AI Article Synopsis

  • The effectiveness of neoadjuvant therapy for improving survival in advanced prostate cancer is still unclear, with existing studies focusing on different endpoints like progression-free survival and symptom relief.
  • This study specifically investigates the use of apalutamide as a neoadjuvant treatment to enhance the surgical resection rate in patients with unresectable prostate tumors.
  • Results showed all 7 patients treated with apalutamide were able to successfully undergo radical prostatectomy without significant increases in complications, though further research is needed to confirm the therapy's overall clinical benefits.

Article Abstract

Whether neoadjuvant therapy confers a survival benefit in advanced prostate cancer (PCa) remains uncertain. The primary endpoints of previous retrospective and phase II clinical studies that used neoadjuvant therapy, including androgen deprivation therapy combined with new-generation androgen receptor signaling inhibitors or chemotherapy, were pathological downstaging, progression-free survival, prostate-specific antigen relief, and local symptom improvement. To the best of our knowledge, no studies have explored the efficacy and safety of neoadjuvant therapy in improving the surgical resection rate in cases of unresectable primary tumors of PCa. We first designed this retrospective study to evaluate the potential value of apalutamide as neoadjuvant therapy in improving the resectability rate of radical prostatectomy (RP). We initially reported 7 patients with unresectable primary lesions who underwent neoadjuvant apalutamide treatment for a median of 4 months, and all of them successfully underwent RP treatment. Our study supported apalutamide as neoadjuvant therapy, which helped improve RP's success rate and did not significantly increase perioperative complications, and the neoadjuvant therapy was controllable. Our findings' clinical value and benefit for survival still need further clinical research to confirm.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10620516PMC
http://dx.doi.org/10.3389/fphar.2023.1284899DOI Listing

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