Stem Cell Transplantation for Participants With Germline RUNX1 Associated Blood Cancers
NCT07524530
Core Binding Factor Alpha Subunits, Hematologic Diseases
Bethesda, Maryland, United States
View Trial DetailsNCT Number: NCT07813585
DECIPHER is a retrospective multicentre observational cohort study using data collected across UKCHART sites. The study will evaluate the impact of ethnicity, socioeconomic deprivation and comorbidity burden on treatment delivery and outcomes in adults diagnosed with DLBCL between 2021 and 2025.
Trial opening soon.
Get Notified18 year and older
All sexes
Observational
Despite the provision of universal healthcare through the National Health Service (NHS), variation in treatment delivery and outcomes among patients with diffuse large B-cell lymphoma (DLBCL) persists. Previous UK population-based studies have demonstrated that socioeconomic factors and multimorbidity influence survival outcomes in aggressive lymphoma, with patients from more deprived backgrounds experiencing poorer outcomes than those from less deprived areas.
Furthermore, multimorbidity has been associated with diagnostic delay and emergency presentation, factors known to adversely affect lymphoma outcomes.
National datasets such as the National Cancer Registration and Analysis Service (NCRAS) and the Systemic Anti-Cancer Therapy (SACT) database provide valuable population-level real-world evidence and have improved understanding of lymphoma outcomes at a national level. However, these datasets often lack the detailed clinical information required to fully explore the impact of ethnicity, socioeconomic deprivation, frailty, comorbidity burden, treatment modifications, and treatment delivery on patient outcomes.
The UK Consortium for Haematology Audit, Real-world Data and Trials (UKCHART) provides a unique opportunity to address these evidence gaps. Through a network of participating NHS organisations serving a large, diverse, and geographically distributed population, UKCHART enables the collection of detailed patient-level clinical data that are not routinely available within national registries. The demographic diversity of the UKCHART population makes it particularly well suited to investigating healthcare inequalities and understanding how ethnicity, deprivation, and comorbidity influence treatment delivery and outcomes in patients with DLBCL.
This study will utilise the UKCHART network to evaluate the impact of ethnicity, socioeconomic deprivation, and comorbidity burden on the delivery of frontline chemoimmunotherapy and subsequent clinical outcomes in patients with newly diagnosed DLBCL. By generating contemporary UK real-world evidence, the study aims to identify potentially modifiable factors contributing to outcome disparities and inform future strategies to improve equity of care for patients with high-grade lymphoma.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Time Period between 2021-2026
Delivered versus planned number of frontline chemoimmunotherapy cycles
Time frame: Time Period between 2021-2026
Occurrence and magnitude (%) of chemotherapy dose reductions, particularly reductions >25% from planned treatment
Time frame: Time Period between 2021-2026
Measured as time from diagnosis (or treatment start, as defined in the SAP) to death from any cause
Time frame: Time Period between 2021-2026
Measured as time from diagnosis/treatment initiation to disease progression, relapse, or death.
Time frame: Time Period between 2021-2026
Measured using Ann Arbor stage recorded at diagnosis
Time frame: Time Period between 2021-2026
Measured as the interval between diagnosis and commencement of first-line treatment.
The Royal Wolverhampton Hospitals NHS Trust
Other Gov
DECIPHER - Impact of Demography, Ethnicity, Co-morbidities and Inequalities on Outcomes in High-Grade Lymphoma Across the UKCHART Network
Acronym: DECIPHER
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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