Estimating progression-free survival in patients with glioblastoma using routinely collected data

被引:39
作者
Kelly, Charlotte [1 ]
Majewska, Paulina [2 ]
Ioannidis, Stefanos [2 ]
Raza, Muhammad Hasan [3 ]
Williams, Matt [1 ,4 ]
机构
[1] Charing Cross Hosp, Dept Clin Oncol, Fulham Palace Rd, London W6 8RF, England
[2] Imperial Coll London, Sch Med, Exhibit Rd, London SW7 2AZ, England
[3] Charing Cross Hosp, Dept Neurosurg, Fulham Palace Rd, London W6 8RF, England
[4] Imperial Coll London, Inst Global Hlth Improvement, Computat Oncol Grp, Exhibit Rd, London SW7 2AZ, England
关键词
Glioblastoma; Routine data; Overall survival; Progression free survival; QUALITY-OF-LIFE; NECK-CANCER; RECURRENCE; CLAIMS; TEMOZOLOMIDE; ONCOLOGY; HEAD; CARE;
D O I
10.1007/s11060-017-2619-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma (GBM) represents 80% of all primary malignant brain tumours in adults. Prognosis is poor, and there is a clear correlation between disease progression and deterioration in functional status. In this pilot study we assess whether we can estimate disease progression and progression free survival (PFS) from routinely collected electronic healthcare data. We identified fifty patients with glioblastoma who had chemo-radiotherapy. For each patient we manually collected a reference data set recording demographics, surgery, radiotherapy, chemotherapy, follow-up and death. We also obtained an electronic routine data set for each patient by combining local data on chemotherapy/radiotherapy and hospital admissions. We calculated overall survival (OS) and PFS using the reference data set, and estimated them using the routine data sets using two different methods, and compared the estimated measures with the reference measures. Overall survival was 68% at 1 year and median OS was 12.8 months. The routine data correctly identified progressive disease in 37 of 40 patients and stable disease in 7 of 10 patients. PFS was 7.4 months and the estimated PFS using routine data was 9.1 and 7.8 months with methods 1 and 2 respectively. There was acceptable agreement between reference and routine data in 49 of 50 patients for OS and 35 of 50 patients for PFS. The event of progression, subsequent treatment and OS are well estimated using our approach, but PFS estimation is less accurate. Our approach could refine our understanding of the disease course and allow us to report PFS, OS and treatment nationally.
引用
收藏
页码:621 / 627
页数:7
相关论文
共 50 条
[21]   The Overall Survival and Progression-Free Survival in Patients with Advanced Adrenocortical Cancer Is Increased after the Multidisciplinary Team Evaluation [J].
Tizianel, Irene ;
Caccese, Mario ;
Torresan, Francesca ;
Lombardi, Giuseppe ;
Evangelista, Laura ;
Crimi, Filippo ;
Sepulcri, Matteo ;
Iacobone, Maurizio ;
Padovan, Marta ;
Galuppini, Francesca ;
Zagonel, Vittorina ;
Scaroni, Carla ;
Ceccato, Filippo .
CANCERS, 2022, 14 (16)
[22]   A microfluidic cell-migration assay for the prediction of progression-free survival and recurrence time of patients with glioblastoma [J].
Wong, Bin Sheng ;
Shah, Sagar R. ;
Yankaskas, Christopher L. ;
Bajpai, Vivek K. ;
Wu, Pei-Hsun ;
Chin, Deborah ;
Ifemembi, Brent ;
ReFaey, Karim ;
Schiapparelli, Paula ;
Zheng, Xiaobin ;
Martin, Stuart S. ;
Fan, Chen-Ming ;
Quinones-Hinojosa, Alfredo ;
Konstantopoulos, Konstantinos .
NATURE BIOMEDICAL ENGINEERING, 2021, 5 (01) :26-+
[23]   Six-month progression-free survival as an alternative primary efficacy endpoint to overall survival in newly diagnosed glioblastoma patients receiving temozolomide [J].
Polley, Mei-Yin C. ;
Lamborn, Kathleen R. ;
Chang, Susan M. ;
Butowski, Nicholas ;
Clarke, Jennifer L. ;
Prados, Michael .
NEURO-ONCOLOGY, 2010, 12 (03) :274-282
[24]   Missing Data and Censoring in the Analysis of Progression-Free Survival in Oncology Clinical Trials [J].
Denne, J. S. ;
Stone, A. M. ;
Bailey-Iacona, R. ;
Chen, T. -T. .
JOURNAL OF BIOPHARMACEUTICAL STATISTICS, 2013, 23 (05) :951-970
[25]   Concordance index: Surrogacy of progression-free survival for overall survival [J].
Fan, Yiwei ;
Yin, Guosheng .
CONTEMPORARY CLINICAL TRIALS, 2021, 104
[26]   Diagnosing Progression in Glioblastoma-Tackling a Neuro-Oncology Problem Using Artificial-Intelligence-Derived Volumetric Change over Time on Magnetic Resonance Imaging to Examine Progression-Free Survival in Glioblastoma [J].
Belue, Mason J. ;
Harmon, Stephanie A. ;
Chappidi, Shreya ;
Zhuge, Ying ;
Tasci, Erdal ;
Jagasia, Sarisha ;
Joyce, Thomas ;
Camphausen, Kevin ;
Turkbey, Baris ;
Krauze, Andra V. .
DIAGNOSTICS, 2024, 14 (13)
[27]   Influence of MMR, MGMT Promotor Methylation and Protein Expression on Overall and Progression-Free Survival in Primary Glioblastoma Patients Treated with Temozolomide [J].
Brawanski, Konstantin R. ;
Sprung, Susanne ;
Freyschlag, Christian F. ;
Hoeftberger, Romana ;
Stroebel, Thomas ;
Haybaeck, Johannes ;
Thome, Claudius ;
Manzl, Claudia ;
Birkl-Toeglhofer, Anna M. .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (07)
[28]   High VEGFA Expression Is Associated with Improved Progression-Free Survival after Bevacizumab Treatment in Recurrent Glioblastoma [J].
Alves, Barbara ;
Peixoto, Joana ;
Macedo, Sofia ;
Pinheiro, Jorge ;
Carvalho, Bruno ;
Soares, Paula ;
Lima, Jorge ;
Lima, Raquel T. .
CANCERS, 2023, 15 (08)
[29]   A Weibull multi-state model for the dependence of progression-free survival and overall survival [J].
Li, Yimei ;
Zhang, Qiang .
STATISTICS IN MEDICINE, 2015, 34 (17) :2497-2513
[30]   Progression-Free Survival as a Surrogate Endpoint of Overall Survival in Patients With Metastatic Renal Cell Carcinoma [J].
Halabi, Susan ;
Rini, Brian ;
Escudier, Bernard ;
Stadler, Walter M. ;
Small, Eric J. .
CANCER, 2014, 120 (01) :52-60