评估Firmagon®(Degarelix)在晚期转移性前列腺癌患者中的临床安全性和PSA反应的审计

N. Vasdev, Patricia McClurey, D. Gray, A. Bhatti, D. Chadwick
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摘要

摘要:目的:评价Firmagon ®(Degarelix)治疗转移性前列腺癌患者的临床安全性和PSA反应,并评估该药物的安全性。患者和方法:根据英国东北和坎布里亚癌症药物审批小组(NECDAG)的指南,对35例PSA水平为bb50的晚期转移性前列腺癌患者进行了审计,这些患者接受了Firmagon ®(Degarelix)治疗。审计使用了英格兰东北部三家医院的结果,目的是评估这种新药的安全性、临床和PSA反应。记录诊断时的基线症状、PSA和开始使用Firmagon ®(Degarelix)时的治疗后参数。我们队列中的所有患者均为同质性,既往未接受过任何治疗,包括任何形式的LHRH类似物治疗。PSA水平最初每6周测量一次,随后每3个月测量一次,以评估对Firmagon ®(Degarelix)治疗的初始和长期反应。结果:即刻给药Firmagon ®(Degarelix)未发生过敏反应或注射部位并发症。在我们的研究中,没有患者出现肾脏或肝脏毒性。所有患者均无肿瘤复发。主要表现为严重骨痛的患者中,共有23%的患者完全缓解了Firmagon ®(Degarelix),不需要双磷酸盐或姑息性放疗等辅助治疗。在使用Firmagon ®(Degarelix)治疗6周和3个月后,PSA水平立即显著降低(p=0.0038)。结论:Firmagon ®(Degarelix)是一种安全的药物,在晚期转移性前列腺癌患者中耐受性良好。在一些广泛骨转移的患者开始使用Firmagon ®(Degarelix)后,骨痛如何完全消退的原因需要评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An Audit to Evaluate the Clinical Safety and PSA Response of Firmagon® (Degarelix) in Patients with Advanced Metastatic Prostate Cancer
Abstract: Objectives : To evaluate the clinical safety and PSA response in patients with metastatic prostate cancer being treated with Firmagon ® ( Degarelix ) and to assess the drug's safety profile. Patients and Methods : This was an audit of 35 patients with PSA levels >50 and advanced metastatic prostate cancer at presentation who received Firmagon ® ( Degarelix ) as per our North East & Cumbria Cancer Drug Approvals Group (NECDAG), UK guidelines. The audit was conducted using results from three hospitals in North East England with an aim to evaluate the safety profile, clinical and PSA response with this new drug. Baseline symptoms at diagnosis, presenting PSA and post treatment parameters on the commencement of with Firmagon ® ( Degarelix ) were recorded. All patients in our cohort were homogenous having had not received any previous treatment including any form of LHRH analogue therapy. PSA levels were measured at 6 weekly intervals initially followed by 3 monthly intervals to evaluate initial and long term response to treatment with Firmagon ® ( Degarelix ). Results : There was no incidence of anaphylaxis or injection site complications on immediate administration of Firmagon ® ( Degarelix ). No of our patients had renal or liver toxicity in our series. There was no incidence of tumour flare in any patient. A total of 23% of patients who presented primarily with severe bone pain described a complete resolution of Firmagon ® ( Degarelix ) and required no adjuvant treatment such as bisphosphonates or palliative radiotherapy. A significant reduction in PSA levels were noted immediately at 6 weeks and 3 months following treatment with Firmagon ® ( Degarelix ) (p=0.0038). Conclusions : Firmagon ® ( Degarelix ) is a safe drug is well tolerated in patients with advanced metastatic prostate cancer. The reason of how bone pain completely resolves in some patients with extensive bone metastasis on the commencement of Firmagon ® ( Degarelix ) needs to be evaluated.
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