oral bisphosphonates are also allowed.
  • Chemo Naive

Exclusion Criteria

  • Patients with prior exposure to Tarceva
  • Patients who have received any prior systemic chemotherapy for prostate cancer. Exposure to chemotherapy for other malignancies is allowed as long as last chemotherapy was completed 3 years prior to study entry.
  • Patients with prior malignancies are excluded except for those who have non-melanoma skin cancers or other cancers that are in remission with the last therapy given 3 years prior to enrollment.
  • Prior exposure to any form of steroids is allowed and is not considered exclusion criteria.
  • Performance status of 3 or above using ECOG scale.
  • Known HIV positive status Known CNS involvement with prostate cancer
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00272038). 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.

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