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Evaluation of the Diagnostic Value of PET (18F-FDG) in Chronic Graft Versus Host Disease (cGVH)

EVALUATION OF THE DIAGNOSTIC VALUE OF PET (18F-FDG) IN CHRONIC GRAFT VERSUS HOST DISEASE (cGVH)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02352064
Acronym
TEP-GVH
Enrollment
26
Registered
2015-02-02
Start date
2015-01-31
Completion date
2018-01-31
Last updated
2017-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Graft Versus Host Disease

Brief summary

Allogeneic stem cell transplantation was developed to cure many patients with hematological malignancies. It results in the development of graft versus host disease (GVHD) in 30-70% of cases. Chronic GVHD diagnosis currently uses biopsies of affected organs (skin, liver, gastrointestinal tract) and / or the observation of typical clinical signs sufficient for diagnosis. However, the anatomical sites for biopsy including the digestive tract are not clearly identified (high or low biopsy) and may present risks in their realization in particular in patients weakened by blood disease or immunosuppression. PET-CT with 18F-FDG has already been evaluated in chronic inflammatory diseases such as Crohns disease with good sensitivity and specificity. It interest in the graft against the host was studied in acute forms of digestive and allows lesion mapping and monitoring the effectiveness of treatment. Among patients with chronic GVHD scleroderma form, PET with 18F-FDG enabled to view musculoskeletal uptakes localized to the affected areas identified with MRI. The investigators propose a study evaluating the sensitivity and specificity of the examination by PET-CT with 18F-FDG in the diagnosis of chronic GVHD compared to conventional diagnostic tools.

Detailed description

Patients will have PET/CT at day 150+/-15d post-hematopoietic stem cell transplantation (HSCT)

Interventions

PROCEDUREPET (18-FDG)

Every patient will have a PET

Sponsors

University Hospital, Caen
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* adult \>18 years * Signed informed consent * subject covered by a social security system * Absence of contraindication to PET (18F-FDG) * Allogeneic stem cell transplantation

Exclusion criteria

* Adult patient under tutelage. * Pregnant or lactating women or women of childbearing potential not currently practicing an adequate method of contraception * Age\<18 years * Evolutive infectious disease * glycemia \>10mmol/L

Design outcomes

Primary

MeasureTime frameDescription
Measure of sensibility and specificity of PET (18F-FDG) for cGVH diagnosis in comparison to standard care5 monthsPresence of pathological 18-FDG uptakes on PET-CT examination in allografted patient compared with standard tests (clinical examination score GVHD, as defined by the NI (with or without targeted organ biopsy) Patient with negative PET-CT and without GVHD signs (NIH classification according to Filipovitch et al) are considered as true negative. Patient with positive PET-CT without GVHD signs are considered as false positive. Patient with clinical GVHD and negative PET-CT are considered as falsse negative and patients with clinical GVHD and positive PET-CT are true positive. The follow-up will determine if PET-CT is positive before the onset of clinical signs of GVHD.

Countries

France

Contacts

Primary ContactSylvain P Chantepie, MD
chantepie-s@chu-caen.fr+33231272073

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026