滤泡性淋巴瘤的治疗顺序和治疗次数对生存期的影响:一项基于全国人口的研究。

EJHaem Pub Date : 2024-04-28 DOI:10.1002/jha2.904
Tove Wästerlid, Caroline E. Dietrich, Anna Oksanen, Linn Deleskog Spångberg, Björn E Wahlin, Gunilla Enblad, Per-Ola Andersson, Eva Kimby, Karin E. Smedby
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摘要

滤泡性淋巴瘤(FL)是一种临床异质性疾病。治疗需求、治疗顺序、治疗次数及其与生存的关系尚未在基于人群的环境中得到描述。我们在瑞典淋巴瘤登记册中确定了2007年至2014年期间确诊的所有FL患者,并随访至2020年,获得了有关进展/复发、转化、第二线和更多线治疗的详细数据。在中位 6.8 年的随访期间,1226 名患者(69%)接受了第一次系统治疗,358 名患者(20%)仅接受了观察和等待(WaW)治疗,188 名患者(10%)接受了放疗,在研究期间无需接受其他治疗。在开始接受系统治疗的患者中,分别有496人(40%)、224人(18%)和88人(7%)接受了二线、三线或四线治疗。病因特异性转化的10年累积发生率为13%。在接受一线R-单药、R-CHOP或BR治疗的患者中,分别有54%、33%和29%需要接受二线治疗。经过一线治疗后,2年内开始后续治疗的累积概率为26%,二线治疗后为35%。经过一线、二线、三线和四线系统治疗后,两年的OS分别为84%、70%、52%和36%,排除转化后的OS仍然相似。我们的结论是,相当一部分 FL 患者可以长期接受 WaW 治疗,而需要多线治疗的患者构成了一个临床需求尚未得到满足的群体。这些结果构成了 FL 有价值的真实世界参考数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Treatment sequencing and impact of number of treatment lines on survival in follicular lymphoma: A national population-based study

Follicular lymphoma (FL) is a clinically heterogeneous disease. The need for treatment, treatment sequencing, number of treatment lines, and its association with survival have not been described in a population-based setting. We identified all patients diagnosed with FL in the Swedish Lymphoma register from 2007 to 2014, followed until 2020, with detailed data on progression/relapse, transformation, and 2nd and further lines of therapy. During a median follow-up of 6.8 years, 1226 patients (69%) received 1st systemic treatment, 358 patients (20%) were managed with watch-and-wait (WaW) only, and 188 (10%) patients were treated with radiotherapy and did not require additional therapy during the study period. Among patients starting systemic treatment, 496 (40%), 224 (18%), and 88 (7%) received 2nd-, 3rd-, or 4th-line therapy, respectively. The 10-year cause-specific cumulative incidence of transformation was 13%. Among patients managed with 1st line R-single, R-CHOP, or BR, 54%, 33%, and 29% required 2nd line, respectively. The cumulative probability of starting subsequent treatment within 2 years was 26% after 1st line and 35% after 2nd line treatment. Two-year OS following 1st, 2nd, 3rd, and 4th line systemic treatment was 84%, 70%, 52%, and 36%, respectively, and remained similar when excluding transformations. We conclude that a substantial proportion of FL patients can be managed with WaW for a long period of time, while patients who require multiple treatment lines constitute a group with a large clinical unmet need. These results constitute valuable real-world reference data for FL.

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