Sintilimab Combined With Chidamide in Treating Peripheral T Cell Lymphoma

Inclusion Criteria:

1. Age range from 18 to 75 years;

2. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2;

3. Pathologically confirmed relapsed/refractory Peripheral T-cell lymphoma (IncludingPTCL-NOS, AITL, anaplastic large cell lymphoma（ALTL）, excluding Nature Killer（NK）/Tcell lymphoma);

4. At least one two-dimensional measurable lesion with a length diameter of at least 1.5cm and vertical diameter of at least 1.0cm (measured by CT or MRI);

5. Adequate medullary hematopoiesis function ( WBC≥3.5×109/L, ANC≥1.5×109/L,PLT≥80×109/L, HB≥90g/L. If the peripheral blood indicators demonstrate abnormal dueto bone marrow or spleen invasion by lymphoma, Enrollment decision can be determinedby the investigator as appropriate;

6. Adequate hepatic function (total serum bilirubin, ALT and AST≤1.5 times of upperlimit of normal);

7. Adequate renal function (serum creatinine≤1.5 times the upper limit of normal,creatinine clearence≥50ml/min);

8. Echocardiography or radionuclide cardia functional test, LVEF≥50%;

9. Patients of child-bearing period agree to use appropriate contraception. The serumpregnancy test of women in childbearing period was negative within 2 weeks beforeenrollment.

10. Willingness to provide pathological tissue specimens (20 pieces of wax or paraffintissue sections);

11. Expectation survival time over 3 months;

12. Willingness to provide written informed consent.

Exclusion Criteria:

1. Patients allergic of any drug in this regimen;

2. Previous treatment with anti-PD-1 antibody combined with HDAC inhibitor (Patientsonly received single agent of treatment regime or sequentially received anti-PD-1and HDAC inhibitor are allowed to enroll);

3. Patients with clinically significant heart disease, including severe cardiacinsufficiency: New York Heart Disease Association (NYHA) grade IV cardiacinsufficiency, unstable angina. And myocardial infarction, congestive heart failure,and QTC interphase > 500ms which occurred before 6 month of screening;

4. Patients who have received grade II or above surgery within 3 weeks beforeenrollment;

5. History of other malignancy within the past 5 years (except for 1. basal cellcarcinoma of the skin and 2. carcinoma in situ of the cervix and 3. patients who hadreceived treatment for the purpose of cure and had not developed a malignant tumorwith a known active disease in the previous 5 years);

6. Patients who had received other antitumor therapy (including corticosteroid therapy,immunotherapy) or participated in other clinical studies within 4 weeks before thestart of the enrollment (if patients received small-molecule targeted drug therapy,they could be included in the study if the drug was discontinued for more than 5half-lives), or had not recovered from the previous toxicity;

7. Patients with significant coagulation abnormality;

8. Patients with autoimmune diseases requiring treatment or with a history of syndromerequiring systemic use of steroid immunosuppressive agents, such as hypophysitis,pneumonia, colitis, hepatitis, nephritis, hyperthyroidism, hypothyroidism, etc;

9. Other serious, uncontrolled concomitant diseases that may affect protocol complianceor interfere with results interpretation, including uncontrolled diabetes, orpulmonary disease (a history of interstitial pneumonia, obstructive pulmonarydisease, and symptomatic bronchospasm);

10. Evidence of central nervous system disease;

11. Patients who received the live vaccine within 4 weeks of the start of theenrollment;

12. Patients with hepatitis B (HBV HBsAg positive and HBV-DNA≥105), hepatitis C (HCV)infection (HCV antibody positive and HCV-RNA detectable); And subjects with otheracquired or congenital immune deficiency diseases, including but not limited tohiv-infected;

13. Pregnant or lactating women;

14. Patients who have had previous organ transplants (except autologous hematopoieticstem cell transplants);

15. Severe or uncontrolled infections;

16. Patients with history of severe neurological or psychiatric illness, includingdementia or epilepsy;

17. Patients with drug abuse, medical, psychological or social conditions that mayinterfere with the study results or the assessment of the study results;

18. Patients are unsuitable for the enrollment according to investigator's judgement.