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Updated: Jun 23, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Single Center Experience with a 4-Week 177Lu-PSMA-617 Treatment Interval in Patients with Metastatic
Jukka Kemppainen1,2, Aki Kangasmäki1, Simona Malaspina2
1Docrates Cancer Center, 00180 Helsinki, Finland.
Lutetium-177 PSMA-617 therapy is safe and effective for metastatic castration-resistant prostate cancer (mCRPC). Nearly 60% of patients showed significant PSA response, correlating with improved overall survival, but better biomarkers are needed for patient selection.
Area of Science:
- Nuclear Medicine
- Oncology
- Radiopharmaceutical Therapy
Background:
- Metastatic castration-resistant prostate cancer (mCRPC) requires effective treatments.
- 177Lu-PSMA-617 offers a promising theragnostic approach for mCRPC.
- Optimal dosing, intervals, and patient selection for 177Lu-PSMA-617 remain unclear.
Purpose of the Study:
- To evaluate the safety and efficacy of 177Lu-PSMA-617 in mCRPC patients.
- To determine the optimal treatment interval and identify predictors of response.
- To assess the association between pre-treatment PSMA PET/CT parameters and treatment outcomes.
Main Methods:
- Retrospective analysis of 62 mCRPC patients treated with 177Lu-PSMA-617.
- Treatment administered in cycles at four-week intervals.
- Evaluation of progression-free survival (PFS), overall survival (OS), and prostate-specific antigen (PSA) response.
Main Results:
- A median of three treatment cycles were administered.
- Progression-free survival was 4.9 months and overall survival was 17.2 months.
- 58.7% of patients achieved a significant PSA response (>50%), associated with longer OS.
- No major adverse events were reported.
- Pre-treatment PSMA PET/CT parameters did not predict treatment response.
Conclusions:
- 177Lu-PSMA-617 therapy at four-week intervals is safe and effective for mCRPC.
- Significant PSA response is a key indicator of improved overall survival.
- Current PSMA PET/CT-derived parameters are insufficient for selecting patients who will respond to treatment; novel biomarkers are necessary.
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