OncoMatch/Clinical Trials/NCT06651853
Large Fraction Radiation Therapy Combined With Lenalidomide, and Glofitamab in Refractory Relapsed DLBCL
Is NCT06651853 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Large fraction radiotherapy in combined with GM-CSF, Lenalidomide, and Glofitamab for diffuse large b-cell lymphoma.
Treatment: Large fraction radiotherapy in combined with GM-CSF, Lenalidomide, and Glofitamab — To prospectively evaluate the efficacy and safety of large fraction radiation therapy combined with granulocyte-macrophage colony-stimulating factor, lenalidomide, and glofitamab monoclonal antibody in the treatment of refractory relapsed diffuse large B-cell lymphoma patients
Check if I qualifyExtracted eligibility criteria
Cancer type
Diffuse Large B-Cell Lymphoma
Non-Hodgkin Lymphoma
Biomarker criteria
Excluded: MS4A1 loss of expression
Performance status
ECOG 0–3(Limited self-care)
Prior therapy
Must have received: systemic therapy — first-line
Patients who have failed first-line standard treatment (patients with relapsed disease < 12 months or primary refractory disease, or relapsed disease > 12 months but are transplant-ineligible after 1 line of systemic therapy, or relapsed disease after 2+ lines of therapy)
Cannot have received: bispecific antibody
Participants must not have received bispecific antibody therapy in the past
Cannot have received: anti-hematologic malignancy treatment
Participants have received anti-hematologic malignancy treatment within 2 weeks before the start of treatment or within 5 half-lives of the drug, whichever is longer
Cannot have received: large fraction radiation therapy
Exception: allowed if >4 weeks before first treatment and no radiation-related toxic reactions, no need for glucocorticoids, excluding radiation pneumonia, hepatitis, enteritis, etc.
Large fraction radiation therapy received within 4 weeks prior to the first treatment. For patients who received radiation therapy more than 4 weeks before the first treatment, all the following conditions must be met to be included: there are currently no radiation-related toxic reactions, no need to take glucocorticoids, excluding radiation pneumonia, radiation hepatitis, radiation enteritis, etc.
Cannot have received: traditional Chinese medicine with anti-tumor indications
Traditional Chinese medicine with anti-tumor indications received within 2 weeks before the first administration
Cannot have received: other clinical trial treatment
Treatment in another clinical trial within 4 weeks before the first administration
Lab requirements
Blood counts
Platelet count ≥30 x 10^9/L; absolute neutrophil count ≥1.0 x 10^9/L; good coagulation function (INR or PT ≤1.5× ULN)
Kidney function
Blood creatinine ≤1.5× ULN and creatinine clearance rate ≥60 ml/min
Liver function
Total bilirubin ≤1.5× ULN; AST and ALT ≤2.5× ULN
laboratory criteria: (1) Total bilirubin ≤1.5× ULN; (2) AST and ALT ≤2.5× ULN; (3) Blood creatinine ≤1.5× ULN and creatinine clearance rate ≥60 ml/min; (4) Good coagulation function, defined as INR or PT ≤1.5× ULN. Bone marrow insufficiency defined by platelet count <30 x 10^9/L or ANC <1.0 x 10^9/L [excluded].
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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