Testing Shorter Duration Radiation Therapy Versus the Usual Radiation Therapy in Patients With High Risk Prostate Cancer

Clinicaltrials.gov ID: NCT05946213
db-list-check Status RECRUITING
b-loader Phase PHASE3
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 1209

Conditions

Stage III Prostate Cancer AJCC v8, Stage IVA Prostate Cancer AJCC v8

Summary

This phase III trial compares stereotactic body radiation therapy (SBRT), (five treatments over two weeks using a higher dose per treatment) to usual radiation therapy (20 to 45 treatments over 4 to 9 weeks) for the treatment of high-risk prostate cancer. SBRT uses special equipment to position a patient and deliver radiation to tumors with high precision. This method may kill tumor cells with fewer doses over a shorter period of time. This trial is evaluating if shorter duration radiation prevents cancer from coming back as well as the usual radiation treatment.

Detailed Description

PRIMARY OBJECTIVE:

I. To compare metastasis-free survival, determined using conventional imaging, between men with high-risk prostate cancer randomized to ultrahypofractionation (stereotactic body radiation therapy [SBRT]) to those randomized to moderate hypofractionation and conventional fractionation.

SECONDARY OBJECTIVES:

I. To compare physician-reported toxicity as measured by Common Terminology Criteria for Adverse Events (CTCAE) version (v)5 between treatment arms.

II. To determine if ultrahypofractionation is non-inferior to moderate hypofractionation and conventional fractionation with respect to patient-reported urinary function (assessed by Expanded Prostate Cancer Index Composite [EPIC]-26 urinary domains).

III. To determine if ultrahypofractionation is non-inferior to moderate hypofractionation and conventional fractionation with respect to patient-reported bowel function (assessed by EPIC-26 bowel domain).

IV. To compare patient-reported fatigue (assessed by Patient Reported Outcomes Measurement Information System [PROMIS]-Fatigue) between treatment arms.

V. To compare patient-reported treatment burden (assessed by COmprehensive Score for financial Toxicity [COST]) between treatment arms.

VI. To compare failure-free survival between treatment arms. VII. To compare metastasis-free survival based on molecular imaging between treatment arms.

VIII. To compare overall survival between treatment arms.

EXPLORATORY OBJECTIVES:

I. To compare patient-reported sexual function (assessed by EPIC-26 sexual domain) between treatment arms.

II. To compare patient-reported quality of life (assessed by European Quality of Life Five Dimension Five Level Scale Questionnaire [EQ-5D-5L]) between treatment arms.

OUTLINE: Patients are randomized to 1 of 2 arms.

ARM I: Patients undergo SBRT for a total of 5 treatments over 2 weeks.

ARM II: Patients undergo external beam radiation treatment (EBRT) for 20-45 treatments over 4 to 9 weeks.

Patients are followed up every 6 months for 5 years.

Locations

66 locations Found with status Recruiting

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 877-642-4691

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 877-642-4691

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 561-745-5768

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 314-996-5569

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 610-988-9323

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 877-405-6866

Principal Investigator

  • Karen E Hoffman

Status

  • RECRUITING

Contact Person

  • Site Public Contact
  • 715-422-7718

Principal Investigator

  • Karen E Hoffman

Eligibility Criteria

Inclusion Criteria:

* Pathologically (histologically or cytologically) proven diagnosis of adenocarcinoma of prostate cancer
* High-risk disease defined as having at least one or more of the following:

* cT3a-T3b by digital exam or imaging (American Joint Committee on Cancer [AJCC] 8th edition [Ed.]) Note: cT4 by imaging or on digital rectal exam is not allowed
* The patient's prostate specific antigen (PSA) > 20 ng/mL prior to starting ADT Note: Patients taking a 5-alpha reductase inhibitor (ex finasteride or dutasteride) are eligible. The baseline PSA value should be doubled for PSAs taken while on 5-alpha reductase inhibitors
* Gleason Score of 8-10
* Pelvic node positive by conventional imaging with a short axis of at least 1.0 cm
* Prostate gland volume less than 100 cc prior to initiation of ADT as reported at time of biopsy or by separate measure with ultrasound or other imaging modalities including MRI or computed tomography (CT) scan
* No definitive clinical or radiologic evidence of metastatic disease outside of the pelvic nodes (M1a, M1b or M1c) on conventional imaging (i.e. bone scan, CT scan, MRI); Negative prostate-specific membrane antigen (PSMA) positron emission tomography (PET) is an acceptable substitute
* Age >= 18
* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-2
* No prior radiotherapy to the region of the study cancer that would result in overlap of radiation therapy fields
* No prior radical prostatectomy
* Prior pharmacologic androgen ablation for prostate cancer is allowed only if the onset of androgen ablation (both luteinizing hormone releasing hormone [LHRH] agonist and oral anti-androgen) is =< 185 days prior to registration
* Patients enrolled in NRG-GU009 must be enrolled in NRG-GU013 prior to radiation therapy treatment planning and start of radiation therapy

Study Plan

Arm I (SBRT)

EXPERIMENTAL

Patients undergo SBRT for a total of 5 treatments over 2 weeks.

  • RADIATION:

    Stereotactic Body Radiation Therapy

    Description:

    Undergo SBRT

Arm II (EBRT)

ACTIVE_COMPARATOR

Patients undergo EBRT for 20 to 45 treatments over 4 to 9 weeks.

  • RADIATION:

    External Beam Radiation Therapy

    Description:

    Undergo EBRT

Outcome Measures

Primary Outcome Measures

Metastasis-Free Survival (MFS)

Time Frame: From randomization to the date of distant metastasis, or death from any cause, assessed up to 15 years

Secondary Outcome Measures

Failure-Free Survival

Time Frame: From randomization to the date of distant metastasis, or death from any cause, assessed up to 15 years

Overall Survival

Time Frame: From the date of randomization to the date of death or last known follow-up date, with patients alive at the last known follow-up time treated as censored, assessed up to 15 years

MFS

Time Frame: From randomization to the date of distant metastasis, or death from any cause, assessed up to 15 years

Incidence of Adverse Events (AEs)

Time Frame: Up to 15 years

Urinary Incontinence domain of the Expanded Prostate Cancer Index Composite (EPIC-26)

Time Frame: Up to 5 years

Urinary Irritative/Obstructive domain of the Expanded Prostate Cancer Index Composite (EPIC-26)

Time Frame: Up to 5 years

Bowel domain of the Expanded Prostate Cancer Index Composite (EPIC-26)

Time Frame: Up to 5 years

Fatigue

Time Frame: Up to 5 years

Cost

Time Frame: Up to 1 year

Timeline

  • Last Updated
    February 7, 2024
  • Start Date
    July 14, 2023
  • Today
    January 22, 2025
  • Completion Date ( Estimated )
    March 31, 2041

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