refractory/relapsed follicular lymphoma
Conditions
Interventions
Group1:Chidamide combined with Linperlisib
Sponsors
The First Aiffiliated hosptical of xiamen University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1.The patients diagnosed as follicular lymphoma with grade 1-3a, have received at least second-line systemic treatment, and at least one of the first-line treatments includes CD20 monoclonal antibody (CD20 monoclonal antibody monotherapy or combined chemotherapy).If the latest histopathological diagnosis is more than 6 months, lymph node or tissue puncture or biopsy (resection or coarse needle puncture) must be performed. 2.Age =18 years old, regardless of gender. 3.The estimated survival time is more than 3 months. 4.ECOG = 2 5.Be able to follow the requirements of the research plan: 6.The patients have at least one measurable lesion (any length of lymph node lesion > 1.5cm or any length of extranodal lesion > 1 cm) examined by computed tomography (CT)/ magnetic resonance imaging (MRI). 7.Be able to understand and voluntarily provide informed consent.
Exclusion criteria
Exclusion criteria: 1.CNS involvement (current or previous). 2.clinical evidence of transformation to a more aggressive subtype of lymphoma 3.Impaired bone marrow function : neutrophils 1.5 x ULN or serum ALT and AST > 2.5x ULN, Patients with liver infiltration by lymphoma, AST and ALT > 5x ULN, Renal glomerular filtration rate (eGFR) 1.5ULN or APTT> 1.5 ULN, Serum amylase or lipase > 1ULN 5.patients with active infection of human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV), if patients with HBV infection with HBsAg or hepatitis B core antibody (HBcAb) positive] but HBV DNA negative can be included, However,these patients need continuous antiviral treatment and HBV DNA PCR detection every cycle after enrollment 6.patients with CMV infection (IgM positive or CMV DNA was positive by PCR.) 7.Meet any of the following criteria related to visceral function: all kinds of clinically significant abnormal rhythm or conduction need clinical pre-diagnosis Hereditary QT interval syndrome or QTcF>480 msec or taking drugs that may cause Qt interval delay or torsade de pointes. A variety of clinically significant cardiovascular diseases, including acute myocardial infarction, unstable angina and coronary artery bypass grafting in the first 6 months of the group, with new york's cardiology (NYHA) classification of grade 3 or above. Left ventricular ejection fraction (LVEF ) 160 mmHg or diastolic blood pressure > 100 mgHg). 8.Have a history of stroke or intracranial hemorrhage within 6 months before drug administration for the first time 9.Major surgery was performed within 4 weeks before enrollment 10.Any PI3K inhibitor has been used before and the disease has progressed during the treatment period (within 6 months after the last use) 11.Received systemic anti-tumor therapy or radiotherapy within 4 weeks before enrollment. 12.The last time you participated in clinical trials of other drugs before enrollment was less than 2 weeks or the last time you used small molecular drugs (such as antibody drugs) was less than 4 weeks 13.The patients received the transplantation of somatic hematopoietic stem cells within 3 months before enrollment. 14.patients received allogeneic hematopoietic stem cell transplantation or having any active graft-versus-host disease within 6 months before drug administration. 15.Take a strong inducer or inhibitor of cytochrome P4503A4 (CYP3A4) within 2 weeks before the first drug administration (3 weeks for Hypericum perforatum) 16.Before the first drug administration, the toxic reaction of previous anti-tumor therapy has not recovered to =1 level (except alopecia) 17.patients with uncontrolled systemic infection requiring intravenous antibiotic treatment 18.Currently suffering from other primary tumors that need active treatment according to the guidelines 19. Inability to take drugs orally, previous surgical history or serious gastrointestinal diseases such as dysphagia and active gastric ulcer may affect the absorption of drugs 20.pregnant (serum pregnancy test results are positive) or lactating women 21.Any other diseases, abnormal metabolism, abnormal physical examination or abnormal laboratory examination with significant clinical significance, according to the researcher's judgm
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| complete response; | — |
Secondary
| Measure | Time frame |
|---|---|
| overall response;Progressive free survival;Overall survival ; | — |
Countries
China
Contacts
Public ContactBing Xu
The First Aiffiliated hosptical of xiamen University
Outcome results
None listed