A Phase I Study of the Oral Platinum Agent Satraplatin in Combination With Weekly Docetaxel

This is a single-center, open-label (sequential-group dose-escalation dose-finding) phase I study of satraplatin and docetaxel in patients who have received prior chemotherapy regimens. Once the MTD is determined, an additional 6 patients, all with chemotherapy-naïve HRPC, will be enrolled. Once a recommended dose(s) (RD(s)) for phase 2 studies has/have been determined, 6 additional patients with chemotherapy-naïve HRPC will be enrolled at the RD to further evaluate safety and efficacy.

Study Overview

• Status: Terminated
• Conditions: Prostate Cancer; Tumors
• Intervention / Treatment: Drug: Satraplatin

Detailed Description

RATIONALE:

Satraplatin is an oral platinum analog that is currently being evaluated in combination with prednisone in a phase III clinical trial in patients with HRPC who have progressed following one prior chemotherapy regimen.

Docetaxel is a taxane that is indicated for the treatment of patients with non-small cell lung, breast, and prostate cancers. Specifically, it was recently approved in combination with prednisone for the treatment of patients with hormone refractory prostate cancer (HRPC). Docetaxel administered every 3 weeks was associated with a survival advantage versus mitoxantrone. Docetaxel administered weekly showed an improvement in survival versus mitoxantrone that was not statistically significant. However, it was better tolerated than docetaxel administered every 3 weeks, with significantly less grade 3 and 4 toxicities, especially neutropenia. The combination of satraplatin and weekly docetaxel may be a feasible regimen for patients with chemotherapy-naïve HRPC and for patients with other malignancies for which these medications show activity.

OBJECTIVE:

The objective of this study is to determine the optimum doses for satraplatin and weekly docetaxel when the 2 drugs are given in combination.

• Study Type: Interventional
• Enrollment (Actual): 25
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Tennessee
    • Nashville, Tennessee, United States
      • Sarah Cannon Research Institute

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Histologically proven advanced solid tumors.
• 2 prior chemotherapy regimens.
• Age greater than or equal to 18 years.
• Eastern Cooperative Oncology Group performance status 0-1.
• Life expectancy greater than 3 months.
• At least 4 weeks between prior surgery or radiotherapy and enrollment.
• Adequate organ function as defined by the following criteria (must be obtained within 1 week of the first day of treatment):

Absolute neutrophil count ≥ 1500/µL. Hemoglobin ≥ 10.0 g/dl. Platelets ≥ 100,000/µL. Serum creatinine ≤ 1.5 upper limit of normal (ULN). Serum bilirubin ≤ ULN. AST/ALT ≤ 1.5 x the ULN.

• Patients must be able to swallow capsules.
• Patients must give written informed consent before study participation.
• No history of another cancer within the past 5 years (except basal or squamous cell carcinoma of the skin).
• No brain or leptomeningeal metastases.
• Female patients must not be pregnant or lactating and must be willing to practice contraception. Males must agree to contraceptive practices.

For HRPC cohort

• Patient must continue to be administered an LHRH agonist if they were receiving it at the time of screening for entry onto this protocol. Patients who have undergone bilateral orchiectomy do not need to be on LHRH agonists.
• Patient must be off of anti-androgen medications for ≥ 6 weeks.
• Patient must have castrate level of testosterone (< 50 ng/dL).

• Progressive HRPC as defined by one of the following:

  • Rising PSA
  • Sequential imaging studies
  • Clinical suspicion in the view of the treating physician

Exclusion Criteria:

• Patients who are unwilling to use contraception.
• Patients with a history of major gastrointestinal surgery.
• Pre-existing peripheral neuropathy > grade 1.
• Pre-existing edema > grade 1.
• Patients with hearing loss or tinnitus > grade 2.
• Prior RT to >25% of the bone marrow.
• Concomitant use of medications that inhibit cytochrome P450 3A4 (including aprepitant).
• Other concurrent chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational (utilized for non-FDA - approved indications and in the context of a research investigation).

• Patients who have not recovered (≥ grade 1) from the following toxicities of previous regimens before enrollment:

  • hematologic toxicities (parameters defined in protocol
  • fatigue
  • mucositis
  • nausea/vomiting/diarrhea.
• Uncontrolled intercurrent illness including, but not limited to, ongoing active infection, uncontrolled congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness that would limit compliance with study requirements.
• History of HIV or AIDS related illness.
• History of severe hypersensitivity reaction to docetaxel, polysorbate, or other drugs formulated with polysorbate 80.
• Evidence of concurrent second malignancy.
• History of bone marrow or major organ transplant.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
To assess the maximum tolerated dose (MTD) of satraplatin administered every 4 weeks in combination with docetaxel administered weekly (3 of 4 weeks)	30 days

Secondary Outcome Measures

Outcome Measure	Time Frame
To assess safety and tolerability (as per NCI-CTCAE version 3.0)	30 days
To assess preliminary antitumor activity	6 months

Collaborators and Investigators

• Sponsor: Agennix
• Investigators: Study Director: Michael Petrone, MD, GPC Biotech Inc.

Study record dates

Study Major Dates

• Study Start: March 1, 2006
• Primary Completion (Actual): March 1, 2009
• Study Completion (Actual): March 1, 2009

Study Registration Dates

• First Submitted: April 10, 2006
• First Submitted That Met QC Criteria: April 11, 2006
• First Posted (Estimate): April 12, 2006

Study Record Updates

• Last Update Posted (Estimate): May 10, 2012
• Last Update Submitted That Met QC Criteria: May 9, 2012
• Last Verified: May 1, 2012

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Neoplasms; Urogenital Neoplasms; Neoplasms by Site; Genital Neoplasms, Male; Prostatic Diseases; Prostatic Neoplasms; Antineoplastic Agents; Satraplatin
• Other Study ID Numbers: SAT1-05-09