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

被引:0
|
作者
Oliva, Esther Natalie [1 ]
Ionova, Tatyana [2 ]
Laane, Edward [3 ]
Csenar, Mario [4 ,5 ]
Schroer, Julia [4 ,5 ]
Behringer, Karolin [5 ,6 ]
Monsef, Ina [4 ,5 ]
Oeser, Annika [4 ,5 ]
Skoetz, Nicole [4 ,5 ,6 ]
Salek, Sam [7 ]
机构
[1] Grande Osped Metropolitano Bianchi Melacrino Morel, Hematol Unit, Reggio Di Calabria, Italy
[2] St Petersburg State Univ Hosp, Qual Life Monitoring Unit, St Petersburg, Russia
[3] Tartu Univ, Hematol Oncol Clin, Tartu, Estonia
[4] Univ Cologne, Fac Med, Dept Internal Med 1, Evidence Based Med, Cologne, Germany
[5] Univ Cologne, Univ Hosp Cologne, Cologne, Germany
[6] Univ Cologne, Fac Med, Ctr Integrated Oncol Aachen Bonn Cologne Duesseldo, Dept Internal Med 1, Cologne, Germany
[7] Univ Hertfordshire, Sch Life & Med Sci, Hatfield, England
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
关键词
Hodgkin lymphoma; patient-reported outcomes; Quality of Life; PRO instrument; psychometric testing; systematic review; validation studies; QUALITY-OF-LIFE; PSYCHOMETRIC EVALUATION; CLINICAL-TRIALS; QLQ-C30; QUESTIONNAIRE; IMPAIRMENT; GUIDELINES; INCLUSION; VALIDITY; PRO;
D O I
10.3389/fonc.2024.1353101
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
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