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基于单一机构连续入选的非选择性患者前瞻性队列的胶质母细胞瘤患者标准治疗预后模型。

A Prognostic Model for Glioblastoma Patients Treated With Standard Therapy Based on a Prospective Cohort of Consecutive Non-Selected Patients From a Single Institution.

作者信息

Abedi Armita Armina, Grunnet Kirsten, Christensen Ib Jarle, Michaelsen Signe Regner, Muhic Aida, Møller Søren, Hasselbalch Benedikte, Poulsen Hans Skovgaard, Urup Thomas

机构信息

Department of Radiation Biology, The Finsen Center, Rigshospitalet, Copenhagen, Denmark.

Department of Oncology, The Finsen Center, Rigshospitalet, Copenhagen, Denmark.

出版信息

Front Oncol. 2021 Feb 25;11:597587. doi: 10.3389/fonc.2021.597587. eCollection 2021.

Abstract

BACKGROUND

Glioblastoma patients administered standard therapies, comprising maximal surgical resection, radiation therapy with concomitant and adjuvant temozolomide, have a variable prognosis with a median overall survival of 15-16 months and a 2-year overall survival of 30%. The aim of this study was to develop a prognostic nomogram for overall survival for glioblastoma patients treated with standard therapy outside clinical trials.

METHODS

The study included 680 consecutive, non-selected glioblastoma patients administered standard therapy as primary treatment between the years 2005 and 2016 at Rigshospitalet, Copenhagen, Denmark. The prognostic model was generated employing multivariate Cox regression analysis modeling overall survival.

RESULTS

The following poor prognostic factors were included in the final prognostic model for overall survival: Age (10-year increase: HR = 1.18, 95% CI: 1.08-1.28, p < 0.001), ECOG performance status (PS) 1 vs. 0 (HR = 1.30, 95% CI: 1.07-1.57, p = 0.007), PS 2 vs. 0 (HR = 2.99, 95% CI: 1.99-4.50, p < 0.001), corticosteroid use (HR = 1.42, 95% CI: 1.18-1.70, p < 0.001), multifocal disease (HR = 1.63, 95% CI: 1.25-2.13, p < 0.001), biopsy vs. resection (HR = 1.35, 95% CI: 1.04-1.72, p = 0.02), un-methylated promoter of the MGMT (O-methylguanine-DNA methyltransferase) gene (HR = 1.71, 95% CI: 1.42-2.04, p < 0.001). The model was validated internally and had a concordance index of 0.65.

CONCLUSION

A nomogram for overall survival was established. This model can be used for risk stratification and treatment planning, as well as improve enrollment criteria for clinical trials.

摘要

背景

接受标准治疗(包括最大程度手术切除、同步放化疗及辅助替莫唑胺治疗)的胶质母细胞瘤患者预后各异,中位总生存期为15 - 16个月,2年总生存率为30%。本研究旨在为非临床试验中接受标准治疗的胶质母细胞瘤患者制定总生存期的预后列线图。

方法

该研究纳入了2005年至2016年间在丹麦哥本哈根的里格霍斯皮塔利特医院连续接受标准治疗作为初始治疗的680例未经筛选的胶质母细胞瘤患者。采用多因素Cox回归分析建立总生存期的预后模型。

结果

最终的总生存期预后模型纳入了以下不良预后因素:年龄(每增加10岁:HR = 1.18,95%CI:1.08 - 1.28,p < 0.001)、东部肿瘤协作组(ECOG)体能状态(PS)1级与0级相比(HR = 1.30,95%CI:1.07 - 1.57,p = 0.007)、PS 2级与0级相比(HR = 2.99,95%CI:1.99 - 4.50,p < 0.001)、使用皮质类固醇(HR = 1.42,95%CI:1.18 - 1.70,p < 0.001)、多灶性病变(HR = 1.63,95%CI:1.25 - 2.13,p < 0.001)、活检与切除相比(HR = 1.35,95%CI:1.04 - 1.72,p = 0.02)、O6 - 甲基鸟嘌呤 - DNA甲基转移酶(MGMT)基因启动子未甲基化(HR = 1.71,95%CI:1.42 - 2.04,p < 0.001)。该模型在内部得到验证,一致性指数为0.65。

结论

建立了总生存期的列线图。该模型可用于风险分层和治疗规划,以及完善临床试验的入组标准。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6838/7946965/e1af2ab2b623/fonc-11-597587-g001.jpg

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