Clinical outcomes in metastatic prostate adenocarcinoma treated with abiraterone and enzalutamide.

IF 1.2 Q4 ONCOLOGY ecancermedicalscience Pub Date : 2024-09-11 eCollection Date: 2024-01-01 DOI:10.3332/ecancer.2024.1763
Misbah Younus Soomro, Saqib Raza Khan, Hashim Ishfaq, Insia Ali, Mirza Rameez Samar, Arif Hameed, Nawazish Zehra, Munira Moosajee, Yasmin Abdul Rashid
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Abstract

Aim: The management of metastatic prostate cancer has progressed immensely in the last decade. This study aims to investigate the real-world clinical outcomes of metastatic prostate adenocarcinoma treated with abiraterone and enzalutamide. The findings will assist healthcare providers in making more informed decisions when choosing between these two drugs for treating these patients.

Methods: A retrospective analysis of 80 patients at our tertiary care hospital was conducted from January 2015 to July 2022. Data were analysed using SPSS version 20.0. An independent sample T-test was used for continuous data and the chi-square test for categorical data. Medians and means were calculated for continuous or ordinal variables. Kaplan-Meier survival curves presented progression-free and overall survival (OS), with comparisons made using the log-rank test. Survival rates with 95% CIs were reported, with p < 0.05 considered significant.

Results: In our final analysis of 80 patients, the median age was 65 years, with 88% having an eastern cooperative oncology group performance status between 0 and 2. Histopathology showed adenocarcinoma in 91% of cases. Grade Group III-IV disease was present in 51.3%, and 67.5% had a Gleason Score of >8. Bilateral orchidectomy was performed in 41 patients (51.25%), with a median Gonadotropin-releasing hormone analogue use of 32 months. Most patients (72.5%) were castration-sensitive. Among the 80 patients, 60 (75%) were treated with abiraterone and 20 (25%) with enzalutamide. The prostate-specific antigen (PSA) doubling time was >6 months in 80% of the abiraterone group and 75% of the enzalutamide group. PSA response rates were similar for both drugs, with comparable rates of progressive disease, partial response, stable disease and complete response (p = 0.036). There was no significant difference in median time to progression (19 months for abiraterone versus 18 months for enzalutamide) (95% CI 9.7-27.9; p = 0.004). The median OS for the entire cohort was 67 months (95% CI 39-94; p = 0.003).

Conclusion: The findings suggest that both abiraterone and enzalutamide are effective in prolonging progression-free and overall survival in this patient population, providing comparable safety. Further studies are recommended to validate these findings and inform clinical decision-making.

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阿比特龙和恩扎鲁胺治疗转移性前列腺癌的临床疗效。
目的:近十年来,转移性前列腺癌的治疗取得了巨大进展。本研究旨在调查阿比特龙和恩杂鲁胺治疗转移性前列腺癌的实际临床疗效。研究结果将有助于医疗服务提供者在选择这两种药物治疗这些患者时做出更明智的决定:2015年1月至2022年7月,我们对本院三级医院的80名患者进行了回顾性分析。数据使用 SPSS 20.0 版进行分析。连续性数据采用独立样本 T 检验,分类数据采用卡方检验。连续或序数变量计算中位数和平均值。卡普兰-梅耶生存曲线显示无进展生存期和总生存期(OS),并使用对数秩检验进行比较。报告的生存率为 95% CI,P < 0.05 为显著:在我们对80名患者的最终分析中,患者的中位年龄为65岁,88%的患者在东部合作肿瘤学组中的表现状态介于0和2之间。组织病理学显示,91%的病例为腺癌。41名患者(51.25%)接受了双侧睾丸切除术,促性腺激素释放激素类似物的中位使用时间为32个月。大多数患者(72.5%)对阉割敏感。在80名患者中,60人(75%)接受了阿比特龙治疗,20人(25%)接受了恩扎鲁胺治疗。80%的阿比特龙组和75%的恩扎鲁胺组患者的前列腺特异性抗原(PSA)倍增时间大于6个月。两种药物的PSA应答率相似,疾病进展率、部分应答率、疾病稳定率和完全应答率相当(p = 0.036)。中位疾病进展时间无明显差异(阿比特龙为19个月,恩杂鲁胺为18个月)(95% CI 9.7-27.9;p = 0.004)。整个队列的中位OS为67个月(95% CI 39-94;p = 0.003):研究结果表明,阿比特龙和恩杂鲁胺都能有效延长该患者群体的无进展生存期和总生存期,且安全性相当。建议进一步开展研究,以验证这些发现并为临床决策提供依据。
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CiteScore
3.80
自引率
5.60%
发文量
138
审稿时长
27 weeks
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