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Central point|For DLBCL patients who achieved partial remission after salvage treatment, the two-year PFS of auto-HCT or CAR-T for consolidation treatment was 52% vs 42%, and the two-year OS was 69% vs 47%, respectively
.
.
Center point | CAR-T
Diffuse large B-cell lymphoma (DLBCL) is a curable disease, and approximately 60% of patients do not require further treatment after initial treatment with anthracycline-based and rituximab-containing therapy
.
However, the prognosis of patients who are not cured by first-line treatment is often poor, and patients with relapsed or refractory DLBCL often need salvage treatment
Lymphoma
At present, the relative efficacy of autologous hematopoietic stem cell transplantation (auto-HCT) and chimeric antigen receptor T cell (CAR-T) therapy as consolidation therapy for DLBCL patients who have achieved partial remission (PR) after salvage chemotherapy is still unclear.
.
Using the registry database of the International Center for Blood and Bone Marrow Transplantation, Mazyar and other researchers screened for auto-HCT (2013-2019) or CAR-T+Axicabtagene Ciloleucel (2018-2019) treatment during PR through CT or PET scans.
Of adult DLBCL patients, and then using univariate and multivariate regression models to compare the clinical outcomes between the two cohorts after adjustment for relevant baseline and clinical factors
.
Prognosis of patients receiving auto-HCT or CAR-T therapy
Prognosis of patients receiving auto-HCT or CAR-T therapyIn univariate analysis, there was no significant difference in 2-year progression-free survival (52% vs 42%; p=0.
1) and 100-day non-relapse mortality (4% vs 2%; p=0.
3) between the two cohorts; but The use of auto-HCT for consolidation therapy was associated with a lower two-year recurrence/progression rate (40% vs 53%; p=0.
05) and an excellent overall survival rate (OS: 69% vs 47%; p=0.
004)
.
05) and an excellent overall survival rate (OS: 69% vs 47%; p=0.
004)
.
The use of auto-HCT for consolidation therapy was associated with a lower two-year recurrence/progression rate (40% vs 53%; p=0.
In multivariate regression analysis, the prognosis of patients receiving auto-HCT or CAR-T therapy
In multivariate regression analysis, the prognosis of patients receiving auto-HCT or CAR-T therapyIn multivariate regression analysis, auto-HCT treatment was associated with a significantly reduced risk of recurrence/progression (HR=1.
49; p=0.
01) and superior OS (HR=1.
63; p=0.
008)
.
49; p=0.
01) and superior OS (HR=1.
63; p=0.
008).
Auto-HCT treatment is associated with a significantly reduced risk of recurrence/progression ( HR=1.
49; p=0.
01) is related to superior OS (HR=1.
63; p=0.
008)
In general, for DLBCL patients who have achieved partial remission after salvage treatment, auto-HCT treatment is associated with a lower recurrence rate and higher OS compared with CAR-T treatment
.
These data support auto-HCT as a consolidation therapy for DLBCL patients who are eligible for transplantation and obtain partial remission after salvage treatment
For DLBCL patients achieved partial remission after salvage therapy, compared with the CAR-T treatment, auto-HCT treatment with a lower recurrence rate and related higher OS for salvage therapy after obtaining section DLBCL patients in remission, and CAR-T Compared with treatment, auto-HCT treatment is associated with lower recurrence rate and higher OS
Original source:
Original source:Shadman Mazyar, Pasquini Marcelo C, Ahn Kwang Woo et al.
Autologous Transplant versus Chimeric Antigen Receptor T- cell Therapy for Relapsed DLBCL in Partial Remission in this message