Progression-free survival versus post-progression survival and overall survival in WHO grade 2 gliomas

被引:0
|
作者
Sagberg, Lisa Millgard [1 ,2 ]
Salvesen, Oyvind [3 ]
Jakola, Asgeir Store [4 ,5 ]
Thurin, Erik [5 ,6 ]
de Dios, Eddie [5 ,6 ]
Nawabi, Noah L. A. [7 ]
Kilgallon, John L. [7 ]
Bernstock, Joshua D. [7 ,8 ]
Kavouridis, Vasileios K. [7 ]
Smith, Timothy R. [7 ,8 ]
Solheim, Ole [2 ,9 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Publ Hlth & Nursing, Trondheim, Norway
[2] Trondheim Reg & Univ Hosp, St Olavs Hosp, Dept Neurosurg, Olav Kyrres gt 17, N-7006 Trondheim, Norway
[3] Norwegian Univ Sci & Technol, Dept Clin & Mol Med, Clin Res Unit, Trondheim, Norway
[4] Sahlgrens Univ Hosp, Dept Neurosurg, Gothenburg, Sweden
[5] Sahlgrens Acad, Inst Neurosci & Physiol, Dept Clin Neurosci, Gothenburg, Sweden
[6] Sahlgrens Univ Hosp, Dept Radiol, Gothenburg, Sweden
[7] Harvard Med Sch, Dept Neurosurg, Brigham & Womens Hosp, Boston, MA USA
[8] MIT, David H Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[9] Norwegian Univ Sci & Technol, Dept Neuromed & Movement Sci, Trondheim, Norway
基金
瑞典研究理事会;
关键词
Brain neoplasms; surrogate endpoints; response assessment criteria; prognostic factors; oncology; QUALITY-OF-LIFE; RESPONSE ASSESSMENT; SURGICAL RESECTION; CLINICAL-TRIALS; END-POINTS; GLIOBLASTOMA; RADIOTHERAPY; BEVACIZUMAB; EFFICACY; OLIGODENDROGLIOMA;
D O I
10.2340/1651-226X.2024.40845
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and purpose: Progression-free survival (PFS) remains to be validated as an outcome measure for diffuse WHO grade 2 gliomas, and knowledge about the relationships between PFS, post-progression survival (PPS), and overall survival (OS) in this subset of tumors is limited. We sought to assess correlations between PFS and OS, and identify factors associated with PFS, PPS, and OS in patients treated for diffuse supratentorial WHO grade 2 gliomas. Material and methods: We included 319 patients from three independent observational cohorts. The correlation between PFS and OS was analyzed using independent exponential distributions for PFS and time from progression to death. Cox proportional hazards models were used to determine the effects of covariates on PFS, PPS, and OS. Results: The overall correlation between PFS and OS was r0.31. The correlation was rs0.37 for astrocytos mas and rs0.19 for oligodendrogliomas. Longer PFS did not predict longer PPS. Patients with astrocytomas had shorter PFS, PPS, and OS. Larger preoperative tumor volume was a risk factor for shorter PFS, while older age was a risk factor for shorter PPS and OS. Patients who received early radio- and chemotherapy had longer PFS, but shorter PPS and OS. Interpretation: We found a weak correlation between PFS and OS in WHO grade 2 gliomas, with the weakest correlation observed in oligodendrogliomas. Our analyses did not demonstrate any association between PFS and PPS. Critically, predictors of PFS are not necessarily predictors of OS. There is a need for validation of PFS as an endpoint in diffuse WHO grade 2 gliomas.
引用
收藏
页码:798 / 804
页数:7
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