[177Lu]Lu-PSMA-617 as first-line systemic therapy in patients with metastatic castration-resistant prostate cancer: a real-world study

Eur J Nucl Med Mol Imaging. 2024 Jul;51(8):2495-2503. doi: 10.1007/s00259-024-06677-y. Epub 2024 Mar 12.

Abstract

Purpose: The use of [177Lu]Lu-PSMA-617 radioligand therapy has become increasingly recognized as a viable therapeutic approach for patients in the advanced stages of metastatic castration-resistant prostate cancer (mCRPC). However, there is limited data regarding its effectiveness and safety in earlier lines. This study aims to present our institution's experience with [177Lu]Lu-PSMA-617 as a first-line systemic therapy for mCRPC.

Methods: We collected and analyzed data from consecutive mCRPC patients who underwent first-line treatment with [177Lu]Lu-PSMA-617 at our center from 2015 to 2023. The various outcome measures included best prostate-specific antigen-response rate (PSA-RR) (proportion of patients achieving a ≥ 50% decline in PSA); objective radiographic response rate (ORR) (proportion of patients achieving complete or partial radiographic responses); radiographic progression-free survival (rPFS) (measured from treatment initiation until radiographic progression or death from any cause); overall survival (OS) (measured from treatment initiation until death from any cause); and adverse events.

Results: Forty treatment-naïve mCRPC patients with PSMA-positive disease on [68Ga]Ga-PSMA-11 PET/CT were included (median age: 68.5 years, range: 45-78; median PSA: 41 ng/mL, range: 1-3028). These patients received a median cumulative activity of 22.2 GBq (range: 5.55-44.4) [177Lu]Lu-PSMA-617 over 1-6 cycles at 8-12 week intervals. A ≥ 50% decline in PSA was observed in 25/40 (62.5%) patients (best PSA-RR). Radiographic responses were evaluated for thirty-eight patients, with thirteen showing partial responses (ORR 34.2%). Over a median follow-up of 36 months, the median rPFS was 12 months (95% confidence interval, CI: 9-15), and the median OS was 17 months (95% CI: 12-22). Treatment-emergent grade ≥ 3 anemia, leucopenia, and thrombocytopenia were noted in 4/40 (10%), 1/40 (2.5%), and 3/40 (7.5%) patients, respectively.

Conclusion: The findings suggest that [177Lu]Lu-PSMA-617 is a safe and effective option as a first-line treatment in mCRPC. Further trials are needed to definitively establish its role as an upfront treatment modality in this setting.

Keywords: First-line; Overall survival; Real-world; [177Lu]Lu-PSMA-617; mCRPC; rPFS.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Dipeptides* / therapeutic use
  • Heterocyclic Compounds, 1-Ring* / therapeutic use
  • Humans
  • Lutetium* / therapeutic use
  • Male
  • Middle Aged
  • Neoplasm Metastasis*
  • Prostate-Specific Antigen
  • Prostatic Neoplasms, Castration-Resistant* / pathology
  • Prostatic Neoplasms, Castration-Resistant* / radiotherapy
  • Radioisotopes / therapeutic use
  • Radiopharmaceuticals / therapeutic use
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Heterocyclic Compounds, 1-Ring
  • Lutetium
  • Dipeptides
  • PSMA-617
  • Pluvicto
  • Prostate-Specific Antigen
  • Lutetium-177
  • Radiopharmaceuticals
  • Radioisotopes