CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Historic Real-World Outcomes and Future Benchmarks for Patients with Diffuse Large B-Cell Lymphoma Receiving First- and Second-Line Therapy in Austria - a Large Single-Center Experience.
Historic Real-World Outcomes and Future Benchmarks for Patients with Diffuse Large B-Cell Lymphoma Receiving First- and Second-Line Therapy in Austria - a Large Single-Center Experience.
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弥漫大B细胞淋巴瘤(DLBCL)是最常见的非霍奇金淋巴瘤。许多患者可治愈,但仍有相当比例患者一线治疗失败,需要二线治疗。目前奥地利DLBCL患者接受标准治疗的真实世界结局数据有限;尽管新疗法不断出现,尚无历史基准可供比较。
对2010—2018年确诊并接受标准治疗的DLBCL患者开展单中心回顾性分析。为建立新疗法疗效基准,采用临床试验和真实世界标准,分析可能符合新型或未来治疗条件患者的结局。
许多患者可通过一线治疗治愈,但结局仍较差,尤其是高危患者。一线治疗失败者,特别是符合嵌合抗原受体(CAR)T细胞治疗适应条件者,结局极差,长期缓解者很少。本研究为可能接受抗体药物偶联物(ADC)或CAR-T 治疗等新型疗法的患者提供了基准结局,可用于未来比较分析。
奥地利DLBCL患者结局与其他真实世界研究相近。总体而言,标准化疗方案对高危患者和一线治疗失败患者疗效不足。如今许多患者符合ADC或CAR-T 等替代一线及二线治疗条件,本研究建立的疗效基准可供未来在奥地利医疗环境中评估这些疗法。
BackgroundDiffuse large B-cell lymphoma (DLBCL) is the most common form of non-Hodgkin-lymphoma. Although it can be cured in many patients, a significant proportion of patients fail the primary treatment and require second-line treatment. Currently, only limited data on real-world outcomes with standard therapies in Austrian patients with DLBCL are available, and while novel therapies are emerging, no historical benchmarks have been established to serve as a reference for these novel treatments. MethodsWe performed a retrospective, single-center analysis of patients with DLBCL diagnosed between 2010 and 2018 who had been treated with standard therapies.
To establish efficacy benchmarks for novel therapies, we applied both clinical-trial and real-world-derived criteria to analyze the outcomes of patients potentially eligible for novel or future treatments. ResultsAlthough many patients can be cured with frontline therapy, outcomes are poor, especially in high-risk patients. Patients failing frontline therapy, especially those fulfilling the chimeric antigen-receptor (CAR) T-cell eligibility criteria, had dismal outcomes, and very few patients achieved long-term remission.
Our data provide benchmark outcomes for patients eligible for novel treatments such as antibody-drug-conjugate (ADC) or CAR T-cell therapy-based treatments for potential future comparative analyses. ConclusionsPatients with DLBCL treated in Austria showed comparable outcomes to those reported in other real-world studies.
Overall, standard chemotherapy-based approaches provide unsatisfactory outcomes in high-risk patients and patients in whom frontline therapy fails. Because many patients are now eligible for alternative first- and second-line treatments, such as ADC-based or CAR T-cell therapy, our efficacy benchmarks can serve for the future evaluation of these therapies in the Austrian healthcare environment.
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