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Abstract Background: Metastatic Prostate cancer (mPCa) mortality rates are high despite numerous treatment options against various mechanisms of action, including targeted therapies, i. e. prostate specific membrane antigen (PSMA) -targeted therapy (Pluvicto) or anti-androgen receptor (AR) (Enzulamide, Biculamide). Further, tumor biomarkers (i. e. PSMA and AR) can change over time and with resistance mechanisms that develop after treatments. This suggests that primary biopsies may not represent later PCa tumors necessitating a way to identify patients that may respond to later line therapies. Blood based biopsies can be used to monitor PCa treatment, which can include circulating tumor cells (CTCs) and the newly discovered cancer associated macrophage like cells (CAMLs), a cancer specific circulating phagocytic stromal cells. Interestingly, while PSMA Part 1 (Regular Abstracts) ; 2024 Apr 5-10; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2024;84 (6Suppl): Abstract nr 3690.
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Dimpal M. Kasabwala
Raymond C. Bergan
R. Katherine Alpaugh
Cancer Research
Memorial Sloan Kettering Cancer Center
Rutgers, The State University of New Jersey
Fox Chase Cancer Center
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Kasabwala et al. (Fri,) studied this question.
www.synapsesocial.com/papers/68e72f4bb6db6435876a88aa — DOI: https://doi.org/10.1158/1538-7445.am2024-3690