New hints towards a precision medicine strategy for IDH wild-type glioblastoma

被引:34
作者
White, K. [1 ]
Connor, K. [1 ]
Clerkin, J. [1 ,2 ]
Murphy, B. M. [3 ]
Salvucci, M. [3 ]
O'Farrell, A. C. [1 ]
Rehm, M. [4 ,5 ]
O'Brien, D. [2 ]
Prehn, J. H. M. [3 ]
Niclou, S. P. [6 ]
Lamfers, M. L. M. [7 ]
Verreault, M. [8 ]
Idbaih, A. [8 ]
Verhaak, R. [9 ]
Golebiewska, A. [6 ]
Byrne, A. T. [1 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Precis Canc Med Grp, Dublin, Ireland
[2] Beaumont Hosp, Natl Neurosurg Dept, Dublin, Ireland
[3] Royal Coll Surgeons Ireland, Dept Physiol & Med Phys, Ctr Syst Med, Dublin, Ireland
[4] Univ Stuttgart, Inst Cell Biol & Immunol, Stuttgart, Germany
[5] Univ Stuttgart, Stuttgart Res Ctr Syst Biol, Stuttgart, Germany
[6] Luxembourg Inst Hlth, Dept Oncol, NORLUX Neurooncol Lab, Luxembourg, Luxembourg
[7] Erasmus MC, Brain Tumor Ctr, Dept Neurosurg, Univ Med Ctr Rotterdam, Rotterdam, Netherlands
[8] Sorbonne Univ, Inst Cerveau & Moelle Epiniere, Hop Univ La Pitie Salpetriere Charles Foix, Serv Neurol, Paris, France
[9] Jackson Lab Genom Med, Farmington, CT USA
基金
欧盟地平线“2020”;
关键词
IDH-wt glioblastoma; tumour microenvironment; multi-omics; precision therapy; NEWLY-DIAGNOSED GLIOBLASTOMA; CENTRAL-NERVOUS-SYSTEM; PHASE-II; T-CELLS; RECURRENT GLIOBLASTOMA; PD-L1; EXPRESSION; TUMOR EVOLUTION; IMMUNE-SYSTEM; GLIOMA; TEMOZOLOMIDE;
D O I
10.1016/j.annonc.2020.08.2336
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma represents the most common primary malignancy of the central nervous system in adults and remains a largely incurable disease. The elucidation of disease subtypes based on mutational profiling, gene expression and DNA methylation has so far failed to translate into improved clinical outcomes. However, new knowledge emerging from the subtyping effort in the IDH-wild-type setting may provide directions for future precision therapies. Here, we review recent learnings in the field, and further consider how tumour microenvironment differences across subtypes may reveal novel contexts of vulnerability. We discuss recent treatment approaches and ongoing trials in the IDH-wildtype glioblastoma setting, and propose an integrated discovery stratagem incorporating multi-omics, single-cell technologies and computational approaches.
引用
收藏
页码:1679 / 1692
页数:14
相关论文
共 116 条
  • [91] The tumor microenvironment underlies acquired resistance to CSF-1R inhibition in gliomas
    Quail, Daniela F.
    Bowman, Robert L.
    Akkari, Leila
    Quick, Marsha L.
    Schuhmacher, Alberto J.
    Huse, Jason T.
    Holland, Eric C.
    Sutton, James C.
    Joyce, Johanna A.
    [J]. SCIENCE, 2016, 352 (6288)
  • [92] Phase I/randomized phase II study of afatinib, an irreversible ErbB family blocker, with or without protracted temozolomide in adults with recurrent glioblastoma
    Reardon, David A.
    Nabors, Louis B.
    Mason, Warren P.
    Perry, James R.
    Shapiro, William
    Kavan, Petr
    Mathieu, David
    Phuphanich, Surasak
    Cseh, Agnieszka
    Fu, Yali
    Cong, Julie
    Wind, Sven
    Eisenstat, David D.
    [J]. NEURO-ONCOLOGY, 2015, 17 (03) : 430 - 439
  • [93] A Phase I/II Trial of Pazopanib in Combination with Lapatinib in Adult Patients with Relapsed Malignant Glioma
    Reardon, David A.
    Groves, Morris D.
    Wen, Patrick Y.
    Nabors, Louis
    Mikkelsen, Tom
    Rosenfeld, Steve
    Raizer, Jeffrey
    Barriuso, Jorge
    McLendon, Roger E.
    Suttle, A. Benjamin
    Ma, Bo
    Curtis, C. Martin
    Dar, Mohammed M.
    de Bono, Johann
    [J]. CLINICAL CANCER RESEARCH, 2013, 19 (04) : 900 - 908
  • [94] CDKN2A Loss Is Associated With Shortened Overall Survival in Lower-Grade (World Health Organization Grades II-III) Astrocytomas
    Reis, Gerald F.
    Pekmezci, Melike
    Hansen, Helen M.
    Rice, Terri
    Marshall, Roxanne E.
    Molinaro, Annette M.
    Phillips, Joanna J.
    Vogel, Hannes
    Wiencke, John K.
    Wrensch, Margaret R.
    Walsh, Kyle M.
    Perry, Arie
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2015, 74 (05) : 442 - 452
  • [95] Oncolytic Viruses: Priming Time for Cancer Immunotherapy
    Russell, Luke
    Peng, Kah Whye
    Russell, Stephen J.
    Diaz, Rosa Maria
    [J]. BIODRUGS, 2019, 33 (05) : 485 - 501
  • [96] Brain immunology and immunotherapy in brain tumours
    Sampson, John H.
    Gunn, Michael D.
    Fecci, Peter E.
    Ashley, David M.
    [J]. NATURE REVIEWS CANCER, 2020, 20 (01) : 12 - 25
  • [97] EGFRvIII mCAR-Modified T-Cell Therapy Cures Mice with Established Intracerebral Glioma and Generates Host Immunity against Tumor-Antigen Loss
    Sampson, John H.
    Choi, Bryan D.
    Sanchez-Perez, Luis
    Suryadevara, Carter M.
    Snyder, David J.
    Flores, Catherine T.
    Schmittling, Robert J.
    Nair, Smita K.
    Reap, Elizabeth A.
    Norberg, Pamela K.
    Herndon, James E., II
    Kuan, Chien-Tsun
    Morgan, Richard A.
    Rosenberg, Steven A.
    Johnson, Laura A.
    [J]. CLINICAL CANCER RESEARCH, 2014, 20 (04) : 972 - 984
  • [98] Neoadjuvant nivolumab modifies the tumor immune microenvironment in resectable glioblastoma
    Schalper, Kurt A.
    Rodriguez-Ruiz, Maria E.
    Diez-Valle, Ricardo
    Lopez-Janeiro, Alvaro
    Porciuncula, Angelo
    Idoate, Miguel A.
    Inoges, Susana
    De Andrea, Carlos
    Lopez-Diaz de Cerio, Ascension
    Tejada, Sonia
    Berraondo, Pedro
    Villarroel-Espindola, Franz
    Choi, Jungmin
    Gurpide, Alfonso
    Giraldez, Miriam
    Goicoechea, Iosune
    Gallego Perez-Larraya, Jaime
    Sanmamed, Miguel F.
    Perez-Gracia, Jose L.
    Melero, Ignacio
    [J]. NATURE MEDICINE, 2019, 25 (03) : 470 - +
  • [99] Glioblastoma: Microenvironment and Niche Concept
    Schiffer, Davide
    Annovazzi, Laura
    Casalone, Cristina
    Corona, Cristiano
    Mellai, Marta
    [J]. CANCERS, 2019, 11 (01):
  • [100] BRAF Mutations and the Utility of RAF and MEK Inhibitors in Primary Brain Tumors
    Schreck, Karisa C.
    Grossman, Stuart A.
    Pratilas, Christine A.
    [J]. CANCERS, 2019, 11 (09)