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Study identifier: NCT07014943 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

High-Dose Gemcitabine, Busulfan, and Thiotepa Followed by ASCT in Primary Central Nervous System Lymphoma

Condition: Primary Central Nervous System Lymphoma (PCNSL)  ·  Sponsor: Sichuan University

PhasePhase 2
Planned participants34
Who can joinAll sexes, 16 Years to 70 Years
Healthy volunteersNo

About this study

The goal of this single-arm, prospective study is to learn if high dose gemcitabine, busulfan and thiotepa with autologous stem cell transplantation to treat primary or relapse central nervous system lymphomas. It will learn about the safety and efficacy of combination therapy. The main question it aims to answer is: Efficacy and safety of the combination of high dose gemcitabine, busulfan and thiotepa as a bridging therapy to ASCT in patients with CNSL. Participants will: Take gemcitabine (2.5 g/m²) was administered intravenously (IV) on Days -9 and -3, Busulfan (3.2 mg/kg) was given IV over 3 hours on Days -9 to -7, and thiotepa (5 mg/kg) was administered IV on Days -5, -4, and -3. Peripheral stem cells were infused on Day 0. Visit the clinic for checkups and tests in accordance with the International Primary CNS Lymphoma Group (IPCG). Researchers will observe the patients receiving GemBuTT regimen as conditioning therapy in CNSL.

This description comes directly from the study's public registry record.

Talk to the study team

Jie Ji, MD  ·  86-28-85422373  ·  jieji@scu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

West China Hospital of Sichuan UniversityChengdu, Sichuan, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07014943