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Prostate cancer is one of the most common cancers in men worldwi.
The PI3K/protein kinase B/mTOR (PI3K/AKT/mTOR) signaling pathway is one of the most frequently activated signaling pathways in solid and hematological malignanci.
Preclinical studies have shown that the PI3K/AKT/mTOR signaling pathway is potentially associated with the androgen receptor (AR) signaling axis in ADT-resistant prostate cancer cel.
This study aimed to evaluate the efficacy and safety of samotolisib, a dual PI3K/mTOR kinase and DNA-dependent protein kinase inhibitor, combined with enzalutamide in patients with mCR.
The primary endpoint was progression-free surviv.
Median PFS and rPFS were significantly longer in both the samotolisib/enzalutamide group compared with the placebo/enzalutamide group (8 vs 8 months, p=003; 12 vs 5 months, p=03.
In conclusion, samotolisib/enzalutamide significantly improved progression-free survival in patients with metastatic-resistant prostate cancer that had progressed on abiraterone, was well tolerated , and was free of androgen receptor splice variantPatients benefit more significant.
Samotolisib/enzalutamide significantly improves progression-free survival in patients with metastatic drug-resistant prostate cancer that has progressed on abiraterone, and is well tolerated Samotolisib/enzalutamide significantly improves abiraterone therapy Progression-free survival in patients with metastatic drug-resistant prostate cancer that progresses and is well tolerated
Original source:
Original source:Christopher.
Christopher.
Sweeney, et .
Phase Ib/II Study of Enzalutamide with Samotolisib (LY3023414) or Placebo in Patients with Metastatic Castration-Resistant Prostate Canc.
Clin Cancer Res OF1–OF1 https://d.
org/11158/1078 -043CCR-21-232 Leave a message here