Inclusion Criteria:
* Pathologically confirmed mantle cell lymphoma
* Age 18-80 years, both genders are eligible..
* Untreated MCL.
* At least one measurable lesion. Measurable disease is defined as a tumor mass measurable in one or two dimensions ≥1.5 cm, as well as measurable spleen lesions.
* Any one of the following factors is present:: MIPI intermediate-high risk, ki67≥30%, blastoid/pleomorphic, TP53 abnormality (mutation/deletion) or p53 protein expression \>50%, large mass (maximum diameter ≥7.5cm), complex karyotype (≥3 chromosomal abnormalities (excluding t(11; 14)))
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 - 2.
* Hematologic function is adequate, defined as:
1. Absolute neutrophil count (ANC) ≥1×109/L, growth factor support must not be used within 7 days prior to testing;
2. Platelet count ≥75×10⁹/L, or ≥50×10⁹/L (if bone marrow involvement), no use of growth factor support or transfusion allowed within 7 days prior to testing.
* Adequate hepatic function per local laboratory reference range as follow:
1. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤2.5× the upper limit of normal (ULN);
2. Bilirubin ≤ 2 × ULN (except for those diagnosed with Gilbert's syndrome, which allows up to 5 × ULN)
* Adequate renal function as demonstrated by:
1. Creatinine clearance ≥60 mL/min (estimated using the Cockcroft-Gault formula or the glomerular filtration rate \[eGFR\] estimated using the Modification of Diet in Renal Disease \[MDRD\] formula)
2. Serum creatinine ≤1.5×ULN
* International Normalized Ratio (INR) ≤ 1.5 × ULN and Activated Partial Thromboplastin Time (APTT) ≤ 1.5 × ULN
* Life expectancy of more than 3 months.
* Ability to provide written informed consent and understand and comply with study requirements.
* Able to comply with the study visit schedule and other protocol requirements
Exclusion Criteria:
* Current central nervous system involvement or suspected patients and those with a history of this condition
* Previously received systemic treatment for MCL, including BTKi.
* Uncontrolled active systemic fungal, bacterial, or viral infections (defined as persistent signs/symptoms related to the infection despite the use of appropriate antibiotics, antiviral therapy, and/or other treatments with no improvement).
* Known human immunodeficiency virus (HIV) infection, or the following serological status indicating active hepatitis B or C virus infection:
1. Subjects with positive hepatitis B virus core antibody (HBcAb) and negative surface antigen (HBsAg) must have a negative polymerase chain reaction (PCR) result prior to the first dose. Subjects with positive HBsAg or HBV-DNA:
2. Subjects with positive hepatitis C antibodies must have an HCV-RNA negative result before the first dose. Subjects with positive hepatitis C PCR results will not be eligible for this study.
* Clinically severe cardiovascular diseases, including:
1. Myocardial infarction occurring within the 6 months prior to screening;
2. Unstable angina occurring within 3 months prior to screening;
3. Clinically significant arrhythmias (e.g., sustained ventricular tachycardia, ventricular fibrillation, torsades de pointes ventricular tachycardia);
4. QTcF (corrected by Fridericia's formula) \> 480 msec;
5. History of second-degree type II atrioventricular (AV) conduction block or third-degree atrioventricular conduction block;
6. III or IV congestive heart failure as defined by the New York Heart Association (NYHA)
* History of severe hemorrhagic disorders, such as hemophilia A, hemophilia B, von Willebrand disease, or a history of spontaneous bleeding requiring blood transfusion or other medical interventions.
* History of deep vein thrombosis (DVT) or pulmonary embolism (PE) in the past 12 months
* History of significant cerebrovascular disease/events within 6 months prior to the first administration of the investigational drug, including stroke or intracranial hemorrhage.
* Unable to swallow capsules or having significant gastrointestinal functional disorders, such as malabsorption syndrome, gastric or small intestine resection, symptomatic inflammatory bowel disease, or partial or complete intestinal obstruction.
* Continuous treatment with strong and moderate CYP3A inhibitors or CYP3A inducers is required. If the patient has taken strong or moderate CYP3A inhibitors or inducers within 7 days prior to the first dose of the investigational drug (or has taken these drugs for less than 5 half-lives), they cannot be enrolled. Patients using moderate CYP3A inhibitors can be considered for the study after at least a 7-day washout period.
* Anticoagulation treatment with warfarin or equivalent vitamin K antagonists (e.g., phenprocoumon) is required within 7 days after the first dose of the investigational drug or receiving anticoagulation therapy.
* Pregnant or breastfeeding women
* Hypersensitivity to any investigational drug
* Any mental or cognitive impairment that may limit their understanding, execution, and compliance with the informed consent form and the study.
* Subjects with drug abuse and alcoholism
