Phase 2 Randomized Trial of Flexible Dosing Schedule of 177Lu-PSMA-617 for the Treatment of Metastatic Castration-Resistant Prostate Cancer (FLEX-MRT)

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexMale
Age18+
SponsorJonsson Comprehensive Cancer Center

About this trial

In advanced metastatic castration resistant prostate cancer (mCRPC) progressing after chemotherapy and androgen receptor (AR)-targeted therapy 177Lu-PSMA-617 is an effective treatment. 177Lu-PSMA-617 RLT is administered with a fixed schedule: 6 treatment cycles, administered every 6 weeks. However, the optimum number of cycles of 177Lu-PSMA in patients who show good response remains unknown. Some patients may benefit from more than 6 cycles of therapy. Additionally, some patients experience a complete or almost complete response before the last cycle. It is unclear whether these patients benefit from the subsequent remaining treatment cycle(s). A treatment holiday period would spare these patients some exposure to the therapy agent and avoid potentially unnecessary toxicity when treatment efficacy is already maximal and additional treatment effect cannot be expected. This randomized phase 2 study compares a group of patients treated with LuPSMA on a flexible and extended dosing schedule including "treatment holiday" periods (investigational arm, up to 12 cycles, as described below) to a control group treated with a fixed dosing schedule of 6 treatments cycles maximum administered every 6 weeks. The flexible dosing schedule in the investigational arm will be based on single photon emission computed tomography (SPECT)/computed tomography (CT) response assessments obtained 24h after injection of LuPSMA therapy cycle. The response assessment during treatment holiday period will be based on positron emission tomography/computed tomography (PET/CT) every 12 weeks. Single-time point SPECT/CT dosimetry protocol at every cycle will be performed and will allow to determine the number of cycles that subjects may receive under the study without exceeding the kidney dose threshold.

Eligibility criteria

Qualifiers

Patients must have prostate cancer proven by histopathology

Patients must have ≥ 1 metastatic lesion by any imaging (CT, magnetic resonance imaging [MRI], bone scan, PET)

Patients must have received at least one regimen of chemotherapy for mCRPC

Patients must have received at least one androgen-receptor signaling inhibitors (ARSI)

Disqualifiers

Prior cycle of 177Lu-PSMA-617 therapy

Less than 6 weeks between last myelosuppressive therapy (including docetaxel, cabazitaxel, strontium-89, samarium-153, rhenium-186, rhenium-188, radium-223, hemi-body irradiation) and first cycle of 177Lu-PSMA-617 therapy

Glomerular filtration rate (GFR) < 50 ml/min

Urinary tract obstruction or marked hydronephrosis

Trial design

Treatments tested in this trial

  • Computed Tomography
  • Gallium Ga 68 Gozetotide
  • Lutetium Lu 177 Vipivotide Tetraxetan
  • Positron Emission Tomography
  • PSMA PET Scan
  • Questionnaire Administration
  • Single Photon Emission Computed Tomography

Treatment groups

90 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Jonsson Comprehensive Cancer Center

Lead sponsor

Novartis Pharmaceuticals

Collaborator