Pediatric Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
Cancer. 2014 Jan 1;120(1):112-25. doi: 10.1002/cncr.28339. Epub 2013 Oct 16.
The delivery of effective treatment for pediatric solid tumors poses a particular challenge to centers in middle-income countries (MICs) that already are vigorously addressing pediatric cancer. The objective of this study was to improve the current understanding of barriers to effective treatment of pediatric solid tumors in MICs.
An ecologic model centered on pediatric sarcoma and expanded to country as the environment was used as a benchmark for studying the delivery of solid tumor care in MICs. Data on resources were gathered from 7 centers that were members of the Central American Association of Pediatric Hematologists and Oncologists (AHOPCA) using an infrastructure assessment tool. Pediatric sarcoma outcomes data were available, were retrieved from hospital-based cancer registries for 6 of the 7 centers, and were analyzed by country. Patients who were diagnosed from January 1, 2000 to December 31, 2009 with osteosarcoma, Ewing sarcoma, rhabdomyosarcoma, and other soft tissue sarcomas were included in the analysis. To explore correlations between resources and outcomes, a pilot performance index was created.
The analyses identified specific deficits in human resources, communication, quality, and infrastructure. The treatment abandonment rate, the proportion of metastatic disease at diagnosis, the relapse rate, and the 4-year abandonment-sensitive overall survival (AOS) rate varied considerably by country, ranging from 1% to 38%, from 15% to 54%, from 24% to 52%, and from 21% to 51%, respectively. The treatment abandonment rate correlated inversely with health economic expenditure per capita (r = -0.86; P = .03) and life expectancy at birth (r = -0.93; P = .007). The 4-year AOS rate correlated inversely with the mortality rate among children aged <5 years (r = -0.80; P = 0.05) and correlated directly with the pilot performance index (r = 0.98; P = 0.005).
Initiatives to improve the effectiveness of treatment for pediatric solid tumors in MICs are warranted, particularly for pediatric sarcomas. Building capacity and infrastructure, improving supportive care and communication, and fostering comprehensive, multidisciplinary teams are identified as keystones in Central America. A measure that meaningfully describes performance in delivering pediatric cancer care is feasible and needed to advance comparative, prospective analysis of pediatric cancer care and to define resource clusters internationally.
为儿科实体瘤提供有效治疗对中低收入国家(MICs)的中心构成了特别的挑战,这些中心已经在积极应对儿科癌症。本研究的目的是提高对 MICs 中儿科实体瘤有效治疗障碍的现有认识。
以小儿肉瘤为中心的生态模型,并扩展为国家环境,作为研究 MICs 中实体肿瘤护理提供情况的基准。使用基础设施评估工具从 7 个中心(均为中美洲儿科血液学家和肿瘤学家协会(AHOPCA)的成员)收集资源数据。获得了小儿肉瘤结局数据,从 7 个中心中的 6 个中心的医院癌症登记处检索到了数据,并按国家进行了分析。本分析纳入了 2000 年 1 月 1 日至 2009 年 12 月 31 日期间被诊断为骨肉瘤、尤文肉瘤、横纹肌肉瘤和其他软组织肉瘤的患者。为了探索资源与结局之间的相关性,创建了一个试点绩效指数。
分析确定了人力资源、沟通、质量和基础设施方面的具体缺陷。治疗放弃率、诊断时转移性疾病的比例、复发率和 4 年敏感总生存率(AOS)的差异在国家间相当大,范围分别为 1%至 38%、15%至 54%、24%至 52%和 21%至 51%。治疗放弃率与人均卫生经济支出呈负相关(r=-0.86;P=0.03),与出生时预期寿命呈负相关(r=-0.93;P=0.007)。4 年 AOS 率与 5 岁以下儿童死亡率呈负相关(r=-0.80;P=0.05),与试点绩效指数呈正相关(r=0.98;P=0.005)。
需要采取措施提高 MICs 中儿科实体瘤治疗的有效性,特别是小儿肉瘤。在中美洲,确定了提高能力和基础设施、改善支持性护理和沟通以及培养全面、多学科团队的重要性。衡量提供儿科癌症护理绩效的措施是可行的,需要用于推进儿科癌症护理的比较性、前瞻性分析,并在国际上确定资源集群。