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A Study Comparing Corticosteroids Alone Versus Corticosteroids and Extracorporal Photopheresis (ECP) as First-line Treatment of Standard II Acute Graft-versus-host Disease

A Multi-center Randomized Phase II Study Comparing Corticosteroids Alone Versus Corticosteroids and Extracorporal Photopheresis (ECP) as First-line Treatment of Standard Risk Grade II Acute Graft-versus-host Disease After Allogeneic Stem Cell Transplantation

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03605940
Acronym
PCE-aGVHD
Enrollment
78
Registered
2018-07-30
Start date
2018-10-01
Completion date
2022-04-01
Last updated
2018-07-30

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

Conditions

Acute-graft-versus-host Disease

Keywords

Acute-graft-versus-host Disease, Extracorporal Photopheresis

Brief summary

Acute graft versus host-disease remains a major cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation. The incidence of grade II to IV acute GVHD ranges from 30 to 50% of the patients transplanted. Steroids remain the standard first line treatment for acute GVHD. Prolonged exposure to steroids is associated to increased risk of infections and of osteoporosis, osteonecrosis and alteration of growth in children. Thus, reducing steroid exposure in order to reduce treatment-related morbidity is another important goal in the management of standard risk aGVHD. Extracoporeal photopheresis (ECP) is active in controlling steroid refractory or dependent acute GVHD. Hypothesis: In this study, the team hypothesizes that addition of ECP to first line treatment with 2 mg/kg steroids of standard risk grade II aGVHD can reduce steroid exposure by increasing the probability of 6 month FFTF including absence of systemic steroids for chronic GVHD.

Interventions

COMBINATION_PRODUCTMethoxsalen + ECP device

2 sessions per week during 4 weeks and 1 session per week during 8 weeks

DRUGCorticosteroids

2 mg/kg/day

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Age ≥ 18 years ; * Having received an allogeneic stem cell transplantation for any malignant or non-malignant hemopathy and whatever the type of donor and graft. * with grade II acute GVHD with skin involvement (stage 1-3 skin +/- stage 1 gastro intestinal) in the 3 months following the allogeneic stem cell transplantation * acute GVHD in the first line treatment * validation of the presence of peripheral or central venous access allowing to perform 2 ECP per week during 3 months. In the absence of a pre-existing and adpated central catheter at the time of inclusion, peripheral venous access will be preferred * Leucocytes \> 1.5 G/L * Platelets \> 30 G/L, Haematocrite \> 27% (allowed transfusions) * Patient affiliated to a French Social Security regimen * information consent form signed.

Exclusion criteria

* acute GVHD of grade I * acute GVHD of grade \> II * progressive hematologic disease at inclusion * uncontrolled ongoing infection at time of inclusion: bacterial or fungal infections, increasing CMV viral load. * patient with HIV positivity or replicative HBV or HCV infection * Contraindications for UVADEX / photopheresis / stéroids / posaconazole / heparin * Patient with a history of deep venous thrombosis * Pregnancy * Women of child bearing potentiel not using contaception

Design outcomes

Primary

MeasureTime frame
Probability of being free of treatment failure (probability of survival without relapse, additional line of treatment for aGVHD and systemic therapy for chronic GVHD)6 months

Secondary

MeasureTime frame
Total T cells numberMonth 3 - Month 6 - Month 12
mean of the cumulative dose of steroidsMonth 1- Month 2 - Month 3 - Month 6 - Month 12
cumulative incidence rate of infectionsMonth 6 - Month 12
cumulative incidence of thromboembolic complicationsMonth 3
incidence of chronic GVHDMonth 6 - Month 12
severity of chronic GVHDMonth 6 - Month 12
incidence rate of non-relapse mortalityMonth 6 - Month 12
scores of health-related quality of life using the French validated FACT-BMTMonth 3 - Month 6 - Month 12
disease-free survivalMonth 6 - Month 12
overall survivalMonth 6 - Month 12
CD4 T cells numberMonth 3 - Month 6 - Month 12
CD8 T cells numberMonth 3 - Month 6 - Month 12
B cells numberMonth 3 - Month 6 - Month 12
NK cells numberMonth 3 - Month 6 - Month 12
gamma globulin numberMonth 3 - Month 6 - Month 12
incidence of disease relapseMonth 6 - Month 12

Contacts

Primary ContactMarie-Thérèse RUBIO, PU-PH
m.rubio@chru-nancy.fr0383153282

Outcome results

None listed

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