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Prediction of Resistance to 177Lu-PSMA Therapy by Assessment of Baseline Circulating Tumor DNA Biomarkers.
Sartor, Oliver; Ledet, Elisa; Huang, Minqui; Schwartz, Jennifer; Lieberman, Alex; Lewis, Brian; Layton, Jodi; Barata, Pedro; Jang, Albert; Hawkins, Madeline; Pocha, Olivia; Lanka, Sree; Harris, Kendra.
Afiliação
  • Sartor O; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana; sartor.oliver@mayo.edu.
  • Ledet E; Department of Medical Oncology, Mayo Clinic, Rochester, Minnesota; and.
  • Huang M; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Schwartz J; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Lieberman A; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Lewis B; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Layton J; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Barata P; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Jang A; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Hawkins M; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Pocha O; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Lanka S; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
  • Harris K; Tulane Cancer Center, Tulane University School of Medicine, New Orleans, Louisiana.
J Nucl Med ; 64(11): 1721-1725, 2023 11.
Article em En | MEDLINE | ID: mdl-37770113
ABSTRACT
177Lu-PSMA-617 and 177Lu-PSMA I&T (collectively termed 177Lu-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.

Methods:

Pretreatment circulating tumor DNA (ctDNA) samples were collected from 44 mCRPC patients receiving 177Lu-PSMA treatment. Prostate-specific antigen responders and nonresponders were assessed relative to the ctDNA findings at baseline.

Results:

The ctDNA findings indicated that nonresponders were more likely to have gene amplifications than were responders (75% vs. 39.2%, P = 0.03). In particular, amplifications in FGFR1 (25% vs. 0%, P = 0.01) and CCNE1 (31.2% vs. 0%, P = 0.001) were more likely to be present in nonresponders. CDK12 mutations were more likely to be present in nonresponders (25% vs. 3.6%, P = 0.05).

Conclusion:

Our analyses indicate that ctDNA assays may contain specific biomarkers predictive of response or resistance for 177Lu-PSMA-treated mCRPC patients. Additional confirmatory studies are required before clinicians can use these findings to make personalized treatment decisions.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias de Próstata Resistentes à Castração / DNA Tumoral Circulante Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias de Próstata Resistentes à Castração / DNA Tumoral Circulante Idioma: En Ano de publicação: 2023 Tipo de documento: Article