Linperlisib-based Treatment Regimen in Newly Diagnosed Nodal T-follicular Helper Cell Lymphoma (nTFHL)

Trial Title: Linperlisib-based Treatment Regimen in Newly Diagnosed Nodal T-follicular Helper Cell Lymphoma (nTFHL)

NCT ID: NCT06347653

Condition: Nodal T-follicular Helper Cell Lymphoma

Conditions: Official terms:
Lymphoma

Conditions: Keywords:
nodal T-follicular helper cell lymphoma
linperlisib
autologous hematopoietic stem cell transplantation
maintenance treatment

Study type: Interventional

Study phase: Phase 2

Overall status: Recruiting

Study design:

Allocation: N/A

Intervention model: Single Group Assignment

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: linperlisib combined with CHOP regimen
Description: Induction therapy: cyclophosphamide 750 mg/m2 day1, doxorubicin 40-50 mg/m2 day1, vincristine 1.4 mg/m2 (max 2 mg) day1, prednisone 100 mg day1-5, linperlisib 80mg once a day，day1-21, repeat every 21 days, for 6 cycle. Consolidation therapy: high dose chemotherapy followed by autologous hematopoietic stem cell transplantation. Maintenance therapy: linperlisib 80 mg day1-28, up to 12 cycles.
Arm group label: linperlisib combined with CHOP regimen

Summary: This study is conducted to evaluate the efficacy and safety of linperlisib combined with CHOP regimen followed by autologous hematopoietic stem cell transplantation and linperlisib monotherapy maintenance for newly diagnosed nTFHL patients.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Histologically confirmed nTFHL classified by WHO-HAEM5, including nodal TFH cell lymphoma, angioimmunoblastic-type, nodal TFH cell lymphoma, follicular-type, Nodal TFH cell lymphoma, NOS 2. Patients planning to receive autologous hematopoietic stem cell transplantation; 3. No previous systemic treatment before enrollment.; 4. There is at least one measurable lesion: the longest diameter (LDi) of the lymph node lesion is greater than 1.5 cm, or the LDi of one extra lymph node lesion is greater than 1 cm (according to the 2014 Lugano classification); 5. Age range from 18 to 65 years old, regardless of gender; 6. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS)≤2; 7. Expected survival time≥12 weeks; 8. Adequate bone marrow and organ functions; For female participants of childbearing period, a negative urine or serum pregnancy test should be performed with 1 week prior to receiving first dose of investigational drug (day 1 of cycle 1). If a urine pregnancy test result cannot be confirmed as negative, a blood pregnancy test is required.WOCBP subjects and male subjects whose partners are WOCBP should agree to use effective contraception from the time of signing the ICF until 6 months after the last dose of study drug. 9. Adequate organ and bone marrow function without severe hematopoietic abnormalities and abnormal heart, lung, liver, kidney, thyroid function and immunodeficiencies (no blood transfusion, granulocyte colony-stimulating factor or other related medical support within 14 days prior to administration of study drug): 1. Routine blood tests (not transfused, not on granulocyte colony-stimulating factor (G-CSF), not corrected with medication within 14 days prior to screening): hemoglobin (Hb) ≥ 90 g/L; neutrophils (ANC) ≥ 1.5 x 10 9/L; platelets (PLT) ≥ 100 x 109/L; 2. Biochemical tests: TBIL <1.5 × upper limit of normal range (ULN); glutamate alanine aminotransferase (ALT) and glutamate aspartate aminotransferase (AST) ≤2.5 × ULN; serum creatinine (Cr) ≤1.25 × ULN or endogenous creatinine clearance ≥60 mL/min (Cockcroft-Gault formula); 3. Coagulation (unless the subject is receiving anticoagulant therapy and coagulation parameters (PT/INR and APTT) are within the expected range for treatment with anticoagulants at screening): international normalized ratio (INR) ≤ 1.5 x ULN; activated partial thromboplastin time (APTT) ≤ 1.5 x ULN. 10. Volunteer to participate in clinical research and sign an informed consent form, willing to follow and capable of completing all trial procedures. Exclusion Criteria: If a patient has any of the following conditions should not be included in this study: 1. Known allergy to the active ingredients or excipients of linperlisib and CHOP regimens. 2. Patients with factors that affect oral medications (such as inability to swallow, chronic diarrhea, and intestinal obstruction); 3. Medical History and comorbidity 1. The subject had any active, known, or suspected autoimmune disease. Subjects who are in a stable state and do not require systemic immunosuppressive therapy are admitted; 2. Known history of interstitial pneumonia; 3. Current or previous history of other malignancies within 2 years prior to study enrollment.Radically treated basal cell carcinoma of the skin, papillary thyroid carcinoma, squamous skin carcinoma, carcinoma in situ of the breast and carcinoma in situ of the cervix, excepted 4. Received systemic antitumor therapy, including chemotherapy, immunotherapy, and biotherapy (tumor vaccines, cytokines, or growth factors used to control cancer) within 28 days prior to study enrollment. 5. Received autologous or allogeneic hematopoietic stem cell transplantation; 6. Patients with active tuberculosis (TB) should be excluded. 7. Severe acute or chronic infections requiring systemic treatment; 8. Patients with hypertension that is not well controlled with antihypertensive medications (systolic blood pressure ≥140 mmHg or diastolic blood pressure ≥90 mmHg) 9. Poor diabetes control (fasting blood glucose (FBG) > 10mmol/L); 10. Patients with heart failure (New York Heart Association standard Class III or IV), poor coronary artery disease control or arrhythmia, or a history of myocardial infarction within the 6 months prior to screening despite receiving appropriate medication; 11. Had clinically significant bleeding symptoms or definite bleeding tendency within 3 months before enrollment, such as gastrointestinal bleeding, hemorrhagic gastric ulcer, stool occult blood ++ or above at baseline, or vasculitis; 12. Renal failure requiring hemodialysis or peritoneal dialysis; 13. Urine routine indicated urinary protein ≥++, and 24-hour urinary protein quantity > 1.0 g； 14. Patients who have had major surgery or severe trauma have had the effects of the surgery or trauma resolved for less than 28 days prior to enrollment； 15. Complicated interstitial lung disease or history of severely impaired lung function; 16. Patients requiring systemic therapy with corticosteroids (> 10 mg/day of prednisone or equivalent) or other immunosuppressive agents within 14 days prior to administration of study drug. Inhaled or topical steroids and adrenal hormone replacement at doses > 10 mg/day prednisone efficacy dose are allowed in the absence of active autoimmune disease; 4. Physical and laboratory findings 1. A known history of human immunodeficiency virus (HIV) infection (i.e., HIV antibody positive). 2. Active hepatitis [Hepatitis B: Hepatitis B virus (HBV) deoxyribonucleic acid (DNA) positive and ALT above the upper limit of detection; Hepatitis C: Hepatitis C virus (HCV) ribonucleic acid (RNA) positive and ALT above the upper limit of detection]; co-infection with Hepatitis B and Hepatitis C; 5. Any medical history or disease evidence that may interfere with the study results or other conditions that investigators consider inappropriate for the study. 6. Pregnant or lactating women.

Gender: All

Minimum age: 18 Years

Maximum age: 65 Years

Healthy volunteers: No

Locations:

Facility:
Name: Bejing Cancer Hospital

Address:
City: Beijing
Country: China

Status: Recruiting

Contact:
Last name: PING WEI LIU, master

Phone: 0086-13522796323

Start date: November 28, 2023

Completion date: January 31, 2030

Lead sponsor:
Agency: Peking University
Agency class: Other

Source: Peking University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06347653