Phase 2
N=29
Single Agent Erlotinib in Chemotherapy-naive Androgen Independent Prostate Cancer
Prostate Cancer
Bottom Line
View on ClinicalTrials.gov: NCT00272038 ↗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
| Outcome | Result | p-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
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.