Zanubrutinib Combined With Rituximab in the Treatment of Secondary HLH in B-cell Lymphoma

Prior treatment

• Have received other experimental drugs and had not completed the drug washout period;

Other illness

• Patients with known severe allergy to rituximab, zanubrutinib, or other BTK inhibitors;
• Severe active infections (including bacterial, viral or fungal infections) or uncontrolled co-infections;
• Combined with other malignant tumors and the expected survival time was less than 3 months;
• any condition that would not be suitable for participation in the study or that might affect adherence, follow-up, or safety assessment, as judged by the investigator.

Lab values

• Severe organ dysfunction including NYHA class III-IV heart failure or severe arrhythmia; Liver function: ALT or AST \>5 times the upper limit, or severe cirrhosis; Renal function: CrCl \<30 mL/min or severe renal insufficiency;

Other

• Pregnant or lactating women, or unwilling to use effective contraception;

• According to the diagnostic criteria of HLH-04, the patients meet the diagnostic criteria of HLH;
• HLH patients with definite or highly suspected evidence of B-cell lymphoma; Or HLH patients whose bone marrow flow cytometry show an increased proportion of CD20-positive B cells;
• Age of 14-80 years old, both sexes;
• Predicted survival beyond 1 month;
• Baseline serum creatinine ≤1.5 times ULN; Fibrinogen could be corrected to ≥0.6g/L by infusion;
• Negative serum HIV antibody; Either negative for HCV antibodies or positive for HCV antibodies but negative for HCV RNA. HBV surface antigen and HBV core antibody were negative. If any of the above was positive, HBV DNA titer in peripheral blood should be tested, and the titer was less than 1×10\^3 copies /ml;
• Left ventricular ejection fraction (LVEF) ≥50% measured by echocardiography;
• The patient have no serious and uncontrollable infections, such as pulmonary infection, intestinal infection, and sepsis;
• Women of childbearing age must be confirmed to be not pregnant by pregnancy test and willing to take effective measures to prevent pregnancy during the study period and ≥12 months after the last dose; Pregnant and lactating women cannot participate; All male subjects took contraceptive measures during the trial and ≥3 months after the last dose;
• Patients should be able to sign informed consent.