The US Food and Drug Administration (FDA) has approved Blue Earth Diagnostics’ prostate-specific membrane antigen (PSMA)-targeted positron emission tomography (PET) imaging agent, POSLUMA (flotufolastat F 18). The high-affinity radiohybrid is the first and only FDA-approved agent of its kind. It will be widely accessible for patients across the United States. ...
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Tumor grade, sarcomatoid features may influence outcomes with adjuvant nivo/ipi in patients with RCC after nephrectomy.
EV plus pembrolizumab continues to demonstrate promising survival trends with durable responses in first-line la/mUC.
The prevalence, outcomes of patients with HRR mutations who initiated 1L mCRPC treatment with a novel hormonal therapy.
PSA nadir ≥0.1 ng/mL within 6 months of RT completion may be prognostic for long-term outcomes in patients receiving ...
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