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Sponsors and Collaborators: |
Evanston Northwestern Healthcare Genentech Northwestern University |
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Information provided by: | Evanston Northwestern Healthcare |
ClinicalTrials.gov Identifier: | NCT00148772 |
The primary objective of this study is to evaluate the effect of erlotinib on the PSA response rate in patients with non-metastatic prostate cancer and a rising PSA on androgen deprivation therapy.
The secondary objectives are to evaluate the effect of erlotinib on the duration of PSA response, to evaluate the effect on the time to PSA progression, to evaluate the toxicity of erlotinib in this patient population, and lastly, to correlate the effect of erlotinib with various epidermal growth factor receptor (EGFR)-related proteins using baseline immunohistochemical (IHC) studies on tissue blocks and peripheral blood mononuclear cells.
Condition | Intervention | Phase |
---|---|---|
Prostate Cancer |
Drug: Erlotinib (Tarceva) |
Phase II |
Study Type: | Interventional |
Study Design: | Prevention, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study |
Official Title: | Phase II Study of Erlotinib in Patients With Non-Metastatic Prostate Cancer With a Rising PSA on Hormone Therapy |
Estimated Enrollment: | 29 |
Study Start Date: | August 2005 |
Patients with prostate cancer who are treated with surgery or radiation often develop recurrence of their cancer which is manifest only by a rising PSA (Prostate Specific Antigen) level. Many of these patients are treated with hormone therapy. After a fall in the PSA, these patients eventually display evidence of tumor progression clearly demonstrated by another rise in PSA level while receiving hormone therapy. Evaluation for evidence of tumor spread is usually negative. There is currently no effective therapy approved for use in these patients.
The drug erlotinib works by blocking the activity of a protein called Epidermal Growth Factor Receptor (EGFR), which is located on the surface of many prostate cancer cells. Blockage of this protein has been shown to inhibit the growth of prostate tumor cells in a laboratory setting and in animal experiments. Erlotinib has been given to patients with other types of cancers. A recently completed study showed that erlotinib improved the survival of patients with advanced lung cancer who failed standard chemotherapy.
There is currently no effective therapy approved for use in patients with this condition. The purpose of this study is to evaluate the effectiveness and side effects of the drug erlotinib in patients with this condition. Erlotinib is an investigational drug that has not yet been approved by the Federal Drug Administration (FDA) for use in prostate cancer, but has been approved for use in lung cancer.
As previously stated: The primary objective of this study is to evaluate the effect of erlotinib on the PSA response rate in patients with non-metastatic prostate cancer and a rising PSA on androgen deprivation therapy.
Secondary objectives are to evaluate the effect of erlotinib on the duration of PSA response, to evaluate the effect on the time to PSA progression, to evaluate the toxicity of erlotinib in this patient population, and lastly, to correlate the effect of erlotinib with various EGFR-related proteins using baseline immunohistochemical (IHC) studies on tissue blocks and peripheral blood mononuclear cells.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Male |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Patients must have adequate major organ function. All values must be obtained within 4 weeks prior to study treatment.
Exclusion Criteria:
Contact: Daniel Shevrin, MD | 847-570-2515 |
United States, Illinois | |
Evanston Northwestern Healthcare | Recruiting |
Evanston, Illinois, United States, 60201 | |
Contact: Erna Kljajo 847-570-1351 | |
Contact: Erik Merwitz, BS 847-570-1597 | |
Principal Investigator: Daniel Shevrin, MD | |
Sub-Investigator: Timothy Kuzel, MD | |
Northwestern University | Recruiting |
Chicago, Illinois, United States, 60611 | |
Contact: Brenda Martone, RN 312-695-1366 | |
Sub-Investigator: Timothy Kuzel, MD |
Principal Investigator: | Daniel Shevrin, MD | Evanston Northwestern Healthcare |
Study ID Numbers: | OSI3316s |
Study First Received: | September 6, 2005 |
Last Updated: | March 28, 2006 |
ClinicalTrials.gov Identifier: | NCT00148772 |
Health Authority: | United States: Food and Drug Administration |
Prostate Cancer Rising PSA Erlotinib Tarceva |
Androgen Deprivation Therapy Hormone Therapy Rising Prostate Specific Antigen (PSA) Non-Metastatic Prostate Cancer |
Erlotinib Prostatic Diseases Genital Neoplasms, Male |
Urogenital Neoplasms Genital Diseases, Male Prostatic Neoplasms |
Neoplasms Neoplasms by Site Molecular Mechanisms of Pharmacological Action |
Enzyme Inhibitors Protein Kinase Inhibitors Pharmacologic Actions |