Department of Anesthesiology and Pain Medicine, National Medical Center, Seoul, Korea.
Division of Biostatistics, Department of R&D Management, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
PLoS One. 2023 Jan 6;18(1):e0280212. doi: 10.1371/journal.pone.0280212. eCollection 2023.
BACKGROUND & AIMS: Fentanyl buccal tablets (FBTs) are a rapid-onset opioid indicated for breakthrough cancer pain (BTcP) and FBT titration is needed to optimize BTcP management. We aimed to predict which patients could tolerate a high dose of FBT (400 μg or more at a time).
A retrospective analysis was performed to assess the final FBT dose. The final FBT doses were compared according to the clinical features. The prediction accuracy of patients tolerant of 400 μg or higher FBT was compared using the area under the receiver operating characteristic (ROC) curves. A risk scoring model based on the odds ratio (OR) was developed from the final multivariable model, and patients were assigned into two groups: low tolerance (0-1 point) and high tolerance (2-3 points).
Among 131 patients, the most frequently effective dose of FBT was 200 μg (54%), followed by 100 μg (30%). The median value of morphine equivalent daily doses (MEDD) was 60 mg/day, and the most common daily use was 3-4 times/day. In multivariable analysis, male sex, younger age, and use of FBTs three or more times per day were independently associated with high-dose FBT. According to the risk scoring model, the patients with a final FBT of 400 μg or higher were significantly more in the high tolerance group (17%) compared to the low tolerance group (3%; p = 0.023).
According to the dose relationship between the final FBT dose and the clinical features, three factors (sex, age, daily use of FBT) were independently associated with the final dose of FBT. Our risk score model could help predict tolerance to high-dose FBT and guide the titration plan for BTcP.
芬太尼口颊贴片(FBT)是一种快速起效的阿片类药物,适用于爆发性癌痛(BTcP),需要进行 FBT 滴定以优化 BTcP 管理。我们旨在预测哪些患者能够耐受高剂量 FBT(每次 400μg 或更高)。
进行了一项回顾性分析,以评估最终 FBT 剂量。根据临床特征比较最终 FBT 剂量。使用受试者工作特征(ROC)曲线下面积比较能够耐受 400μg 或更高 FBT 的患者的预测准确性。基于比值比(OR)的风险评分模型是从最终多变量模型中开发的,患者被分为两组:低耐受(0-1 分)和高耐受(2-3 分)。
在 131 名患者中,FBT 最有效的剂量是 200μg(54%),其次是 100μg(30%)。等效吗啡日剂量(MEDD)的中位数为 60mg/天,最常见的日用量为 3-4 次/天。在多变量分析中,男性、年龄较小和每天使用 FBT 三次或更多次与高剂量 FBT 独立相关。根据风险评分模型,最终 FBT 为 400μg 或更高的患者在高耐受组中明显更多(17%),而在低耐受组中则较少(3%;p=0.023)。
根据最终 FBT 剂量与临床特征之间的剂量关系,三个因素(性别、年龄、每日使用 FBT)与 FBT 的最终剂量独立相关。我们的风险评分模型可以帮助预测对高剂量 FBT 的耐受程度,并指导 BTcP 的滴定计划。