Prostate-specific antigen kinetics and metastasis-free survival in patients treated with external beam radiotherapy combined with high-dose-rate brachytherapy boost and androgen deprivation therapy for localized prostate cancer

被引:3
|
作者
Miszczyk, Marcin [1 ]
Magrowski, Lukasz [1 ]
Masri, Oliwia [1 ]
Jablonska, Iwona [1 ]
Nowicka, Zuzanna [2 ]
Krzysztofiak, Tomasz [3 ]
Wojcieszek, Piotr [3 ]
Lipka-Rajwa, Aleksandra [1 ]
Ciepal, Jakub [1 ]
Depowska, Gabriela [1 ]
Chimiak, Krystyna [1 ]
Bylica, Gabriela [1 ]
Ploszka, Katarzyna [2 ]
Laszczych, Mateusz [2 ]
Majewski, Wojciech [4 ]
机构
[1] Maria Sklodowska Curie Natl Res Inst Oncol, Radiotherapy & Chemotherapy Dept 3, Wybrzeze Armii Krajowej 15, PL-44102 Gliwice, Poland
[2] Med Univ, Dept Biostat & Translat Med, Lodz, Poland
[3] Maria Sklodowska Curie Natl Res Inst, Brachytherapy Dept, Gliwice Branch, Gliwice, Poland
[4] Maria Sklodowska Curie Natl Res Inst Oncol, Radiotherapy Dept, Gliwice, Poland
关键词
prostate cancer; radiotherapy; brachytherapy; PSA bounce; PSA nadir; SURROGATE END-POINTS; PSA BOUNCE; PREDICTS; MEN;
D O I
10.5114/jcb.2022.113546
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Serum prostate-specific antigen (PSA) kinetics has been linked to prognosis in prostate cancer (PCa) patients. Our goal was to analyze the association between PSA kinetics and metastasis-free survival (MFS) in patients with localized PCa treated with high-dose-rate (HDR) brachytherapy (BT) boost combined with external beam radiotherapy (EBRT). Material and methods: We retrospectively analyzed multiple PSA kinetics related to PSA nadir (nPSA), PSA bouncing, and biochemical recurrence (BCR) in 186 PCa patients treated with neoadjuvant androgen deprivation therapy (ADT), followed by EBRT combined with HDR-BT boost. Uni- and multivariate Cox regression models were cal- culated to assess the value of PSA-related parameters for the prediction of MFS. Results: 5-and 10-year MFS were 95% and 84%, respectively. Median nPSA was 0.011 (IQR, 0.007-0.057) ng/ml and predicted MFS in multivariable analysis. Implementation of nPSA improved c-index of baseline model from 0.8 to 0.68. nPSA of 0.2 ng/ml offered the most optimal discriminatory ability for identifying patients with better prognoses. Time to nPSA (median, 11 months; IQR, 8-18 months) and PSA bounce, which occurred in 12.4% of patients, were not significantly associated with MFS. Conclusions: Lower values of nPSA are significantly associated with decreased risk of developing metastases in patients treated with EBRT combined with HDR-BT boost and ADT, and improve the accuracy of a clinical model for MFS.
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收藏
页码:15 / 22
页数:8
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