Clinical Trials Directory

Trials / Terminated

TerminatedNCT00348816

Docetaxel, Radiation Therapy, and Prednisone in Treating Patients Who Have Undergone Surgery For Prostate Cancer

A Phase II Study to Assess the Feasibility and Activity of Concomitant Radiation and Docetaxel Chemotherapy Followed by Docetaxel Chemotherapy in Prostate Cancer Patients With a Persistent or Rising PSA After Radical Prostatectomy

Status
Terminated
Phase
Phase 2
Study type
Interventional
Enrollment
21 (actual)
Sponsor
The University of Texas Health Science Center at San Antonio · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel and prednisone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Docetaxel may make tumor cells more sensitive to radiation therapy. Giving docetaxel together with radiation therapy and prednisone after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well giving docetaxel together with radiation therapy and prednisone works in treating patients who have undergone surgery for prostate cancer.

Detailed description

OBJECTIVES: Primary * Determine the rate of prostate-specific antigen (PSA) decline and the number of patients reaching a PSA nadir of zero after treatment with chemoradiotherapy comprising docetaxel and external-beam radiotherapy followed by docetaxel and prednisone in patients with hormone-naive prostate cancer who have a persistent or rising PSA after radical prostatectomy. Secondary * Determine the tolerability of this regimen in these patients. * Determine the progression-free survival, based on PSA progression, of these patients. * Determine the overall survival of patients treated with chemoradiotherapy for rising PSA after radical prostatectomy. * Determine if the velocity of subsequent PSA failure impacts survival of these patients. Tertiary * Document subsequent therapy for patients whose previous treatment has failed and if there is a response to that therapy. Quaternary: To collect data on a contemporary cohort to those on study that received radiation alone. We will match cancer and patient characteristics to determine if the variable of chemotherapy has any impact on outcomes. OUTLINE: Patients receive docetaxel IV over 1 hour on days 1, 8, 15, 22, 29, 36, and 43 and undergo external-beam radiotherapy on days 1-5, 8-12, 15-19, 22-26, 29-33, 36-40, and 43-47. Beginning within 6 weeks after completion of chemoradiotherapy, patients receive docetaxel IV over 1 hour on day 1 and oral prednisone twice daily on days 1-21. Treatment repeats every 21 days for 4 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed at 1 month, every 4 months for 2 years, and then every 6 months for 3 years. PROJECTED ACCRUAL: A total of 50 patients will be accrued for this study.

Conditions

Interventions

TypeNameDescription
DRUGdocetaxelDocetaxel 20mg/m2/week IV every week during standard of care radiation treatment (7 cycles). Post radiation: docetaxel 75mg/m2 IV every 21 days for 4 cycles plus prednisone 5mg PO BID QD.
DRUGprednisoneDocetaxel 20mg/m2/week IV every week during radiation treatment (7 cycles). Post radiation: docetaxel 75mg/m2 IV every 21 days for 4 cycles plus prednisone 5mg PO BID QD.
PROCEDURERadical prostatectomyRadical prostatectomy as part of standard care
RADIATIONRadiation therapyDoses for standard care radiation therapy: The initial target volume will be the lower pelvis followed by a boost to the prostate fossa and immediate periprostatic tissue. The initial dose will be 4500 cGy. With the final boost, the total dose will be 6840-6900 cGy. (4500/25 plus 2340/13 or 2400/12) with a total of 37 or 38 fractions.

Timeline

Start date
2006-05-01
Primary completion
2016-07-08
Completion
2016-07-08
First posted
2006-07-06
Last updated
2017-12-08
Results posted
2017-05-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00348816. Inclusion in this directory is not an endorsement.