接受利妥昔单抗联合苯达莫司汀治疗不显性 B 细胞淋巴瘤患者的临床效果:一项单中心机构研究。

Journal of cancer & allied specialties Pub Date : 2024-08-16 eCollection Date: 2024-01-01 DOI:10.37029/jcas.v10i2.677
Zurrya Fasih Khan, Nabiha Saeed, Hamzah Jehanzeb, Faryal Jahangir, Usman Shaikh, Salman Adil, Mehmood Alam Khan, Muhammad Daniyal, Mian Muinuddin Jamshed, Maria Ali, Natasha Ali
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引用次数: 0

摘要

简介惰性非霍奇金淋巴瘤(NHL)是一种以慢性复发-缓解病程为特征的多种恶性肿瘤。在现代,患者通常会接受苯达莫司汀联合利妥昔单抗作为初始疗法,也就是所谓的R-Benda疗法。虽然临床试验证明 R-Benda 优于其他方案,但我们的研究旨在深入了解 R-Benda 治疗的实际效果:我们对巴基斯坦卡拉奇阿迦汗大学医院接受 R-Benda 治疗的非淋菌性 NHL 患者进行了一项回顾性研究,研究时间为 2015 年 1 月至 2022 年 7 月。所有患者都通过正电子发射断层扫描和计算机断层扫描(CT)成像进行了治疗前后评估。采用卡普兰-梅耶尔生存分析法评估治疗反应,并评估总生存期(OS)和无进展生存期(PFS):我们共招募了 118 名患者,其中大多数为老年男性(64%)。2年随访率为76.3%(n = 90),中位随访时间为29个月。最常见的组织病理学是滤泡性淋巴瘤(52%)和 IV 期疾病(56%)。约 73% 的患者对治疗产生了完全代谢反应。其中,31.4%的患者随后复发。此外,17.7%的患者获得了部分应答,7%的患者患有难治性疾病。平均生存期为140个月(95% CI:120-160),下四分位值为50个月。另一方面,中位PFS为80个月(95% CI:43-N/A):我们的研究表明,接受 R-Benda 治疗的患者临床疗效良好,绝大多数患者的生存期超过了 50 个月。此外,76.1%的患者在最初的两年中疾病没有进展。该研究补充了现有的文献,这些文献表明,在现实世界中,R-Benda 治疗的结果优于早期随机对照试验的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Outcome of Patients Receiving Rituximab in Combination with Bendamustine in Indolent B-cell Lymphomas: A Single-center Institutional Study.

Introduction: Indolent non-Hodgkin's lymphomas (NHLs) are a diverse category of malignancies characterized by a chronic relapsing-remitting disease course. In the modern era, patients usually receive a combination of bendamustine plus rituximab as the initial therapy, otherwise known as an R-Benda regimen. While clinical trials have demonstrated R-Benda to be superior to other regimens, our study aims to provide insight into real-world outcomes of R-Benda therapy.

Materials and methods: We conducted a retrospective study for January 2015-July 2022 among patients receiving R-Benda for indolent NHLs at the Aga Khan University Hospital, Karachi, Pakistan. All patients underwent pre- and post-treatment assessment through positron emission tomography scan and computed tomography (CT) imaging. The response to treatment was assessed, and the overall survival (OS) and progression-free survival (PFS) were assessed using a Kaplan-Meier survival analysis.

Results: We enrolled 118 patients, out of which the majority were elderly males (64%). The 2-year follow-up rate was 76.3% (n = 90), and the median follow-up time was 29 months. The most common histopathology encountered was follicular lymphoma (52%) presenting with stage IV disease (56%). Approximately 73% experienced a complete metabolic response to the treatment. Of these, 31.4% subsequently experienced a relapse. In addition, 17.7% of patients underwent a partial response, while 7% had refractory disease. The mean OS was 140 months (95% CI: 120-160), while the lower quartile value was 50 months. On the other hand, the median PFS was 80 months (95% CI: 43-N/A).

Conclusion: Our study demonstrated that patients on R-Benda had good clinical outcomes, with the vast majority living beyond 50 months. Moreover, 76.1% had no disease progression for the first 2 years. It adds to the existing body of literature that demonstrates that in real-world experience, the outcomes of R-Benda treatment are better than those reported by earlier randomized-control trials.

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