复发/难治性大 B 细胞淋巴瘤 CAR-T 治疗失败后双特异性抗体治疗的结局

Patients with large B-cell lymphoma (LBCL) who experience relapsed disease after CD19-directed chimeric antigen receptor (CAR) T-cell (CAR-T) therapy have a poor prognosis. Bispecific antibodies (BsAbs) induce complete remissions in 35% of these cases. Hypothesizing overlapping LBCL-intrinsic resistance mechanisms as well as common poor prognosis predictors to CAR-T and BsAb therapy, we conducted a multicenter retrospective analysis including 92 patients with relapsed/refractory (R/R) LBCL treated with BsAbs after CAR-T failure.

Overall response rate (ORR) was 43%, with a progression-free survival (PFS) of 2. 8 months. Patients receiving BsAbs during early relapse ( 3 months) achieved a significantly worse outcome (ORR, 29%; PFS, 2. 2 months) compared with patients with an intermediate (4-6 months; ORR, 54%; PFS, 3.

7 months) or a late relapse (>6 months; ORR, 60%; PFS, 10. 5 months). The benefit of later relapse was particularly notable in patients receiving BsAbs as first salvage therapy compared with those receiving a BsAb in subsequent lines (PFS not reached vs 2. 7 months; overall survival not reached vs 9. 1 months, respectively).

In addition to early R/R state before BsAbs, elevated lactate dehydrogenase and higher International Prognostic Index score were significant predictors of poor outcomes to BsAb in multivariate Cox regression analyses. The finding that patients with early relapse after CAR-T respond particularly poorly to BsAb highlights the necessity for alternative treatment options in this high-risk patient cohort.