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Updated: Aug 5, 2026

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A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Rechallenge With 177Lu-PSMA Radioligand Therapy in Metastatic Castration-resistant and Hormone-sensitive Prostate
Faeze Rabani1, Nikoo Rezaei, Amin Tanha Saber
1Nuclear Medicine Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Clinical Nuclear Medicine
|August 3, 2026
Summary
Four prostate cancer patients showed significant improvement with 177Lu-PSMA-617 radioligand therapy (RLT). Retreatment after progression was safe and effective, demonstrating RLT rechallenge feasibility in metastatic prostate cancer.
Area of Science:
- Oncology
- Nuclear Medicine
- Radiopharmaceutical Therapy
Background:
- Metastatic prostate cancer, including hormone-sensitive (mHSPC) and castration-resistant (mCRPC) forms, presents significant treatment challenges.
- 177Lu-PSMA-617 radioligand therapy (RLT) has emerged as a promising treatment modality for advanced prostate cancer.
Purpose of the Study:
- To evaluate the efficacy and safety of 177Lu-PSMA-617 RLT in patients with metastatic prostate cancer.
- To assess the feasibility and outcomes of RLT rechallenge in patients who progressed after initial treatment.
Main Methods:
- Retrospective case series of 4 patients with mHSPC or mCRPC treated with 177Lu-PSMA-617 RLT.
- Patients received initial RLT, and some were retreated upon disease progression.
Main Results:
- Initial RLT resulted in significant prostate-specific antigen (PSA) declines, pain relief, and radiographic responses.
- Rechallenge with 177Lu-PSMA-617 led to further PSA reductions, sustained symptom improvement, and favorable safety.
- No grade III-IV hematologic or renal toxicities were observed during rechallenge.
Conclusions:
- 177Lu-PSMA-617 RLT is effective in both mHSPC and mCRPC settings.
- RLT rechallenge is feasible and effective, even after prior progression, supporting its dynamic application across disease stages.
