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Not yet recruitingNCT07813585DECIPHERUpdated Sep 25, 2026

Impact of Demography, Ethnicity, Co-morbidities and Inequalities on Outcomes in DLBCL Across the UKCHART Network

An observational study in Lymphoma, sponsored by The Royal Wolverhampton Hospitals NHS Trust. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-25.

Sponsored by The Royal Wolverhampton Hospitals NHS Trust · Observational

Updated Sep 25, 2026Title changedGo to Updates ↓
Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
2,000
Ages
18 Years and older
Sex
All
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Study summary

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.

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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.

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Conditions studied

  • Lymphoma

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03

In context

Lymphoma

3,018 studies on the registry are indexed under Lymphoma; 434 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 167 across 393 observational studies indexed under Lymphoma.

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Lead sponsor

The Royal Wolverhampton Hospitals NHS Trust is the lead sponsor of 51 studies on the registry; 16 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Data will be collected retrospectively by the 21 individual trusts which make up UKCHART. The population catchment is around 18 million.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adults aged ≥18 years.
  • Newly diagnosed DLBCL.
  • Managed within participating UKCHART sites.

Exclusion criteria

Exclusion Criteria:

  • Transformed lymphoma.
  • Insufficient linkage data.
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Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
2,000 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Treatment completion

    Delivered versus planned number of frontline chemoimmunotherapy cycles

    Time frame: Time Period between 2021-2026

  2. Dose intensity reduction

    Occurrence and magnitude (%) of chemotherapy dose reductions, particularly reductions \>25% from planned treatment

    Time frame: Time Period between 2021-2026

Secondary outcomes

  1. Overall Survival (OS)

    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

  2. Progression-Free Survival (PFS)

    Measured as time from diagnosis/treatment initiation to disease progression, relapse, or death.

    Time frame: Time Period between 2021-2026

  3. Stage at Diagnosis

    Measured using Ann Arbor stage recorded at diagnosis

    Time frame: Time Period between 2021-2026

  4. Time to Treatment Initiation

    Measured as the interval between diagnosis and commencement of first-line treatment.

    Time frame: Time Period between 2021-2026

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Study locations

No study locations are listed for this record.

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Updates

1 registry update since Sep 25, 2026
Title
Impact of Demography, Ethnicity, Co-morbidities and Inequalities on Outcomes in High-Grade LymphomaDLBCL Across the UKCHART Network
Sep 25, 2026
Show all 1 update
  1. Sep 25, 2026
    Title Impact of Demography, Ethnicity, Co-morbidities and Inequalities on Outcomes in High-Grade LymphomaDLBCL Across the UKCHART Network

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

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Registry details

Key details

Study ID
NCT07813585
Lead sponsor
The Royal Wolverhampton Hospitals NHS Trust
Responsible party
Sponsor
First posted
Sep 10, 2026
Start date
Oct 2026 (estimated)
Primary completion
Sep 2027 (estimated)
Completion
Sep 2027 (estimated)
Last update
Sep 25, 2026
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

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