Institute for Cancer Outcomes and Survivorship, University of Alabama at Birmingham, Birmingham.
Department of Population Sciences, City of Hope, Duarte, California.
JAMA Netw Open. 2020 Aug 3;3(8):e2014205. doi: 10.1001/jamanetworkopen.2020.14205.
Suboptimal adherence to oral mercaptopurine treatment in children with acute lymphoblastic leukemia (ALL) increases the risk of relapse. A frequently expressed barrier to adherence is forgetfulness, which is often overcome by parental vigilance.
To determine whether a multicomponent intervention, compared with education alone, will result in a higher proportion of patients with ALL who have mercaptopurine adherence rates 95% or higher, for all study participants and among patients younger than 12 years and vs those aged 12 years and older.
DESIGN, SETTING, AND PARTICIPANTS: The adherence intervention trial was an investigator-initiated, multi-institutional, parallel-group, unblinded, randomized clinical trial conducted between July 16, 2012, and August 8, 2018, at 59 Children's Oncology Group institutions in the US, enrolling patients with ALL diagnosed through age 21 years and receiving mercaptopurine for maintenance. The date of final follow-up was January 2, 2019. Data analysis was performed from February to October 2019.
Patients were randomized 1:1 to education alone or the intervention package, which consisted of education and personalized text message reminders daily to prompt directly supervised therapy. Four weeks of baseline adherence monitoring were followed with a 16-week intervention.
The primary end point was the proportion of patients with adherence rates 95% or higher over the duration of the intervention for all study participants, and for those younger than 12 years vs those aged 12 years and older.
There were 444 evaluable patients (median age, 8.1 years; interquartile range, 5.3-14.3 years), including 230 in the intervention group and 214 in the education group. Three hundred two patients (68.0%) were boys, 180 (40.5%) were non-Hispanic White, 170 (38.3%) were Hispanic, 43 (9.7%) were African American, and 51 (11.5%) were Asian or of mixed race/ethnicity. The proportion of patients with adherence rates 95% or higher did not differ between the intervention vs education groups (65% vs 59%; odds ratio, 1.33; 95% CI, 1.0-2.0; P = .08). Exploratory analyses showed that among patients aged 12 years and older, those in the intervention group had higher mean (SE) adherence rates than those in the education group (93.1% [1.1%] vs 90.0% [1.3%]; difference, 3.1%; 95% CI, 0.1%-6.0%; P = .04). In particular, among patients aged 12 years and older with baseline adherence less than 90%, those in the intervention group had higher mean (SE) adherence rates than those in the education group (83.4% [2.5%] vs 74.6% [3.4%]; difference, 8.8%; 95% CI, 2.2%-15.4%; P = .008). No safety concerns were identified.
Although this multicomponent intervention did not result in an increase in the proportion of patients with ALL who had mercaptopurine adherence rates 95% or higher, it did identify a high-risk subpopulation to target for future adherence intervention strategies: adolescents with low baseline adherence.
ClinicalTrials.gov Identifier: NCT01503632.
儿童急性淋巴细胞白血病(ALL)患者口服巯嘌呤治疗的依从性不理想会增加复发的风险。忘记服药是导致依从性差的常见原因,而这种情况通常可以通过父母的监督来克服。
确定与单纯教育相比,多组分干预是否会导致 ALL 患者中更高比例的患者具有更高的巯嘌呤依从率,即在所有研究参与者中以及在 12 岁以下和 12 岁及以上的患者中达到 95%或更高的依从率。
设计、地点和参与者:这项依从性干预试验是由研究者发起的、多机构、平行组、非盲、随机临床试验,于 2012 年 7 月 16 日至 2018 年 8 月 8 日在美国 59 家儿童肿瘤学组机构进行,招募的患者年龄在 21 岁以下且接受巯嘌呤维持治疗。最后一次随访日期为 2019 年 1 月 2 日。数据分析于 2019 年 2 月至 10 月进行。
患者以 1:1 的比例随机分为单纯教育组或干预组,干预组包括教育和每天个性化的短信提醒,以提示直接监督治疗。在干预前进行了 4 周的依从性监测,然后进行了 16 周的干预。
主要终点是所有研究参与者在干预期间达到巯嘌呤依从率 95%或更高的比例,以及 12 岁以下和 12 岁及以上的患者比例。
共有 444 例可评估患者(中位年龄为 8.1 岁;四分位间距为 5.3-14.3 岁),其中 230 例患者接受干预,214 例患者接受教育。302 例患者(68.0%)为男性,180 例(40.5%)为非西班牙裔白人,170 例(38.3%)为西班牙裔,43 例(9.7%)为非裔美国人,51 例(11.5%)为亚洲人或混合种族/民族。干预组和教育组的患者中,依从率达到 95%或更高的比例没有差异(65%与 59%;比值比,1.33;95%置信区间,1.0-2.0;P=0.08)。探索性分析显示,在 12 岁及以上的患者中,干预组的平均(SE)依从率高于教育组(93.1%[1.1%]与 90.0%[1.3%];差异,3.1%;95%置信区间,0.1%-6.0%;P=0.04)。特别是在基线依从率低于 90%的 12 岁及以上的患者中,干预组的平均(SE)依从率高于教育组(83.4%[2.5%]与 74.6%[3.4%];差异,8.8%;95%置信区间,2.2%-15.4%;P=0.008)。没有发现安全问题。
尽管这种多组分干预并没有增加 ALL 患者中达到巯嘌呤依从率 95%或更高的比例,但它确实确定了一个高危亚人群,需要针对未来的依从性干预策略进行目标定位:基线依从性较低的青少年。
ClinicalTrials.gov 标识符:NCT01503632。