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OncoMatch/Clinical Trials/NCT07680933

Orelabrutinib Combined With Standard Immunochemotherapy With or Without Autologous Hematopoietic Stem Cell Transplantation (Auto-HSCT) for Newly Diagnosed Diffuse Large B-cell Lymphoma (DLBCL)

Is NCT07680933 recruiting? Yes, currently enrolling (Jul 2026). This Phase 2 trial studies Orelabrutinib combined with standard immunochemotherapy with or without auto-HSCT for dlbcl - diffuse large b cell lymphoma.

Phase 2RecruitingThe Affiliated Hospital of Xuzhou Medical UniversityNCT07680933Data as of Jul 2026Location: China

Treatment: Orelabrutinib combined with standard immunochemotherapy with or without auto-HSCTThis study is a prospective, open-label, multicenter study in previously untreated participants with CD20-positive DLBCL. Orelabrutinib combined with standard immunochemotherapy with or without autologous hematopoietic stem cell transplantation (auto-HSCT) for newly diagnosed diffuse large B-cell lymphoma (DLBCL). The primary objective is to explore the 1-year progression-free survival (PFS) of orelabrutinib combined with standard immunochemotherapy with or without auto-HSCT in newly diagnosed DLBCL.

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Extracted eligibility criteria

Treatments studied

Other

Orelabrutinib combined with standard immunochemotherapy with or without auto-HSCT

Cancer type

Diffuse Large B-Cell Lymphoma

Non-Hodgkin Lymphoma

Biomarker criteria

Required: MS4A1 expression

Pathologically confirmed CD20-positive DLBCL

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 80

Lab requirements

Blood counts

Hemoglobin ≥90 g/L within 7 days prior to enrollment without packed red blood cell transfusion; ANC ≥1.0 × 10⁹/L; Platelet count ≥75 × 10⁹/L

Kidney function

Creatinine ≤ 1.5× ULN; creatinine clearance ≥ 60 mL/min (estimated by Cockcroft-Gault formula)

Liver function

ALT or AST ≤ 2× ULN; ALP and bilirubin ≤ 1.5× ULN

Cardiac function

Left ventricular ejection fraction (LVEF) ≥50% as assessed by MUGA scan or ECHO

Adequate hematologic function...Hemoglobin ≥90 g/L...ANC ≥1.0 × 10⁹/L; Platelet count ≥75 × 10⁹/L. Adequate organ function. LVEF ≥50% as assessed by MUGA scan or ECHO

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07680933 currently recruiting?

Yes, this trial is currently recruiting patients.

Does this trial require MS4A1?

Yes, MS4A1 expression is a required biomarker for enrollment.

Is there an age limit?

Yes. Patients must be 80 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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