Study on the Treatment of Double/Triple-hit DLBCL With Chidamide and Lisaftoclax in Combination W… (NCT07552324) | Clinical Trial Compass
Not Yet RecruitingPhase 2
Study on the Treatment of Double/Triple-hit DLBCL With Chidamide and Lisaftoclax in Combination With Pola-R-CHP
28 participantsStarted 2026-05-01
Plain-language summary
This is an open-label, multicenter clinical study for patients aged 65 and above with double/triple-hit diffuse large B-cell lymphoma who are not suitable for transplantation. The study employs a 6-cycle CL-Pola-R-CHP regimen, with cycles repeated every 21 days.
Who can participate
Age range65 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Histopathological diagnosis confirmed as diffuse large B-cell lymphoma, with CD20 positivity;
* Double or triple hit confirmed by pathology;
* Age ≥ 65 years old;
* ECOG performance status score of 0, 1, or 2;
* No history of malignant tumor; no concurrent occurrence of other tumors;
* Patients whose life expectancy is at least 6 months, as determined by the researcher;
* The patient or their legal guardian must provide written informed consent before undergoing any special examinations or procedures in the study.
* International Prognostic Index (IPI) \> 1 point.
Exclusion Criteria:
* There is a history of other malignant tumors, excluding basal cell carcinoma and cervical carcinoma in situ;
* Accompanied by uncontrolled cardiovascular and cerebrovascular diseases, coagulation disorders, connective tissue diseases, severe infectious diseases, etc;
* Primary central nervous system lymphoma;
* Left ventricular ejection fraction (LVEF) is less than or equal to 50%;
* Laboratory test values during screening: (unless caused by lymphoma); A. Neutrophil count \<1.5\*10\^9/L; B. Platelet count \<75\*10\^9/L; C. ALT or AST is more than twice the upper limit of normal, and AKP and bilirubin are more than 1.5 times the upper limit of normal; D. Creatinine level is higher than 1.5 times the upper limit of normal;
* Other concurrent and uncontrolled medical conditions that the researcher believes will affect the patient's participation in the study.
* Patients wi…
What they're measuring
1
Complete remission (CR) rate
Timeframe: End of treatment visit (6-8 weeks after last dose on Day 1 of Cycle 6 [Cycle length=21 days]