TY - JOUR
T1 - Treating De novo metastatic castration sensitive prostate cancer with visceral metastases: an evolving issue
AU - Roviello, Giandomenico
AU - Petrioli, Roberto
AU - Villari, Donata
AU - D'Angelo, Alberto
PY - 2021/2/1
Y1 - 2021/2/1
N2 - Visceral metastasis is widely considered a prognostic factor for overall survival of men with
metastatic castration-sensitive prostate cancer (mCSPC) and has been historically
managed with androgen deprivation therapy (ADT). More recently, this therapeutic
scenario has been enriched by the possibility to integrate ADT with chemotherapy or novel
androgen-signalling–targeted inhibitors. In order to define the effect of
chemotherapy/androgen-signalling–targeted inhibitors plus ADT, we performed a pooled
analysis on patients with mCSPC and visceral metastases revealing that survival was
significantly improved in patients without visceral metastasis (HR=0.64 95%CI: 0.56-0.74;
p<0.01) compared with men with visceral metastases (HR=0.68; 95%CI: 0.51-0.91;
p<0.01). Although several limitations do not allow to draw definitive conclusions, our
analysis confirms the efficacy of chemotherapy/androgen-signalling–targeted inhibitors in
combination with ADT also in mCSPC with visceral metastases. In the absence of specific
randomized controlled trials, symptoms, toxicity, cost, patients’ preference and clinical
experience should guide the decision to add chemotherapy or androgen receptor-targeted
therapy to ADT in patients with visceral metastases from mCSPC.
AB - Visceral metastasis is widely considered a prognostic factor for overall survival of men with
metastatic castration-sensitive prostate cancer (mCSPC) and has been historically
managed with androgen deprivation therapy (ADT). More recently, this therapeutic
scenario has been enriched by the possibility to integrate ADT with chemotherapy or novel
androgen-signalling–targeted inhibitors. In order to define the effect of
chemotherapy/androgen-signalling–targeted inhibitors plus ADT, we performed a pooled
analysis on patients with mCSPC and visceral metastases revealing that survival was
significantly improved in patients without visceral metastasis (HR=0.64 95%CI: 0.56-0.74;
p<0.01) compared with men with visceral metastases (HR=0.68; 95%CI: 0.51-0.91;
p<0.01). Although several limitations do not allow to draw definitive conclusions, our
analysis confirms the efficacy of chemotherapy/androgen-signalling–targeted inhibitors in
combination with ADT also in mCSPC with visceral metastases. In the absence of specific
randomized controlled trials, symptoms, toxicity, cost, patients’ preference and clinical
experience should guide the decision to add chemotherapy or androgen receptor-targeted
therapy to ADT in patients with visceral metastases from mCSPC.
U2 - 10.1016/j.clgc.2020.06.001
DO - 10.1016/j.clgc.2020.06.001
M3 - Article
VL - 19
SP - 83
EP - 86
JO - Clinical Genitourinary Cancer
JF - Clinical Genitourinary Cancer
IS - 1
ER -