TY - JOUR
T1 - Prognostic impact of lung metastasis in patients treated with androgen receptor signaling inhibitors for castration-sensitive prostate cancer
T2 - data from the ULTRA-Japan Consortium
AU - Uchimoto, Taizo
AU - Hirosuna, Kensuke
AU - Niigawa, Heima
AU - Kakumae, Sho
AU - Morinaka, Hirofumi
AU - Fukuokaya, Wataru
AU - Yoshizawa, Atsuhiko
AU - Saruta, Masanobu
AU - Fujimoto, Saizo
AU - Morita, Tsuyoshi
AU - Yamamoto, Yutaka
AU - Sakamoto, Moritoshi
AU - Nishimura, Kazuki
AU - Maenosono, Ryoichi
AU - Tsujino, Takuya
AU - Nishio, Kyosuke
AU - Yoshikawa, Yuki
AU - Ichihashi, Atsushi
AU - Yamamoto, Shutaro
AU - Iwatani, Kosuke
AU - Urabe, Fumihiko
AU - Mori, Keiichiro
AU - Yanagisawa, Takafumi
AU - Tsuduki, Shunsuke
AU - Takahara, Kiyoshi
AU - Inamoto, Teruo
AU - Fujita, Kazutoshi
AU - Azuma, Haruhito
AU - Kimura, Takahiro
AU - Komura, Kazumasa
N1 - Publisher Copyright:
© The Author(s) 2025. Published by Oxford University Press. All rights reserved.
PY - 2026/1/1
Y1 - 2026/1/1
N2 - Background Androgen receptor signaling inhibitors (ARSIs) have become the standard treatment for metastatic castration-sensitive prostate cancer (mCSPC). While visceral metastases, including lung metastases (LMs), are considered poor prognostic factors, their impact on clinical outcomes in mCSPC remains unclear. This study aimed to evaluate the prognostic significance of LM in mCSPC patients treated with ARSI-based doublet therapy. Methods This retrospective study analyzed a multi-institutional cohort of 453 mCSPC patients treated with ARSIa-based doublet therapy. Results The median overall survival (OS) and time to castration resistance (TTCR) were 80 and 41 months, respectively, with a median follow-up of 20 months. The total cohort included 117 patients (25.8%) with LM and 336 patients (74.2%) without LM. LATITUDE high-risk and CHAARTED high-volume criteria classified 380 patients (83.9%) and 356 patients (78.6%), respectively. Although not statistically significant, OS and TTCR showed a trend toward better outcomes in the LM group compared to the non-LM group in LATITUDE high-risk (n = 380: P =.097 for OS and P =.104 for TTCR) and CHAARTED high-volume (n = 356: P =.064 for OS and P =.086 for TTCR). In the propensity score matching cohort (n = 218 and n = 206 for LATITUDE and CHAARTED criteria, respectively), OS and TTCR remained comparable between the LM and non-LM groups. Conclusions LM does not appear to be related to OS or TTCR in mCSPC patients treated with ARSI-based doublet therapy, indicating that its prognostic value may need to be reevaluated.
AB - Background Androgen receptor signaling inhibitors (ARSIs) have become the standard treatment for metastatic castration-sensitive prostate cancer (mCSPC). While visceral metastases, including lung metastases (LMs), are considered poor prognostic factors, their impact on clinical outcomes in mCSPC remains unclear. This study aimed to evaluate the prognostic significance of LM in mCSPC patients treated with ARSI-based doublet therapy. Methods This retrospective study analyzed a multi-institutional cohort of 453 mCSPC patients treated with ARSIa-based doublet therapy. Results The median overall survival (OS) and time to castration resistance (TTCR) were 80 and 41 months, respectively, with a median follow-up of 20 months. The total cohort included 117 patients (25.8%) with LM and 336 patients (74.2%) without LM. LATITUDE high-risk and CHAARTED high-volume criteria classified 380 patients (83.9%) and 356 patients (78.6%), respectively. Although not statistically significant, OS and TTCR showed a trend toward better outcomes in the LM group compared to the non-LM group in LATITUDE high-risk (n = 380: P =.097 for OS and P =.104 for TTCR) and CHAARTED high-volume (n = 356: P =.064 for OS and P =.086 for TTCR). In the propensity score matching cohort (n = 218 and n = 206 for LATITUDE and CHAARTED criteria, respectively), OS and TTCR remained comparable between the LM and non-LM groups. Conclusions LM does not appear to be related to OS or TTCR in mCSPC patients treated with ARSI-based doublet therapy, indicating that its prognostic value may need to be reevaluated.
KW - androgen-receptor signaling inhibitors
KW - lung metastasis
KW - metastatic castration-sensitive prostate cancer
KW - overall survival
KW - time to castration resistance
UR - https://www.scopus.com/pages/publications/105027204440
UR - https://www.scopus.com/pages/publications/105027204440#tab=citedBy
U2 - 10.1093/jjco/hyaf161
DO - 10.1093/jjco/hyaf161
M3 - Article
C2 - 41110124
AN - SCOPUS:105027204440
SN - 0368-2811
VL - 56
SP - 80
EP - 88
JO - Japanese journal of clinical oncology
JF - Japanese journal of clinical oncology
IS - 1
ER -