← 返回

弥漫大 B 细胞淋巴瘤各治疗线的患者特征、医疗资源利用与费用——德国理赔数据研究

英文原题:Patient characteristics, healthcare resource utilization and costs across treatment lines in diffuse large B-cell lymphoma - a German claims data study.

查看英文原题

Patient characteristics, healthcare resource utilization and costs across treatment lines in diffuse large B-cell lymphoma - a German claims data study.

PubMed 2025/08/13(内容时间) J Comp Eff Res Q2 · IF 2.8(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

鉴于德国真实世界弥漫性大B细胞淋巴瘤(DLBCL)数据有限,我们利用德国索赔数据评估了DLBCL跨治疗线的基线特征、治疗、临床并发症、医疗资源利用和成本。

在一项使用德国疾病基金(AOK PLUS)索赔数据的回顾性队列研究中,我们识别了2012年至2022年间新发DLBCL诊断的患者。使用基于德国治疗指南的算法,患者被分层为一线(1L)、二线(2L)和三线(3L)治疗。然后我们描述性分析了基线特征、治疗、临床并发症、医疗资源利用和成本。

共有2423例接受1L治疗的DLBCL患者纳入研究(49.1%女性;平均年龄:69.7岁;平均CCI:7.0;中位随访:29.3个月)。共有1209例(49.7%)和505例(20.8%)患者分别进展至2L和3L。共有209例患者接受了干细胞移植(SCT;平均年龄:56.1岁);37例接受了CAR-T 细胞疗法(CAR-T;平均年龄:60.8岁)。大多数患者在随访期间至少有一次DLBCL相关住院(1L:79.2%;2L:60.0%;3L:71.9%;平均住院时间[天/患者年]:1L:15.2;2L:6.4;3L:14.2),相应的住院成本为每患者年12,777(1L)、5993(2L)和17,408(3L)。临床并发症常见,尤其是在3L,包括中性粒细胞减少症(1L:31.9%;2L:27.0%;3L:46.9%)、肺炎(1L:19.6%;2L:16.8%;3L:30.3%)、贫血(1L:17.8%;2L:18.7%;3L:35.2%)、血小板减少症(1L:17.3%;2L:21.8%;3L:45.1%)和脓毒症(1L:14.6%;2L:13.0%;3L:23.2%)。

二线或更后线治疗患者比例高(提示复发/难治性疾病)、SCT数量少以及大量临床并发症和医疗资源使用,凸显了对新型有效且耐受性良好的DLBCL治疗选择的需求。这篇文章是关于什么的?弥漫性大B细胞淋巴瘤(DLBCL)是一种快速生长的癌症,通常首先接受称为R-CHOP的化疗和免疫治疗联合方案。虽然R-CHOP对大多数患者有帮助,但部分患者的癌症会复发或对治疗无应答。本研究试图更好地了解DLBCL在真实世界中的治疗情况,考察DLBCL患者的治疗、并发症和医疗服务使用情况。我们使用了来自德国一家大型健康保险基金的数据,覆盖2010年至2022年的350万人。在本研究中,我们纳入了2012年至2022年间首次诊断为DLBCL的患者,并随访至2022年或直至其死亡。患者按不同治疗线进行追踪。结果如何?我们识别出2432例接受一线治疗的患者,平均年龄为69.7岁。其中近半数患者需要进一步的治疗线。大多数患者(一线治疗中约85%)接受了化疗联合利妥昔单抗。少数通常较年轻的患者接受了先进疗法,如干细胞移植或所谓的CAR-T 细胞疗法。患者住院很常见,每年约6至15个住院日,费用约为每年6000至17,000,具体取决于治疗线。常见并发症包括中性粒细胞减少症、肺炎、贫血、血小板减少症和脓毒症。血液和血小板输注也很常见,尤其是在后线治疗中。这些结果意味着什么?由于近一半患者接受了多线治疗,我们的研究表明,许多患者出现复发或对初始治疗反应不佳。我们还观察到大量住院和并发症,显示尽管有当前治疗,DLBCL仍带来负面影响。这凸显了对n的需求

展开英文摘要原文

Aim: Given the limited availability of real world diffuse large B-cell lymphoma (DLBCL) data in Germany, we assessed the baseline characteristics, treatments, clinical complications, healthcare resource utilization and costs of DLBCL across treatment lines using German claims data.

Materials & methods: In a retrospective cohort study using claims data from a German sickness fund (AOK PLUS), we identified patients with an incident DLBCL diagnosis between 2012 and 2022. Using an algorithm based on German treatment guidelines, patients were stratified into first (1L), second (2L) and third line (3L) treatment.

We then descriptively analyzed baseline characteristics, treatments, clinical complications, healthcare resource utilization and costs. Results: A total of 2423 patients with DLBCL and 1L treatment were included in the study (49. 1% female; mean age: 69. 7 years; mean CCI: 7. 0; median follow-up: 29. 3 months). A total of 1209 (49. 7%) and 505 (20. 8%) patients progressed to 2L and 3L, respectively. A total of 209 patients received a stem cell transplant (SCT; mean age: 56. 1 years); 37 received a chimeric antigen receptor T-cell therapy (CAR-T; mean age: 60. 8 years). Most patients had at least one DLBCL related hospitalization during follow-up (1L: 79. 2%; 2L: 60. 0%; 3L: 71. 9%; mean length of stay [days/patient year]: 1L: 15. 2; 2L: 6. 4; 3L: 14. 2), with corresponding hospitalization costs of 12,777 (1L), 5993 (2L) and 17,408 (3L) per patient year.

Clinical complications were common, particularly in 3L, including neutropenia (1L: 31. 9%; 2L: 27. 0%; 3L: 46. 9%), pneumonia (1L: 19. 6%; 2L: 16. 8%; 3L: 30. 3%), anemia (1L: 17. 8%; 2L: 18. 7%; 3L: 35. 2%), thrombocytopenia (1L: 17. 3%; 2L: 21. 8%; 3L: 45. 1%) and sepsis (1L: 14. 6%; 2L: 13. 0%; 3L: 23. 2%).

Conclusion: The high proportion of patients with second or later-line treatment (indicating a relapse or refractory disease), the low number of SCTs together with many clinical complications and healthcare resource use underscore the need for novel effective and well-tolerated DLBCL treatment options.

What is this article about? Diffuse large B-cell lymphoma (DLBCL) is a fast-growing cancer that is usually first treated with a combination of chemotherapy and immunotherapy called R-CHOP. While R-CHOP helps most patients, for some patients the cancer returns or they do not respond to the treatment.

This study tries to better understand how DLBCL is treated in the real world, looking at treatments, complications, and the use of healthcare services among DLBCL patients.

We used data from a large German health insurance fund, covering 3. 5 million people from 2010 to 2022. For the study, we included patients diagnosed with DLBCL for the first time between 2012 and 2022 and followed them until 2022 or until they died. Patients were tracked through different lines of therapy. What were the results?

We identified 2432 patients with first-line treatment, with an average age of 69. 7 years. Nearly half of these patients needed further treatment lines. Most patients (about 85% in first-line treatment) received chemotherapy combined with rituximab. A small number of typically younger patients received advanced therapies like stem cell transplants or so-called chimeric antigen receptor T-cell therapy.

Hospitalizations among patients were common, with around 6 to 15 hospital days per year and costs ranging from around 6000 to 17,000 per year, depending on the treatment line. Common complications included neutropenia, pneumonia, anemia, thrombocytopenia and sepsis. Blood and platelet transfusions were also common, especially in later treatment lines. What do the results mean? With nearly half of the patients having more than one line of treatment, our study indicates that many patients experience relapses or do not respond well to treatment initially.

We also observed a high number of hospitalizations and complications, showing the negative impact of DLBCL despite current treatments. This highlights the need for n

论文信息

作者
Greth K、Lehne M、Ghiani M、Mevius A、Jiang W、Russell A、Gokhale M
第一作者单位
Cytel Inc., Berlin, Germany.Germany
通讯作者单位
Pfizer Inc, Collegeville, PA, USA.United States
文献类型
非美国政府资助研究
期刊
Journal of comparative effectiveness research2025 Sep
原文标识
PubMed 40801820 · DOI 10.57264/cer-2024-0218