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在使用阿比特龙和恩杂鲁胺进行一线治疗的四周时,早期前列腺特异性抗原(PSA)变化可预测转移性去势抵抗性前列腺癌的早期/原发耐药。

Early Prostate-Specific Antigen (PSA) Change at Four Weeks of the First-Line Treatment Using Abiraterone and Enzalutamide Could Predict Early/Primary Resistance in Metastatic Castration-Resistant Prostate Cancer.

作者信息

Uchimoto Taizo, Komura Kazumasa, Fukuokaya Wataru, Kimura Takahiro, Takahashi Kazuhiro, Nishimura Kazuki, Nakamori Keita, Fujiwara Yuya, Matsunaga Tomohisa, Tsutsumi Takeshi, Tsujino Takuya, Maenosono Ryoichi, Yoshikawa Yuki, Taniguchi Kohei, Tanaka Tomohito, Uehara Hirofumi, Ibuki Naokazu, Hirano Hajime, Nomi Hayahito, Takahara Kiyoshi, Inamoto Teruo, Egawa Shin, Azuma Haruhito

机构信息

Department of Urology, Osaka Medical College, Osaka 569-8686, Japan.

Translational Research Program, Osaka Medical College, Osaka 569-8686, Japan.

出版信息

Cancers (Basel). 2021 Jan 30;13(3):526. doi: 10.3390/cancers13030526.

DOI:10.3390/cancers13030526
PMID:33573172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7866532/
Abstract

The identification of early or primary resistance to androgen signaling inhibitors (ASIs) is of great value for the treatment of metastatic castration-resistant prostate cancer (mCRPC). This study evaluates the predictive value of prostate-specific antigen (PSA) response at dour weeks of first-line ASIs treatment for mCRPC patients. A total of 254 patients treated with ASIs (abiraterone acetate: AA and enzalutamide: Enz) at the first-line treatment are retrospectively analyzed. Patients are stratified according to the achievement of >30% PSA decline at 4 and 12 weeks from the treatment initiation. At four weeks of the treatment, 157 patients (61.8%) achieved >30% PSA decline from the baseline. Thereafter, 177 patients (69.7%) achieved >30% PSA decline at 12 weeks of the treatment. A multivariate analysis exhibits >30% PSA decline at four weeks as an independent predictor for overall survival (OS). We note that 30 of 97 (30.9%) patients who did not achieve >30% PSA decline at four weeks consequently achieved >30% PSA decline at 12 weeks, and had a comparable favorable three years OS rate as the 147 patients achieving >30% PSA decline at both 4 and 12 weeks. To identify the variables that discriminate the patient survival in 97 patients without achieving >30% PSA decline at four weeks, a multivariate analysis is performed. The duration of androgen deprivation therapy before CRPC ≤ 12 months and Eastern Cooperative Oncology Group Performance Status ≥ 1 are identified as independent predictors for shorter OS for those patients. These data offer a concept of early treatment switch after four weeks of first-line ASIs when not observing >30% PSA decline at four weeks-particularly in patients with a modest effect of ADT and poor performance status.

摘要

鉴定对雄激素信号抑制剂(ASI)的早期或原发性耐药对于转移性去势抵抗性前列腺癌(mCRPC)的治疗具有重要价值。本研究评估一线ASI治疗4周时前列腺特异性抗原(PSA)反应对mCRPC患者的预测价值。对254例接受一线ASI(醋酸阿比特龙:AA和恩杂鲁胺:Enz)治疗的患者进行回顾性分析。根据治疗开始后4周和12周时PSA下降>30%的情况对患者进行分层。治疗4周时,157例患者(61.8%)PSA较基线下降>30%。此后,177例患者(69.7%)在治疗12周时PSA下降>30%。多变量分析显示4周时PSA下降>30%是总生存期(OS)的独立预测因素。我们注意到,97例在4周时未实现PSA下降>30%的患者中有30例(30.9%)在12周时实现了PSA下降>30%,并且其三年总生存率与4周和12周时PSA下降>30%的147例患者相当。为了确定在4周时未实现PSA下降>30%的97例患者中区分患者生存情况的变量,进行了多变量分析。CRPC之前雄激素剥夺治疗的持续时间≤12个月以及东部肿瘤协作组体能状态≥1被确定为这些患者较短OS的独立预测因素。这些数据提出了一线ASI治疗4周后早期治疗转换的概念,即在4周时未观察到PSA下降>30%的情况下,特别是在雄激素剥夺治疗效果中等且体能状态较差的患者中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/b58d8a0eab9c/cancers-13-00526-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/ed21c76f2c25/cancers-13-00526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/0dc0e9c97913/cancers-13-00526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/ce0e0c95ca14/cancers-13-00526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/7c304a2a3602/cancers-13-00526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/b58d8a0eab9c/cancers-13-00526-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/ed21c76f2c25/cancers-13-00526-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/0dc0e9c97913/cancers-13-00526-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/ce0e0c95ca14/cancers-13-00526-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/7c304a2a3602/cancers-13-00526-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c5e/7866532/b58d8a0eab9c/cancers-13-00526-g005.jpg

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