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Shorter Duration Radiotherapy to Treat Prostate Cancer After Removal of the Prostate (HypoFX)

Primary Purpose

Prostate Cancer

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Hypofractionated therapy
Sponsored by
Timothy Showalter, MD
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring Radiotherapy, hypofractionated, Salvage therapy, Radiotherapy, adjuvant

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • diagnosis of prostate adenocarcinoma and
  • have had a prostatectomy
  • have detectable PSA
  • 18 years of age or older

Exclusion Criteria:

  • are receiving chemotherapy or other agents intended for cancer treatment
  • history of rectal surgery or lower gastrointestinal bleed
  • history of bleeding diathesis or abnormal sensitivity to ionizing radiation
  • had prior pelvic irradiation or are scheduled to receive pelvic nodal irradiation

Sites / Locations

  • University of Virginia Health System
  • Southwest Virginia Regional Cancer Center
  • Virginia Commonwealth University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Dose Level 1

Dose Level 2

Dose Level 3

Dose Level 4

Arm Description

Hypofractionated therapy, 26 treatments at 2.5 Gy

Hypofractionated therapy, 20 treatments at 2.83Gy

Hypofractionated therapy,15 treatments at 3.36 Gy

Hypofractionated therapy, 10 treatments at 4.26 Gy

Outcomes

Primary Outcome Measures

Dose limiting toxicity
Incidence of GU (genitourinary) and GI (gastrointestinal) toxicities of CTCAE (Common Terminology Criteria for Adverse Events) grade 3 or greater
Quality of life measure
To compare quality of life post-procedure from baseline

Secondary Outcome Measures

Biochemical failure rate
A biochemical failure is defined as an increase in prostate serum antigen concentration to nadir plus 2ng/mL or 3 consecutive increases in PSA

Full Information

First Posted
May 14, 2013
Last Updated
April 26, 2021
Sponsor
Timothy Showalter, MD
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1. Study Identification

Unique Protocol Identification Number
NCT01868386
Brief Title
Shorter Duration Radiotherapy to Treat Prostate Cancer After Removal of the Prostate
Acronym
HypoFX
Official Title
Hypofractionated Post-prostatectomy Radiotherapy for Prostate Cancer to Reduce Toxicity and Improve Patient Convenience: A Phase I/II Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
April 2013 (undefined)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
December 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Timothy Showalter, MD

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Radiation therapy is one of the standard treatments for men with prostate cancer who have detectable levels of prostate specific antigen (PSA, a prostate cancer specific marker) after surgery. When radiation therapy is given to patients who have an increase in PSA after surgery, it is called "salvage radiation therapy". Currently the standard radiation therapy course length for this type of cancer is around 7 ½ -8 weeks. Sometimes, radiation therapy after prostate removal causes unpleasant side effects. A shorter course of radiation therapy, known as a "hypofractionated" course, gives fewer but higher doses of radiation than standard radiation. The purpose of this study is to test the safety of a shorter course of radiation therapy at progressively lower dose levels and shorter lengths of treatment (hypofractionated) with patients who have had their prostate removed. The study will assess whether the hypofractionated course works better without causing additional side effects to the remaining cancer cells in the prostate bed.
Detailed Description
Primary Objectives: To determine the shortest dose-fractionation schedule (Dose Schedule) with acceptable grade ¡Ã 3 GU/GI toxicity rate for salvage HypoFx RT to maintain a constant, high BED for prostate cancer response while reducing the BED for late GU and GI toxicity To assess health-related quality of life (HRQOL) of the recommended Dose Schedule of salvage HypoFx RT by demonstrating no significant change in 1-year disease specific QoL, as compared to baseline Secondary Objectives: To evaluate and characterize the acute and late genitourinary (GU) and gastrointestinal (GI) adverse effects associated with postoperative, hypofractionated radiation therapy. To evaluate biochemical failure rate, defined separately as nadir plus 2 ng/mL and as three consecutive rises in PSA, at 2 years after hypofractionated, post-prostatectomy radiation therapy. To evaluate health utilities at 1 year after HypoFx salvage RT, as measured by the EQ-5D instrument. To evaluate changes in sexual domain of EPIC quality of life instrument at 1 year after HypoFx salvage RT. To evaluate the treatment burden for patients undergoing salvage HypoFx RT, in order to examine whether HypoFx RT results in less burdensome treatment for patients, as measured by patient-reported direct and indirect (i.e., transportation) health care costs and lost productivity due to treatment, as evaluated by the Work Productivity and Activity Impairment Questionnaire¢-General Health (WPAI-GH).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Radiotherapy, hypofractionated, Salvage therapy, Radiotherapy, adjuvant

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dose Level 1
Arm Type
Experimental
Arm Description
Hypofractionated therapy, 26 treatments at 2.5 Gy
Arm Title
Dose Level 2
Arm Type
Experimental
Arm Description
Hypofractionated therapy, 20 treatments at 2.83Gy
Arm Title
Dose Level 3
Arm Type
Experimental
Arm Description
Hypofractionated therapy,15 treatments at 3.36 Gy
Arm Title
Dose Level 4
Arm Type
Experimental
Arm Description
Hypofractionated therapy, 10 treatments at 4.26 Gy
Intervention Type
Radiation
Intervention Name(s)
Hypofractionated therapy
Intervention Description
Shorter courses of increasing doses of radiation therapy will be assessed in each subsequent arm
Primary Outcome Measure Information:
Title
Dose limiting toxicity
Description
Incidence of GU (genitourinary) and GI (gastrointestinal) toxicities of CTCAE (Common Terminology Criteria for Adverse Events) grade 3 or greater
Time Frame
over a period of 2 years
Title
Quality of life measure
Description
To compare quality of life post-procedure from baseline
Time Frame
over a period of 2 years
Secondary Outcome Measure Information:
Title
Biochemical failure rate
Description
A biochemical failure is defined as an increase in prostate serum antigen concentration to nadir plus 2ng/mL or 3 consecutive increases in PSA
Time Frame
over a period of 2 years
Other Pre-specified Outcome Measures:
Title
Acute and late GU and GI toxicity
Time Frame
over a period of two years
Title
Health Utilities
Time Frame
1 year after radiation treatment
Title
EPIC Prostate Cancer-Specific QOL instrument
Description
looking at changes in sexual and hormonal domains
Time Frame
over a period of two years
Title
Ancillary financial burden
Description
estimating out-of-pocket costs and lost wages for patients during treatment
Time Frame
over a period of two years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosis of prostate adenocarcinoma and have had a prostatectomy have detectable PSA 18 years of age or older Exclusion Criteria: are receiving chemotherapy or other agents intended for cancer treatment history of rectal surgery or lower gastrointestinal bleed history of bleeding diathesis or abnormal sensitivity to ionizing radiation had prior pelvic irradiation or are scheduled to receive pelvic nodal irradiation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Timothy Showalter, MD
Organizational Affiliation
University of Virginia School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Virginia Health System
City
Charlottesville
State/Province
Virginia
ZIP/Postal Code
22908
Country
United States
Facility Name
Southwest Virginia Regional Cancer Center
City
Norton
State/Province
Virginia
ZIP/Postal Code
24273
Country
United States
Facility Name
Virginia Commonwealth University
City
Richmond
State/Province
Virginia
ZIP/Postal Code
23220
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
33227441
Citation
Wages NA, Sanders JC, Smith A, Wood S, Anscher MS, Varhegyi N, Krupski TL, Harris TJ, Showalter TN. Hypofractionated Postprostatectomy Radiation Therapy for Prostate Cancer to Reduce Toxicity and Improve Patient Convenience: A Phase 1/2 Trial. Int J Radiat Oncol Biol Phys. 2021 Apr 1;109(5):1254-1262. doi: 10.1016/j.ijrobp.2020.11.009. Epub 2020 Nov 21.
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Shorter Duration Radiotherapy to Treat Prostate Cancer After Removal of the Prostate

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