Radiation Medicine Program, The Ottawa Hospital Cancer Centre, Ottawa, Ontario, Canada; Radiation Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland, USA.
Radiation Medicine Program, The Ottawa Hospital Cancer Centre, Ottawa, Ontario, Canada; Division of Radiation Oncology, University of Ottawa, Ottawa, Ontario, Canada.
Clin Oncol (R Coll Radiol). 2021 Mar;33(3):181-190. doi: 10.1016/j.clon.2020.09.005. Epub 2020 Sep 29.
Several classes of concomitant medications have been shown to affect oncological outcomes in patients with prostate cancer (PCa). We assessed the association between the use of commonly prescribed concomitant medications and biochemical relapse-free survival (bRFS) in patients with localised PCa treated with radiotherapy and androgen deprivation therapy (ADT).
A secondary pooled analysis of two phase III randomised trials was carried out. In the first trial, patients with localised PCa with clinical stage T1b-T3, prostate-specific antigen <30 ng/ml and Gleason score ≤7 were treated with radical radiotherapy and 6 months of ADT starting 4 months before or concomitantly with radiotherapy. In the second trial, patients with high-risk PCa were treated with radical radiotherapy and 36 months of ADT with randomisation to three-dimensional conformal or intensity-modulated radiotherapy. Information on concomitant medications was collected from the medical record. Univariable and multivariable Cox regression was used to identify factors associated with bRFS.
Overall, 486 patients were evaluable. The median follow-up was 125 months; 10-year bRFS was 83.7%. On univariable analysis, receipt of metformin was significantly associated with worse bRFS. Ten-year bRFS was 73% and 85% for patients with and without concomitant metformin (adjusted hazard ratio 2.11, 95% confidence interval 1.03-4.33). Similar evidence of an association was observed with sulfonamide-based α1-receptor blockers (adjusted hazard ratio 2.72, 95% confidence interval 1.31-5.66). However, no such association was seen with receipt of quinazoline-based α1-receptor blockers (adjusted hazard ratio 1.09, 95% confidence interval 0.42-2.82). There was no significant association between bRFS and receipt of all other medication classes considered.
In this population of patients with localised PCa treated with radiotherapy and ADT, receipt of concomitant metformin and sulfonamide-based α1-receptor blockers was associated with inferior biochemical outcome. Randomised trials are required to assess the true effect of these medications on oncological outcomes in localised PCa.
已有几类伴随药物被证明会影响前列腺癌(PCa)患者的肿瘤学结局。我们评估了在接受放疗和雄激素剥夺治疗(ADT)的局限性 PCa 患者中,常用伴随药物的使用与生化无复发生存(bRFS)之间的关系。
对两项 III 期随机试验进行了二次汇总分析。在第一项试验中,局部 PCa 患者的临床分期为 T1b-T3,前列腺特异性抗原(PSA)<30ng/ml 和 Gleason 评分≤7,接受根治性放疗和 6 个月 ADT,从放疗前 4 个月开始或同时开始 ADT。在第二项试验中,高危 PCa 患者接受根治性放疗和 36 个月 ADT,并随机分为三维适形或强度调制放疗。伴随药物信息从病历中收集。采用单变量和多变量 Cox 回归分析确定与 bRFS 相关的因素。
总共 486 例患者可评估。中位随访时间为 125 个月;10 年 bRFS 为 83.7%。单变量分析显示,接受二甲双胍治疗与 bRFS 较差显著相关。接受二甲双胍治疗的患者 10 年 bRFS 为 73%,未接受二甲双胍治疗的患者为 85%(调整后的危险比 2.11,95%置信区间 1.03-4.33)。类似的关联证据也见于磺酰胺类α1 受体阻滞剂(调整后的危险比 2.72,95%置信区间 1.31-5.66)。然而,喹唑啉类α1 受体阻滞剂的使用与 bRFS 之间没有显著关联(调整后的危险比 1.09,95%置信区间 0.42-2.82)。考虑的其他所有药物类别与 bRFS 之间没有显著关联。
在接受放疗和 ADT 治疗的局限性 PCa 患者中,接受二甲双胍和磺酰胺类α1 受体阻滞剂治疗与生化结局较差相关。需要进行随机试验来评估这些药物对局限性 PCa 肿瘤学结局的真正影响。