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NCT03569241Active, not recruitingPhase 2

PEACE V: Salvage Treatment of OligoRecurrent Nodal Prostate Cancer Metastases

PEACE V: a Randomized Phase II Trial for the Salvage Treatment of OligoRecurrent Nodal Prostate Cancer Metastases (STORM)

Source: ClinicalTrials.gov · Last updated 9 Dec 2024

Brief summary (registry, in English)

A proportion of prostate cancer (PCa) patients develop relapse following curative local treatment. Regional nodal recurrence is an emerging clinical situation since the introduction of new molecular imaging methods in the restaging of recurrent prostate cancer. More specifically, a subgroup of these patients is being diagnosed with a recurrence confined to the regional lymph nodes and limited in number (oligorecurrence) using choline or PSMA PET-CT. As there are no specific treatment recommendations for these type of patients, different treatment approaches are currently used, mostly focusing on local ablative treatments using radiotherapy or surgery. These treatments are coined metastasisdirected therapy (MDT). MDT in combination with or without temporary ADT could delay the subsequent risk of progression, and even cure limited regional nodal recurrences. Consequently, lifelong palliative ADT, with its toxicity and excess in non-cancer mortality might be postponed. The proposed trial randomizes patients with oligorecurrent nodal prostate cancer following primary PCa treatment to either metastasis-directed therapy (MDT) (salvage lymph node dissection, sLND or stereotactic body radiotherapy, SBRT) or MDT plus whole pelvis radiotherapy (WPRT: 45 Gy in 25 fractions).

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
196 (actual)
First submitted
14 Jun 2018
Start date
27 Apr 2018
Primary completion date
30 Apr 2023
Lead sponsor
University Hospital, Ghent
NCT number
NCT03569241

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 196
  • From 27 Apr 2018 to the primary completion date, 30 Apr 2023
  • 29 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous irradiation of the pelvic and or para-aortic nodes
  • Lymph node metastases in previously irradiated areas resulting in dose constraint violation
  • Contraindications to androgen deprivation therapy
  • PSA rise while on active treatment with (LHRH-agonist, LHRH-antagonist, anti-androgen, estrogen
  • Previous treatment with cytotoxic agent for PCa
  • Treatment during the past month with products known to influence PSA levels (e.g. fluconazole, finasteride, corticosteroids,…)

Other illness

  • Contraindications to pelvic radiotherapy (chronic pelvic inflammatory bowel disease)
  • Other active malignancy, except non-melanoma skin cancer or other malignancies with a documented disease-free survival for a minimum of 3 years before randomization.

Lab values

  • Serum testosterone level \<50ng/dl or 1.7 nmol/L at time of randomization

Other

  • Bone or visceral metastases
  • Para-aortic lymph node metastases (above the aortic bifurcation)
  • Local relapse in the prostate gland or prostate bed not suitable for a curative treatment
  • Symptomatic metastases

Who the study is looking for

  • Histologically proven initial diagnosis of adenocarcinoma of the prostate
  • Biochemical relapse of prostate cancer following radical local prostate treatment (radical prostatectomy, primary radiotherapy or radical prostatectomy +/- prostate bed adjuvant/ salvage radiotherapy) according to the EAU guidelines 2016.
  • Following radical prostatectomy, patients with a biochemical relapse are eligible in case a nodal relapse is detected in the pelvis even in the absence of prior postoperative prostate bed radiotherapy (adjuvant or salvage).
  • In case of a suspected local recurrence following primary radiotherapy, a biopsy should confirm local recurrence and patients with a confirmed local recurrence are eligible in case they also undergo a local salvage therapy. If imaging rules out local relapse, patients are eligible.
  • Nodal relapse in the pelvis on choline, PSMA or FACBC PET-CT with a maximum of 3 positive nodal lymph nodes. The upper limit of the pelvis is defined as the aortic bifurcation.
  • WHO performance state 0-1
  • Age \>18 years
  • Absence of any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be discussed with the patient before registration in the trial
  • Before patient registration/randomization, written informed consent must be given according to ICH/GCP, and national/local regulations.

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (29)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Epworth Healthcare
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MelbourneAustraliaUnknown status
GZA
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AntwerpBelgiumUnknown status
AZ St-Jan Brugge
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BrugesBelgiumUnknown status
AZ St-Lucas
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BrugesBelgiumUnknown status
Institut Jules Bordet
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BrusselsBelgiumUnknown status
AZ Maria Middelares
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GhentBelgiumUnknown status
University Hospital Ghent
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GhentBelgiumUnknown status
AZ Groeninge
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KortrijkBelgiumUnknown status
UZ Leuven
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LeuvenBelgiumUnknown status
CH Mouscron
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MouscronBelgiumUnknown status
Universitätsspital Basel
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BaselSwitzerlandUnknown status
Universitätsklinik für Radio-Onkologie
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BernSwitzerlandUnknown status
Hôpitaux universitaires de Genève
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GenevaSwitzerlandUnknown status
Kantonsspital St. Gallen
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Sankt GallenSwitzerlandUnknown status
Universitätsspital Zürich
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ZurichSwitzerlandUnknown status
Cruces University Hospital
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BarakaldoSpainUnknown status
Clínica Universitaria IMQ
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BilbaoSpainUnknown status
Hospital Ramón y Cajal
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MadridSpainUnknown status
Hospital Universitario la Princesa
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MadridSpainUnknown status
Universitario Quironsalud
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MadridSpainUnknown status
Hospitalario de Navarra
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NavarroSpainUnknown status
Hospital Clínico de Santiago
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SantiagoSpainUnknown status
Hospital Universitari i Politécnic La Fe
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ValenciaSpainUnknown status
Humanitas Research Hospital
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MilanItalyUnknown status
Vita-Salute San Raffaele University
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MilanItalyUnknown status
Istituto Nazionale Tumori IRCCS
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NaplesItalyUnknown status
Fondazione IRCCS Policlinico S. Matteo
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PaviaItalyUnknown status
Ospedale Sacro Cuore-Don Calabria
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VeronaItalyUnknown status
Oslo University Hospital
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OsloNorwayUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.