Optimizing PSMA Radioligand Therapy for Patients with Metastatic Castration-Resistant Prostate Cancer. A Systematic Review and Meta-Analysis

Int J Mol Sci. 2020 Nov 28;21(23):9054. doi: 10.3390/ijms21239054.

Abstract

The aim of the review was to evaluate patient and treatment characteristics for patients with metastatic castration-resistant prostate cancer (mCRPC) treated with PSMA radioligand therapy (PRLT) associated with above-average outcome. The systematic review and meta-analysis followed recommendations by the Preferred Reporting Items for Systematic reviews and Meta-Analysis (PRISMA). We searched for publications in PubMed, Embase, and ClinicalTrials.gov up to 31 September 2020. Thirty-six publications and four duplicates reported 2346 patients. Nearly two-thirds of the patients had bone metastases. Median overall survival (OS) was 16 months. Asymptomatic patients and patients with only lymph node metastases lived longer than symptomatic patients and patients with more extensive metastases. Patients treated with an intensified schedule of 177Lu PRLT lived longer than those treated with a conventional schedule. Half of the patients obtained a PSA decline ≥ 50% and these patients lived longer than those with less PSA decline. Approximately 10% of the patients developed hematologic toxicity with anemia grade 3 as the most severe adverse effect. Characteristics for patients, cancer, restaging, and PRLT predict above average overall survival following treatment with PRLT.

Keywords: adverse effects; decline of prostate specific antigen; metastases; overall survival; predictive factors; prostate cancer; prostate-specific membrane antigen; theranostics.

Publication types

  • Meta-Analysis
  • Systematic Review

MeSH terms

  • Humans
  • Male
  • Prostate-Specific Antigen / metabolism*
  • Prostatic Neoplasms, Castration-Resistant / therapy*
  • Publication Bias
  • Radiopharmaceuticals / adverse effects
  • Radiopharmaceuticals / therapeutic use*
  • Survival Analysis
  • Treatment Outcome

Substances

  • Radiopharmaceuticals
  • Prostate-Specific Antigen