Stem the blood flow: beneficial impact of bevacizumab on survival of subventricular zone glioblastoma patients.

Angiogenesis Bevacizumab Glioblastoma Glioma stem cells Subventricular zone

Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
24 Sep 2024
Historique:
received: 16 08 2024
accepted: 10 09 2024
medline: 24 9 2024
pubmed: 24 9 2024
entrez: 24 9 2024
Statut: aheadofprint

Résumé

Angiogenesis is a crucial step in tumorigenesis of glioblastoma (GBM). Bevacizumab, an anti-vascular endothelial growth factor drug, is approved for second-line therapy for GBM. Glioma stem cells, presumably the cell of origin of GBM, take an active role in angiogenesis. The subventricular zone (SVZ) is the brain's largest reservoir of neural stem cells, and GBM near this region (SVZ GBM) is associated with a poor prognosis. This study aims to evaluate the potential impact of second-line bevacizumab treatment on survival in patients with SVZ GBM. The electronic medical records of adult patients with newly diagnosed SVZ GDM under treated between 1/2011 and 12/2021 were retrospectively reviewed. Clinical, surgical, radiological, and outcome parameters were compared between patients treated with bevacizumab after first relapse to patients without such treatment. The cohort included 67 patients. 45 (67.1%) were treated with bevacizumab after the first relapse while 22 (32.9%) were not. The only statistically significant difference between groups was the rate of re-surgery, which was higher in the non-bevacizumab group (40.9% vs. 15.6%; p = 0.023), indicating that the groups were quite homogenous. In general, bevacizumab as a second-line treatment did not affect OS in SVZ GBM cases. However, it significantly prolongs survival time from 1st relapse by an average of more than 4 months, including after adjustment to re-surgery variable (HR = 0.57, 95% CI 0.34-0.94, p = 0.028 and HR = 0.57, 95%CI = 0.34-0.97, PV = 0.038; respectively). Furthermore, when adjusting to time from diagnosis to 1st relapse, bevacizumab treatment was also associated with prolonged OS (HR = 0.58; p = 0.043). In a subgroup analysis, comparing patients treated with both re-surgery and bevacizumab to patients treated in any other way, patients with the combined treatment had the longest mean OS of the entire cohort (22.16 ± 7.81 m vs. 13.60 ± 6.86, p = 0.049; HR = 0.361 95%CI 0.108-1.209, p = 0.085). The use of bevacizumab as a second-line therapy in SVZ GBM cases may positively affect survival after relapse, even when given as a monotherapy. Additionally, in certain yet-to-be-identified sub-populations, bevacizumab may even extend overall survival. Further research is required to accurately identify SVZ GBM patients who would benefit most from anti-angiogenic therapy.

Identifiants

pubmed: 39316315
doi: 10.1007/s11060-024-04828-7
pii: 10.1007/s11060-024-04828-7
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2024. The Author(s).

Références

Berendsen S, van Bodegraven E, Seute T et al (2019) Adverse prognosis of glioblastoma contacting the subventricular zone: Biological correlates. PLoS ONE 14:e0222717
pubmed: 31603915 pmcid: 6788733 doi: 10.1371/journal.pone.0222717
Woo P, Ho J, Lam S et al (2018) A comparative analysis of the usefulness of Survival Prediction models for patients with Glioblastoma in the Temozolomide era: the importance of Methylguanine Methyltransferase Promoter Methylation, extent of Resection, and Subventricular Zone Location. World Neurosurg 115:e375–e385
pubmed: 29678708 doi: 10.1016/j.wneu.2018.04.059
Beiriger J, Habib A, Jovanovich N et al (2022) The Subventricular Zone in Glioblastoma: Genesis, maintenance, and modeling. Front Oncol 12:790976
pubmed: 35359410 pmcid: 8960165 doi: 10.3389/fonc.2022.790976
Lee JH, Lee JE, Kahng JY et al (2018) Human glioblastoma arises from subventricular zone cells with low-level driver mutations. Nature 560:243–247
pubmed: 30069053 doi: 10.1038/s41586-018-0389-3
Bao S, Wu Q, Sathornsumetee S et al (2006) Stem cell-like glioma cells promote tumor angiogenesis through vascular endothelial growth factor. Cancer Res 66:7843–7848
pubmed: 16912155 doi: 10.1158/0008-5472.CAN-06-1010
D’Alessio A, Proietti G, Lama G et al (2016) Analysis of angiogenesis related factors in glioblastoma, peritumoral tissue and their derived cancer stem cells. Oncotarget 7:78541–78556
pubmed: 27705944 pmcid: 5346658 doi: 10.18632/oncotarget.12398
Mistry AM (2019) Clinical correlates of subventricular zone-contacting glioblastomas: a meta-analysis. J Neurosurg Sci 63:581–587
pubmed: 29205011 doi: 10.23736/S0390-5616.17.04274-6
Mistry AM, Dewan MC, White-Dzuro GA et al (2017) Decreased survival in glioblastomas is specific to contact with the ventricular-subventricular zone, not subgranular zone or corpus callosum. J Neurooncol 132:341–349
pubmed: 28074322 pmcid: 5771712 doi: 10.1007/s11060-017-2374-3
Comas S, Luguera E, Molero J et al (2021) Influence of glioblastoma contact with the subventricular zone on survival and recurrence patterns. Clin Transl Oncol 23:554–564
pubmed: 32728970 doi: 10.1007/s12094-020-02448-x
Daniele Armocidaa AP, Mauro Palmieria GD, Andread M, Salvatib A, Santoroa A, Frati (2021) Periventricular Zone involvement as a predictor of survival in glioblastoma patients: a single centre cohort-comparison investigation concerning a distinct clinical entity, vol 25. Advanced Techniques and Case Management, Interdisciplinary Neurosurgery
Jafri NF, Clarke JL, Weinberg V, Barani IJ, Cha S (2013) Relationship of glioblastoma multiforme to the subventricular zone is associated with survival. Neuro Oncol 15:91–96
pubmed: 23095230 doi: 10.1093/neuonc/nos268
Pellerino A, Bruno F, Soffietti R, Rudà R (2023) Antiangiogenic therapy for malignant brain tumors: does it still Matter? Curr Oncol Rep 25:777–785
pubmed: 37071295 pmcid: 10256654 doi: 10.1007/s11912-023-01417-1
Kazazi-Hyseni F, Beijnen JH, Schellens JH, Bevacizumab (2010) Oncologist 15:819–825
Rajaratnam V, Islam MM, Yang M, Slaby R, Ramirez HM, Mirza SP (2020) Glioblastoma: Pathogenesis and current status of Chemotherapy and other Novel treatments. Cancers (Basel) 12
Narayana A, Gruber D, Kunnakkat S et al (2012) A clinical trial of bevacizumab, temozolomide, and radiation for newly diagnosed glioblastoma. J Neurosurg 116:341–345
pubmed: 22035272 doi: 10.3171/2011.9.JNS11656
Wick W, Gorlia T, Bendszus M et al (2017) Lomustine and Bevacizumab in Progressive Glioblastoma. N Engl J Med 377:1954–1963
pubmed: 29141164 doi: 10.1056/NEJMoa1707358
Chinot OL, Wick W, Mason W et al (2014) Bevacizumab plus radiotherapy-temozolomide for newly diagnosed glioblastoma. N Engl J Med 370:709–722
pubmed: 24552318 doi: 10.1056/NEJMoa1308345
Gilbert MR, Dignam JJ, Armstrong TS et al (2014) A randomized trial of bevacizumab for newly diagnosed glioblastoma. N Engl J Med 370:699–708
pubmed: 24552317 pmcid: 4201043 doi: 10.1056/NEJMoa1308573
Wirsching HG, Roelcke U, Weller J et al (2021) MRI and (18)FET-PET predict Survival Benefit from Bevacizumab Plus Radiotherapy in patients with isocitrate dehydrogenase wild-type Glioblastoma: results from the Randomized ARTE Trial. Clin Cancer Res 27:179–188
pubmed: 32967939 doi: 10.1158/1078-0432.CCR-20-2096
Louis DN, Ohgaki H, Wiestler OD et al (2007) The 2007 WHO classification of tumours of the central nervous system. Acta Neuropathol 114:97–109
pubmed: 17618441 pmcid: 1929165 doi: 10.1007/s00401-007-0243-4
Louis DN, Perry A, Reifenberger G et al (2016) The 2016 World Health Organization Classification of Tumors of the Central Nervous System: a summary. Acta Neuropathol 131:803–820
pubmed: 27157931 doi: 10.1007/s00401-016-1545-1
Louis DN, Perry A, Wesseling P et al (2021) The 2021 WHO classification of tumors of the Central Nervous System: a summary. Neuro Oncol 23:1231–1251
pubmed: 34185076 pmcid: 8328013 doi: 10.1093/neuonc/noab106
Stupp R, Mason WP, van den Bent MJ et al (2005) Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med 352:987–996
pubmed: 15758009 doi: 10.1056/NEJMoa043330
Perry JR, Laperriere N, O’Callaghan CJ et al (2017) Short-course Radiation plus Temozolomide in Elderly patients with Glioblastoma. N Engl J Med 376:1027–1037
pubmed: 28296618 doi: 10.1056/NEJMoa1611977
Wen PY, Macdonald DR, Reardon DA et al (2010) Updated response assessment criteria for high-grade gliomas: response assessment in neuro-oncology working group. J Clin Oncol 28:1963–1972
pubmed: 20231676 doi: 10.1200/JCO.2009.26.3541
Karschnia P, Young JS, Dono A et al (2023) Prognostic validation of a new classification system for extent of resection in glioblastoma: a report of the RANO resect group. Neuro Oncol 25:940–954
pubmed: 35961053 doi: 10.1093/neuonc/noac193
Ameratunga M, Pavlakis N, Wheeler H, Grant R, Simes J, Khasraw M (2018) Anti-angiogenic therapy for high-grade glioma. Cochrane Database Syst Rev 11:Cd008218
pubmed: 30480778
Zikou A, Sioka C, Alexiou GA, Fotopoulos A, Voulgaris S, Argyropoulou MI (2018) Radiation Necrosis, Pseudoprogression, Pseudoresponse, and Tumor Recurrence: Imaging Challenges for the Evaluation of Treated Gliomas. Contrast Media Mol Imaging 2018:6828396
Gilbert MR, Pugh SL, Aldape K et al (2017) NRG oncology RTOG 0625: a randomized phase II trial of bevacizumab with either irinotecan or dose-dense temozolomide in recurrent glioblastoma. J Neurooncol 131:193–199
pubmed: 27770279 doi: 10.1007/s11060-016-2288-5
Raizer JJ, Giglio P, Hu J et al (2016) A phase II study of bevacizumab and erlotinib after radiation and temozolomide in MGMT unmethylated GBM patients. J Neurooncol 126:185–192
pubmed: 26476729 pmcid: 4826294 doi: 10.1007/s11060-015-1958-z
Zhuang H, Shi S, Yuan Z, Chang JY (2019) Bevacizumab treatment for radiation brain necrosis: mechanism, efficacy and issues. Mol Cancer 18:21
pubmed: 30732625 pmcid: 6367784 doi: 10.1186/s12943-019-0950-1
Balana C, De Las Penas R, Sepúlveda JM et al (2016) Bevacizumab and temozolomide versus temozolomide alone as neoadjuvant treatment in unresected glioblastoma: the GENOM 009 randomized phase II trial. J Neurooncol 127:569–579
pubmed: 26847813 doi: 10.1007/s11060-016-2065-5
Herrlinger U, Schäfer N, Steinbach JP et al (2016) Bevacizumab Plus Irinotecan Versus Temozolomide in newly diagnosed O6-Methylguanine-DNA methyltransferase nonmethylated Glioblastoma: the Randomized GLARIUS Trial. J Clin Oncol 34:1611–1619
pubmed: 26976423 doi: 10.1200/JCO.2015.63.4691
Lee EQ, Kaley TJ, Duda DG et al (2015) A Multicenter, Phase II, Randomized, Noncomparative Clinical Trial of Radiation and Temozolomide with or without Vandetanib in newly diagnosed Glioblastoma patients. Clin Cancer Res 21:3610–3618
pubmed: 25910950 pmcid: 4790106 doi: 10.1158/1078-0432.CCR-14-3220
Nabors LB, Fink KL, Mikkelsen T et al (2015) Two cilengitide regimens in combination with standard treatment for patients with newly diagnosed glioblastoma and unmethylated MGMT gene promoter: results of the open-label, controlled, randomized phase II CORE study. Neuro Oncol 17:708–717
pubmed: 25762461 pmcid: 4482861 doi: 10.1093/neuonc/nou356
Stupp R, Hegi ME, Gorlia T et al (2014) Cilengitide combined with standard treatment for patients with newly diagnosed glioblastoma with methylated MGMT promoter (CENTRIC EORTC 26071– 22072 study): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol 15:1100–1108
pubmed: 25163906 doi: 10.1016/S1470-2045(14)70379-1
Gil-Gil MJ, Mesia C, Rey M, Bruna J (2013) Bevacizumab for the treatment of glioblastoma. Clin Med Insights Oncol 7:123–135
pubmed: 23843722 pmcid: 3682734 doi: 10.4137/CMO.S8503
Lu-Emerson C, Duda DG, Emblem KE et al (2015) Lessons from anti-vascular endothelial growth factor and anti-vascular endothelial growth factor receptor trials in patients with glioblastoma. J Clin Oncol 33:1197–1213
pubmed: 25713439 pmcid: 4517055 doi: 10.1200/JCO.2014.55.9575
Doetsch F, Caillé I, Lim DA, García-Verdugo JM, Alvarez-Buylla A (1999) Subventricular zone astrocytes are neural stem cells in the adult mammalian brain. Cell 97:703–716
pubmed: 10380923 doi: 10.1016/S0092-8674(00)80783-7
Spiteri I, Caravagna G, Cresswell GD et al (2019) Evolutionary dynamics of residual disease in human glioblastoma. Ann Oncol 30:456–463
pubmed: 30452544 doi: 10.1093/annonc/mdy506
Matarredona ER, Pastor AM (2019) Neural stem cells of the Subventricular Zone as the origin of human glioblastoma stem cells. Therapeutic Implications Front Oncol 9:779
pubmed: 31482066 doi: 10.3389/fonc.2019.00779
Dalemans DJZ, Berendsen S, Draaisma K, Robe PA, Snijders TJ (2021) Glioblastomas within the Subventricular Zone Are Region-Specific enriched for mesenchymal transition markers: an Intratumoral Gene expression analysis. Cancers (Basel) 13
Oka N, Soeda A, Inagaki A et al (2007) VEGF promotes tumorigenesis and angiogenesis of human glioblastoma stem cells. Biochem Biophys Res Commun 360:553–559
pubmed: 17618600 doi: 10.1016/j.bbrc.2007.06.094
Cheng L, Huang Z, Zhou W et al (2013) Glioblastoma stem cells generate vascular pericytes to support vessel function and tumor growth. Cell 153:139–152
pubmed: 23540695 pmcid: 3638263 doi: 10.1016/j.cell.2013.02.021
Şuşman S, Leucuţa DC, Kacso G, Florian ŞI (2019) High dose vs low dose irradiation of the subventricular zone in patients with glioblastoma-a systematic review and meta-analysis. Cancer Manag Res 11:6741–6753
pubmed: 31410064 pmcid: 6645358 doi: 10.2147/CMAR.S206033
Kahng JY, Kang BH, Lee ST et al (2023) Clinicogenetic characteristics and the effect of radiation on the neural stem cell niche in subventricular zone-contacting glioblastoma. Radiother Oncol 186:109800
pubmed: 37423479 doi: 10.1016/j.radonc.2023.109800

Auteurs

Yosef Laviv (Y)

Neurosurgery department, Beilinson hospital, Rabin Medical Center, 39 Zeev Jabotinsky St, Petach Tikva, 4941492, Israel. yossilaviv@gmail.com.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel. yossilaviv@gmail.com.

Ohad Regev (O)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Meir Medical Center, Kfar Saba, Israel.

Andrew A Kanner (AA)

Neurosurgery department, Beilinson hospital, Rabin Medical Center, 39 Zeev Jabotinsky St, Petach Tikva, 4941492, Israel.
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Susana Fichman (S)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Pathology department, Beilinson hospital, Rabin Medical Center, Petah Tikva, Israel.

Dror Limon (D)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Neuro-Oncology Unit, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Tali Siegal (T)

Neuro-Oncology Unit, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.
Hebrew University, Jerusalem, Israel.

Shlomit Yust-Katz (S)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Neuro-Oncology Unit, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Alexandra Benouaich-Amiel (A)

Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Neuro-Oncology Unit, Davidoff Cancer Center, Beilinson Hospital, Rabin Medical Center, Petah Tikva, Israel.

Classifications MeSH