Lymphoblastic Lymphoma, Adult

2

Review clinical trials related to Lymphoblastic Lymphoma, Adult. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Thiotepa, Cyclophosphamide, Clarithromycin and Cytarabine

This study is an observational study on the efficacy and safety of auto-HSCT in adult patients with Burkitt lymphoma, lymphoblastic lymphoma, and acute lymphoblastic leukemia who received TCCA conditioning regimen. The study plans to include 28 patients who received the TCCA regimen for pre-transplantation pretreatment before auto-HSCT. Maintenance treatment will be carried out after transplantation for 1 year to observe the efficacy and safety.

Participants needed: 28
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Fifth Affiliated Hospital, Sun Yat-Sen UniversityUpdated: Mar 6, 2025Locations: 1
Eligibility criteria

1. Voluntarily sign the informed consent form, which must be signed by the patie...

Have a history of uncontrolled or symptomatic angina; [+7]

Status: Recruiting

BCL-2 Inhibitors Combined with the HyperCVAD Regimen for Newly Diagnosed T-lymphoblastic Leukemia/lymphoma.

The experimental group included patients diagnosed with T-ALL/LBL (T-lymphoblastic leukemia/ lymphoma) at initial diagnosis, who received treatment with BCL-2 inhibitors combined with the Hyper CVAD regimen. The control group consisted of patients diagnosed with T-ALL/LBL from multiple centers, for whom basic information, disease information, treatment details, and efficacy data were collected. Propensity score matching was conducted with historical data (matching factors included age, gender, initial LDH levels, and the presence or absence of a large mediastinal mass at diagnosis) to compare the advantages and disadvantages of the experimental regimen with previous induction treatment protocols. The primary endpoint was the complete remission (CR) rate after induction chemotherapy, while secondary endpoints included duration of remission (DOR), progression-free survival (PFS), overall survival (OS), and the occurrence of adverse events. This study aims to provide a more effective and safer treatment option for patients with T-LBL.

Participants needed: 206
Trial details
Phase: Phase 2Age: 18-60Biological sex: AllType: InterventionalSponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of MedicineUpdated: Sep 24, 2024Locations: 1
Eligibility criteria

Not listed