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Phase I Trial of Fixed Dose STI571 (Imatinib Mesylate) With Escalating Doses of Docetaxel in Patients With Metastatic Androgen-Independent Prostate Cancer

Phase 1
Not Enrolling
Prostate Cancer

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Trial Information

Phase I Trial of Fixed Dose STI571 (Imatinib Mesylate) With Escalating Doses of Docetaxel in Patients With Metastatic Androgen-Independent Prostate Cancer


1. To define the maximum tolerated dose of weekly docetaxel in combination with fixed-dose
oral STI571 in adult men with metastatic androgen-independent prostate cancer (AIPC).

2. To determine the qualitative and quantitative toxicity of the combination of oral
STI571 and docetaxel.

3. Evaluate PSA modulation with STI571 alone at thirty days in patients with AIPC.

4. Obtain a preliminary estimate of the response rate in AIPC to the combination of STI571
and docetaxel.

5. Obtain tissue for correlative science studies (these are optional studies).

Inclusion Criteria


- Patients with histologic proof of adenocarcinoma of the prostate and must have
progressed on conventional hormonal therapy.

- Patients must have bone metastases which can be demonstrated by bone scans. Lytic
bone lesions should be considered for biopsy if there is a clinical suspicion of
histologic conversion to small cell carcinoma.

- Patients must have evidence of progression of disease. PSA- progression is defined as
2 consecutive increments in PSA (an absolute change of at least 1ng/mL) over 4 weeks.
An increase by 25% of the product of bidimensional disease qualifies as progression.
An increase in the number of metastatic lesions on bone scan qualifies as

- All patients must have a minimum PSA of 1ng/ml.

- Patients on antiandrogens should be discontinued from flutamide or nilutamide for at
least 4 weeks and bicalutamide for 8 weeks. If progression is documented as below
prior to this time interval, patients are eligible.

- Patients must have a performance status of < 2 (ECOG).

- Patients must have an expected survival from cancer or co-morbidity of at least three

- Patients may receive no concurrent chemotherapy, immunotherapy or ketoconazole.

- Patients should not have received prior chemotherapy or radiation within the last 30
days and no Strontium or Samarium within the last 90 days.

- Patients must have castrate serum testosterone levels (< 30ng/dl). For patients who
are medically castrated, luteinizing hormone releasing hormone analog must continue
to maintain testicular suppression.

- Patients must have adequate bone marrow function defined as an absolute peripheral
granulocyte count of > 1,500/mm3 and platelet count of > 100,000/mm3.

- Patients should have adequate hepatic function defined with a bilirubin of < 1.5
mg/dl and AST/ALT < 2X the upper limits of normal.

- Patients should have adequate renal function defined as serum creatinine clearance >
40 cc/min (measured or calculated by Cockcroft and Gault formula) or serum creatinine
< 1.5 X upper limit of normal.

- Fully recovered from any previous surgery (at least 4 weeks since major surgery.

- Patients must sign an informed consent indicating that they are aware of the
investigational nature of this study, in keeping with the policies of the
institution. The only approved consent is attached to this protocol.


- Patients with severe intercurrent infection.

- Patients whose tumors contain small cell or sarcomatoid elements.

- Patients with NYHA Class III/IV CHF, unstable angina or MI in the last 6 months or
evidence of active myocardial ischemia on ECG.

- CNS metastases that are uncontrolled.

- Prior hypersensitivity or dose-limiting toxicity with docetaxel.

- Oxygen-dependent lung disease

- Contraindications to corticosteroids.

- Uncontrolled severe hypertension or uncontrolled diabetes mellitus.

- Second malignancies (except non-melanoma skin cancer) unless disease-free for 3

- Overt psychosis or mental disability or otherwise incompetent to give informed

- Patients with a history of non-compliance with medical regimens or who are considered
potentially unreliable.

Type of Study:


Study Design:

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


United States: Food and Drug Administration

Study ID:




Start Date:

October 2001

Completion Date:

September 2005

Related Keywords:

  • Prostate Cancer
  • Prostate Cancer
  • bone metastasis
  • Prostatic Neoplasms



U.T. M.D. Anderson Cancer Center Houston, Texas  77030