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Prostate CancerPhase 2NCT00006002

SU5416 Compared to Dexamethasone in Treating Patients With Progressive Prostate Cancer That Has Not Responded to Hormone Therapy

A Phase 2 study testing dexamethasone and semaxanib in people with Prostate Cancer, run by University of Chicago at 18 sites in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

RATIONALE: SU5416 may stop the growth of prostate cancer by stopping blood flow to the tumor. Dexamethasone may be effective in slowing the growth of prostate cancer cells. It is not yet known whether SU5416 or dexamethasone is more effective in treating progressive prostate cancer. Read more about this study

Who is it for?
Ages 18 years and older, men only
Conditions the study is for
Prostate Cancer
What is being tested?
dexamethasone and semaxanib
Could I receive a placebo?
No, everyone receives an active treatment
How many people
36 participants
Where
18 sitesUnited States
Study dates
Jun 2000to Jan 2006
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • Men only
  • No healthy volunteers
  • Adult, Older adult

DISEASE CHARACTERISTICS:

  • Histologically confirmed prostate cancer not amenable to curative treatment with surgery or radiotherapy
  • Progressive disease defined by 1 of the following criteria:
  • New bone scan lesions
  • New or progressive radiologic lesions
  • Sequential increases in PSA on at least 2 successive measurements no less than 2 weeks apart of at least 50% above nadir on prior therapy provided absolute value at time of enrollment is at least 5 ng/mL
  • Progressive disease, as defined above, despite adequate hormonal therapy defined by all of the following:
  • Continued treatment with an LHRH agonist or prior orchiectomy
  • Sequential or concurrent treatment with an antiandrogen (e.g., flutamide, nilutamide, or bicalutamide)
  • Trial of antiandrogen withdrawal at least 4 weeks prior to study
  • CNS metastasis allowed if:
  • Previously treated
  • Neurologically stable
  • Oral or intravenous steroids or anticonvulsants not required
  • Brain scan (CT or MRI) within the past 2 weeks shows no active or residual disease
  • Negative brain scan required if neurologic signs or symptoms suggestive of CNS metastasis

PATIENT CHARACTERISTICS:

Age:

  • 18 and over

Performance status:

  • WHO 0-1

Life expectancy:

  • Not specified

Hematopoietic:

  • WBC at least 3,000/mm^3
  • Platelet count at least 75,000/mm^3

Hepatic:

  • Bilirubin no greater than 1.5 mg/dL
  • Transaminases no greater than 2.5 times upper limit of normal

Renal:

  • Creatinine no greater than 2.0 mg/dL OR
  • Creatinine clearance at least 60 mL/min

Cardiovascular:

  • No uncompensated coronary artery disease
  • No history of myocardial infarction or severe unstable angina within the past 6 months
  • No severe peripheral vascular disease associated with diabetes mellitus
  • No deep venous or arterial thrombosis within the past 3 months

Pulmonary:

  • No pulmonary embolism within the past 3 months

Other:

  • Not pregnant
  • Fertile patients must use effective contraception
  • No significant uncontrolled underlying medical or psychiatric illness
  • No serious active infection
  • No other prior or concurrent malignancy except nonmelanoma skin cancer unless completed therapy and considered to be at less than 30% risk of relapse
  • No history of severe allergic or anaphylactic reactions to paclitaxel or docetaxel

PRIOR CONCURRENT THERAPY:

Biologic therapy:

  • Not specified

Chemotherapy:

  • No prior systemic chemotherapy
  • No other concurrent chemotherapy
  • No other concurrent investigational antineoplastic drugs

Endocrine therapy:

  • See Disease Characteristics

Radiotherapy:

  • See Disease Characteristics
  • At least 4 weeks since prior radiotherapy
  • No concurrent radiotherapy

Surgery:

  • See Disease Characteristics
  • At least 4 weeks since prior major surgery

Trial locations and contacts

18 sites in 1 country.

18 sites in 1 country

United States18 sites
  • University of Illinois at Chicago

    Chicago, Illinois, 60612

  • University of Chicago Cancer Research Center

    Chicago, Illinois, 60637-1470

  • Louis A. Weiss Memorial Hospital

    Chicago, Illinois, 60640

  • Cancer Care Specialists of Central Illinois, S.C.

    Decatur, Illinois, 62526

  • Cancer Center and Beckman Research Institute, City of Hope

    Duarte, California, 91010-3000

  • Veterans Affairs Medical Center - Durham

    Durham, North Carolina, 27705

  • Evanston Northwestern Health Care

    Evanston, Illinois, 60201

  • Fort Wayne Medical Oncology and Hematology, Inc.

    Fort Wayne, Indiana, 46885-5099

  • Ingalls Memorial Hospital

    Harvey, Illinois, 60426

  • LaGrange Memorial Hospital

    LaGrange, Illinois, 60525

  • USC/Norris Comprehensive Cancer Center and Hospital

    Los Angeles, California, 90033-0804

  • Loyola University Medical Center

    Maywood, Illinois, 60153

  • Division of Hematology/Oncology

    Park Ridge, Illinois, 60068

  • City of Hope Medical Group

    Pasadena, California, 91105

  • Oncology/Hematology Associates of Central Illinois, P.C.

    Peoria, Illinois, 61602

  • Oncology Care Associates, P.L.L.C.

    Saint Joseph, Michigan, 49085

  • Michiana Hematology/Oncology P.C.

    South Bend, Indiana, 46617

  • Central Illinois Hematology Oncology Center

    Springfield, Illinois, 62701

Other trials in United States

About this study

Official title: A Phase II Trial of SU5416 (NSC# 686819) in Patients With Hormone Refractory Prostate Cancer

RATIONALE: SU5416 may stop the growth of prostate cancer by stopping blood flow to the tumor. Dexamethasone may be effective in slowing the growth of prostate cancer cells. It is not yet known whether SU5416 or dexamethasone is more effective in treating progressive prostate cancer.

PURPOSE: Randomized phase II trial to compare the effectiveness of SU5416 with that of dexamethasone in treating patients who have progressive prostate cancer that has not responded to hormone therapy.

Read the detailed description

OBJECTIVES:

  • Compare the time to progression in patients with hormone refractory prostate cancer treated with dexamethasone with or without SU5416.
  • Determine the differences in PSA kinetics and PSA hazard score between these two regimens in this patient population.
  • Determine the objective response rate and time to development of new lesions in these patients treated with SU5416.
  • Determine the toxicity of SU5416 in these patients.

OUTLINE: This is a randomized study. Patients are randomized to one of two treatment arms.

  • Arm I: Patients receive oral dexamethasone once a day 6 days a week. Treatment continues until disease progression, at which time patients cross over to arm II.
  • Arm II: Patients receive oral dexamethasone as in arm I followed by SU5416 IV over 60 minutes twice weekly for 4 weeks. A smaller dose of dexamethasone is administered the day after SU5416. Treatment continues for a minimum of 2 courses in the absence of unacceptable toxicity or disease progression.

PROJECTED ACCRUAL: A total of 60 patients (30 per arm) will be accrued for this study within 16 months.

Conditions
Prostate Cancer
Being tested
dexamethasone, semaxanib
Keywords
stage IV prostate cancer, recurrent prostate cancer
Medical subject headings
Prostatic Neoplasms

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT00006002
Study groupRoleWhat they receive
Arm BExperimentaldexamethasone followed by SU5416 done twice weekly (Monday and Thursday or Tuesday and Friday) every week for 4 weeks (a total of 8 doses). Four weeks of treatment (8 doses) is considered 1 cycle of treatment if tumor grows.
Receives: Drug: dexamethasone; Drug: semaxanib
Arm AExperimentalSU5416 done twice weekly (Monday and Thursday or Tuesday and Friday) every week for 4 weeks (a total of 8 doses). Four weeks of treatment (8 doses) is considered 1 cycle of treatment
Receives: Drug: semaxanib

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Objective response rate

    Measured: 3 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted29 Aug 2003 (estimated)
  2. Study startJun 2000
  3. Primary completionSep 2002
  4. Study completionJan 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Single group
Masking
None (open label)
Enrolment
36 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00006002
Sponsor's protocol ID
10428
Other IDs
UCCRC-10428, UCCRC-NCI-49, NCI-49
Status last verified
Sep 2013
First submitted
5 Jul 2000
Last updated
5 Sep 2013
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing dexamethasone and semaxanib in people with Prostate Cancer, run by University of Chicago at 18 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 5 Sep 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 18 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Objective response rate (time frame: 3 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Sep 2013; AzTrials last refreshed its copy on 1 Nov 2026.

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