Real-world effectiveness and safety of goserelin 10.8-mg depot in Chinese patients with localized or locally advanced prostate cancer.

IF 5.6 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Cancer Biology & Medicine Pub Date : 2024-02-05 DOI:10.20892/j.issn.2095-3941.2023.0335
Nanhui Chen, Zengjun Wang, Ming Chen, Qi Ma, Yi He, Yujie Wang, Xin Li, Mingxing Qiu, Lei Shi, Shaoxing Zhu, Qun Xie, Xiuheng Liu, Benkang Shi, Guowen Lin, Weizhong Yang, Yongbin Liao, Haibin Zhang, Shusheng Wang, Jiexian Li, Shaogang Wang, Lijun Dong, Hui Chen, Jiaju Lu, Yongyi Cheng, Xiaoping Zhang, Lulin Ma, Liqun Zhou, He Wang, Shen Li, Dingwei Ye
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Abstract

Objective: Real-word data on long-acting luteinizing hormone-releasing hormone (LHRH) agonists in Chinese patients with prostate cancer are limited. This study aimed to determine the real-world effectiveness and safety of the LHRH agonist, goserelin, particularly the long-acting 10.8-mg depot formulation, and the follow-up patterns among Chinese prostate cancer patients.

Methods: This was a multicenter, prospective, observational study in hormone treatment-naïve patients with localized or locally advanced prostate cancer who were prescribed goserelin 10.8-mg depot every 12 weeks or 3.6-mg depot every 4 weeks with or without an anti-androgen. The patients had follow-up evaluations for 26 weeks. The primary outcome was the effectiveness of goserelin in reducing serum testosterone and prostate-specific antigen (PSA) levels. The secondary outcomes included testosterone and PSA levels, attainment of chemical castration (serum testosterone <50 ng/dL), and goserelin safety. The exploratory outcome was the monitoring pattern for serum testosterone and PSA. All analyses were descriptive.

Results: Between September 2017 and December 2019, a total of 294 eligible patients received ≥ 1 dose of goserelin; 287 patients (97.6%) were treated with goserelin 10.8-mg depot. At week 24 ± 2, the changes from baseline [standard deviation (95% confidence interval)] in serum testosterone (n = 99) and PSA (n = 131) were -401.0 ng/dL [308.4 ng/dL (-462.5, -339.5 ng/dL)] and -35.4 ng/mL [104.4 ng/mL (-53.5, -17.4 ng/mL)], respectively. Of 112 evaluable patients, 100 (90.2%) achieved a serum testosterone level < 50 ng/dL. Treatment-emergent adverse events (TEAEs) and severe TEAEs occurred in 37.1% and 10.2% of patients, respectively. The mean testing frequency (standard deviation) was 1.6 (1.5) for testosterone and 2.2 (1.6) for PSA.

Conclusions: Goserelin 10.8-mg depot effectively achieved and maintained castration and was well-tolerated in Chinese patients with localized and locally advanced prostate cancer.

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戈舍瑞林 10.8 毫克去势药物在中国局部或局部晚期前列腺癌患者中的实际有效性和安全性。
目的:长效促黄体生成素释放激素(LHRH)激动剂在中国前列腺癌患者中的实际应用数据有限。本研究旨在确定 LHRH 激动剂戈舍瑞林(尤其是 10.8 毫克长效去势制剂)在中国前列腺癌患者中的实际有效性和安全性,以及随访模式:这是一项多中心、前瞻性、观察性研究,研究对象是激素治疗无效的局部或局部晚期前列腺癌患者,他们接受了戈舍瑞林10.8毫克去势剂每12周一次或3.6毫克去势剂每4周一次的治疗,同时服用或不服用抗雄激素。患者接受了为期 26 周的随访评估。主要结果是戈舍瑞林在降低血清睾酮和前列腺特异性抗原(PSA)水平方面的有效性。次要结果包括睾酮和 PSA 水平、达到化学阉割的程度(血清睾酮 结果)、前列腺特异性抗原(PSA)水平和睾酮水平:2017年9月至2019年12月期间,共有294名符合条件的患者接受了≥1次戈舍瑞林治疗;287名患者(97.6%)接受了戈舍瑞林10.8毫克去势治疗。在第 24±2 周,血清睾酮(n = 99)和 PSA(n = 131)与基线相比的变化[标准偏差(95% 置信区间)]分别为-401.0 ng/dL [308.4 ng/dL (-462.5, -339.5 ng/dL)] 和 -35.4 ng/mL [104.4 ng/mL (-53.5, -17.4 ng/mL)]。在 112 名可评估的患者中,100 人(90.2%)的血清睾酮水平低于 50 ng/dL。分别有 37.1% 和 10.2% 的患者发生了治疗突发不良事件 (TEAE) 和严重 TEAE。睾酮的平均检测频率(标准偏差)为1.6(1.5)次,PSA的平均检测频率(标准偏差)为2.2(1.6)次:结论:戈舍瑞林10.8毫克去势药物能有效实现并维持阉割,对中国局部和局部晚期前列腺癌患者的耐受性良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer Biology & Medicine
Cancer Biology & Medicine Medicine-Oncology
CiteScore
9.80
自引率
3.60%
发文量
1143
审稿时长
12 weeks
期刊介绍: Cancer Biology & Medicine (ISSN 2095-3941) is a peer-reviewed open-access journal of Chinese Anti-cancer Association (CACA), which is the leading professional society of oncology in China. The journal quarterly provides innovative and significant information on biological basis of cancer, cancer microenvironment, translational cancer research, and all aspects of clinical cancer research. The journal also publishes significant perspectives on indigenous cancer types in China.
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