Akagi Naoki, Obayashi Riki, Yamamoto Akihiro, Nagoshi Akihiko, Fujiwara Tasuku, Igarashi Atsushi, Hattori Yuto, Shibasaki Noboru, Kawakita Mutsushi, Yamasaki Toshinari
Department of Urology, Kobe City Medical Center General Hospital, 2-1-1, Minatojimaminami-cho, Chuo-ku, Kobe-shi, Hyogo, Japan.
Jpn J Clin Oncol. 2025 Aug 3;55(8):963-969. doi: 10.1093/jjco/hyaf082.
Common adverse events associated with apalutamide include skin rashes and occur more frequently in Japanese patients. This study used relative dose intensity (RDI) and body surface area (BSA) to investigate the risk of skin adverse events and the efficacy of apalutamide in patients with prostate cancer.
We retrospectively reviewed data from 63 patients with prostate cancer who were treated with an initial dose of 240 mg apalutamide, and RDI (%) was calculated. Patient backgrounds were compared, and factors contributing to rash development were analyzed. Progression-free survival (PFS), defined as the time to castration-resistant prostate cancer, was analyzed using overall RDI/BSA in metastatic castration-sensitive prostate cancer (mCSPC) patients.
The receiver operating characteristic curve analysis showed that RDI/BSA had a slightly stronger association with rash occurrence than RDI/kg. Univariate analysis identified age and RDI/BSA as significant risk factors for rash occurrence, particularly when both an age cutoff of 72 years and a RDI/BSA cutoff of 56 were met. PFS in mCSPC patients showed no significant differences among tRDI/BSA groups (<36, 36-55, >55) or between patients with and without dose reductions. Cutoff points (36 and 55) were based on the maximum tRDI/BSA values assuming continuous administration of 120 mg or 180 mg apalutamide in patients with a minimum BSA of 1.36 m2.
Age and RDI/BSA were associated with rash occurrence, suggesting a need for dose reduction of apalutamide. A dose reduction to 180 or 120 mg may be appropriate in such cases when considering efficacy.
阿帕鲁胺常见的不良事件包括皮疹,且在日本患者中更频繁出现。本研究使用相对剂量强度(RDI)和体表面积(BSA)来调查前列腺癌患者发生皮肤不良事件的风险以及阿帕鲁胺的疗效。
我们回顾性分析了63例接受初始剂量240mg阿帕鲁胺治疗的前列腺癌患者的数据,并计算了RDI(%)。比较了患者背景,并分析了导致皮疹发生的因素。无进展生存期(PFS)定义为至去势抵抗性前列腺癌的时间,在转移性去势敏感性前列腺癌(mCSPC)患者中使用总体RDI/BSA进行分析。
受试者工作特征曲线分析表明,RDI/BSA与皮疹发生的关联略强于RDI/kg。单因素分析确定年龄和RDI/BSA是皮疹发生的重要风险因素,特别是当年龄临界值为72岁且RDI/BSA临界值为56时。mCSPC患者的PFS在不同的tRDI/BSA组(<36、36 - 55、>55)之间或有剂量减少和无剂量减少的患者之间无显著差异。临界值(36和55)基于假设最小体表面积为1.36m²的患者持续服用120mg或180mg阿帕鲁胺时的最大tRDI/BSA值。
年龄和RDI/BSA与皮疹发生有关,提示需要降低阿帕鲁胺的剂量。在考虑疗效的情况下,这种情况下将剂量减至180mg或120mg可能是合适的。