ClinicalTrials.gov record NCT05898477
Describing Treatment Outcomes and Responses in Lymphoma-associated Hemophagocytic Lymphohistiocytosis
Describing Treatment Outcomes and Responses in Lymphoma-associated Hemophagocytic Lymphohistiocytosis
AI summaryWhat this study is about, in plain languageShow ▾Hide ▴
AI-written from the registry record, not the study's own wording. May contain errors or omissions. Check the registry text on this page and the original record ↗ before acting on it.
This retrospective, multi-institutional study reviews past medical records of people who had hemophagocytic lymphohistiocytosis (HLH) in the setting of lymphoma. It describes clinical features, laboratory findings, treatments, and outcomes. The investigators will look for factors—including treatments and timing—associated with survival at 180 days after the malignancy diagnosis.
What it is studying. Which clinical features, laboratory findings, treatments, and treatment timing are associated with 180‑day overall survival in people with lymphoma-associated HLH.
What the researchers hope to learn. To describe clinical features, laboratory parameters, treatments, and outcomes of HLH occurring with lymphoma; to determine which factors predict 180‑day overall survival; and to identify possible therapeutic strategies for future study.
What this study is about
The study's own summary, as published on ClinicalTrials.gov. Underlined terms have a short explanation.
The purpose of the study is to describe Hemophagocytic lymphohistiocytosis (HLH) in patients with lymphoma to identify possible therapeutic strategies to improve overall survival of the patients with lymphoma associated hemophagocytic lymphohistiocytosis.
Eligibility
The criteria exactly as listed on ClinicalTrials.gov. Only the study team can say whether they apply to you.
Inclusion criteria
- Patients with lymphoma that are fulfilling at least one of the following:
- A. Meeting 5 of 8 HLH-2004 diagnostic criteria OR B. Are OHI index positive (sCD25>3,900 U/mL and ferritin>1,000 ng/mL)
Exclusion criteria
- Patients developing HLH> 1 month after lymphoma diagnosis (for aggressive lymphomas)
- Patients with incomplete treatment and response documentation
Study description and what participation involves
The study's detailed description, as published on ClinicalTrials.gov.
Detailed description from the registry
Retrospective, multi-institutional study focused on describing the clinical features, laboratory parameters, treatments, and outcomes among individuals presenting with HLH in the setting of a lymphoma
AI summaryWhat participation may involve, in plain languageShow ▾Hide ▴
AI-written from the registry record, not the study's own wording. May contain errors or omissions. Check the registry text on this page and the original record ↗ before acting on it.
This is a retrospective review of medical records. Investigators will collect past clinical information, laboratory results (including sCD25 and ferritin when available), treatments received, treatment responses, and outcomes; survival at 180 days from the malignancy diagnosis will be assessed. The registry describes data collection from existing records rather than new study procedures or experimental treatments. Records that lack required treatment or response documentation are excluded.
How the study is structured. A retrospective observational cohort study that collects and analyzes past medical records from multiple centers to describe features, treatments, and outcomes for lymphoma-associated HLH.
Questions you could ask
These questions are suggestions for a conversation with the study team or your own clinician, not advice.
- The registry lists this study under Lymphoma; Hemophagocytic Lymphohistiocytoses. Does it apply to my diagnosis?
- This is an observational study, so the study itself gives no treatment. What would taking part involve for me, and would it change my usual care?
- The listed sites are in United States. Is any of them reachable for me, and does the study help with travel?
- Which of the eligibility criteria would need to be checked with tests before I could join?
More on hemophagocytic lymphohistiocytosis
Important dates
- Study start
- May 1, 2023
- Primary completion
- January 2028 (estimated)
- Study completion
- July 2028 (estimated)
- Target enrollment
- 2000 participants (estimated)
- Last updated on registry
- Jan 22, 2026
- Data verified
- Oct 10, 2026
Sponsor and research team
The lead sponsor funds and oversees the trial. A pharmaceutical or biotech company sponsor typically means the study is testing that company's drug or device; a hospital, university, or government agency usually indicates investigator-initiated or publicly funded research.
- Lead sponsor
- University of Alabama at Birmingham
- Principal investigator
- Gaurav Goyal, Principal Investigator
University of Alabama at Birmingham
Central study contact
If you're interested in participating, the central contact can answer general questions about the study — including eligibility requirements and how to find a recruiting site near you. Actual eligibility is determined by the site's medical team.
- Gaurav Goyal, MD 📞 205-934-1816 ✉ ggoyal@uabmc.edu
Participating sites (1)
- University of Alabama at BirminghamRecruiting
Birmingham, Alabama, 35294 · United States
- Gaurav Goyal, MD · 2059346770 · ggoyal@uabmc.edu
Terms used on this page · explanations by MedicalUpdates.ai
- overall survival
- The length of time from the start of the study or treatment that participants are alive, whatever the cause of death.
- Inclusion Criteria
- The conditions a person must meet to be considered for the study, for example a confirmed diagnosis, an age range or a test result.
- Exclusion Criteria
- The conditions that rule a person out even if they meet the inclusion criteria, for example other illnesses, certain medicines or pregnancy.
The study record on this page is reproduced from ClinicalTrials.gov, a database of the U.S. National Library of Medicine, where it was submitted by the study sponsor. MedicalUpdates.ai does not own this content, is not affiliated with or endorsed by ClinicalTrials.gov, NIH, or the U.S. Government, and does not verify the record. Plain-language notes, the glossary and the questions above are added by this site; text in the boxes marked "AI summary" was written by an AI model and may contain errors. Registry records change over time. Check the original record for the current version and discuss eligibility or participation with a qualified healthcare professional.
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