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
相关论文
共 50 条
  • [41] OVERALL SURVIVAL (OS) VERSUS PROGRESSION-FREE SURVIVAL (PFS): IS THERE A RATIONAL FOR REPLACING ONE OUTCOME FOR THE OTHER?
    Teich, V
    Fernandes, R. A.
    VALUE IN HEALTH, 2017, 20 (09) : A863 - A863
  • [42] Radiographic Progression-Free Survival and Clinical Progression-Free Survival as Potential Surrogates for Overall Survival in Men With Metastatic Hormone-Sensitive Prostate Cancer
    Halabi, Susan
    Roy, Akash
    Rydzewska, Larysa
    Guo, Siyuan
    Godolphin, Peter
    Hussain, Maha
    Tangen, Catherine
    Thompson, Ian
    Xie, Wanling
    Carducci, Michael A.
    Smith, Matthew R.
    Morris, Michael J.
    Gravis, Gwenaelle
    Dearnaley, David P.
    Verhagen, Paul
    Goto, Takayuki
    James, Nick
    Buyse, Marc E.
    Tierney, Jayne F.
    Sweeney, Christopher
    JOURNAL OF CLINICAL ONCOLOGY, 2024, 42 (09)
  • [43] Impact of Clinical Versus Biochemical Progression on Post-Progression Survival in Multiple Myeloma
    Chakraborty, Rajshekhar
    Liu, Hien D.
    Rybicki, Lisa
    Dean, Robert M.
    Faiman, Beth M.
    Kalaycio, Matt
    Khouri, Jack
    Samaras, Christy J.
    Majhail, Navneet S.
    Valent, Jason
    BLOOD, 2018, 132
  • [44] Progression-free or overall survival...revisited in BOLERO-2
    Gupta, Sudeep
    INDIAN JOURNAL OF MEDICAL AND PAEDIATRIC ONCOLOGY, 2014, 35 (01) : 1 - 2
  • [45] TERT as a prognostic factor for gliomas progression-free survival (PFS)
    Solis Hernandez, M. P.
    Faez, L.
    Cantero, D.
    Hernandez Lain, A.
    Sanchez Gomez, P.
    Ruano, Y.
    Galera, M. D. M.
    Sepulveda Sanchez, M.
    ANNALS OF ONCOLOGY, 2016, 27
  • [46] Detecting Overall Survival Benefit Derived From Survival Postprogression Rather Than Progression-Free Survival
    Morita, Satoshi
    Sakamaki, Kentaro
    Yin, Guosheng
    JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2015, 107 (08):
  • [47] IS PROGRESSION-FREE SURVIVAL A GOOD INDICATOR OF OVERALL SURVIVAL FOR PAZOPANIB IN PATIENTS WITH SYNOVIAL SARCOMA?
    Han, J.
    Lee, S.
    Cho, E.
    VALUE IN HEALTH, 2022, 25 (12) : S489 - S490
  • [48] Progression-free survival, overall survival and quality of life: What is their medicoeconomic importance in oncology?
    Pavlovic, Mira
    Garnier, Jerome
    Durand-Zaleski, Isabelle
    Bilbault, Pascal
    Gaudin, Anne-Francoise
    Le Jeunne, Claire
    Lalaude, Olivier
    Roze, Stephane
    De Sahb, Rima
    Sapede, Claudine
    THERAPIE, 2016, 71 (01): : 59 - 67
  • [49] Progression-free survival as a surrogate for overall survival in oncology trials: a methodological systematic review
    Belin, Lisa
    Tan, Aidan
    De Rycke, Yann
    Dechartres, Agnes
    BRITISH JOURNAL OF CANCER, 2020, 122 (11) : 1707 - 1714
  • [50] Individual-level data on the relationships of progression-free survival, post-progression survival and tumor response with overall survival in patients with advanced non-squamous non-small cell lung cancer
    Imai, H.
    Takahashi, T.
    Mori, K.
    Ono, A.
    Akamatsu, H.
    Shukuya, T.
    Taira, T.
    Kenmotsu, H.
    Naito, T.
    Murakami, H.
    Endo, M.
    Nakajima, T.
    Yamamoto, N.
    NEOPLASMA, 2014, 61 (02) : 233 - 240