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23-02-2016 | Glioblastoma multiforme | Article

Recurrent glioblastoma: who receives tumor specific treatment and how often?

Journal: Journal of Neuro-Oncology

Authors: Rieke Steffens, Sabine Semrau, Godehard Lahmer, Florian Putz, Sebastian Lettmaier, Ilker Eyüpoglu, Michael Buchfelder, Rainer Fietkau

Publisher: Springer US

Abstract

The recurrence of glioblastoma (rGBM) is inevitable and often short-term. Therefore, information on the prognosis and effectiveness of tumor-specific versus purely palliative approaches should be more in-depth than a mere list of available treatment options for patients in this situation. However, follow-up data on the course of the disease in unselected patient populations after completion of primary treatment are scarce. This single-center analysis investigated the rate and number of glioblastoma recurrences after initial radiotherapy in 189 consecutive GM patients, focusing on the incidence of early death and the frequency of tumor-specific treatment (TST) versus best-supportive care (BSC) as well as the outcomes for the different approaches. In 61 % of initial population first recurrence (rGBM) could be determined by histology or imaging. 47 % received TST. 58 % of the patients with rGBM and TST were diagnosed with a second recurrence. Up to five recurrences were treated. 35–45 % of patients died before undergoing imaging studies to confirm the next recurrence. Multivariate analysis identified male sex and KPS score as independent factors (p < 0.01) for the choice of TST over BSC. Median overall survival from the diagnosis of first recurrence was 267 days in the TST group versus 65 days in patients receiving BSC (p < 0.0001). Nearly half of all rGBM patients received second-line TST, but a remarkably high proportion died early. Gender and KPS played a role in the choice of TST over BSC for recurrence treatment.
Literature
1.
Stupp R, Mason WP, van den Bent MJ et al (2005) Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med 352:987–996CrossRefPubMed
2.
Dolecek TA, Propp JM, Stroup NE, Kruchko C (2012) CBTRUS statistical report: primary brain and central nervous system tumors diagnosed in the United States in 2005–2009. Neuro Oncol 14(Suppl 5):1–49CrossRef
3.
Stummer W, Pichlmeier U, Meinel T et al (2006) Fluorescence-guided surgery with 5-aminolevulinic acid for resection of malignant glioma: a randomised controlled multicentre phase III trial. Lancet Oncol 7:392–401CrossRefPubMed
4.
Walker MD, Strike TA, Sheline GE (1979) An analysis of dose-effect relationship in the radiotherapy of malignant gliomas. Int J Radiat Oncol Biol Phys 5:1725–1731CrossRefPubMed
5.
Weller M, Tabatabai G, Kastner B et al (2015) MGMT promoter methylation is a strong prognostic biomarker for benefit from dose-intensified temozolomide rechallenge in progressive glioblastoma: the DIRECTOR trial. Clin Cancer Res 21:2057–2064CrossRefPubMed
6.
Combs SE, Edler L, Rausch R et al (2013) Generation and validation of a prognostic score to predict outcome after re-irradiation of recurrent glioma. Acta Oncol 52:147–152CrossRefPubMed
7.
Park JK, Hodges T, Arko L et al (2010) Scale to predict survival after surgery for recurrent glioblastoma multiforme. J Clin Oncol 28:3838–3843CrossRefPubMedPubMedCentral
8.
Taal W, Oosterkamp HM, Walenkamp AM et al (2014) Single-agent bevacizumab or lomustine versus a combination of bevacizumab plus lomustine in patients with recurrent glioblastoma (BELOB trial): a randomised controlled phase 2 trial. Lancet Oncol 15:943–953CrossRefPubMed
9.
Fokas E, Wacker U, Gross MW et al (2009) Hypofractionated stereotactic reirradiation of recurrent glioblastomas: a beneficial treatment option after high-dose radiotherapy? Strahlenther Onkol 185:235–240CrossRefPubMed
10.
Levin VA, Mendelssohn ND, Chan J et al (2015) Impact of bevacizumab administered dose on overall survival of patients with progressive glioblastoma. J Neurooncol 122:145–150CrossRefPubMed
11.
Fietkau R, Putz F, Lahmer G et al (2013) Can MGMT promoter methylation status be used as a prognostic and predictive marker for glioblastoma multiforme at the present time? A word of caution. Strahlenther Onkol 189:993–995CrossRefPubMed
12.
Gorlia T, Stupp R, Brandes AA et al (2012) New prognostic factors and calculators for outcome prediction in patients with recurrent glioblastoma: a pooled analysis of EORTC Brain Tumour Group phase I and II clinical trials. Eur J Cancer 48:1176–1184CrossRefPubMed
13.
Balducci M, Diletto B, Chiesa S et al (2014) Low-dose fractionated radiotherapy and concomitant chemotherapy for recurrent or progressive glioblastoma: final report of a pilot study. Strahlenther Onkol 190:370–376CrossRefPubMed
14.
Macdonald DR, Cascino TL, Schold SC Jr, Cairncross JG (1990) Response criteria for phase II studies of supratentorial malignant glioma. J Clin Oncol 8:1277–1280PubMed
15.
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 28:1963–1972CrossRefPubMed
16.
Brodbelt A, Greenberg D, Winters T, Williams M, Vernon S, Collins VP, National Cancer Information Network Brain Tumour G (2015) Glioblastoma in England: 2007–2011. Eur J Cancer 51:533–542CrossRefPubMed
17.
Ho VK, Reijneveld JC, Enting RH, Bienfait HP, Robe P, Baumert BG, Visser O, Dutch Society for N-O (2014) Changing incidence and improved survival of gliomas. Eur J Cancer 50:2309–2318CrossRefPubMed
18.
Barone DG, Lawrie TA, Hart MG (2014) Image guided surgery for the resection of brain tumours. Cochrane Database Syst Rev 28:1
19.
Stupp R, Hegi ME, Mason WP et al (2009) Effects of radiotherapy with concomitant and adjuvant temozolomide versus radiotherapy alone on survival in glioblastoma in a randomised phase III study: 5-year analysis of the EORTC-NCIC trial. Lancet Oncol 10:459–466CrossRefPubMed
20.
Kim HR, Kim KH, Kong DS, Seol HJ, Nam DH, Lim DH, Lee JI (2015) Outcome of salvage treatment for recurrent glioblastoma. J Clin Neurosci 22:468–473CrossRefPubMed
21.
Krex D, Klink B, Hartmann C et al (2007) Long-term survival with glioblastoma multiforme. Brain 130:2596–2606CrossRefPubMed
22.
Su D, Stimpson JP, Wilson FA (2015) Racial disparities in mortality among middle-aged and older men: does marriage matter? Am J Mens Health 9:289–300CrossRefPubMed
23.
Ening G, Huynh MT, Schmieder K, Brenke C (2015) Repeat-surgery at glioblastoma recurrence, when and why to operate? Clin Neurol Neurosurg 136:89–94CrossRefPubMed
24.
Hasan S, Chen E, Lanciano R et al (2015) Salvage fractionated stereotactic radiotherapy with or without chemotherapy and immunotherapy for recurrent glioblastoma multiforme: a single institution experience. Front Oncol 15:106
25.
Bakitas MA, Tosteson TD, Li Z et al (2015) Early versus delayed initiation of concurrent palliative oncology care: patient outcomes in the ENABLE III randomized controlled trial. J Clin Oncol 33:1438–1445CrossRefPubMedPubMedCentral
26.
Tieu MT, Lovblom LE, McNamara MG et al (2015) Impact of glycemia on survival of glioblastoma patients treated with radiation and temozolomide. J Neurooncol 124:119–126CrossRefPubMedPubMedCentral
27.
Silvani A, Gaviani P, Lamperti E et al (2011) Metabolic, electrolytes disorders and tromboembolic risk in malignant glioma patients. Neurol Sci 32(Suppl 2):229–231CrossRef
28.
Mayer A, Vaupel P, Struss HG et al (2014) Strong adverse prognostic impact of hyperglycemic episodes during adjuvant chemoradiotherapy of glioblastoma multiforme. Strahlenther Onkol 190:933–938CrossRefPubMed
29.
Pan E, Tsai JS, Mitchell SB (2009) Retrospective study of venous thromboembolic and intracerebral hemorrhagic events in glioblastoma patients. Anticancer Res 29:4309–4313PubMed
30.
Goerig NL, Gaipel U, Frey B et al (2015) Cytomegalovirus-Encephalitis als Ursache neurologischer Verschlechterung während der Radiotherapie und/oder Chemotherapie des Cerebrums. Strahlenther Onkol 191(Suppl 1):39