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将患者报告的结局纳入青少年和青年 III 期治疗试验:对 ClinicalTrials.gov 上注册的癌症临床试验的分析。

Inclusion of Patient-Reported Outcomes in Adolescent and Young Adult Phase III Therapeutic Trials: An Analysis of Cancer Clinical Trials Registered on ClinicalTrials.gov.

机构信息

Department of Pediatrics, Duke University School of Medicine, Durham, NC, USA.

Department of Social Sciences and Health Policy, Wake Forest School of Medicine, Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, NC, USA.

出版信息

Value Health. 2021 Dec;24(12):1820-1827. doi: 10.1016/j.jval.2021.06.012. Epub 2021 Aug 8.

Abstract

OBJECTIVES

There is a paucity of research on the impact of cancer treatment on the health-related quality of life (HRQOL) of adolescent and young adult (AYA) patients with cancer. Patient-reported outcomes (PROs) are self-report measures used to assess HRQOL and symptom burden. The extent to which PROs have been included in trials that include common AYA cancer types has not been previously assessed.

METHODS

Therapeutic phase 3 trials among common AYA cancer types (Hodgkin lymphoma, non-Hodgkin lymphoma, acute lymphoblastic leukemia, sarcomas, and germ cell tumors) initiated between 2007 and 2020 were identified on ClinicalTrials.gov. The proportions and characteristics of trials including a PRO endpoint were assessed. For comparison with an older population, the proportion of breast and colorectal therapeutic phase 3 trials including PRO endpoints were assessed.

RESULTS

Eighty-seven studies met the inclusion criteria. Overall, 20.7% of therapeutic phase 3 AYA trials included a PRO endpoint, and only one trial published PRO data. Germ cell tumors (42.9%) and non-Hodgkin lymphoma (40%) trials had the highest proportions of PRO inclusion. The European Organization for Research and Treatment of Cancer generic, cancer-specific quality of life questionnaire was the most commonly used PRO measure; nevertheless, the measures used varied within and between cancer types. The proportion of trials including a PRO endpoint did not change significantly between 2007 to 2013 and 2014 to 2020 (18.6% vs 22.7%, P=.79).

CONCLUSIONS

Few therapeutic phase 3 AYA cancer trials include PRO endpoints, fewer publish PRO data, and there is no homogeneity in the measures administered. Therapeutic trials represent an underused opportunity to capture PRO data in the AYA population with the goal of improving HRQOL outcomes.

摘要

目的

针对癌症治疗对青少年和年轻成人(AYA)癌症患者健康相关生活质量(HRQOL)的影响,目前相关研究较为匮乏。患者报告的结果(PRO)是一种自我报告的衡量标准,用于评估 HRQOL 和症状负担。目前尚未对包含常见 AYA 癌症类型的试验中 PRO 的纳入程度进行评估。

方法

在 ClinicalTrials.gov 上,确定了 2007 年至 2020 年间启动的常见 AYA 癌症类型(霍奇金淋巴瘤、非霍奇金淋巴瘤、急性淋巴细胞白血病、肉瘤和生殖细胞瘤)的治疗阶段 3 试验。评估了纳入 PRO 终点的试验的比例和特征。为了与老年人群进行比较,还评估了纳入 PRO 终点的乳腺癌和结直肠癌治疗阶段 3 试验的比例。

结果

符合纳入标准的研究共 87 项。总体而言,20.7%的治疗阶段 3 AYA 试验纳入了 PRO 终点,仅有一项试验发表了 PRO 数据。生殖细胞瘤(42.9%)和非霍奇金淋巴瘤(40%)试验中纳入 PRO 的比例最高。欧洲癌症研究与治疗组织的通用型、癌症特异性生活质量问卷是最常用的 PRO 衡量标准;然而,在癌症类型内和癌症类型之间,使用的衡量标准存在差异。2007 年至 2013 年和 2014 年至 2020 年期间,纳入 PRO 终点的试验比例没有显著变化(18.6%比 22.7%,P=.79)。

结论

在治疗阶段 3 AYA 癌症试验中,很少有试验纳入 PRO 终点,更少的试验发表 PRO 数据,且使用的衡量标准并不统一。治疗试验代表了在 AYA 人群中利用 PRO 数据的一个未充分利用的机会,旨在改善 HRQOL 结果。

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