Rokitka Denise A, Curtin Colleen, Heffler Jennifer E, Zevon Michael A, Attwood Kris, Mahoney Martin C
1 Department of Pediatric Oncology, Roswell Park Cancer Institute , Buffalo, New York.
2 Jacobs School of Medicine and Biomedical Sciences, State University at Buffalo , Buffalo, New York.
J Adolesc Young Adult Oncol. 2017 Mar;6(1):67-73. doi: 10.1089/jayao.2016.0023. Epub 2016 Aug 16.
Surveillance for long-term complications related to previous cancer therapy can help diagnose/manage chronic health conditions in childhood cancer survivors and improve survivor quality of life. However, a challenge to delivering long-term care to childhood cancer survivors is loss to follow-up; many patients discontinue care at specialized survivor care centers. The purpose of this study was to examine patterns of loss to follow-up among a cohort of childhood cancer survivors.
This retrospective study examined follow-up patterns among a nonrandom representative sample of 370 childhood cancer survivors among 1116 patients from a single institution. The median age of patients at diagnosis was 10.2 years (range <1-21). Factors potentially related to follow-up were utilized to evaluate patterns of follow-up across 5-year intervals following completion of active therapy. The association between patient characteristics and follow-up was evaluated using univariate and multivariate binomial regression models.
The probability of follow-up 1-5 years post-treatment was 91.2% (89.7%-92.5%) but dropped to 68.5% (66.2%-70.8%) during years 6-10, 47.7% (45.0%-50.3%) during years 11-15, and continued to steadily decrease over time. Overall, white race, diagnoses at younger ages, patients with lymphomas/leukemias, and decade of diagnosis were each associated with somewhat better rates of follow-up.
These findings highlight the lack of follow-up by adult survivors of childhood cancer with only approximately one-half of patients returning for follow-up 10 years after completion of therapy. Interventions focused on educating both patients and primary care physicians may help to increase long-term follow-up care among this at-risk population.
监测与既往癌症治疗相关的长期并发症有助于诊断/管理儿童癌症幸存者的慢性健康状况,并提高幸存者的生活质量。然而,为儿童癌症幸存者提供长期护理面临的一个挑战是失访;许多患者在专门的幸存者护理中心停止接受护理。本研究的目的是检查一组儿童癌症幸存者的失访模式。
这项回顾性研究检查了来自单一机构的1116名患者中370名儿童癌症幸存者的非随机代表性样本的随访模式。患者诊断时的中位年龄为10.2岁(范围<1-21岁)。利用可能与随访相关的因素来评估积极治疗结束后5年间隔内的随访模式。使用单变量和多变量二项式回归模型评估患者特征与随访之间的关联。
治疗后1-5年的随访概率为91.2%(89.7%-92.5%),但在6-10年期间降至68.5%(66.2%-70.8%),在11-15年期间降至47.7%(45.0%-50.3%),并随着时间的推移持续稳步下降。总体而言,白人、较年轻年龄诊断的患者、淋巴瘤/白血病患者以及诊断年代与随访率略高相关。
这些发现凸显了儿童癌症成年幸存者缺乏随访,治疗完成10年后只有约一半的患者返回接受随访。针对患者和初级保健医生的教育干预措施可能有助于增加这一高危人群的长期随访护理。