Johns Hopkins School of Medicine, 600 N Wolfe St, Phipps 281, Baltimore, MD 21287, USA.
Cerner Enviza, 51 Valley Stream Pkwy, Malvern, PA 19355, USA.
Future Oncol. 2022 Feb;18(4):491-503. doi: 10.2217/fon-2021-0567. Epub 2021 Dec 8.
To understand the preferences of US patients and oncologists for PARP inhibitors as second-line maintenance (2LM) for epithelial ovarian cancer. A discrete choice experiment was conducted to assess the preferences of treatment attributes. The most valued attributes were risk of grade 3/4 adverse events (AEs; patients, n = 204) and progression-free survival (PFS; oncologists, n = 151). To accept a 37% increased risk of grade 3/4 AEs, PFS would need to increase by 27.9 months (patients) and 6.3 months (oncologists). The least valued attributes were dosing form/frequency (patients) and grade 3/4 anemia risk (oncologists). Patients' and oncologists' willingness to make benefit-risk trade-offs in the 2LM setting suggests that the PFS gains observed in selected studies of poly (ADP-ribose) polymerase inhibitors in BRCA-mutated disease are worth the toxicity risk.
为了了解美国患者和肿瘤学家对聚 ADP 核糖聚合酶抑制剂(PARP 抑制剂)作为上皮性卵巢癌二线维持(2LM)治疗的偏好。采用离散选择实验评估了治疗属性的偏好。最有价值的属性是 3/4 级不良事件(AE;患者,n=204)和无进展生存期(PFS;肿瘤学家,n=151)的风险。为了接受 37%的 3/4 级 AE 风险增加,PFS 需要增加 27.9 个月(患者)和 6.3 个月(肿瘤学家)。最不重要的属性是剂量形式/频率(患者)和 3/4 级贫血风险(肿瘤学家)。在 2LM 环境下,患者和肿瘤学家愿意进行获益-风险权衡,这表明在 BRCA 突变疾病中,聚(ADP-核糖)聚合酶抑制剂的选定研究中观察到的 PFS 获益值得承受毒性风险。