Real-world outcomes with novel therapies in relapsed/refractory diffuse large B-cell lymphoma

被引:1
作者
Crombie, Jennifer L. [1 ]
Jun, Monika [2 ]
Wang, Tongsheng [2 ]
Mutebi, Alex [2 ]
Wang, Anthony [3 ]
Chhibber, Anindit [2 ]
Kamalakar, Rajesh [3 ]
Ukropec, Jon [2 ]
Blaedel, Julie [2 ]
Kalsekar, Anupama [2 ]
机构
[1] Dana Farber Canc Inst, 450 Brookline Ave, Boston, MA 02215 USA
[2] Genmab, Plainsboro, NJ USA
[3] AbbVie, N Chicago, IL USA
关键词
Diffuse large B-cell lymphoma; electronic health records; real-world; non-Hodgkin lymphoma; retrospective studies; SINGLE-ARM; OPEN-LABEL; MULTICENTER; TRANSPLANTATION;
D O I
10.1080/10428194.2024.2371472
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This study used COTA de-identified data (2010-2021) of patients in the US to explore outcomes of novel therapies in relapsed/refractory (R/R) diffuse large B-cell lymphoma (DLBCL) in real-world settings. Demographics, clinical characteristics, and clinical outcomes of patients with R/R DLBCL who received novel treatments including chimeric antigen receptor T-cell (CAR T) therapy and tafasitamab- or polatuzumab-based therapies were evaluated. Overall, 175 patients with R/R DLBCL were analyzed; 73, 69, and 27 received CAR T therapy, polatuzumab-based regimens, and tafasitamab-based regimens, respectively. In patients who had >= 1 prior lines of therapy (i.e. starting second-line or later therapy; 2 L+), CAR T, polatuzumab-based regimens, and tafasitamab-based regimens achieved a median overall survival of 26.5, 7.8, and 6.3 months, respectively. Outcomes were particularly poor for patients with relapse following CAR T, indicating that polatuzumab- and tafasitamab-based regimens in 2 L + R/R DLBCL have suboptimal outcomes in the real world. Additional treatment options are needed.
引用
收藏
页码:1623 / 1633
页数:11
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