Suppr超能文献

霍奇金淋巴瘤试验中患者报告的结局:一项系统评价

Patient-reported outcomes in Hodgkin lymphoma trials: a systematic review.

作者信息

Oliva Esther Natalie, Ionova Tatyana, Laane Edward, Csenar Mario, Schroer Julia, Behringer Karolin, Monsef Ina, Oeser Annika, Skoetz Nicole, Salek Sam

机构信息

Hematology Unit, Grande Ospedale Metropolitano Bianchi Melacrino Morelli, Reggio di Calabria, Italy.

Quality of Life Monitoring Unit, Saint Petersburg State University Hospital, Saint Petersburg, Russia.

出版信息

Front Oncol. 2024 Mar 13;14:1353101. doi: 10.3389/fonc.2024.1353101. eCollection 2024.

Abstract

BACKGROUND

Lymphoma treatment can lead to long-term consequences such as fatigue, infertility and organ damage. In clinical trials, survival outcomes, clinical response and toxicity are extensively reported while the assessment of treatment on quality of life (QoL) and symptoms is often lacking.

OBJECTIVE

We evaluated the use and frequency of patient-reported outcome (PRO) instruments used in randomized controlled trials (RCTs) for Hodgkin lymphoma (HL) and their consistency of reporting.

METHODS

MEDLINE, CENTRAL and trial registries for RCTs investigating HL were systematically searched from 01/01/2016 to 31/05/2022. Following trial selection, trial, patient characteristics and outcome data on the use of PRO measures (PROMs) and reporting of PROs using a pre-defined extraction form were extracted. To assess reporting consistency, trial registries, protocols and publications were compared.

RESULTS

We identified 4,222 records. Following screening, a total of 317 reports were eligible for full-text evaluation. One hundred sixty-six reports of 51 ongoing/completed trials were included, of which 41% of trials were completed and 49% were ongoing based on registry entries. Full-text or abstract were available for 33 trials. Seventy percent of trials were conducted in the newly diagnosed disease setting, the majority with advanced HL. In 32 trials with published follow-up data, the median follow-up was 5.2 years. Eighteen (35%) completed/ongoing trials had mentioned PRO assessment in registry entries, protocol or publications. Twelve trials (67%) had published results and only 6 trials (50%) reported on PROs in part with the exception of 1 trial where PROs were evaluated as secondary/exploratory outcome. The most referenced global PROM was the EORTC-QLQ-C30 (12 studies), the EQ-5D (3 studies) and the FACT-Neurotoxicity (3 studies). FACT-Lymphoma, a disease-specific PROM for non-HL was mentioned in one ongoing trial. None of the trials referenced the EORTC QLQ-HL27, another disease-specific PROM developed specifically for HL patient's QoL assessment.

DISCUSSIONS

Only one-third of RCTs in HL report PROs as an outcome and only half present the outcome in subsequent publications, showcasing the underreporting of PROs in trials. Disease-specific PROMs are underutilized in the assessment of QoL in HL patients. Guidance on the assessment of PROs is needed to inform on comprehensive outcomes important to patients.

SYSTEMATIC REVIEW REGISTRATION

https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=391552, identifier CRD42023391552.

摘要

背景

淋巴瘤治疗可能导致疲劳、不孕和器官损伤等长期后果。在临床试验中,生存结果、临床反应和毒性被广泛报道,而对生活质量(QoL)和症状的治疗评估往往缺失。

目的

我们评估了随机对照试验(RCT)中用于霍奇金淋巴瘤(HL)的患者报告结局(PRO)工具的使用情况和频率,以及它们报告的一致性。

方法

对2016年1月1日至2022年5月31日期间调查HL的RCT的MEDLINE、CENTRAL和试验注册库进行系统检索。在试验选择后,提取试验、患者特征以及使用PRO测量工具(PROMs)和使用预定义提取表报告PROs的结局数据。为评估报告的一致性,对试验注册库、方案和出版物进行了比较。

结果

我们识别出4222条记录。筛选后,共有317份报告符合全文评估条件。纳入了51项正在进行/已完成试验的166份报告,其中根据注册库记录,41%的试验已完成,49%正在进行。33项试验有全文或摘要。70%的试验是在新诊断疾病的情况下进行的,大多数是晚期HL。在32项有发表随访数据的试验中,中位随访时间为5.2年。18项(35%)已完成/正在进行的试验在注册库记录、方案或出版物中提及了PRO评估。12项试验(67%)发表了结果,只有6项试验(50%)部分报告了PROs,1项试验除外,该试验将PROs作为次要/探索性结局进行评估。引用最多的总体PROM是EORTC-QLQ-C30(12项研究)、EQ-5D(3项研究)和FACT-神经毒性(3项研究)。一项正在进行的试验中提到了FACT-淋巴瘤,这是一种针对非HL的疾病特异性PROM。没有试验引用EORTC QLQ-HL27,这是另一种专门为评估HL患者QoL而开发的疾病特异性PROM。

讨论

HL的RCT中只有三分之一将PROs作为结局报告,后续出版物中只有一半呈现了结局,这表明试验中PROs报告不足。疾病特异性PROMs在HL患者QoL评估中未得到充分利用。需要关于PROs评估的指导,以了解对患者重要的综合结局。

系统评价注册

https://www.crd.york.ac.uk/PROSPERO/display_record.php?RecordID=391552,标识符CRD42023391552。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f7c/10965683/d0c999c75b57/fonc-14-1353101-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验