不适合移植的大 B 细胞淋巴瘤二线使用 axicabtagene ciloleucel:ALYCANTE 最终分析
Second-line axicabtagene ciloleucel in large B-cell lymphoma ineligible for transplantation: ALYCANTE final analysis.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Epidemiology and Real-World Treatment of Incident Diffuse Large B-cell Lymphoma (DLBCL): A German Claims Data Analysis.
Epidemiology and Real-World Treatment of Incident Diffuse Large B-cell Lymphoma (DLBCL): A German Claims Data Analysis.
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尽管该领域取得了进展,DLBCL 仍存在高度未满足的医疗需求。治疗格局非常异质,尤其是在二线或后线治疗中,很少有患者在一线之后接受潜在治愈性治疗。DLBCL 的治疗,尤其是对于不适合移植的患者,仍然具有挑战性。
本研究的目的是在真实世界环境中调查弥漫性大B细胞淋巴瘤(DLBCL)的患病率、发病率及治疗模式(治疗方案、换药、持续时间)。
这是一项针对2012年1月1日至2020年12月31日期间诊断为DLBCL的患者的德国回顾性理赔数据分析。得出了2019/2020年DLBCL的患病率和累积发病率。描述了从首次DLBCL诊断到随访结束的治疗线数(LOT)和治疗环境。计算了自DLBCL诊断和治疗线开始以来的Kaplan-Meier总生存期(OS)估计值。
总体共识别出2633例新发DLBCL病例(中位年龄75岁,51%为男性)。其中,2119例患者接受了至少一种DLBCL相关治疗(LOT1),1567例患者在随访期间死亡。2019/2020年,DLBCL的患病率和累积发病率分别为每100,000例患者34.8/36.7例和每100,000例患者14.0/12.7例。对于LOT1,1922例患者接受了以化疗为基础的治疗方案(1530例联合CD20抗体)。共有403例患者接受了二线治疗(LOT2),其中183例患者接受了含CD20抗体的化疗方案,100例患者接受了干细胞移植或嵌合抗原受体(CAR)-T治疗。在136例LOT3+治疗中,74例为化疗方案(54例联合CD20抗体),18例为激酶抑制剂。治疗线之间的中位时间小于6个月。在至少接受LOT2的患者中,约50%在诊断后第一年内接受了超过一种LOT。约25%的接受治疗患者在治疗开始后6个月内死亡。在2633例纳入患者中,自诊断起的中位OS为31.0个月(接受治疗患者:46.8个月,未接受治疗患者:3.0个月)。
This was a retrospective German claims data analysis of patients with DLBCL diagnosed between January 1, 2012, and December 31, 2020. The prevalence and cumulative incidence of DLBCL were found for 2019/2020. Line of treatment (LOT) and treatment setting from first DLBCL diagnosis to end of follow-up were described. Kaplan-Meier overall survival (OS) estimates since DLBCL diagnosis and start of treatment lines were calculated.
Overall, 2633 incident DLBCL cases were identified (median age 75 years, 51% male). Of these, 2119 patients received at least one DLBCL-related treatment (LOT1), and 1567 patients died during follow-up. In 2019/2020, the prevalence and cumulative incidence of DLBCL was 34.8/36.7 per 100,000 patients and 14.0/12.7 per 100,000 patients, respectively. For LOT1, 1922 patients were given a chemotherapy-based regimen (1530 with CD20 antibodies). A total of 403 patients were administered a second line (LOT2), of which 183 patients received a CD20 antibody-containing chemotherapy regimen and 100 patients received stem cell transplantation or chimeric antigen receptor (CAR)-T therapy. Of the 136 LOT3+ treatments, 74 were chemotherapy regimens (54 with CD20 antibodies) and 18 were kinase inhibitors. The median time between treatment lines was less than 6 months. Among patients with at least LOT2, approximately 50% received more than one LOT during the first year after diagnosis. Approximately 25% of treated patients died within 6 months of treatment initiation. Of the 2633 included patients, the median OS from diagnosis was 31.0 months (treated patients: 46.8 months, untreated patients: 3.0 months).
Despite advances in the field, high unmet medical need in DLBCL remains. The treatment landscape is very heterogeneous, particularly in second- or later-line treatments, with few patients receiving potentially curative treatment beyond the first line. Treatment for DLBCL, particularly for transplant-ineligible patients, remains challenging.
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