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NCT Number: NCT06737835

Metabolic Insights: the Impact of F-18 FDG PET/CT in Adult Lymphoma

1. To assess staging accuracy of F-18 FDG PET/CT in lymphoma 2. Determine the role of F-18 FDG PET/CT in monitoring treatment response and detecting relapse or residual disease in lymphoma 3. To evaluate FDG uptake correlation with histopathological subtypes and immunophenotypes as a prognostic factor.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

About this study

The incidence of lymphoma in Egypt has been increasing in recent years, with a noticeable rise in both Hodgkin's and non-Hodgkin's lymphoma cases. This increase is due to better healthcare, awareness, and diagnostic advancements. Risk factors include infections, lifestyle, genetics, and immune system issues.

Lymphoma is now the fourth most prevalent cancer among Egyptian adults, accounting for approximately 8.4% of all new cancer cases annually. As the burden of lymphoma grows, it becomes essential to develop effective strategies for its diagnosis and management.

Flurodeoxyglucose F-18 (F-18 FDG) is a radiolabeled glucose analog that accumulates in metabolically active cells, such as lymphoma cells, making F-18 FDG positron emission tomography / computed tomography scan (PET/CT) highly sensitive for detecting malignant lesions. It plays a key role in staging lymphoma by assessing the extent of disease spread.

Additionally, F-18 FDG PET/CT is essential for assessing treatment response, detecting relapses early, and evaluating the prognosis of patients, offering prognostic value by evaluating residual disease and predicting recurrence. Its ability to monitor disease progression and detect recurrent lymphoma provides critical insights that guide therapeutic decisions and long-term outcomes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: Patient must be older than 18 years.
  • Confirmed Diagnosis of Lymphoma: Patient must have a confirmed diagnosis of lymphoma based on histopathology and immunophenotyping.

Exclusion criteria

  • Patients with Known concomitant malignancy.
  • Pregnancy: Pregnant women due to the potential risks associated with radiation exposure from the PET/CT scan.
  • Severe Renal or Hepatic Impairment: Patients with significant renal or hepatic dysfunction that could affect FDG metabolism or excretion.
  • Uncontrolled Diabetes: Patients with uncontrolled diabetes (blood glucose >200 mg/dL), as it can affect FDG uptake and PET/CT results.

Treatment and study plan

18 FDG

Device

18 flurodeoxy glucose PET/CT

Primary outcomes

  1. primary

    Time frame: 3 years

    Treatment Response Using Deauville Score for FDG Uptake Evaluation:

    Evaluate FDG uptake using the 5-point scale:

    • No uptake above background
    • Uptake ≤ mediastinum
    • Uptake > mediastinum but ≤ liver
    • Moderately increased compared to liver
    • Markedly increased compared to liver X: New uptake, unlikely related to lymphoma

Secondary outcomes

  1. secondary

    Time frame: 3 years

    Detect early relapse or residual disease using F-18 FDG PET/CT using SUVmax, maximum standardized uptake value(g/mL )

Study contacts

Contact information is provided by the study sponsor or research team.

Aya A Ahmed Ali ALsanory, MSc

CONTACT

[email protected]

00201063490867

Mohamed A Mekkawy, Prof

CONTACT

[email protected]

00201011580757

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Dec 17, 2024
Registry last updated
Dec 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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