Mustafa Mahmoud, Rass Honood Abu, Yahya Mothafr, Hamdan Khaleel, Eiss Yazan
Urology Department, Faculty of Medicine and Health Science, An-Najah National University, Nablus, West Bank, Palestine.
Pathology Department, Faculty of Medicine and Health Science, An-Najah National University, Nablus, West Bank, Palestine.
World J Surg Oncol. 2021 Jan 4;19(1):5. doi: 10.1186/s12957-020-02111-3.
To define the efficacy of standard androgen deprivation therapy (ADT) in the treatment of metastatic prostate cancer (PCa).
Fifty patients with mean age of 70.48 ± 9.95 years old (range 52-87) who had metastatic PCa and received ADT between 2014 and 2019 were retrospectively evaluated. Median values of pre-therapeutic PSA and Gleason scores were 50 ng/ml (range 8-1201) and 8 (range 6-9), respectively. All patients received luteinizing hormone-releasing hormone (LHRH) analogue and anti-androgen. The patients were evaluated in terms of age, pre-therapeutic PSA serum levels, Gleason scores, presence of metastasis, number and percentage of cores involved, nadir PSA, time to nadir PSA, duration of ADT, and PSA at last follow-up. Multivariate analysis was used to define the factors which have impact on ADT response. The mean follow-up period was 13.87 ± 7.78 months, (range 2-32).
All patients showed reduction in serum PSA level after initiation of ADT, and the median value of nadir PSA was 1.12 ng/ml (range 0.02-50). The mean value of time to nadir PSA was 3.85 ± 1.57 months (range 2-7). The median value of PSA at last follow-up was 2 ng/ml (range 0.02-50.21). Multi-variant analysis showed that nadir PSA have a significant correlation with pre-therapeutic PSA, PSA at last follow-up, age, and Gleason scores (p < .05).
Standard ADT is a feasible option in the treatment of metastatic PCa. Gleason scores, age, pre-therapeutic PSA, and PSA at last follow-up have significant impact on outcomes of ADT. Further studies of high number of patients with long-term follow-up including other chemo-hormonal therapy and androgen receptor blockers should be carried out to confirm and improve efficacy of ADT.
确定标准雄激素剥夺疗法(ADT)在治疗转移性前列腺癌(PCa)中的疗效。
回顾性评估了2014年至2019年间50例平均年龄为70.48±9.95岁(范围52 - 87岁)的转移性PCa患者,这些患者接受了ADT治疗。治疗前前列腺特异性抗原(PSA)和 Gleason评分的中位数分别为50 ng/ml(范围8 - 1201)和8(范围6 - 9)。所有患者均接受促黄体生成素释放激素(LHRH)类似物和抗雄激素药物治疗。对患者进行了年龄、治疗前PSA血清水平、Gleason评分、转移情况、受累核心的数量和百分比、最低PSA值、达到最低PSA值的时间、ADT持续时间以及最后一次随访时的PSA等方面的评估。采用多变量分析来确定对ADT反应有影响的因素。平均随访期为13.87±7.78个月(范围2 - 32个月)。
所有患者在开始ADT治疗后血清PSA水平均降低,最低PSA值的中位数为1.12 ng/ml(范围0.02 - 50)。达到最低PSA值的平均时间为3.85±1.57个月(范围2 - 7个月)。最后一次随访时PSA的中位数为2 ng/ml(范围0.02 - 50.21)。多变量分析表明,最低PSA值与治疗前PSA、最后一次随访时的PSA、年龄和Gleason评分具有显著相关性(p <.05)。
标准ADT是治疗转移性PCa的一种可行选择。Gleason评分、年龄、治疗前PSA以及最后一次随访时的PSA对ADT的结果有显著影响。应进行更多患者的长期随访研究,包括其他化疗 - 激素疗法和雄激素受体阻滞剂,以确认并提高ADT的疗效。