Extensive brainstem infiltration, not mass effect, is a common feature of end-stage cerebral glioblastomas

被引:59
作者
Drumm, Michael R. [1 ]
Dixit, Karan S. [2 ]
Grimm, Sean [2 ]
Kumthekar, Priya [2 ]
Lukas, Rimas V. [2 ]
Raizer, Jeffrey J. [2 ]
Stupp, Roger [2 ]
Chheda, Milan G. [3 ]
Kam, Kwok-Ling [4 ]
McCord, Matthew [4 ]
Sachdev, Sean [5 ]
Kruser, Timothy [5 ]
Steffens, Alicia [1 ]
Javier, Rodrigo [1 ]
McCortney, Kathleen [1 ]
Horbinski, Craig [1 ,4 ]
机构
[1] Northwestern Univ, Dept Neurol Surg, Chicago, IL 60611 USA
[2] Northwestern Univ, Dept Neurol, Chicago, IL 60611 USA
[3] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[4] Northwestern Univ, Dept Pathol, Chicago, IL 60611 USA
[5] Northwestern Univ, Dept Radiat Oncol, Chicago, IL 60611 USA
关键词
glioblastoma; midbrain; pons; medulla; brainstem; postmortem; autopsy; SUPRATENTORIAL GLIOBLASTOMA; TEMOZOLOMIDE; BEVACIZUMAB; DISSEMINATION; POSTMORTEM; MULTIFORME; INVASION; PHASE; TRIAL;
D O I
10.1093/neuonc/noz216
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. Progress in extending the survival of glioblastoma (GBM) patients has been slow. A better understanding of why patient survival remains poor is critical to developing new strategies. Postmortem studies on GBM can shed light on why patients are dying. Methods. The brains of 33 GBM patients were autopsied and examined for gross and microscopic abnormalities. Clinical-pathologic correlations were accomplished through detailed chart reviews. Data were compared with older published autopsy GBM studies that predated newer treatment strategies, such as more extensive surgical resection and adjuvant temozolomide. Results. In older GBM autopsy series, mass effect was observed in 72% of brains, with herniation in 50% of all cases. Infiltration of tumor into the brainstem was noted in only 21% of those older cases. In the current series, only 10 of 33 (30%) GBMs showed mass effect (P = 0.0003), and only 1 (3%) showed herniation (P < 0.0001). However, extensive GBM infiltration of the brainstem was present in 22 cases (67%, P < 0.0001), with accompanying destruction of the pons and white matter tracts. There was a direct correlation between longer median patient survival and the presence of brainstem infiltration (16.1 mo in brainstem-invaded cases vs 9.0 mo in cases lacking extensive brainstem involvement; P = 0.0003). Conclusions. With improving care, severe mass effect appears to be less common in GBM patients today, whereas dissemination, including life-threatening brainstem invasion, is now more pronounced. This has major implications regarding preclinical GBM models, as well as the design of clinical trials aimed at further improving patient survival.
引用
收藏
页码:470 / 479
页数:10
相关论文
共 32 条
  • [11] Hamza Ameer, 2017, Autops Case Rep, V7, P1, DOI 10.4322/acr.2017.036
  • [12] MGMT gene silencing and benefit from temozolomide in glioblastoma
    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
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (10) : 997 - 1003
  • [13] What do we know about IDH1/2 mutations so far, and how do we use it?
    Horbinski, Craig
    [J]. ACTA NEUROPATHOLOGICA, 2013, 125 (05) : 621 - 636
  • [14] Diffusion Tensor Tractography of the Human Brain Cortico-Ponto-Cerebellar Pathways: A Quantitative Preliminary Study
    Kamali, Arash
    Kramer, Larry A.
    Frye, Richard E.
    Butler, Ian J.
    Hasan, Khader M.
    [J]. JOURNAL OF MAGNETIC RESONANCE IMAGING, 2010, 32 (04) : 809 - 817
  • [15] IMAGING-BASED STEREOTAXIC SERIAL BIOPSIES IN UNTREATED INTRACRANIAL GLIAL NEOPLASMS
    KELLY, PJ
    DAUMASDUPORT, C
    KISPERT, DB
    KALL, BA
    SCHEITHAUER, BW
    ILLIG, JJ
    [J]. JOURNAL OF NEUROSURGERY, 1987, 66 (06) : 865 - 874
  • [16] VEGF Inhibits Tumor Cell Invasion and Mesenchymal Transition through a MET/VEGFR2 Complex
    Lu, Kan V.
    Chang, Jeffrey P.
    Parachoniak, Christine A.
    Pandika, Melissa M.
    Aghi, Manish K.
    Meyronet, David
    Isachenko, Nadezda
    Fouse, Shaun D.
    Phillips, Joanna J.
    Cheresh, David A.
    Park, Morag
    Bergers, Gabriele
    [J]. CANCER CELL, 2012, 22 (01) : 21 - 35
  • [17] Leptomeningeal dissemination in glioblastoma; an inspection of risk factors, treatment, and outcomes at a single institution
    Mandel, Jacob J.
    Yust-Katz, Shlomit
    Cachia, David
    Wu, Jimin
    Liu, Diane
    de Groot, John F.
    Yung, Alfred W. K.
    Gilbert, Mark R.
    [J]. JOURNAL OF NEURO-ONCOLOGY, 2014, 120 (03) : 597 - 605
  • [18] Nemetz Peter N, 2006, MedGenMed, V8, P80
  • [19] Targeted next-generation sequencing panel (GlioSeq) provides comprehensive genetic profiling of central nervous system tumors
    Nikiforova, Marina N.
    Wald, Abigail I.
    Melan, Melissa A.
    Roy, Somak
    Zhong, Shan
    Hamilton, Ronald L.
    Lieberman, Frank S.
    Drappatz, Jan
    Amankulor, Nduka M.
    Pollack, Ian F.
    Nikiforov, Yuri E.
    Horbinski, Craig
    [J]. NEURO-ONCOLOGY, 2016, 18 (03) : 379 - 387
  • [20] Initial and cumulative recurrence patterns of glioblastoma after temozolomide-based chemoradiotherapy and salvage treatment: a retrospective cohort study in a single institution
    Ogura, Kengo
    Mizowaki, Takashi
    Arakawa, Yoshiki
    Ogura, Masakazu
    Sakanaka, Katsuyuki
    Miyamoto, Susumu
    Hiraoka, Masahiro
    [J]. RADIATION ONCOLOGY, 2013, 8