Majeed Muhammad Awais, Alam Ayesha, Imran Maryam, Muzaffar Shakeel, Jamil Muhammad Ahsan, Ul Ain Noor, Shabbir Muhammad Usman, Salman Umer, Bin Naeem Sameen
Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, PAK.
Physiology, Al-Aleem Medical College, Lahore, PAK.
Cureus. 2025 Jun 22;17(6):e86518. doi: 10.7759/cureus.86518. eCollection 2025 Jun.
Background Metastatic castration-sensitive prostate cancer is defined as prostate cancer with de novo metastatic disease that responds to androgen deprivation therapy by keeping the testosterone levels low. Endogenous androgen synthesis is further blocked by abiraterone acetate along with prednisolone and indicated in patients with metastatic castration-sensitive prostate cancer. However, over time, these patients will become castration-resistant. The time from castration-sensitive to castration-resistant in our population is short, which calls for further investigation on a larger scale to explore factors such as genetics and environmental influences that may play a significant role. Methodology This retrospective study involved 47 adult patients aged 40 years and older. It focused exclusively on patients who were presented with de novo metastatic castration-sensitive disease and were treated with upfront abiraterone acetate. The study was carried out at the Department of Medical Oncology, Shaukat Khanum Memorial Cancer Hospital and Research Centre, Lahore, Pakistan. Patient data spanning 10 years, from 2014 to 2024, was collected from hospital records. Results The cohort demonstrated a median progression-free survival (PFS) of 20.7 months and a median overall survival (OS) of 38.4 months. These outcomes represent the entire study population, irrespective of subgroup classification. Different subgroup analyses do not show any statistically significant difference. Conclusion In our study, OS and PFS were lower than those reported in landmark studies conducted on similar populations in Western countries. This disparity highlights the need for further research in subcontinental populations to investigate potential contributing factors, including environmental influences or genetic variations.
转移性去势敏感性前列腺癌被定义为患有新发转移性疾病且通过维持低睾酮水平对雄激素剥夺疗法有反应的前列腺癌。醋酸阿比特龙与泼尼松龙一起可进一步阻断内源性雄激素合成,并适用于转移性去势敏感性前列腺癌患者。然而,随着时间的推移,这些患者会变得去势抵抗。在我们的人群中,从去势敏感到去势抵抗的时间很短,这就需要进行更大规模的进一步研究,以探索可能起重要作用的遗传和环境影响等因素。
这项回顾性研究纳入了47名年龄在40岁及以上的成年患者。该研究仅关注那些患有新发转移性去势敏感性疾病并接受一线醋酸阿比特龙治疗的患者。该研究在巴基斯坦拉合尔的沙卡特·汗姆纪念癌症医院和研究中心的医学肿瘤学部门进行。从医院记录中收集了2014年至2024年这10年间的患者数据。
该队列的中位无进展生存期(PFS)为20.7个月,中位总生存期(OS)为38.4个月。这些结果代表了整个研究人群,无论亚组分类如何。不同的亚组分析未显示出任何统计学上的显著差异。
在我们的研究中,总生存期和无进展生存期低于在西方国家对类似人群进行的里程碑式研究中报告的结果。这种差异凸显了在次大陆人群中进行进一步研究以调查潜在影响因素的必要性,包括环境影响或基因变异。