Douma Joeri A J, Buffart Laurien M, Sedhom Ramy, Labots Mariette, Menke-van der Houven van Oordt Willemien C, Skardhamar Mikkjal, De Felice Anthony, Lee Esther, Dharmaraj Divya, Azad Nilofer S, Carducci Michael A, Verheul Henk M W
Cancer Center Amsterdam, Amsterdam University Medical Center, Department of Medical Oncology, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands.
Department of Physiology, Radboudumc, 6525 GA Nijmegen, The Netherlands.
Cancers (Basel). 2021 May 11;13(10):2304. doi: 10.3390/cancers13102304.
Despite stringent eligibility criteria for trial participation, early discontinuation often occurs in phase I trials. To better identify patients unlikely to benefit from phase I trials, we investigated predictors for early trial discontinuation. Data from 415 patients with solid tumors who participated in 66 trials were pooled for the current analysis. Early trial discontinuation was defined as (i) trial discontinuation within 28 days after start of treatment or (ii) discontinuation before administration of the first dosage in eligible patients. Multilevel logistic regression analyses were conducted to identify predictors for early trial discontinuation. Eighty-two participants (20%) demonstrated early trial discontinuation. Baseline sodium level below the lower limit of normal (OR = 2.95, 95%CI = 1.27-6.84), elevated alkaline phosphatase level > 2.5 times the upper limit of normal (OR = 2.72, 95%CI = 1.49-4.99), performance score ≥ 1 (OR = 2.07, 95%CI = 1.03-4.19) and opioid use (OR = 1.82, 95%CI = 1.07-3.08) were independent predictors for early trial discontinuation. Almost 50% of the patients with hyponatremia and all four patients in whom all four predictors were present together discontinued the trial early. Hyponatremia, elevated alkaline phosphatase level, performance score ≥ 1 and opioid use were identified as significant predictors for early trial discontinuation. Hyponatremia was the strongest predictor and deserves consideration for inclusion in eligibility criteria for future trials.
尽管参与试验有严格的入选标准,但在I期试验中早期停药情况仍经常发生。为了更好地识别不太可能从I期试验中获益的患者,我们研究了早期试验停药的预测因素。将参与66项试验的415例实体瘤患者的数据汇总用于当前分析。早期试验停药定义为:(i)治疗开始后28天内停药,或(ii)符合条件的患者在首次给药前停药。进行多水平逻辑回归分析以确定早期试验停药的预测因素。82名参与者(20%)出现早期试验停药。基线钠水平低于正常下限(OR = 2.95,95%CI = 1.27 - 6.84)、碱性磷酸酶水平升高>正常上限的2.5倍(OR = 2.72,95%CI = 1.49 - 4.99)、体能状态评分≥1(OR = 2.07,95%CI = 1.03 - 4.19)以及使用阿片类药物(OR = 1.82,95%CI = 1.07 - 3.08)是早期试验停药的独立预测因素。几乎50%的低钠血症患者以及所有四项预测因素均存在的4名患者均提前停药。低钠血症、碱性磷酸酶水平升高、体能状态评分≥1以及使用阿片类药物被确定为早期试验停药的显著预测因素。低钠血症是最强的预测因素,值得考虑纳入未来试验的入选标准。