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RecruitingNCT07895927BL-TOXUpdated Oct 26, 2026

Toxicity of Intensive First-Line Treatment for Adult Burkitt Lymphoma: A Retrospective Observational Study

An observational study in Adult Burkitt Lymphoma, Chemotherapy-Related Toxicity and Overall and Progression-Free Survival, sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-26.

Sponsored by University Hospital, Strasbourg, France · Observational

From the registry’s dates

  • Started Feb 2026; still recruiting 8 months later.
Updated Oct 26, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
25
Ages
18 Years and older
Sex
All
01

Study summary

Burkitt lymphoma is a rare, highly aggressive B-cell non-Hodgkin lymphoma in adults. Although intensive multi-agent chemotherapy can achieve high complete remission rates, it is associated with substantial toxicity, morbidity, and sometimes treatment-related mortality. This retrospective, single-center observational study aims to characterize the short- and long-term complications of intensive first-line treatment in adults with Burkitt lymphoma managed at Strasbourg University Hospitals.

The study will evaluate treatment-related toxicities, overall survival at five years, and progression-free survival at 24 months. Secondary objectives include assessing treatment delays, chemotherapy dose reductions, and their associations with toxicity, disease location at diagnosis, and survival.

All eligible adult patients diagnosed with Burkitt lymphoma or managed for this condition at Strasbourg University Hospitals and the ICANS between January 1, 2009, and December 31, 2025, will be considered. The study will use retrospective medical record data, with no a priori sample size calculation because of the rarity of the disease and the single-center design.

02

Conditions studied

  • Adult Burkitt Lymphoma
  • Chemotherapy-Related Toxicity
  • Overall and Progression-Free Survival

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Keywords

  • Burkitt Lymphoma
  • Intensive First-Line Treatment
  • Treatment-Related Toxicity
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In context

Burkitt Lymphoma

407 studies on the registry are indexed under Burkitt Lymphoma; 117 are open to participants now.

This study's planned enrollment of 25 is below the median of 203 across 27 observational studies indexed under Burkitt Lymphoma.

Browse Burkitt Lymphoma studies →

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 994 studies on the registry; 353 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
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Adult patients with Burkitt lymphoma managed at Strasbourg University Hospitals and/or ICANS between January 1, 2009, and December 31, 2025, whose medical records are available and who meet the eligibility criteria

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 or older.
  • Patients diagnosed with Burkitt lymphoma at Strasbourg University Hospitals between January 1, 2009, and December 31, 2025, and/or managed by the Hematology Department of Strasbourg University Hospitals or ICANS for Burkitt lymphoma during this period.
  • No written objection documented in the medical record to the reuse of personal data for scientific research.

Exclusion criteria

Exclusion Criteria:

  • Patients who have objected to the reuse of their personal data for scientific research.
  • Patients diagnosed with another B-cell non-Hodgkin lymphoma other than Burkitt lymphoma.
  • Patients for whom accessible data are unavailable.
  • Individuals under legal protection (sauvegarde de justice).
  • Individuals under guardianship or curatorship (tutelle or curatelle).
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Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
25 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Treatment-Related Toxicity

    Incidence of different toxicities during intensive first-line treatment for adult Burkitt lymphoma

    Time frame: Retrospective assessment of patients treated between January 1, 2009, and December 31, 2025

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Study locations

1 of 1 sites recruiting
  • Service d'Hématologie et d'Oncologie - CHU de Strasbourg, France
    Strasbourg, 67091, France
    Recruiting
08

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 26, 2026
Show all 1 update
  1. Oct 26, 2026
    First appeared on the registry

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
NCT07895927
Responsible party
Sponsor
First posted
Oct 26, 2026
Start date
Feb 11, 2026
Primary completion
Feb 11, 2027 (estimated)
Completion
Apr 11, 2027 (estimated)
Last update
Oct 26, 2026

Study contacts

Marie-Pierre Marie-Pierre, MD
Contact
mariepierre.ledoux@chru-strasbourg.fr
33 3 68 76 74 07

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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