Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outline
Published Results
Related Publications
Trial Contact Information
Registry Information
Radiation Therapy After Prostatectomy in Treating Patients With Stage III Prostate Cancer
| Phase | Type | Status | Age | Sponsor | Protocol IDs |
|---|---|---|---|---|---|
| Phase III | Treatment | Completed | any age | NCI | SWOG-8794 CAN-NCIC-PR2, CLB-9493, EST-9887, NCCTG-895251, RTOG-9019, INT-0086, NCT00394511, PR2 |
Objectives
I. Compare disease-free survival rates of patients randomly assigned to adjuvant external-beam radiotherapy vs. no adjuvant therapy following radical prostatectomy and pelvic lymphadenectomy for surgical Stage C (T3 N0 M0) adenocarcinoma of the prostate. II. Determine the qualitative and quantitative toxicities associated with this adjuvant therapy.
Entry Criteria
Disease Characteristics:
Pathologically documented Stage C (T3 N0 M0) adenocarcinoma of the prostate
following radical prostatectomy and pelvic lymphadenectomy for clinical Stage
A/B disease
Ineligible for SWOG protocols of higher priority
At least 1 of the following on pathologic examination:
Presence of cancer in the seminal vesicles
Evidence of cancer at the inked surgical margin of the prostate
Extension of tumor beyond the prostatic capsule
Negative preoperative metastatic survey within 6 months prior to registration,
including the following:
Normal bone scan
No palpable evidence of extraprostatic tumor extension
Bilateral lymph node dissection histologically negative for cancer
Nodal sampling not required with the following stage/biopsy specimen Gleason
score/preoperative PSA:
Stage T1a/2-6/<10 ng/ml
Stage T1b-c/2-5/<10 ng/ml
Stage T2a/2-6/<10 ng/ml
Stage T2b/2-6/<6 ng/ml
Stage T2c/2-6/<4 ng/ml
Free from the following postoperative complications:
Total urinary incontinence
Intraoperative rectal injury
Persistent urinary extravasation
Pelvic infection
Concurrent registration on protocol SWOG-9205 (serum repository protocol)
optional
Concurrent registration on protocol SWOG-8994 (quality-of-life study) required
of English-speaking and Spanish-speaking patients enrolled by SWOG
Prior/Concurrent Therapy:
Biologic therapy: Not specified Chemotherapy: No prior chemotherapy for prostate cancer Endocrine therapy: No more than 3 months of hormonal therapy prior to prostatectomy allowed Radiotherapy: No prior radiotherapy for prostate cancer Surgery: Radical prostatectomy and pelvic lymphadenectomy within 16 weeks prior to registration required
Patient Characteristics:
Age:
Any age
Performance status:
SWOG 0-2
Life expectancy:
At least 2 years
Hematopoietic:
WBC at least institutional LLN
Platelets at least institutional LLN
Hepatic:
SGOT no more than 2 x ULN
Renal:
Not specified
Other:
No second malignancy within 5 years except adequately treated
nonmelanomatous skin cancer
Expected Enrollment
408 eligible patients will be entered over about 8.5 years.
Outline
Randomized study. Randomization takes place when the patient is physically able to begin treatment, any time within 16 weeks after surgery. Arm I: Radiotherapy. Irradiation of the prostatic bed using megavoltage equipment with effective photon energies of greater than 4 MV. Arm II: No further treatment.Published Results
Moinpour CM, Hayden KA, Unger JM, et al.: Health-related quality of life results in pathologic stage C prostate cancer from a Southwest Oncology Group trial comparing radical prostatectomy alone with radical prostatectomy plus radiation therapy. J Clin Oncol 26 (1): 112-20, 2008.[PUBMED Abstract]
Swanson GP, Goldman B, Tangen CM, et al.: The prognostic impact of seminal vesicle involvement found at prostatectomy and the effects of adjuvant radiation: data from Southwest Oncology Group 8794. J Urol 180 (6): 2453-7; discussion 2458, 2008.[PUBMED Abstract]
Swanson GP, Hussey MA, Tangen CM, et al.: Predominant treatment failure in postprostatectomy patients is local: analysis of patterns of treatment failure in SWOG 8794. J Clin Oncol 25 (16): 2225-9, 2007.[PUBMED Abstract]
Swanson GP, Hussey MA, Thompson IM, et al.: Pre radiation PSA predicts for outcome of adjuvant radiation in SWOG 8794. [Abstract] American Urological Association: Annual Meeting, May 20-25, 2006, Atlanta, GA A-668, 2006.
Thompson IM Jr, Tangen CM, Paradelo J, et al.: Adjuvant radiotherapy for pathologically advanced prostate cancer: a randomized clinical trial. JAMA 296 (19): 2329-35, 2006.[PUBMED Abstract]
Swanson GP, Thompson IM, Tangem C, et al.: Phase III randomized study of adjuvant radiation therapy versus observation in patients with pathologic T3 prostate cancer (SWOG 8794). [Abstract] Int J Radiat Oncol Biol Phys 63 (Suppl 1): A-1, S1, 2005.
Related PublicationsShowalter TN, Foley KA, Jutkowitz E, et al.: Costs of early adjuvant radiation therapy after radical prostatectomy: a decision analysis. Ann Oncol : , 2011.[PUBMED Abstract]
Ganswindt U, Stenzl A, Bamberg M, et al.: Adjuvant radiotherapy for patients with locally advanced prostate cancer--a new standard? Eur Urol 54 (3): 528-42, 2008.[PUBMED Abstract]
Thompson IM, Paradelo JC, Crawford ED, et al.: An opportunity to determine optimal treatment of pT3 prostate cancer: the window may be closing. Urology 44 (6): 804-11, 1994.[PUBMED Abstract]
Trial Lead Organizations
Southwest Oncology Group
| Ian Thompson, MD, Protocol chair |
| |||
Eastern Cooperative Oncology Group
| Edward Messing, MD, FACS, Protocol chair |
| |||
NCIC-Clinical Trials Group
| Joseph Chin, MD, Protocol chair |
| |||
North Central Cancer Treatment Group
| John Bolton, MD, Protocol chair |
| |||
Radiation Therapy Oncology Group
| Arthur Porter, MD, Protocol chair |
| ||
Cancer and Leukemia Group B
| Parvesh Kumar, MD, Protocol chair (Contact information may not be current) |
| ||
| Registry Information | ||
| Official Title | Phase III Randomized Evaluation of Adjuvant Radiotherapy vs No Adjuvant Therapy Following Radical Prostatectomy and Pelvic Lymphadenectomy in Surgical Stage C Adenocarcinoma of the Prostate | |
| Trial Start Date | 1988-08-15 | |
| Registered in ClinicalTrials.gov | NCT00394511 | |
| Date Submitted to PDQ | 1988-08-15 | |
| Information Last Verified | 2011-07-07 | |
| NCI Grant/Contract Number | CA21115, CA21661, CA25224, CA31946, CA32102 | |
Note: The purpose of most clinical trials listed in this database is to test new cancer treatments, or new methods of diagnosing, screening, or preventing cancer. Because all potentially harmful side effects are not known before a trial is conducted, dose and schedule modifications may be required for participants if they develop side effects from the treatment or test. The therapy or test described in this clinical trial is intended for use by clinical oncologists in carefully structured settings, and may not prove to be more effective than standard treatment. A responsible investigator associated with this clinical trial should be consulted before using this protocol.
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