The Detection and Negative Reversion of Circulating Tumor Cells as Prognostic Biomarkers for Metastatic Castration-Resistant Prostate Cancer with Bone Metastases Treated by Enzalutamide

• Published in: Cancers Vol. 16; no. 4; p. 772
• Main Authors: Nakamura, So, Nagata, Masayoshi, Nagaya, Naoya, Ashizawa, Takeshi, Hirano, Hisashi, Lu, Yan, Ide, Hisamitsu, Horie, Shigeo
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.02.2024
• Subjects: Androgen receptors; Androgens; Biological markers; Biomarkers; Biopsy; Bone cancer; Cancer therapies; Care and treatment; Castration; Development and progression; Ethylenediaminetetraacetic acid; Hemoglobin; Medical prognosis; Medical research; Medicine, Experimental; Metastases; Metastasis; Mortality; Patients; Prognosis; Prostate cancer; Surveys; Tumor cells; Tumors; Japan; bone metastases; androgen receptor signaling inhibitor; castration-resistant prostate cancer; circulating tumor cells (CTCs); enzalutamide
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers16040772

Enzalutamide is a second-generation androgen receptor inhibitor that increases overall survival (OS) rates in patients with metastatic castration-resistant prostate cancer (mCRPC). This study evaluates the efficacy of circulating tumor cell (CTC) status as a prognostic biomarker following enzalutamide administration. A retrospective subgroup analysis and prognostic survey were conducted on 43 patients with mCRPC and bone metastases treated in Juntendo University-affiliated hospitals from 2015 to 2022. Patients were treated with 160 mg enzalutamide daily. CTC analyses on blood samples were performed regularly before and every three months after treatment. The relationship between the patients’ clinical factors and the OS rate was analyzed using the log-rank test; the median OS was 37 months. Patients with no detected CTCs at baseline showed significantly longer OS than those with detectable CTCs at baseline. Furthermore, patients demonstrating negative reversion of CTCs during enzalutamide treatment had significantly longer OS than patients with CTC-positivity. Two biomarkers—higher hemoglobin at baseline and achieving negative reversion of CTCs—were significantly associated with prolonged OS. This study suggests that patients achieving CTC-negative reversion during treatment for mCRPC with bone metastases exhibit improved long-term OS. Chronological measurement of CTC status might be clinically useful in the treatment of mCRPC.