Study of Chidamide, Decitabine and Immune Checkpoint Inhibitors in R/R NHL and Advanced Solid Tumors

Advanced Solid Tumors Clinical Trial

Official title:

A PhaseⅠ/Ⅱ Trial of Chidamide，Decitabine and Immune Checkpoint Inhibitors in Relapsed/Refractory Non-Hodgkin Lymphoma and Advanced Solid Tumors

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05320640
• Other study ID #: CHN-PLAGH-BT-069
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: March 30, 2022
• Est. completion date: April 1, 2025

Study information

• Verified date: April 2022
• Source: Chinese PLA General Hospital
• Contact: Weidong Han, Professor
• Phone: +86-10-55499341
• Email: hanwdrsw[@]163.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase I/II trial aims to evaluate safety and efficacy of Chidamide, Decitabine and Immune checkpoint inhibitors in relapsed/refractory Non-Hodgkin Lymphoma and advanced solid tumors.

Description:

Chidamide is a novel and orally active benzamide class of HDAC inhibitor that selectively inhibits activity of HDAC1, 2, 3 and 10, which can induce tumor-cell apoptosis, suppress cell proliferation and enhance immune surveillance. Low-dose decitabine inhibits the activity of DNA methyltransferase, which can increase the expression of tumor antigens and HLA molecules, enhance antigen processing, promote T cell infiltration, and boost effector T cell function. Immune checkpoint inhibitors (ICIs) have emerged as effective therapies for many cancers by promoting the reactivation and restoring function of T cells. In conclusion, we speculate that the chemotherapy free regimen of Chidamide, Decitabine and Immune checkpoint inhibitors may explore a new avenue for therapeutic intervention in relapsed/refractory Non-Hodgkin Lymphoma and advanced solid tumors.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: April 1, 2025
• Est. primary completion date: April 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 16 Years to 80 Years

Eligibility

Inclusion Criteria:

1. 16 to 80 years of age.

2. ECOG performance of less than 3.

3. Life expectancy of at least 3 months.

4. Histopathological confirmed Non-Hodgkin Lymphoma and solid tumors.

5. Patients are relapsed/refractory Non-Hodgkin Lymphoma with ineligible for autologous hematopoietic stem cell transplantation.

6. The guidelines(ASCO/CSCO)recommend patients to participate in clinical trials.

7. Subjects must have at least one measureable target lesion.

8. Willingness to provide written informed consent for the study.

Exclusion Criteria:

1. Active, known or suspected autoimmune diseases.

2. Subjects are being treated with either corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of enrollment.

3. History of severe hypersensitive reactions to other monoclonal antibodies.

4. History of allergy or intolerance to study drug components.

5. Substance abuse, medical, psychological or social conditions that may interfere with the patient's participation in the study or evaluation of the study results.

6. History or concurrent condition of interstitial lung disease of any grade or severely impaired pulmonary function.

7. Uncontrolled intercurrent illness, including ongoing or active systemic infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia (excluding insignificant sinus bradycardia and sinus tachycardia) or psychiatric illness/social situations and any other illness that would limit compliance with study requirements and jeopardize the safety of the patient.

8. History of human immunodeficiency virus (HIV) infection or acquired immunodeficiency syndrome (AIDS).

9. Pregnant or breast-feeding. Women of childbearing potential must have a pregnancy test performed within 7 days before the enrollment, and a negative result must be documented.

10. Vaccination within 30 days of study enrollment.

11. Active bleeding or known hemorrhagic tendency.

Related Conditions & MeSH terms

• Advanced Solid Tumors
• Lymphoma
• Lymphoma, Non-Hodgkin
• Relapsed/Refractory Non-Hodgkin Lymphoma

Intervention

Drug:
• Chidamide
Chidamide is a novel and orally active benzamide class of HDAC inhibitor that selectively inhibits activity of HDAC1, 2, 3 and 10, which can induce tumor-cell apoptosis, suppress cell proliferation and enhance immune surveillance.
• Decitabine
Low-dose decitabine inhibits the activity of DNA methyltransferase, which can increase tumor antigens and HLA expression, enhance antigen processing, promote T cell infiltration, and boost effector T cell function.
• Immune checkpoint inhibitors(anti-PD1/PD-L1/CTLA4 antibodies)
Immune checkpoint inhibitors (ICIs) have emerged as effective therapies for many cancers by promoting the reactivation and restoring function of T cells.

Locations

Country	Name	City	State
China	Biotherapeutic Department, Chinese PLA General Hospital	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Chinese PLA General Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Biomarkers predictive of response	Biomarkers from tumor cells, lymphocytes and tumor microenvironment will be assessed for their potential in predicting clinical response.	3 years
Primary	Objective response rate (ORR)	The percentage of patients with CR or PR was determined according to the revised lymphoma efficacy evaluation criteria (Lugano 2014 criteria) and Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).	3 years
Primary	Adverse events	Incidence, nature, and severity of adverse events are graded according to the National Cancer Institute Common Terminology Criteria for adverse events (version5.0).	3 years
Secondary	Duration of response (DOR)	Time from the first recording of CR or PR evidence to disease progression or death from any cause was determined according to the revised lymphoma efficacy evaluation criteria (Lugano 2014 criteria) and Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1).	3 years
Secondary	Progression-free survival (PFS)	Time from the date of first administration of the study drug to disease progression or death from any cause.	3 years