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Hypofractionated Stereotactic Body Radiation Therapy (SBRT)

A Study of Hypofractionated Stereotactic Body Radiation Therapy (SBRT) Using Continuous Real-time Evaluation of Prostate Motion

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01288534
Enrollment
68
Registered
2011-02-02
Start date
2011-01-31
Completion date
2016-01-31
Last updated
2017-10-24

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 evaluate the safety and tolerability of using radiation therapy with 5 fractions of radiation to treat prostate cancer with guidance of radiation using the Calypso 4D Treatment System (Calypso).A number of recent studies have used 5 radiation fraction to treat prostate cancer over 2-3 weeks as compared to the typical treatment which would involve 40-42 smaller radiation fractions over 8-9 weeks. This type of radiation using a smaller number of treatments has been called hypofractionated radiation therapy. The Calypso is a new technique which uses beacons implanted into the prostate which using radio signals are able to localize and track the position of the prostate continuously during radiation therapy. The Calypso system has been approved by the United States Food and Drug Administration (FDA) for guidance of radiation therapy during the treatment of prostate cancer and is being utilized all across the United States. However, it has not been tested for hypofractionated radiation therapy.

Interventions

RADIATIONRadiation Therapy

Patients will receive 5 fractions of radiation (you will not receive radiation therapy on two consecutive days). Each fraction size will be 7.4 Gy. The total dose will be 37 Gy. The 5 treatments will be scheduled to be delivered 2 fractions per business week (Monday through Friday). The total duration of treatment will be no shorter than 15 days and no longer than 19 days.

Sponsors

Fox Chase Cancer Center
CollaboratorOTHER
Cedars-Sinai Medical Center
CollaboratorOTHER
Washington University School of Medicine
CollaboratorOTHER
University of Michigan Rogel Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* 18 years of age or older * Histologically confirmed diagnosis of adenocarcinoma of the prostate within 180 days of enrollment * Signed informed consent * Gleason score ≤ 7 * If Gleason 7 (3+4=7 or 4+3=7) then \<50% of biopsy cores must be positive for any pathologic grade of prostate cancer * If Gleason score \<7 then there is no limit on the percentage of biopsy cores involved by prostate cancer * PSA (within 90 days prior to enrollment) * ≤ 15 ng/ml prior to start of therapy if Gleason ≤ 6 and * ≤ 10 ng/ml prior to start of therapy if Gleason 7 * No plan to use hormone therapy prior to evidence of biochemical failure(ie: No neoadjuvant or adjuvant ADT) * Tumor stage: T1a, T1b, T1c, T2a, T2b * ECOG Performance Status 0-1

Exclusion criteria

* A history of other malignancy diagnosed within the previous 60 months except for non-melanoma skin cancer. * Any patients who have received other investigational therapy within the last 60 days * Individuals that have previously been implanted with permanent Beacon transponders * Patients that have any prosthetic implants in the pelvic region that contain metal or conductive materials (e.g., an artificial hip) * Patients with implanted pacemaker or defibrillators * Patients who are felt to have body habitus not conducive to tracking with Calypso beacons * Positive lymph nodes or metastatic disease from prostate cancer * Tumor stage: T2c, T3, or T4 * Previous pelvic radiation therapy * Previous surgery or chemotherapy for prostate cancer * Previous transuretheral resection of the prostate (TURP) or cryotherapy to the prostate * Prior hormone therapy or plans for concurrent or post treatment adjuvant hormonal therapy or chemotherapy * Hormone therapy to include LHRH agonist or oral anti-androgen * Finasteride and Dutasteride use not excluded * Concomitant antineoplastic therapy (including surgery, cryotherapy, conventionally fractionated radiation therapy, and chemotherapy) while on this protocol * History of Crohn's Disease or Ulcerative Colitis

Design outcomes

Primary

MeasureTime frameDescription
Percentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)24 monthsTo evaluate the safety of the proposed hyperfractionation regimen of 5 fractions of radiation to treat prostate cancer with guidance of radiation using the Calypso 4D Treatment System (Calypso, and to compare it to that expected from conventional treatment, which would involve 40-42 smaller radiation fractions over 8-9 weeks. Percentage of patients with a MDD in Quality of Life (QOL) surveys for urinary incontinence (UI), urinary obstructive (UO), bowel (BS), and sexual (SS) domains were reviewed at 6 months and 24 months.

Secondary

MeasureTime frameDescription
Percentage of Patients With a PSA Nadir of <3.35 ng/ml at 12 Months1 YearTo estimate one year prostate specific antigen (PSA)control of prostate cancer when treated with stereotactic body radiotherapy (SBRT) using continuous real-time evaluation of prostate motion.
Relation Between Dose Distribution and Toxicities.5 yearsTo look at the relation between dose distribution and toxicities and to determine if reconstructed delivered doses are more predictive of toxicity than planned doses.
Relation Between Reconstructed Delivered Dose Distributions.5 yearsTo determine the relation between reconstructed delivered dose distributions, accounting for prostate translation and rotation, and tumor control probabilities.
Frequency of Required Interventions.5 yearsTo assess the frequency of required interventions (interruptions) based on real-time prostate translations and rotations to verify that the proposed planning target volume(PTV) margins and action level are appropriate and practical. This will be assessed by the percentage of patients with no interventions for any fraction, the percentage of patients with 1-2 fractions interrupted and the percentage of patients with more than two fractions interrupted and the percentage of patients that had an interruption of the beam at least once for all 5 fractions.

Countries

United States

Participant flow

Participants by arm

ArmCount
Radiation Treatment
Radiation Therapy: Patients will receive 5 fractions of radiation (you will not receive radiation therapy on two consecutive days). Each fraction size will be 7.4 Gy. The total dose will be 37 Gy. The 5 treatments will be scheduled to be delivered 2 fractions per business week (Monday through Friday). The total duration of treatment will be no shorter than 15 days and no longer than 19 days.
68
Total68

Baseline characteristics

CharacteristicRadiation Treatment
Age, Continuous63 years
Sex: Female, Male
Female
0 Participants
Sex: Female, Male
Male
68 Participants

Adverse events

Event typeEG000
affected / at risk
deaths
Total, all-cause mortality
— / —
other
Total, other adverse events
62 / 68
serious
Total, serious adverse events
5 / 68

Outcome results

Primary

Percentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)

To evaluate the safety of the proposed hyperfractionation regimen of 5 fractions of radiation to treat prostate cancer with guidance of radiation using the Calypso 4D Treatment System (Calypso, and to compare it to that expected from conventional treatment, which would involve 40-42 smaller radiation fractions over 8-9 weeks. Percentage of patients with a MDD in Quality of Life (QOL) surveys for urinary incontinence (UI), urinary obstructive (UO), bowel (BS), and sexual (SS) domains were reviewed at 6 months and 24 months.

Time frame: 24 months

ArmMeasureGroupValue (NUMBER)
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)UI by MDD, 6 Months, n=4617 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)UI by MDD, 24 Months, n=3418 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)UO by MDD, 6 Months, n=4641 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)UO by MDD, 24 Months, n=3619 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)BS by MDD, 6 Months, n=4533 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)BS by MDD, 24 Months, n=3123 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)SS by MDD, 6 Months, n=4439 percentage of patients
Radiation TreatmentPercentage of Patients With a Minimally Detected Decline (MDD) in Quality of Life (QOL)SS by MDD, 24 Months, n=3543 percentage of patients
Secondary

Frequency of Required Interventions.

To assess the frequency of required interventions (interruptions) based on real-time prostate translations and rotations to verify that the proposed planning target volume(PTV) margins and action level are appropriate and practical. This will be assessed by the percentage of patients with no interventions for any fraction, the percentage of patients with 1-2 fractions interrupted and the percentage of patients with more than two fractions interrupted and the percentage of patients that had an interruption of the beam at least once for all 5 fractions.

Time frame: 5 years

ArmMeasureGroupValue (NUMBER)
Radiation TreatmentFrequency of Required Interventions.No interruptions for any fraction24 percentage of participants
Radiation TreatmentFrequency of Required Interventions.1-2 fractions interrupted23 percentage of participants
Radiation TreatmentFrequency of Required Interventions.More than 2 fractions interrupted53 percentage of participants
Radiation TreatmentFrequency of Required Interventions.At least 1 interruption for all 5 fractions24 percentage of participants
Secondary

Percentage of Patients With a PSA Nadir of <3.35 ng/ml at 12 Months

To estimate one year prostate specific antigen (PSA)control of prostate cancer when treated with stereotactic body radiotherapy (SBRT) using continuous real-time evaluation of prostate motion.

Time frame: 1 Year

ArmMeasureValue (NUMBER)
Radiation TreatmentPercentage of Patients With a PSA Nadir of <3.35 ng/ml at 12 Months89 percentage of patients
Secondary

Relation Between Dose Distribution and Toxicities.

To look at the relation between dose distribution and toxicities and to determine if reconstructed delivered doses are more predictive of toxicity than planned doses.

Time frame: 5 years

Population: Data was not collected in full by some centers for their patients and these endpoints couldn't be analyzed.

Secondary

Relation Between Reconstructed Delivered Dose Distributions.

To determine the relation between reconstructed delivered dose distributions, accounting for prostate translation and rotation, and tumor control probabilities.

Time frame: 5 years

Population: Data was not collected in full by some centers for their patients and these endpoints couldn't be analyzed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026