ESMO 2021: Cisplatin (Cis)-Related Immunomodulation and Efficacy with Atezolizumab + Cis- vs Carboplatin-Based Chemotherapy in Metastatic Urothelial Cancer (mUC)

(UroToday.com)Cisplatin-based chemotherapy is associated with improved responses and more durable outcomes than carboplatin in mUC, though the mechanisms for this are poorly characterized. An exploratory subset analysis of the IMvigor130 trial suggested that the addition of atezolizumab to cisplatin-based chemotherapy had more efficacy (hazard ratio for overall survival 0.73 (0.54 – 0.98) with cisplatin versus […]

Loss of SNAI2 in Prostate Cancer Correlates with Clinical Response to Androgen Deprivation Therapy – Expert Commentary

The time between diagnosis of organ-confined prostate cancer and definitive therapy with radical prostatectomy provides an interval for intervention, with the benefit of pre- (biopsy specimen) and post-intervention (surgical specimen) tissue for comparison. The authors of “Loss of SNAI2 in Prostate Cancer Correlates with Clinical Response to Androgen Deprivation Therapy” present molecular studies from their […]

Maintenance therapy and beyond with avelumab…

Avelumab initially received regulatory approval for patients with metastatic urothelial carcinoma in the post-platinum chemotherapy setting based on an objective response rate of 16.5%.1  In the post-platinum chemotherapy setting, both nivolumab and pembrolizumab also currently retain their regulatory approval status.  However, the situation where avelumab has the strongest data is in the maintenance-switch setting.  I […]

Loss of SNAI2 in Prostate Cancer Correlates With Clinical Response to Androgen Deprivation Therapy.

Androgen receptor (AR) signaling is important in prostate cancer progression, and therapies that target this pathway have been the mainstay of treatment for advanced disease for over 70 years. Tumors eventually progress despite castration through a number of well-characterized mechanisms; however, little is known about what determines the magnitude of response to short-term pathway inhibition.

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