Clinical Trials Directory

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UnknownNCT03733327

BUCYE Conditioning Regimen for PCNSL Undergoing Auto-HSCT

Busulfan+ Cyclophosphamide+ Etoposide Conditioning Regimen for Primary Central Nervous System Lymphoma Undergoing Autologous Hematopoietic Stem Cell Transplantation

Status
Unknown
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Nanfang Hospital, Southern Medical University · Academic / Other
Sex
All
Age
14 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the safety and efficacy of BUCYE conditioning regimens in primary central nervous system lymphoma undergoing autologous hematopoietic stem cell transplantation.

Detailed description

The prognosis of patients with primary central nervous system lymphoma (PCNSL) is poor. Recent studies have demonstrated that autologous hematopoietic stem cell transplantation (auto-HSCT) could improve the prognosis of these patients. However, the optimal conditioning regimen of auto-HSCT remains unclear. In this study, the investigators evaluated the safety and efficacy of BUCYE conditioning regimens in PCNSL undergoing auto-HSCT.

Conditions

Interventions

TypeNameDescription
DRUGBusulfan (BU)Busulfan was administered at 3.2 mg/kg/day on days-7 to -4.
DRUGCyclophosphamide (CY)Cyclophosphamide was administered at 60 mg/kg/day on days -3 to -2.
DRUGEtoposide (VP-16)Etoposide was administered at 15 mg/kg/day on days -3 to -2.

Timeline

Start date
2018-11-01
Primary completion
2021-10-01
Completion
2021-10-01
First posted
2018-11-07
Last updated
2018-11-07

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03733327. Inclusion in this directory is not an endorsement.