Section of Pediatric Hematology/Oncology, Yale School of Medicine, New Haven, CT.
Cancer Outcomes, Public Policy, and Effectiveness Research (COPPER) Center, Yale Cancer Center, Yale School of Medicine, New Haven, CT.
J Natl Cancer Inst. 2018 Dec 1;110(12):1352-1359. doi: 10.1093/jnci/djy057.
A survivorship care plan (SCP), that is, individualized treatment summary and schedule of off-therapy surveillance, will be mandated by January 2019. It is unclear whether SCPs improve adherence to recommended follow-up care in the community. In this trial, we evaluated the impact of randomly assigning childhood cancer survivors to 1) SCPs to be taken to their primary care physician (PCP) to implement or 2) survivorship clinic (SC) on health care quality measures.
Eligibility included cancer diagnosis younger than age 18 years (2000-2012), cancer free, one or more years off therapy, and no prior survivorship clinic attendance. At 12 months, the random assignment groups were compared (SCP+PCP vs SC) by intent-to-treat analysis with two-sided statistical tests in terms of patient adherence to guideline-recommended surveillance tests (eg, echocardiogram) and number of newly identified late complications of therapy.
From 2011 to 2013, 96 participants (46.9% female, mean age = 15.9 ± 6.1 years) were randomly assigned. Adherence to 14 evaluated guideline-recommended surveillance tests ranged from 0% to 46.9% in the SCP+PCP group (n = 47) and from 50.0% to 86.4% in the SC group (n = 47). Adherence to 10 tests was statistically significantly different between the groups (all P < .05). One mild new late complication was identified in the SCP+PCP group compared with 21 late complications, ranging from mild to severe, identified in 11 patients in the SC group (2.1% vs 23.4% of patients, respectively, P = .003).
Our randomized trial suggests that empowering childhood cancer survivors with SCPs to be implemented by their PCPs is not sufficient to meet consensus follow-up recommendations.
自 2019 年 1 月起,将强制要求制定生存者关怀计划(SCP),即个性化的治疗总结和治疗后监测计划。目前尚不清楚 SCP 是否能提高社区中遵循推荐的随访护理的比例。在这项试验中,我们评估了将儿童癌症幸存者随机分配到以下两种方案对改善医疗质量的影响:1)SCP 由幸存者本人带到初级保健医生(PCP)处执行;2)SCP 由幸存者带到生存者诊所(SC)处执行。
符合条件的参与者包括在 2000 年至 2012 年期间诊断患有癌症且年龄小于 18 岁、癌症已治愈、已停药一年或一年以上且从未参加过生存者诊所的患者。在 12 个月时,通过意向治疗分析比较了随机分组(SCP+PCP 组与 SC 组)之间的差异,使用双侧统计检验评估患者对指南推荐的监测测试(例如,超声心动图)的依从性以及新发现的治疗后晚期并发症的数量。
2011 年至 2013 年期间,共纳入 96 名参与者(46.9%为女性,平均年龄=15.9±6.1 岁)。在 SCP+PCP 组(n=47)中,有 14 项评估的指南推荐监测测试的依从率为 0%至 46.9%,在 SC 组(n=47)中,有 50.0%至 86.4%的患者依从。两组间 10 项测试的依从率有统计学显著差异(均 P<.05)。在 SCP+PCP 组中发现 1 例轻度新的晚期并发症,而在 SC 组中发现 11 例患者中有 21 例轻度至重度晚期并发症,发生率分别为 2.1%和 23.4%(P=.003)。
我们的随机试验表明,让儿童癌症幸存者获得 SCP 并由其 PCP 执行并不足以满足共识随访建议。