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High-Dose Lymph Node Intensity Modulated Radiation Therapy and Hypofractionated Prostate (SIB)

A Phase II Trial of High-Dose Pelvic Lymph Node IMRT( Intensity Modulated Radiation Therapy) and Hypofractionated Prostate IMRT for High Risk Prostate Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02177292
Acronym
SIB
Enrollment
80
Registered
2014-06-27
Start date
2010-06-23
Completion date
2026-08-17
Last updated
2026-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Cancer

Brief summary

The purpose of this study is to find out the effects (good and bad) of using newer technologies that allow very precise delivery of radiation. These newer technologies are Intensity Modulated Radiation Therapy (IMRT) and Image Guided Radiation Therapy (IGRT).

Detailed description

In this study the treating physicians will deliver a high dose of radiation to pelvic lymph nodes of 56 Gy (Gy/Gray = measure of amount of radiation) and at the same time give a boost (additional) radiation to the prostate itself (to 70 Gy). The study will evaluate the response of the cancer and side effects of radiation to pelvic lymph nodes and to the prostate. It is hoped that these newer technologies will: 1. allow a higher daily dose of radiation to the tumor and pelvic nodes 2. avoid nearby normal tissue and organs like the rectum and bladder 3. prevent the cancer from spreading or coming back

Interventions

RADIATIONRadiation Therapy

A high dose of radiation to the pelvic lymph nodes of 56 Gy (Gy/Gray = measure of amount of radiation) and at the same time give a boost (additional) radiation to the prostate itself (to 70 Gy).

Sponsors

Medical College of Wisconsin
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Histologically confirmed, adenocarcinoma of the prostate * T1-2N0M0 with risk of pelvic lymph nodes involvement \>25% by Roach formula \[(2/3xPSA) + (Gleason Score - 6)x10\], or any T3-4N0M0 * Karnofsky Performance Scale \> 70. * Prostate tumor biopsy grading by Gleason score classification is mandatory prior to registration. * No prior pelvic or prostate radiation or chemotherapy for any reason; induction hormonal therapy prior to registration is acceptable. * Patients must sign a study-specific consent form prior to registration. * No evidence of distant metastases (Bone scanning)

Exclusion criteria

* Clinical or pathological evidence of distant metastases (M1). * Radical surgery for carcinoma of the prostate * History of prior chemotherapy * History of prior pelvic radiation therapy * Children (age \< 18).

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline PSA level4 monthsPSA level in blood is measured in units of nanograms per milliliter.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORWilliam Hall, MD

Medical College of Wisconsin

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 27, 2026