Incorporating Supramaximal Resection into Survival Stratification of IDH-wildtype Glioblastoma: A Refined Multi-institutional Recursive Partitioning Analysis.

IF 10 1区 医学 Q1 ONCOLOGY Clinical Cancer Research Pub Date : 2024-11-01 DOI:10.1158/1078-0432.CCR-23-3845
Yae Won Park, Kyu Sung Choi, Martha Foltyn-Dumitru, Gianluca Brugnara, Rouzbeh Banan, Sooyon Kim, Kyunghwa Han, Ji Eun Park, Tobias Kessler, Martin Bendszus, Sandro Krieg, Wolfgang Wick, Felix Sahm, Seung Hong Choi, Ho Sung Kim, Jong Hee Chang, Se Hoon Kim, Doonyaporn Wongsawaeng, Jeffrey Michael Pollock, Seung-Koo Lee, Ramon Francisco Barajas, Philipp Vollmuth, Sung Soo Ahn
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Abstract

Purpose: To propose a novel recursive partitioning analysis (RPA) classification model in patients with IDH-wildtype glioblastomas that incorporates the recently expanded conception of the extent of resection (EOR) in terms of both supramaximal and total resections.

Experimental design: This multicenter cohort study included a developmental cohort of 622 patients with IDH-wildtype glioblastomas from a single institution (Severance Hospital) and validation cohorts of 536 patients from three institutions (Seoul National University Hospital, Asan Medical Center, and Heidelberg University Hospital). All patients completed standard treatment including concurrent chemoradiotherapy and underwent testing to determine their IDH mutation and MGMTp methylation status. EORs were categorized into either supramaximal, total, or non-total resections. A novel RPA model was then developed and compared with a previous Radiation Therapy Oncology Group (RTOG) RPA model.

Results: In the developmental cohort, the RPA model included age, MGMTp methylation status, Karnofsky performance status, and EOR. Younger patients with MGMTp methylation and supramaximal resections showed a more favorable prognosis [class I: median overall survival (OS) 57.3 months], whereas low-performing patients with non-total resections and without MGMTp methylation showed the worst prognosis (class IV: median OS 14.3 months). The prognostic significance of the RPA was subsequently confirmed in the validation cohorts, which revealed a greater separation between prognostic classes for all cohorts compared with the previous RTOG RPA model.

Conclusions: The proposed RPA model highlights the impact of supramaximal versus total resections and incorporates clinical and molecular factors into survival stratification. The RPA model may improve the accuracy of assessing prognostic groups. See related commentary by Karschnia et al., p. 4811.

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将超极限切除纳入 IDH 野生型胶质母细胞瘤的生存分层:一种经过改进的多机构递归分区分析。
目的:针对IDH-野生型胶质母细胞瘤患者提出一种新的递归分区分析(RPA)分类模型,该模型结合了最近扩大的切除范围(EOR)概念,即超大切除范围和全切除范围:这项多中心队列研究包括来自一家机构(Severance 医院)的 622 名 IDH 野生型胶质母细胞瘤患者组成的发展队列,以及来自三家机构(首尔国立大学医院、牙山医疗中心和海德堡大学医院)的 536 名患者组成的验证队列。所有患者都完成了标准治疗,包括同期化疗和放疗,并接受了 IDH 突变和 MGMTp 甲基化状态检测。EORs被分为超小切除、全切除或非全切除。然后建立了一个新的RPA模型,并与之前的RTOG RPA模型进行了比较:在发展队列中,RPA模型包括年龄、MGMTp甲基化状态、KPS和EOR。有MGMTp甲基化和上颌骨切除的年轻患者预后较好(I级:中位总生存期[OS]57.3个月),而无MGMTp甲基化和非全切的低水平患者预后最差(IV级:中位OS 14.3个月)。RPA的预后意义随后在验证队列中得到了证实,与之前的RTOG RPA模型相比,验证队列显示所有队列的预后分级之间的差异更大:结论:所提出的 RPA 模型强调了超全切与全切的影响,并将临床和分子因素纳入生存分层。RPA模型可提高评估预后分组的准确性。
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来源期刊
Clinical Cancer Research
Clinical Cancer Research 医学-肿瘤学
CiteScore
20.10
自引率
1.70%
发文量
1207
审稿时长
2.1 months
期刊介绍: Clinical Cancer Research is a journal focusing on groundbreaking research in cancer, specifically in the areas where the laboratory and the clinic intersect. Our primary interest lies in clinical trials that investigate novel treatments, accompanied by research on pharmacology, molecular alterations, and biomarkers that can predict response or resistance to these treatments. Furthermore, we prioritize laboratory and animal studies that explore new drugs and targeted agents with the potential to advance to clinical trials. We also encourage research on targetable mechanisms of cancer development, progression, and metastasis.
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