Treatment-related survival patterns in diffuse intrinsic pontine glioma using a historical cohort: A report from the European Society for Pediatric Oncology DIPG/DMG Registry.

IF 3.7 Q1 CLINICAL NEUROLOGY
Neuro-oncology advances Pub Date : 2024-09-10 eCollection Date: 2024-01-01 DOI:10.1093/noajnl/vdae155
Joshua N Baugh, Sophie Veldhuijzen van Zanten, Marta Fiocco, Niclas Colditz, Marion Hoffmann, Geert O Janssens, Chiara Valentini, Darren Hargrave, Maria Wiese, André O von Bueren, Michael Karremann, Thomas Perwein, Gunther Nussbaumer, Martin Benesch, Dominik Sturm, Gerrit H Gielen, Mechthild Krause, Matthias Eyrich, Eelco W Hoving, Brigitte Bison, Dannis G van Vuurden, Christof M Kramm
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引用次数: 0

Abstract

Background: Our aim is to investigate the association of treatment with survival in patients with diffuse intrinsic pontine glioma (DIPG) by examining 6 historical treatment paths.

Methods: We retrospectively analyzed data from 409 patients with radiologically centrally reviewed DIPG, sourced from the German Society of Pediatric Oncology and Hematology HIT-HGG trial database and the SIOPE-DIPG/DMG Registry. Survival outcomes were estimated using the Kaplan-Meier method, and univariable and multivariable Cox proportional hazard models were estimated to study treatment effects.

Results: The median overall survival (OS) from diagnosis was 11.2 months (95% confidence interval [CI], 10.5-11.9). Patients who by choice received no frontline treatment had an OS of 3.0 months (95% CI, 2.0-4.0), while those treated with radiation therapy (RT) alone had a median OS of 10.4 months (95% CI, 9.1-11.8). Those receiving RT combined with chemotherapy had the longest median OS of 11.7 months (95% CI, 10.8-12.6). The median post-progression survival (PPS) was 4.1 months (95% CI, 3.5-4.7). Patients who relapsed and did not receive treatment had a PPS of 2.2 months (95% CI, 1.8-2.6), while those treated with chemotherapy alone had a PPS of 4.4 months (95% CI, 3.7-5.0), and those who underwent reirradiation, with or without chemotherapy, had the longest survival after relapse of 6.6 months (95% CI, 5.3-8.0). Treatment differences remained significant in multivariable analysis adjusted for age and symptom duration in both diagnosis and relapse setting.

Conclusions: This study shows increased survival outcomes associated with radiation and chemotherapy treatment or a combination thereof, at diagnosis and relapse, in a historical DIPG cohort.

利用历史队列研究弥漫性固有脑桥胶质瘤的治疗相关生存模式:欧洲儿科肿瘤学会 DIPG/DMG 登记处的报告。
背景:我们的目的是通过研究6种历史治疗路径,探讨弥漫性内生性桥脑胶质瘤(DIPG)患者的治疗与生存之间的关系:我们回顾性分析了409例经放射学中心复查的DIPG患者的数据,这些数据来自德国儿科肿瘤与血液学会HIT-HGG试验数据库和SIOPE-DIPG/DMG登记处。采用卡普兰-梅耶法估算生存结果,并通过单变量和多变量考克斯比例危险模型研究治疗效果:中位总生存期(OS)为 11.2 个月(95% 置信区间 [CI],10.5-11.9)。选择不接受前线治疗的患者的OS为3.0个月(95% CI,2.0-4.0),而单独接受放射治疗(RT)的患者的中位OS为10.4个月(95% CI,9.1-11.8)。接受RT联合化疗的患者的中位生存期最长,为11.7个月(95% CI,10.8-12.6)。中位进展后生存期(PPS)为4.1个月(95% CI,3.5-4.7)。复发但未接受治疗的患者的中位生存期为2.2个月(95% CI,1.8-2.6),而仅接受化疗的患者的中位生存期为4.4个月(95% CI,3.7-5.0),接受或不接受化疗的患者复发后的生存期最长,为6.6个月(95% CI,5.3-8.0)。在根据年龄和症状持续时间对诊断和复发情况进行调整的多变量分析中,治疗差异仍有意义:这项研究表明,在DIPG历史队列中,诊断和复发时放疗和化疗或两者联合治疗可提高生存率。
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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来源期刊
CiteScore
6.20
自引率
0.00%
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0
审稿时长
12 weeks
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