Prostate-specific antigen doubling time predicts the efficacy of site-directed therapy for oligoprogressive castration-resistant prostate cancer

In recent years, site-directed therapies (SDTs) targeting progressive lesions in patients with oligometastatic prostate cancer have attracted attention. However, whether they effectively treat oligoprogressive castration-resistant prostate cancer (CRPC) remains unclear. Here, we investigated the eff...

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Veröffentlicht in:Prostate international 2023-12, Vol.11 (4), p.239-246
Hauptverfasser: Kawai, Taketo, Taguchi, Satoru, Nozaki, Keina, Kimura, Naoki, Oshina, Takahiro, Iwaki, Takuya, Matsui, Hotaka, Niimi, Aya, Kamei, Jun, Akiyama, Yoshiyuki, Yamada, Yuta, Sato, Yusuke, Yamada, Daisuke, Kaneko, Tomoyuki, Sawayanagi, Subaru, Nakayama, Hidetsugu, Minamimoto, Ryogo, Yamashita, Hideomi, Miyazaki, Hideyo, Fujimura, Tetsuya, Nakagawa, Tohru, Kume, Haruki
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Sprache:eng
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Zusammenfassung:In recent years, site-directed therapies (SDTs) targeting progressive lesions in patients with oligometastatic prostate cancer have attracted attention. However, whether they effectively treat oligoprogressive castration-resistant prostate cancer (CRPC) remains unclear. Here, we investigated the efficacy of SDT in patients with oligoprogressive CRPC and identified prognostic factors. We reviewed 59 patients with oligoprogressive CRPC who underwent SDT targeting prostate or metastatic lesions between April 2014 and March 2022. We evaluated the associations between several pretreatment clinical variables and treatment procedures and a >50% prostate-specific antigen (PSA) response, progression-free survival (PFS), and time to next treatment (TTNT). A PSA response of >50% was observed in 66% of patients. The median PFS and TTNT were 8.3 months and 9.9 months, respectively. Patients with PSA doubling time ≥6 months showed a higher >50% PSA response rate (87% vs. 45%;  
ISSN:2287-8882
2287-903X
DOI:10.1016/j.prnil.2023.10.002