Phase II Trial of PSA Response-based Androgen Deprivation Therapy and Nodal Coverage for Prostate Cancer Early Salvage Radiotherapy (RANGER)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexMale
Age18+
SponsorUniversity of Texas Southwestern Medical Center

About this trial

This Phase II, single arm study evaluates a PSA-response-adapted approach to salvage radiotherapy after radical prostatectomy for prostate cancer. All participants will receive hypo-fractionated stereotactic radiotherapy to the prostate fossa. At 5 weeks, biochemical response will be assessed. responders will proceed to observation, while non responders will receive sequential pelvic nodal radiotherapy and 4 months of androgen deprivation therapy (ADT). The study aims to determine whether this response base approach achieves non inferior 2 year freedom from progression compared with historical outcomes using routine pelvic nodal radiotherapy and ADT in all patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Men aged ≥18 years with histologically confirmed prostate adenocarcinoma treated with prostatectomy in the localized setting within 10 years, with post-operative PSA (persistent or rising) of ≥0.05ng/mL.

Radical prostatectomy ≥4 months prior to enrollment without nodal involvement (pN0 or pNx)

Performance status ECOG 0-2

PSA>=0.2ng/mL: positron emission tomography (PET) with FDA-approved advanced imaging agent for prostate cancer (e.g. PSMA) required.

Disqualifiers

Prior androgen deprivation therapy (ADT) > 3 months OR anti-androgen therapy (AAT) of > 30 days. For shorter courses of either, at least 30 day "wash out" period is required with confirmation of resolved castration of testosterone to >50ng/mL.

Ongoing testosterone replacement therapy (TRT) with refusal to discontinue (must be stopped with demonstration of detectable PSA ≥0.05ng/mL and non-castrate testosterone >50ng/mL after 14 days of TRT cessation)

Prior pelvic radiotherapy

Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that, in the opinion of the investigator, would limit compliance with study requirements.

Trial design

Design model

Single group

Treatments tested in this trial

  • Prostate Fossa Radiotherapy

    Radiation

    Stereotactic ultra hypofractionanted radiotherapy delivered to the prostate fossa using the Ethos online adaptive platform. Total dose of 32.5 Gy administered in 5 fractions over 2-4 weeks.

  • Pelvic nodal Radiotherapy

    Radiation

    Sequential pelvic nodal radiotherapy delivered only to PSA non responders. Dose of 25 Gy given in 5 fractions over 4 weeks using the same stereotactic technique as prostate fossa RT.

  • Androgen Deprivation Therapy (ADT)

    Drug

    GnRH agonist or antagonist (leuprolide, goserelin, degarelix) administered as per institutional standard. Therapy duration is 4 months, starting before or within 14 days of pelvic nodal RT initiation.

Treatment groups

68 Participants
are divided into 1 treatment group
Group A: Single Arm: PSA Response Adapted Salvage RadiotherapyExperimental treatment 3 interventions

Trial outcomes

Primary outcomes

1

Freedom from failure

first occurrence of rise of PSA of 2 ng/dL above post-salvage RT nadir, clinical progression (local/regional/distant) or death due to any cause.

Time frame
2 years from end of radiotherapy

Secondary outcomes

1

EPIC-26 hormonal summary domain score

Patient reported hormonal symptom severity measure by the EPIC-26 questionnaire

Time frame
Baseline and regular intervals during 2 year follow up
2

EPIC-26 Genitourinary (GU) summary domain score

Patient reported genitourinary symptom severity measure by EPIC-26

Time frame
Baseline and regular intervals during 2 year follow up
3

EPIC-26 Gastrointestinal (GI) summary domain score

Patient reported gastrointestinal severity measured by EPIC-26

Time frame
Baseline and regular intervals during 2 year follow up
4

CTCAE v5.0 toxicity GU and GI

GI and GU adverse events will be assessed and graded according to the National Cancer Institute Common Technology Criteria for Adverse Events (CTCAE), version 5.0.

Time frame
Baseline and regular intervals during 2 year follow up

Other outcomes

Sponsors and contacts

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