Molecular features of glioblastomas in long-term survivors compared to short-term survivors-a matched-pair analysis

被引:15
作者
Sommerlath, Vivien N. [1 ]
Buergy, Daniel [1 ]
Etminan, Nima [2 ]
Brehmer, Stefanie [2 ]
Reuss, David [3 ]
Sarria, Gustavo R. [4 ]
Guiot, Marie-Christin [5 ]
Hanggi, Daniel [6 ]
Wenz, Frederik [7 ]
Petrecca, Kevin [8 ]
Giordano, Frank A. [4 ]
机构
[1] Heidelberg Univ, Univ Med Ctr Mannheim, Dept Radiat Oncol, Heidelberg, Germany
[2] Heidelberg Univ, Univ Med Ctr Mannheim, Dept Neurosurg, Heidelberg, Germany
[3] Heidelberg Univ, Inst Pathol, Dept Neuropathol, Heidelberg, Germany
[4] Univ Bonn, Univ Hosp Bonn, Dept Radiat Oncol, Venusberg Campus 1, D-53127 Bonn, Germany
[5] Montreal Neurol Inst, Dept Pathol, Montreal, PQ, Canada
[6] Heinrich Heine Univ, Dept Neurosurg, Dusseldorf, Germany
[7] Freiburg Med Ctr, Freiburg, Germany
[8] Montreal Neurol Inst, Dept Neurosurg, Montreal, PQ, Canada
关键词
Glioblastoma; GBM; Prognostic factors; GFAP; MGMT; CENTRAL-NERVOUS-SYSTEM; TOPOISOMERASE-II-ALPHA; ACIDIC PROTEIN GFAP; ADJUVANT TEMOZOLOMIDE; PROGNOSTIC-FACTORS; DIAGNOSTIC MARKER; CLASSIFICATION; TUMORS; BRAIN; ASTROCYTOMAS;
D O I
10.1186/s13014-022-01984-w
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Although glioblastoma (GB) is associated with a devastating prognosis, a small proportion of patients achieve long-term survival rates. We herein present a matched-pair analysis of molecular factors found in long- and short-term survivors (LTS, STS). Methods We performed a cross-institutional analysis of 262 patient records and matched a group of 91 LTS (>= 3 years) with two groups of STS (STS-1, n = 91; STS-2, n = 80). Matching was performed according to age, Karnofsky Performance Status, initial therapy and adjuvant therapy. Molecular factors were compared between LTS (total of 91 patients) v. STS-1, and LTS (subgroup of 80 patients) v. STS-2. We included glial fibrillary acidic protein (GFAP), O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation, isocitrate dehydrogenase 1 (IDH-1); furthermore, the proliferation index was analyzed (Ki-67/MIB-1). Results IDH-1 and decreased Ki-67 were numerically associated with LTS but the difference was only significant compared to STS-1 (n.s. v. STS-2). LTS was associated with MGMT promoter hypermethylation (p = 0.013 and p = 0.022) and GFAP expression (p < 0.001 and p = 0.001). Positivity for both factors combined compared to negativity for one factor occurred more often in the LTS group (p = 0.002 and p = 0.006); negativity for both factors combined did not occur in the LTS group. Conclusion In this retrospective analysis, GFAP expression and MGMT promoter methylation were associated with LTS. Given the hypothesis-generating nature of our study, these observations should be confirmed in prospective clinical trials.
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页数:8
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共 30 条
[1]   High expression of DNA topoisomerase IIα and Ki-67 antigen is associated with prolonged survival glioblastoma patients [J].
Bredel, M ;
Piribauer, M ;
Marosi, C ;
Birner, P ;
Gatterbauer, B ;
Fischer, I ;
Ströbel, T ;
Rössler, K ;
Budka, H ;
Hainfellner, JA .
EUROPEAN JOURNAL OF CANCER, 2002, 38 (10) :1343-1347
[2]   Prognostic factors for survival in 676 consecutive patients with newly diagnosed primary glioblastoma [J].
Filippini, Graziella ;
Falcone, Chiara ;
Boiardi, Amerigo ;
Broggi, Giovanni ;
Bruzzone, Maria G. ;
Caldiroli, Dario ;
Farina, Rita ;
Farinotti, Mariangela ;
Fariselli, Laura ;
Finocchiaro, Gaetano ;
Giombini, Sergio ;
Polio, Bianca ;
Savoiardo, Mario ;
Solero, Carlo L. ;
Valsecchi, Maria G. .
NEURO-ONCOLOGY, 2008, 10 (01) :79-87
[3]   GFAP IN BRAIN-TUMOR DIAGNOSIS - POSSIBILITIES AND LIMITATIONS [J].
GULLOTTA, F ;
SCHINDLER, F ;
SCHMUTZLER, R ;
WEEKSSEIFERT, A .
PATHOLOGY RESEARCH AND PRACTICE, 1985, 180 (01) :54-60
[4]   PROLIFERATIVE ASSESSMENT OF GFAP-POSITIVE AND GFAP-NEGATIVE GLIOMA-CELLS BY NUCLEOLAR ORGANIZER REGION STAINING [J].
HARA, A ;
SAKAI, N ;
YAMADA, H ;
NIIKAWA, S ;
OHNO, T ;
TANAKA, T ;
MORI, H .
SURGICAL NEUROLOGY, 1991, 36 (03) :190-194
[5]   Patients with IDH1 wild type anaplastic astrocytomas exhibit worse prognosis than IDH1-mutated glioblastomas, and IDH1 mutation status accounts for the unfavorable prognostic effect of higher age: implications for classification of gliomas [J].
Hartmann, Christian ;
Hentschel, Bettina ;
Wick, Wolfgang ;
Capper, David ;
Felsberg, Joerg ;
Simon, Matthias ;
Westphal, Manfred ;
Schackert, Gabriele ;
Meyermann, Richard ;
Pietsch, Torsten ;
Reifenberger, Guido ;
Weller, Michael ;
Loeffler, Markus ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2010, 120 (06) :707-718
[6]   Type and frequency of IDH1 and IDH2 mutations are related to astrocytic and oligodendroglial differentiation and age: a study of 1,010 diffuse gliomas [J].
Hartmann, Christian ;
Meyer, Jochen ;
Balss, Joerg ;
Capper, David ;
Mueller, Wolf ;
Christians, Arne ;
Felsberg, Joerg ;
Wolter, Marietta ;
Mawrin, Christian ;
Wick, Wolfgang ;
Weller, Michael ;
Herold-Mende, Christel ;
Unterberg, Andreas ;
Jeuken, Judith W. M. ;
Wesseling, Peter ;
Reifenberger, Guido ;
von Deimling, Andreas .
ACTA NEUROPATHOLOGICA, 2009, 118 (04) :469-474
[7]   MGMT gene silencing and benefit from temozolomide in glioblastoma [J].
Hegi, ME ;
Diserens, A ;
Gorlia, T ;
Hamou, M ;
de Tribolet, N ;
Weller, M ;
Kros, JM ;
Hainfellner, JA ;
Mason, W ;
Mariani, L ;
Bromberg, JEC ;
Hau, P ;
Mirimanoff, RO ;
Cairncross, JG ;
Janzer, RC ;
Stupp, R .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (10) :997-1003
[8]   Correlation of O6-Methylguanine methyltransferase (MGMT) promoter methylation with clinical outcomes in glioblastoma and clinical strategies to modulate MGMT activity [J].
Hegi, Monika E. ;
Liu, Lili ;
Herman, James G. ;
Stupp, Roger ;
Wick, Wolfgang ;
Weller, Michael ;
Mehta, Minesh P. ;
Gilbert, Mark R. .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (25) :4189-4199
[9]   MIB-1 and DNA topoisomerase IIα could be helpful for predicting long-term survival of patients with glioblastoma [J].
Ho, DMT ;
Hsu, CY ;
Ting, LT ;
Chiang, H .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2003, 119 (05) :715-722
[10]   Use of MIB-1 (Ki-67) immunoreactivity in differentiating grade II and grade III gliomas [J].
Hsu, DW ;
Louis, DN ;
Efird, JT ;
HedleyWhyte, ET .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1997, 56 (08) :857-865