利妥昔单抗和化疗治疗新诊断的滤泡性淋巴瘤:波兰淋巴瘤研究组的真实世界报告

IF 2 4区 医学 Q3 ONCOLOGY
Chemotherapy Pub Date : 2022-03-04 DOI:10.1159/000523921
E. Paszkiewicz-Kozik, M. Debowska, Natalia Jakacka, M. Kotarska, M. Szymanski, K. Wiśniewski, A. Końska, Malgorzata Jarzembowska, J. Drozd-Sokołowska, J. Romejko-Jarosińska, A. Szumera-Ciećkiewicz, G. Rymkiewicz, B. Ziarkiewicz-Wróblewska, E. Lech-Maranda, J. Walewski, I. Hus
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引用次数: 0

摘要

滤泡性淋巴瘤(Follicular lymphoma, FL)是最常见的一种惰性b细胞淋巴瘤,大多数患者预后良好。诱导治疗仍以利妥昔单抗和化疗为基础,尽管最近引入了新的抗cd20抗体和无化疗方案。本研究的目的是分析在现实世界中新诊断的FL患者的治疗、结果和预后的决定因素。方法:回顾性分析3家血液学中心2011-2015年5年间连续诊断为FL患者的资料。变量比较酌情采用Mann-Whitney检验或χ2检验,生存终点采用Kaplan-Meier法计算。结果:181例患者纳入研究。患者诊断时的中位年龄为56.6岁。62.1%的患者有低组织学分级(G1-G2), 77.0%的患者有临床晚期。57.1%的患者观察到ECOG 0表现状态。中位随访时间为5.91年。最初,31.5%的患者符合观察等待(W&W)策略,观察期间,整个患者组有84.0%的患者接受了全身治疗。诱导治疗方面,分别有53.9%和41.4%的患者接受RCVP和RCHOP方案;39.8%的患者在一线治疗后接受了利妥昔单抗维持治疗。随访期间,7.2%的患者转化为侵袭性淋巴瘤。中位总生存期(OS)未达到,中位无进展生存期(PFS)为8.28年(95% CI;7.35, NA), 19.6%的患者在治疗开始后的24个月内复发(POD24)。POD24组的中位PFS为1.1年(95% CI;0.56, 1.45),中位生存期大于8年。ECOG 0、低PRIMA PI和未发现POD24是延长PFS和OS的决定因素。结论:我们的临床实践数据表明,利妥昔单抗和化疗仍然是治疗FL的有效方法,大多数患者自诊断后生存期超过8年。RCVP方案加RM是一线治疗的合理选择,特别是在低/中级组患者中。POD24患者的预后明显较差。因此,有必要寻找精确的初始临床和生物学标志物,并开发治疗方法来改善POD24患者的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rituximab and Chemotherapy for Newly Diagnosed Follicular Lymphoma: Real-World Report of Polish Lymphoma Research Group
Introduction: Follicular lymphoma (FL) is the most common type of indolent B-cell lymphoma with a favorable prognosis in the majority of patients. The induction treatment is still based on rituximab and chemotherapy, though new anti-CD20 antibody and chemo-free regimen have been recently introduced. The aim of the study was to analyze the management, outcomes, and determinants of prognosis of newly diagnosed patients with FL in real-world experience. Methods: Data of consecutive patients diagnosed with FL in 5 years period (2011–2015) in three oncohematological centers were reviewed. Variables were compared using Mann-Whitney or χ2 test as appropriate, survival outpoints were calculated using Kaplan-Meier method. Results: One hundred eighty-one patients were included in the study. The median patients’ age at diagnosis was 56.6 years. Low histological grade (G1–G2) was found in 62.1% of patients and advanced clinical stage in 77.0% of patients. ECOG 0 performance status was observed in 57.1% of patients. The median follow-up was 5.91 years. Initially, 31.5% of the patients were qualified to watch-and-wait (W&W) strategy, and 84.0% of the whole patients’ group received systemic treatment during the observation period. As induction treatment, 53.9% and 41.4% of patients received RCVP and RCHOP regimens, respectively; 39.8% received rituximab maintenance (RM) after first-line therapy. During follow-up, transformation to aggressive lymphoma occurred in 7.2% of patients. Median overall survival (OS) was not achieved, and median progression-free survival (PFS) was 8.28 years (95% CI; 7.35, NA), 19.6% of patients relapsed during 24 months from the start of the treatment (POD24). Median PFS for POD24 group was 1.1 years (95% CI; 0.56, 1.45) with a median OS longer than 8 years. ECOG 0, low PRIMA PI, and no POD24 were found as determinants of longer PFS and OS. Conclusions: Our data from clinical practice showed that rituximab and chemotherapy is still an effective method of FL treatment resulting in survival more than 8 years from diagnosis in most patients. RCVP protocol followed with RM is a reasonable choice for the first-line therapy especially in low/intermediate group of patients. The prognosis was significantly worse in patients with POD24. Therefore, searching for precise initial clinical and biological markers is warranted and development therapies to improve prognosis of POD24 patients.
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来源期刊
Chemotherapy
Chemotherapy 医学-药学
CiteScore
5.80
自引率
0.00%
发文量
34
审稿时长
6-12 weeks
期刊介绍: This journal publishes original research articles and state-of-the-art reviews on all aspects of antimicrobial and antitumor chemotherapy. The results of experimental and clinical investigations into the microbiological and pharmacologic properties of antibacterial, antiviral and antitumor compounds are major topics of publication. Papers selected for the journal offer data concerning the efficacy, toxicology, and interactions of new drugs in single or combined applications. Studies designed to determine the pharmacokinetic and pharmacodynamics properties of similar preparations and comparing their efficacy are also included. Special emphasis is given to the development of drug-resistance, an increasing problem worldwide.
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