Prediction of Resistance to <sup>177</sup>Lu-PSMA Therapy by Assessment of Baseline Circulating Tumor DNA Biomarkers.
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- Record sourced from PubMed, PMID 37770113.
- Also identified by DOI 10.2967/jnumed.123.266167.
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Abstract
<sup>177</sup>Lu-PSMA-617 and <sup>177</sup>Lu-PSMA I&T (collectively termed <sup>177</sup>Lu-PSMA) are currently being used for the treatment of selected metastatic castration-resistant prostate cancer (mCRPC) patients with PSMA PET-positive disease, but biomarkers for these agents remain incompletely understood. <b>Methods:</b> Pretreatment circulating tumor DNA (ctDNA) samples were collected from 44 mCRPC patients receiving <sup>177</sup>Lu-PSMA treatment. Prostate-specific antigen responders and nonresponders were assessed relative to the ctDNA findings at baseline. <b>Results:</b> The ctDNA findings indicated that nonresponders were more likely to have gene amplifications than were responders (75% vs. 39.2%, <i>P</i> = 0.03). In particular, amplifications in <i>FGFR1</i> (25% vs. 0%, <i>P</i> = 0.01) and <i>CCNE1</i> (31.2% vs. 0%, <i>P</i> = 0.001) were more likely to be present in nonresponders. <i>CDK12</i> mutations were more likely to be present in nonresponders (25% vs. 3.6%, <i>P</i> = 0.05). <b>Conclusion:</b> Our analyses indicate that ctDNA assays may contain specific biomarkers predictive of response or resistance for <sup>177</sup>Lu-PSMA-treated mCRPC patients. Additional confirmatory studies are required before clinicians can use these findings to make personalized treatment decisions.
Medical subject headings
- Circulating Tumor DNA
- Prostatic Neoplasms, Castration-Resistant