PEACE-6 Poor Responders is an international, multicenter, open-label, controlled, randomized, phase III trial to evaluate the efficacy and safety of 177Lu-PSMA-617 when administered on top of the ongoing standard systemic treatment compared to standard systemic treatment alone in patients with de novo metastatic hormone-sensitive prostate cancer (mHSPC) who do not present with a satisfactory response characterized by a serum prostatic specific antigen (PSA) level of ≥ 0.2 ng/mL at 6 to 8 months after systemic treatment initiation for mHSPC (i.e. poor responders) in the absence of evidence of cancer progression (including a rising PSA level).
The study plans to enroll 500 patients over 63 months who will be randomized (1:1) to receive either: (i) Control arm: SoC (ADT+ ARSI (second-generation androgen receptor signaling inhibitors) +/- RT or ADT+ ARSI +/- RT) or (ii) Experimental arm: 177Lu-PSMA-617 + SoC (ADT+ ARSI +/- RT or ADT+ docetaxel + ARSI +/- RT). Response to treatment will be assessed according to the Prostate Cancer Clinical Trials Working Group 3 (PCWG3) criteria. Treatment will be continued at least until castration-resistant prostate cancer (CRPC) stage is reached, defined by evidence of cancer progression (either a confirmed PSA rise or a radiographic progression) with serum testosterone being at castrated levels (\<0.50 ng/mL). This systemic treatment may be continued after CRPC is reached, based on patient benefit and the investigator's opinion. Treatment may also be terminated at the initiative of either the patient or the investigator for any reason that would be beneficial to the patient, including: unacceptable toxicity, intercurrent conditions that preclude continuation of treatment, or patient request. At the end of treatment period, the follow-up period will last for 102 months (8.5 years). The overall trial duration, including the follow-up, is expected to last 18.5 years.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
500
Once every 6 weeks, 7400 MBq 177Lu-PMSA-617 will be administered for up to a total of 4 cycles.
ADT, abiraterone and each ARSI (Apalutamide, Darolutamide, Enzalutamide) will be administrated according to the standard of care
Institut de Cancérologie de l'Ouest
Angers, France
NOT_YET_RECRUITINGInstitut Bergonié
Bordeaux, France
NOT_YET_RECRUITINGCHRU Brest
Brest, France
NOT_YET_RECRUITINGCentre Francois Baclesse
Caen, France
NOT_YET_RECRUITINGCHU Henri Mondor
Créteil, France
NOT_YET_RECRUITINGCentre Georges-François Leclerc
Dijon, France
NOT_YET_RECRUITINGCHU Grenoble
Grenoble, France
NOT_YET_RECRUITINGCentre Léon Berard
Lyon, France
NOT_YET_RECRUITINGInstitut Paoli-Calmettes
Marseille, France
RECRUITINGCHRU Nancy
Nancy, France
NOT_YET_RECRUITING...and 15 more locations
Overall survival (OS)
Overall survival (OS) is defined as the time from the date of randomization to the date of death due to any cause.
Time frame: From randomization to death due to any cause, up to 8.5 years
Radiographic progression-free survival (rPFS)
Radiographic progression-free survival (rPFS) is defined as the time from randomization to the date of radiographic progression according to PCWG3 criteria by investigator assessment, or death, whichever occurs first.
Time frame: From randomization to radiographic progression or death, up to 8.5 years
Castration-Resistance Prostate Cancer-Free Survival (CRPC-FS)
Castration-Resistance Prostate Cancer-Free Survival (CRPC-FS) is defined as the time from randomization to the onset of castration-resistance or death from any cause, whichever occurs first.
Time frame: From randomization to onset of castration-resistance or death, up to 8.5 years
Prostate Cancer-Specific Survival (PCSS)
Prostate Cancer-Specific Survival (PCSS) is defined as the time from the date of randomization to the date of death due to prostate cancer.
Time frame: From the date of randomization to a PCSS event, up to 8.5 years
PSA response
PSA response will be assessed by the maximum change of PSA (rise or fall) from baseline over the treatment period. A complete PSA response is defined by an undetectable level of serum PSA.
Time frame: From baseline over the treatment period, up to 8.5 years
Skeletal-related event-free survival (SRE-FS)
Skeletal-related event-free survival (SRE-FS) is defined as the time from the randomization date to the date of diagnosis of either a skeletal-related event (SRE) (fracture, or bone pain requiring radiation therapy, or spinal cord compression, or preventive surgery to the bones) or death, whichever occurs first.
Time frame: From randomization to the onset of a SRE-FS event, up to 8.5 years
Time to severe urinary event (SUE)
Time to severe urinary event (SUE) is defined as the time from the randomization date to the date of diagnosis of either one of the following SUE, whichever occurs first: urinary retention with need for a urinary catheter, suprapubic catheter, double J stent, nephrostomy, treatment of the prostate by radiotherapy or trans-urethral resection of the prostate (TURP) or prostatectomy done to relieve patients with local symptoms.
Time frame: From randomization to the onset of a SUE event, up to 8.5 years
Time to initiation of first subsequent anti-cancer systemic therapy for CRPC (TTSST1)
TTSST1 is defined as the time from the randomization date to the date of initiation of the first anti-cancer systemic therapy for CRPC.
Time frame: From randomization to initiation of the first anti-cancer systemic therapy for CRPC, up to 10 years
Time to initiation of second subsequent anti-cancer systemic therapy for CRPC (TTSST2)
TTSST2 is defined as the time from the randomization date to the date of initiation of the second anti-cancer systemic therapy for CRPC.
Time frame: From randomization to initiation of the second anti-cancer systemic therapy for CRPC, up to 10 years
Efficacy of first subsequent anti-cancer systemic therapy for CRPC
Efficacy of subsequent anti-cancer systemic therapy for CRPC will be defined as the time from first anti-cancer systemic therapy for CRPC to disease progression or death from any cause, whichever comes first.
Time frame: From first anti-cancer systemic therapy for CRPC to disease progression or death, up to 10 years
Efficacy of second subsequent anti-cancer systemic therapy for CRPC
Efficacy of second subsequent anti-cancer systemic therapy for CRPC will be defined as the time from second anti-cancer systemic therapy for CRPC to disease progression or death from any cause, whichever comes first.
Time frame: Fromsecond anti-cancer systemic therapy for CRPC to disease progression or death, up to 10 years
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