Association Between Perioperative Hyperglycemia and Survival in Patients With Glioblastoma

被引:18
作者
Hagan, Katherine [1 ]
Bhavsar, Shreyas [1 ]
Arunkumar, Radha [1 ]
Grasu, Roxana [1 ]
Dang, Anh [1 ]
Carlson, Richard [1 ]
Cowles, Charles [1 ]
Arnold, Benjamin [1 ]
Potylchansky, Yuri [1 ]
Rahlfs, Thomas F. [1 ]
Lipski, Ian [1 ]
Walsh, Caroline [4 ]
Jimenez, Federico [1 ]
Nguyen, Anh T. [1 ]
Feng, Lei [2 ]
Cata, Juan P. [1 ,3 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Anesthesiol & Perioperat Med, 1515 Holcombe Blvd, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Anesthesiol & Surg Oncol Res Grp, Houston, TX USA
[4] Colgate Univ, Hamilton, NY 13346 USA
关键词
glioblastoma multiforme; hyperglycemia; overall survival; progression free survival; NEWLY-DIAGNOSED GLIOBLASTOMA; PREOPERATIVE GLUCOSE; DEXAMETHASONE; ASTROCYTOMAS; TEMOZOLOMIDE; GLYCEMIA; SURGERY; CELLS;
D O I
10.1097/ANA.0000000000000339
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Several studies have examined the association between hyperglycemia in the first 10 to 12 weeks following surgery and postoperative survival in glioblastoma multiforme (GBM) patients. We hypothesize that episodes of hyperglycemia before, during and/or following surgery for primary GBM are independent predictors of disease progression and mortality. Materials and Methods: A total of 162 adult patients were included in the analysis. All patients received adjuvant temozolamide. The progression free survival (PFS) and overall survival (OS) rates at 1 and 5 years were analyzed using different glycemic cutoff values. Multivariate analyses were conducted to test the association between preoperative, intraoperative and postoperative hyperglycemia with PFS and OS. Results: Kaplan-Meier curves revealed a trend toward increased PFS and OS with lower glucose concentrations with the exception of glucose concentrations >180 mg/dL in the intraoperative/postoperative day 0 time period. Univariate analysis of blood glucose levels did not demonstrate a statistically significant effect on PFS in any time period, however hyperglycemia was statistically significant for OS in the preoperative time period. Although, multivariate analysis showed no statistically significant association with hyperglycemia on PFS, a statistically significant decrease in OS was seen for plasma glucose concentrations >112 mg/dL (P=0.01) and >180 mg/dL (P=0.01) in the preoperative period. There was a decreasing effect on OS with blood glucose concentrations greater than the median in multiple time periods (P=0.02). Conclusions: Preoperative hyperglycemia is associated with poor OS after GBM surgery.
引用
收藏
页码:21 / 29
页数:9
相关论文
共 23 条
[1]   Preoperative blood glucose concentrations and postoperative outcomes after elective non-cardiac surgery: an observational study [J].
Abdelmalak, B. B. ;
Knittel, J. ;
Abdelmalak, J. B. ;
Dalton, J. E. ;
Christiansen, E. ;
Foss, J. ;
Argalious, M. ;
Zimmerman, R. ;
Van den Berghe, G. .
BRITISH JOURNAL OF ANAESTHESIA, 2014, 112 (01) :79-88
[2]   Persistent outpatient hyperglycemia is independently associated with survival, recurrence and malignant degeneration following surgery for hemispheric low grade gliomas [J].
Chaichana, Kaisorn L. ;
McGirt, Matthew J. ;
Woodworth, Graeme F. ;
Datoo, Ghazala ;
Tamargo, Rafael J. ;
Weingart, John ;
Olivi, Alessandro ;
Brem, Henry ;
Quinones-Hinojosa, Alfredo .
NEUROLOGICAL RESEARCH, 2010, 32 (04) :442-448
[3]   Association Between Hyperglycemia and Survival in Patients With Newly Diagnosed Glioblastoma [J].
Derr, Rachel L. ;
Ye, Xiaobu ;
Islas, Melissa U. ;
Desideri, Serena ;
Saudek, Christopher D. ;
Grossman, Stuart A. .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (07) :1082-1086
[4]   Intensive versus Conventional Glucose Control in Critically Ill Patients [J].
Finfer, S. ;
Blair, D. ;
Bellomo, R. ;
McArthur, C. ;
Mitchell, I. ;
Myburgh, J. ;
Norton, R. ;
Potter, J. ;
Chittock, D. ;
Dhingra, V. ;
Foster, D. ;
Cook, D. ;
Dodek, P. ;
Hebert, P. ;
Henderson, W. ;
Heyland, D. ;
McDonald, E. ;
Ronco, J. ;
Schweitzer, L. ;
Peto, R. ;
Sandercock, P. ;
Sprung, C. ;
Young, J. D. ;
Su, S. ;
Heritier, S. ;
Li, Q. ;
Bompoint, S. ;
Billot, L. ;
Crampton, L. ;
Darcy, F. ;
Jayne, K. ;
Kumarasinghe, V. ;
Little, L. ;
McEvoy, S. ;
MacMahon, S. ;
Pandey, S. ;
Ryan, S. ;
Shukla, R. ;
Vijayan, B. ;
Atherton, S. ;
Bell, J. ;
Hadfield, L. ;
Hourigan, C. ;
McArthur, C. ;
Newby, L. ;
Simmonds, C. ;
Buhr, H. ;
Eccleston, M. ;
McGuinness, S. ;
Parke, R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (13) :1283-1297
[5]   Insulin-mediated signaling promotes proliferation and survival of glioblastoma through Akt activation [J].
Gong, Yuanying ;
Ma, Yufang ;
Sinyuk, Maksim ;
Loganathan, Sudan ;
Thompson, Reid C. ;
Sarkaria, Jann N. ;
Chen, Wenbiao ;
Lathia, Justin D. ;
Mobley, Bret C. ;
Clark, Stephen W. ;
Wang, Jialiang .
NEURO-ONCOLOGY, 2016, 18 (01) :48-57
[6]   The Effect of Timing of Concurrent Chemoradiation in Patients With Newly Diagnosed Glioblastoma [J].
Han, Seunggu J. ;
Rutledge, W. Caleb ;
Molinaro, Annette M. ;
Chang, Susan M. ;
Clarke, Jennifer L. ;
Prados, Michael D. ;
Taylor, Jennie W. ;
Berger, Mitchel S. ;
Butowski, Nicholas A. .
NEUROSURGERY, 2015, 77 (02) :248-253
[7]   Dietary sugar intake increases liver tumor incidence in female mice [J].
Healy, Marin E. ;
Lahiri, Sujoy ;
Hargett, Stefan R. ;
Chow, Jenny D. Y. ;
Byrne, Frances L. ;
Breen, David S. ;
Kenwood, Brandon M. ;
Taddeo, Evan P. ;
Lackner, Carolin ;
Caldwell, Stephen H. ;
Hoehn, Kyle L. .
SCIENTIFIC REPORTS, 2016, 6
[8]   Delay in radiotherapy shortens survival in patients with high grade glioma [J].
Irwin, Chris ;
Hunn, Martin ;
Purdie, Gordon ;
Hamilton, David .
JOURNAL OF NEURO-ONCOLOGY, 2007, 85 (03) :339-343
[9]   Glucose withdrawal induces oxidative stress followed by apoptosis in glioblastoma cells but not in normal human astrocytes [J].
Jelluma, Nannette ;
Yang, Xiaodong ;
Stokoe, David ;
Evan, Gerard I. ;
Dansen, Tobias B. ;
Haas-Kogan, Daphne A. .
MOLECULAR CANCER RESEARCH, 2006, 4 (05) :319-330
[10]  
Kreth FW, 1997, CANCER, V79, P370, DOI 10.1002/(SICI)1097-0142(19970115)79:2<370::AID-CNCR21>3.0.CO