Leukemia Clinical Trials

Find Leukemia Clinical Trials Near You

Safety and Efficacy Study of Demethylating Agents With Venetoclax in Preventing Recurrence of High-risk T-cell Lymphoblastic Lymphoma/Leukemia After Transplantation

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This study is a prospective, phase II clinical trial with the primary objective of assessing the effectiveness of demethylating agents combined with venetoclax in the prevention of recurrence after allogeneic hematopoietic stem cell transplantation (allo-HSCT) of high risk T-lymphoblastic lymphoma/leukemia (T-LBL/ALL) patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 14
Maximum Age: 55
Healthy Volunteers: f
View:

• 1.14-55 years old, male,or female.

• 2.Patients with allo-HSCT due to T-LBL/ALL, the donor type is not limited.

• 3.ECOG score is 0-2 points.

• 4.Blood routine: ANC ≥ 1.0 × 109/L, PLT ≥ 50 × 109/L.

• 5.One of the following high-risk factors:

• a. Age of initial diagnosis ≥ 35 years old.

• b. Initial diagnosis of WBC ≥ 100 × 109/L.

• c. Initial diagnosis of LDH exceeding the upper limit of normal values.

• d. Initial diagnosis of bone marrow involvement (blast cells ≥ 5%).

• e. Initial diagnosis of a bulky in the mediastinum (longest diameter ≥ 10cm).

• f. ETP immunophenotype.

• g. During the induction chemotherapy process, 2 courses did not achieve partial remission and/or 4 courses did not achieve complete remission.

• h. Residual lesions before transplantation: Flow cytometry analysis showed that the proportion of abnormal lymphoid cells in the bone marrow was greater than 0.01%; Positive detection of minimal residual lesions in molecular biology; PET-CT scan shows that residual lesions are still active.

• i. Based on the ELN recommendation based on adult T-ALL: gene mutations involving myeloid related genes, RAS/PI3K/AKT, JAK/STAT signaling pathway, and epigenetics, such as FLT3, NRAS/KRAS, PTEN, IL7R, JAK1, JAK3, DNMT3A, IDH1, IDH2; TP53, BCL2 mutations; t (8; 14) (q24; q11)/MYC rearrangement; t (7; 19) (q34; p13)/TCR-LYL1,TCR-MEF2C; del(5q) (q14).

• j. High risk subgroups based on NGS definition: PI3K signaling pathway/NRAS, KRAS/TP53/IKZF1/DNTM3A/IDH1, IDH2 gene mutation with or without NOTCH1, FBXW7/PHF6/EP300 gene mutation.

Locations
Other Locations
China
Shanghai General Hospital
RECRUITING
Shanghai
Contact Information
Primary
Xianmin Song
shongxm@139.com
+8613501672508
Time Frame
Start Date: 2024-10-30
Estimated Completion Date: 2028-10-30
Participants
Target number of participants: 59
Treatments
Experimental: combination therapy
There is only 1 arm. Combination therapy arm included venetoclax combined with hypomethylating agents such as azacitidine or decitabine. 1. venetoclax: 400mg/d, po, days 1-7 of each 28-day cycle. 2.For patients without TP53 mutation, azacitidine was administered: 32mg/m2/d, ih, days 1-5 of each 28-day cycle; for patients with TP53 mutation, decitabine was administered: 5mg/m2/d, iv, days 1-5 of each 28-day cycle.
Sponsors
Leads: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

This content was sourced from clinicaltrials.gov

Similar Clinical Trials