Roessler Navid, Miszczyk Marcin, Matsukawa Akihiro, Dematteis Alessandro, Alfarhan Ahmed R, Cormio Angelo, Alqahtani Abdulrahman S, Rajwa Pawel, Schuettfort Victor M, Vetterlein Malte W, Soeterik Timo F W, Fazekas Tamás, Fisch Margit, Leapman Michael S, Karakiewicz Pierre I, Shariat Shahrokh F
Department of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Eur Urol Open Sci. 2025 Sep 8;80:48-56. doi: 10.1016/j.euros.2025.08.008. eCollection 2025 Oct.
PARP inhibitor (PARPi) agents, alone or in combination with antiandrogens, are considered a standard of care for patients with metastatic castration-resistant prostate cancer (mCRPC). This meta-analysis evaluates the impact of PARPi agents on health-related quality of life (HRQoL) using data from prospective trials.
In this prospectively registered systematic review and meta-analysis (PROSPERO: CRD420251011282), we searched the MEDLINE, Embase, and Web of Science databases in March 2025 for prospective trials assessing the impact of PARPi on patient HRQoL in mCRPC. Results for the mean differences (MD) in Functional Assessment of Cancer Therapy-Prostate (FACT-P) total scores at early and late time points were pooled using a random-effects model.
Reports for seven prospective trials (2861 patients) were included. The PROfound trial ( = 387) demonstrated a clinically meaningful improvement in global HRQoL (MD from baseline: 6.7, 95% confidence interval [CI] 1.5-12), while the remaining six studies ( = 2474) did not show a clinically meaningful impact individually. In pooled analysis for the PROpel, MAGNITUDE, and NCT01972217 randomised controlled trials ( = 911), no clinically meaningful differences in the change in FACT-P total score were observed at early (weeks 8-9: MD -1.4, 95%CI -3.0 to 0.2) or late (weeks 96-101: MD -2.1, 95%CI -8.9 to 4.8) time points. Six studies were rated as having some/moderate concerns regarding bias, and one was considered at high risk of bias because of baseline stratification by symptom status.
We observed no statistically or clinically meaningful deterioration in HRQoL with PARPi treatment in patients with mCRPC, with one study suggesting a potential benefit. Predefined thresholds may not capture the individual and complex nature of HRQoL in the palliative mCRPC setting, where even modest changes can have important clinical and personal significance, which underscores the importance of nuanced interpretation of HRQoL data in guiding treatment decisions.
We did not find evidence that drugs called PARP inhibitors have a negative effect on health-related quality of life (HRQoL) for men with advanced prostate cancer. However, the current tools used to measure HRQoL may not fully reflect the individual and complex experiences of patients receiving palliative treatment for their cancer.
聚(ADP-核糖)聚合酶抑制剂(PARPi)药物单独使用或与抗雄激素药物联合使用,被认为是转移性去势抵抗性前列腺癌(mCRPC)患者的标准治疗方案。本荟萃分析使用前瞻性试验数据评估PARPi药物对健康相关生活质量(HRQoL)的影响。
在这项前瞻性注册的系统评价和荟萃分析(PROSPERO:CRD420251011282)中,我们于2025年3月检索了MEDLINE、Embase和科学网数据库,以查找评估PARPi对mCRPC患者HRQoL影响的前瞻性试验。使用随机效应模型汇总早期和晚期时间点癌症治疗功能评估-前列腺(FACT-P)总分的平均差异(MD)结果。
纳入了7项前瞻性试验(2861例患者)的报告。PROfound试验(n = 387)显示总体HRQoL有临床意义的改善(与基线相比MD:6.7,95%置信区间[CI] 1.5 - 12),而其余6项研究(n = 2474)单独未显示出临床意义的影响。在PROpel、MAGNITUDE和NCT01972217随机对照试验(n = 911)的汇总分析中,在早期(第8 - 9周:MD -1.4,95%CI -3.0至0.2)或晚期(第96 - 101周:MD -2.1,95%CI -8.9至4.8)时间点,FACT-P总分变化未观察到临床意义的差异。6项研究被评为对偏倚有一些/中度担忧,1项由于按症状状态进行基线分层而被认为有高偏倚风险。
我们观察到mCRPC患者接受PARPi治疗时,HRQoL在统计学或临床上均无有意义的恶化,有一项研究提示可能有益。预定义阈值可能无法捕捉姑息性mCRPC环境中HRQoL的个体和复杂性质,在这种情况下,即使是适度变化也可能具有重要的临床和个人意义,这强调了在指导治疗决策时对HRQoL数据进行细致解读的重要性。
我们没有发现证据表明称为PARP抑制剂的药物对晚期前列腺癌男性的健康相关生活质量(HRQoL)有负面影响。然而,目前用于测量HRQoL的工具可能无法完全反映接受癌症姑息治疗患者的个体和复杂经历。