School of Public Health, University of Texas Health Science Center at Houston (UTHealth), Houston, TX, USA.
Department of Population and Data Sciences, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Cancer Med. 2021 Sep;10(17):5917-5924. doi: 10.1002/cam4.4140. Epub 2021 Aug 18.
As use of oral cancer therapies increases, patient adherence has become critical when evaluating the effectiveness of therapy. In a phase III trial for renal cell carcinoma, we: (a) characterized adherence to sorafenib, sunitinib, and/or placebo and (b) identified factors associated with non-adherence.
ECOG-ACRIN E2805 was a double-blind, placebo-controlled, randomized trial comparing adjuvant sorafenib or sunitinib in patients with resected primary renal cell carcinoma at high risk for recurrence. We used patient-completed pill diaries to measure adherence as the number of pills taken divided by the number of pills prescribed. Log-binomial regression was used to identify correlates of non-adherence (<80% of prescribed pills reported as taken).
Mean adherence was 90.7% among those assigned to sunitinib (n = 613) and 84.8% among those assigned to sorafenib (n = 616). Among those assigned to placebo, mean adherence was 94.9% and 92.4% to sunitinib and sorafenib placebo, respectively. Non-adherence was associated with race/ethnicity (non-Hispanic Black: prevalence ratio [PR] 2.22, 95% CI 1.63, 3.01; Hispanic: PR 1.54, 95% CI 1.05, 2.26), high volume enrollment (≥10 patients: PR 1.30, 95% CI 1.03, 1.64), treatment group (sunitinib: PR 2.24, 95% CI 1.66, 3.02; sorafenib: PR 2.37, 95% CI 1.74, 3.22), and skin rash (PR 1.36, 95% CI 1.03, 1.80).
Among patients participating in a randomized clinical trial, adherence to oral cancer therapies was lower compared to placebo. Adherence was also worse in racial/ethnic minorities, those experiencing toxicities, and high volume enrolling sites. Our findings highlight several challenges to address in clinical practice as use of oral therapies continues to increase.
This trial is registered with ClinicalTrials.gov, number NCT00326898.
随着口腔癌治疗方法的应用增加,在评估治疗效果时,患者的依从性变得至关重要。在一项针对肾细胞癌的 III 期试验中,我们:(a)描述了索拉非尼、舒尼替尼和/或安慰剂的依从性,(b)确定了与不依从相关的因素。
ECOG-ACRIN E2805 是一项双盲、安慰剂对照、随机试验,比较了辅助索拉非尼或舒尼替尼在高复发风险的肾细胞癌切除后的原发性肾细胞癌患者中的应用。我们使用患者完成的药丸日记来衡量依从性,即服用的药丸数除以规定的药丸数。对数二项式回归用于确定不依从(报告服用的药丸数<80%规定的药丸数)的相关因素。
索拉非尼组(n=613)的平均依从率为 90.7%,舒尼替尼组(n=616)为 84.8%。索拉非尼安慰剂组和舒尼替尼安慰剂组的平均依从率分别为 94.9%和 92.4%。种族/民族(非西班牙裔黑人:患病率比[PR]2.22,95%CI1.63,3.01;西班牙裔:PR1.54,95%CI1.05,2.26)、高容量入组(≥10 例患者:PR1.30,95%CI1.03,1.64)、治疗组(舒尼替尼:PR2.24,95%CI1.66,3.02;索拉非尼:PR2.37,95%CI1.74,3.22)和皮疹(PR1.36,95%CI1.03,1.80)与不依从相关。
在参加随机临床试验的患者中,口服癌症治疗的依从性低于安慰剂。在少数族裔、出现毒性反应和高容量入组的患者中,依从性更差。我们的发现强调了随着口服治疗的应用不断增加,在临床实践中需要解决几个挑战。
本试验在 ClinicalTrials.gov 注册,编号为 NCT00326898。