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CHiR Therapy for Elderly DLBCL Intolerant to Chemo

F

First Affiliated Hospital of Ningbo University

Status and phase

Enrolling
Phase 2

Conditions

Diffuse Large B-Cell Lymphoma

Treatments

Drug: CHiR-DEL

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT06764017
2024-164A-02

Details and patient eligibility

About

The objective of exploring the application of CHiR is to evaluate its therapeutic efficacy and safety in newly diagnosed elderly patients with diffuse large B-cell lymphoma (DLBCL) aged 70 and above, and to investigate the genetic subtypes that may benefit from CHiR. The primary endpoint is the complete remission rate (CRR) at the end of 8 cycles.

Enrollment

30 estimated patients

Sex

All

Ages

70 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  1. Age ≥ 70 years;
  2. ECOG score of 0-3;
  3. Rated as unfit or frail on the simplified geriatric assessment (sGA);
  4. Histologically confirmed CD20-positive diffuse large B-cell lymphoma (diagnostic criteria according to WHO 2016), excluding transformed type 2 DLBCL;
  5. Immunohistochemically confirmed positive expression of MYC and BCL2 (MYC ≥ 40%, BCL2 ≥ 50% by immunohistochemistry);
  6. Previously untreated patients;
  7. Cardiac, hepatic, and renal function: creatinine < 2 times the upper limit of normal (ULN); ALT (alanine aminotransferase)/AST (aspartate aminotransferase) < 2.5 ULN; total bilirubin < 2 ULN;
  8. At least one measurable lesion;
  9. Unable to tolerate standard CHOP regimen chemotherapy or unwilling to receive chemotherapy;
  10. Adequate understanding and voluntary signing of the informed consent form. Exclusion Criteria:

1.Patients with central nervous system involvement at the time of onset; 2.Known human immunodeficiency virus (HIV) infection; 3.Pregnant or lactating women; 4.Other tumors requiring treatment; 5.Uncontrollable active infection; 6.Active hepatitis with HBV-DNA copy number not controlled within 2*1000/mL despite antiviral treatment; 7.Inability to understand, comply with the study protocol, or sign the informed consent form.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

CHiR
Experimental group
Description:
The combined regimen of chidamide, zanubrutinib, and lenalidomide (CHiR) is employed to treat elderly patients with double-expressor lymphoma. This study aims to explore the efficacy and safety of this regimen in newly diagnosed elderly patients with diffuse large B-cell lymphoma (DLBCL) who are intolerant to chemotherapy.
Treatment:
Drug: CHiR-DEL

Trial contacts and locations

1

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Central trial contact

Lixia Chief Physician

Data sourced from clinicaltrials.gov

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