Additional Local Therapy for Liver Metastases in Patients with Metastatic Castration-Resistant Prostate Cancer Receiving Systemic PSMA-Targeted Therapy.
Where this comes from
- Record sourced from PubMed, PMID 31601703.
- Also identified by DOI 10.2967/jnumed.119.233429.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
The aim of this study was to evaluate the efficacy of <sup>177</sup>Lu-prostate-specific membrane antigen (PSMA)-617 (<sup>177</sup>Lu-PSMA) and selective internal radiation therapy (SIRT) for the treatment of liver metastases of castration-resistant prostate cancer. <b>Methods:</b> Safety and survival of patients with metastatic castration-resistant prostate cancer and liver metastases assigned to <sup>177</sup>Lu-PSMA alone (<i>n</i> = 31) or in combination with SIRT (<i>n</i> = 5) were retrospectively analyzed. Additionally, a subgroup (<i>n</i> = 10) was analyzed using morphologic and molecular response criteria. <b>Results:</b> Median estimated survival was 5.7 mo for <sup>177</sup>Lu-PSMA alone and 8.4 mo for combined sequential <sup>177</sup>Lu-PSMA and SIRT. <sup>177</sup>Lu-PSMA achieved discordant therapy responses with both regressive and progressive liver metastases in the same patient (best vs. worst responding metastases per patient: -35% vs. +63% diameter change; <i>P</i> < 0.05). SIRT was superior to <sup>177</sup>Lu-PSMA for the treatment of liver metastases (0% vs. 56% progression). <b>Conclusion:</b> The combination of <sup>177</sup>Lu-PSMA and SIRT is efficient and feasible for the treatment of advanced prostate cancer. <sup>177</sup>Lu-PSMA alone seems to have limited response rates in the treatment of liver metastases.
Medical subject headings
- Dipeptides
- Heterocyclic Compounds, 1-Ring
- Liver Neoplasms
- Prostatic Neoplasms, Castration-Resistant