Overview

CHP-BV Followed by Consolidation With High-dose Therapy / ASCT as Frontline Treatment of Patients With EATL Type 1.

Status:
Recruiting

Trial end date:
2024-02-06

Target enrollment:
0

Participant gender:
All

Summary

It has been recently reported that EATL type 1, but not refractory coeliac disease, strongly expressed CD30 and might benefit from brentuximab vedotin. Since the safety profile of the combination brentuximab vedotin and CHP is known and since the role of etoposide as part of induction regimen is not demonstrated, the investigator will assess the efficacy and toxicity of the combination brentuximab vedotin and CHP followed by HDT/ASCT, as frontline treatment of EATL.

Phase:

Phase 2

Accepts Healthy Volunteers?

Details

Lead Sponsor:

Imagine Institute

Collaborator:

Takeda

Treatments:

Antibodies, Monoclonal
Brentuximab Vedotin

Criteria

Main Inclusion Criteria:

1. Histologically confirmed diagnosis of EATL based on criteria established by the World
Health Organization (WHO) 2016 Classification of Tumors of Haematopoietic and Lymphoid
Tissues.

2. EATL should be CD30-positive with a threshold of 10%.

3. Patients aged ≥ 18 years and < 70 years at the time of study entry.

4. ECOG performance status 0 to 3 at time of study entry.

5. Left Ventricular Ejection Fraction (LVEF) ≥ 45% measured by bidimensional echography
or radionuclide ventriculography (MUGA scan).

Main Exclusion Criteria:

1. Participants must not have been treated with any prior chemotherapy for EATL. Patients
with previous treatment for refractory celiac disease (i.e., immunosuppressive or
immunoregulatory drugs) may be included.

2. Known central nervous system involvement by EATL.

3. Active chronic hepatitis B or C.

4. HIV positive serology.

5. HTLV-1 positive serology.