A Study of BEBT-908 in Combination With Chemotherapy in Patients With Previously Untreated Peripheral T-Cell Lymphoma (PTCL)

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Participants must meet all of the following inclusion criteria:

1. Participants must fully understand the study and voluntarily sign an informed consent form (ICF).
2. Age 18 to 75 years (inclusive), either sex.
3. Histologically confirmed peripheral T-cell lymphoma (PTCL), including not otherwise specified (PTCL-NOS), angioimmunoblastic T-cell lymphoma (AITL), anaplastic large cell lymphoma (ALCL) deemed by the investigator to be ineligible for or unable to receive anti-CD30 monoclonal antibody therapy (e.g., brentuximab vedotin) due to economic burden or intolerable toxicity (if ALK-positive, International Prognostic Index [IPI] score must be ≥2), subcutaneous panniculitis-like T-cell lymphoma (SPTCL), enteropathy-associated T-cell lymphoma (EATL), hepatosplenic T-cell lymphoma (HSTL), and other T-cell lymphomas deemed appropriate for enrollment by the investigator.
4. No prior systemic anti-PTCL therapy.
5. Life expectancy >6 months.
6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
7. At least one measurable and evaluable tumor lesion (per Lugano 2014 criteria: nodal lesions must have a longest diameter >1.5 cm; extranodal lesions must have a longest diameter >1.0 cm).
8. At screening, laboratory parameters must meet the following standards, unless the investigator determines the abnormality is due to lymphoma (with no corrective or supportive treatment for the following parameters within 2 weeks prior to assessment):

Peripheral Blood: a) Absolute Neutrophil Count (ANC) ≥1.5×10⁹/L (≥1.0×10⁹/L for patients with bone marrow involvement); b) White Blood Cell count (WBC) ≥3.0×10⁹/L (≥2.0×10⁹/L for patients with bone marrow involvement); c) Hemoglobin (HGB) ≥80 g/L; d) Platelet count (PLT) ≥75×10⁹/L (≥50×10⁹/L for patients with bone marrow involvement).

Hepatic and Renal Function: a) Serum total bilirubin ≤1.5×Upper Limit of Normal (ULN) (≤3.0×ULN for patients with liver involvement); b) Serum creatinine \<1.5×ULN; c) Alanine Aminotransferase (ALT) and Aspartate Aminotransferase (AST) ≤2.5×ULN, or ≤5×ULN if the investigator determines the elevation is due to hepatic infiltration.

Exclusion Criteria:

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Participants who meet any of the following exclusion criteria are not eligible for enrollment:

1. History or current diagnosis of immune thrombocytopenia, autoimmune hemolytic anemia, aplastic anemia, or other primary or secondary hematologic disorders that may affect bone marrow function, other than the primary malignancy.
2. Receipt of transfusion, recombinant human thrombopoietin (rhTPO), erythropoietin (EPO), granulocyte colony-stimulating factor (G-CSF), or similar treatments within 2 weeks prior to the first dose of study drug.
3. Active bleeding within 2 months prior to the first dose, or current use of anticoagulant medications (e.g., warfarin, phenprocoumon), or evidence of a clear bleeding tendency as determined by the investigator (e.g., esophageal varices at risk of bleeding, active localized ulcerative lesions, fecal occult blood >2+), except for bleeding attributed by the investigator to lymphoma itself (e.g., gastrointestinal bleeding caused by gastrointestinal lymphoma).
4. Participation in another interventional clinical trial within 3 months prior to the first dose.
5. PTCL with involvement of special sites such as testis, breast, or ovary; extranodal natural killer/T-cell lymphoma (ENKTL); cutaneous T-cell lymphoma (except subcutaneous panniculitis-like T-cell lymphoma [SPTCL]); or concurrent hemophagocytic lymphohistiocytosis (HLH).
6. Receipt of the following treatments within 7 days prior to study entry: drugs known to be strong cytochrome P450 3A4 (CYP3A4) inhibitors or inducers, or drugs known to significantly prolong the QT interval.
7. Major surgery requiring general anesthesia within 4 weeks prior to enrollment, or surgery requiring local/epidural anesthesia within 2 weeks prior to enrollment with incomplete recovery (excluding bone marrow biopsy or local lymphoid tissue biopsy).
8. Active infection requiring systemic treatment (oral or intravenous) within 2 weeks prior to the first dose, or imaging findings suggestive of interstitial lung disease (ILD), pulmonary fibrosis, or pneumonia (infectious or non-infectious) requiring treatment: participants receiving prophylactic antibiotic therapy (e.g., for interstitial pneumonia) are eligible for enrollment; participants with patchy changes from old or previously treated lesions, determined by the investigator to not affect lung function and not require treatment, are eligible for enrollment.

9. Corticosteroid use >30 mg/day prednisone or equivalent for purposes other than lymphoma symptom control; the following permitted scenarios must meet corresponding requirements:

   If currently receiving corticosteroid therapy at ≤30 mg/day prednisone or equivalent, documented evidence of stable dosing for at least 4 weeks prior to initiation of study drug is required.

   If urgent corticosteroid therapy is needed prior to the first dose to control lymphoma symptoms, prednisone up to 100 mg/day or equivalent may be used for a maximum of 7 days; however, all tumor assessments must be completed before initiation of corticosteroid therapy.

10. Mean corrected QT interval (QTc) >450 msec (male) or >470 msec (female) derived from 3 electrocardiogram (ECG) recordings at rest (repeat testing and averaging of 3 corrected values is required only when the first ECG indicates QTc >450 msec [male] or >470 msec [female]); history of long QT syndrome or confirmed family history of long QT syndrome; history of clinically significant ventricular arrhythmia, or current use of antiarrhythmic drugs or implanted defibrillator for treatment of ventricular arrhythmia.
11. Inability to discontinue during the study period medications that may cause QT prolongation (e.g., antiarrhythmic drugs).
12. Tumor invasion of surrounding vital organs or vessels (e.g., heart and pericardium, trachea, esophagus, aorta, superior vena cava) with risk of bleeding, or risk of esophagotracheal fistula or esophagopleural fistula.
13. Participants with clinically symptomatic pleural effusion, ascites, or pericardial effusion that remains poorly controlled despite repeated treatment.
14. Comorbid conditions: a) Cerebrovascular accident within 6 months prior to the first dose, or history of deep vein thrombosis (DVT), arterial thrombosis, or pulmonary embolism (PE). b) History of other malignancy within 3 years prior to enrollment that does not meet criteria for clinical cure. Exceptions: locally treatable and cured basal cell carcinoma or squamous cell carcinoma of the skin, superficial bladder cancer, cervical carcinoma in situ, ductal carcinoma in situ of the breast, and papillary thyroid carcinoma. c) Concurrent central nervous system (CNS) lymphoma or meningeal involvement, or history of or current CNS disorders including but not limited to: epilepsy, paralysis, stroke, severe brain injury, dementia, Parkinson's disease, cerebellar disease, organic brain syndrome. d) Poorly controlled diabetes mellitus (random blood glucose ≥11.1 mmol/L despite anti-diabetic treatment, or glycated hemoglobin [HbA1c] ≥8.5%). e) Uncontrolled hypertension [systolic blood pressure (SBP) ≥160 mmHg and/or diastolic blood pressure (DBP) ≥100 mmHg despite standard treatment, or history of hypertensive crisis or, hypertensive encephalopathy, or history of cerebrovascular accident]. f) Significant cardiac disease [including any of the following: 1) congestive heart failure above NYHA Class II (i.e., Class III or IV), unstable angina, symptomatic pericarditis, or myocardial infarction within 6 months prior to the first dose of study drug; 2) arrhythmia requiring treatment, or left ventricular ejection fraction (LVEF) \<50% at screening; 3) primary cardiomyopathy (e.g., dilated cardiomyopathy, hypertrophic cardiomyopathy, arrhythmogenic right ventricular cardiomyopathy, restrictive cardiomyopathy, unclassified cardiomyopathy); 4) symptomatic coronary artery disease requiring medication at screening; 5) other cardiovascular diseases deemed by the investigator as inappropriate for enrollment]. g) Significant renal or hepatic dysfunction. h) Uncontrolled active hepatitis B or hepatitis C disease [clinically significant active infections including hepatitis B virus (HBV) and hepatitis C virus (HCV). Active hepatitis B is defined as: hepatitis B surface antigen (HBsAg) or hepatitis B e antigen (HBeAg) positive with HBV DNA ≥2000 IU/mL (equivalent to 10⁴ copies/mL); (if HBsAg or HBeAg positive with HBV DNA \<2000 IU/mL, per infectious disease control requirements, the participant must continue entecavir until one year after study completion or as recommended by an infectious disease specialist). Active hepatitis C is defined as: HCV RNA above the lower limit of quantification]. i) Human immunodeficiency virus (HIV) positive or syphilis (anti-treponemal antibody [Anti-TP]) positive. j) History of immunodeficiency, including other acquired or congenital immunodeficiency disorders, or history of organ transplantation. k) History of psychiatric disorder, family history of psychiatric disorder, or mood disorder as determined by the investigator or psychologist [including medical records of depressive episodes, bipolar disorder (Type I or II), obsessive-compulsive disorder, schizophrenia, history of suicide attempt or suicidal ideation, or homicidal ideation (immediate risk of harm to others), or anxiety grade 3 or above, etc.].
15. Known severe hypersensitivity to BEBT-908 for injection or any component of CHOP regimen or any excipient in their formulations.
16. Female participants who are pregnant or breastfeeding, or participants who cannot guarantee use of contraceptive measures during the study and for at least 6 months after the last dose of study drug.
17. Any unstable condition or condition that may jeopardize participant safety or compliance with the study, as determined by the investigator.
18. Participants deemed by the investigator as unsuitable for treatment under this protocol.