Phase I/IIa study of cilengitide and temozolomide with concomitant radiotherapy followed by cilengitide and temozolomide maintenance therapy in patients with newly diagnosed glioblastoma.


Autoria(s): Stupp Roger; Hegi Monika E.; Neyns Bart; Goldbrunner Roland; Schlegel Uwe; Clement Paul M. J.; Grabenbauer Gerhard G.; Ochsenbein Adrian F.; Simon Matthias; Dietrich Pierre-Yves; Pietsch Torsten; Hicking Christine; Tonn Joerg-Christian; Diserens Annie-Claire; Pica Alessia; Hermisson Mirjam; Krueger Stefan; Picard Martin; Weller Michael
Data(s)

2010

Resumo

Purpose: Invasion and migration are key processes of glioblastoma and are tightly linked to tumor recurrence. Integrin inhibition using cilengitide has shown synergy with chemotherapy and radiotherapy in vitro and promising activity in recurrent glioblastoma. This multicenter, phase I/IIa study investigated the efficacy and safety of cilengitide in combination with standard chemoradiotherapy in newly diagnosed glioblastoma. Patients and Methods: Patients (age >= 18 to >= 70 years) were treated with cilengitide (500 mg) administered twice weekly intravenously in addition to standard radiotherapy with concomitant and adjuvant temozolomide. Treatment was continued until disease progression or for up to 35 weeks. The primary end point was progression-free survival (PFS) at 6 months. Results: Fifty-two patients ( median age, 57 years; 62% male) were included. Six- and 12-month PFS rates were 69% (95% CI, 54% to 80%) and 33% ( 95% CI, 21% to 46%). Median PFS was 8 months ( 95% CI, 6.0 to 10.7 months). Twelve- and 24-month overall survival ( OS) rates were 68% ( 95% CI, 53% to 79%) and 35% ( 95% CI, 22% to 48%). Median OS was 16.1 months ( 95% CI, 13.1 to 23.2 months). PFS and OS were longer in patients with tumors with O-6-methylguanine-DNA methyltransferase (MGMT) promoter methylation (13.4 and 23.2 months) versus those without MGMT promoter methylation (3.4 and 13.1 months). The combination of cilengitide with temozolomide and radiotherapy was well tolerated, with no additional toxicity. No pharmacokinetic interactions between temozolomide and cilengitide were identified. Conclusion: Compared with historical controls, the addition of concomitant and adjuvant cilengitide to standard chemoradiotherapy demonstrated promising activity in patients with glioblastoma with MGMT promoter methylation. J Clin Oncol 28:2712-2718. (C) 2010 by American Society of Clinical Oncology

Identificador

http://serval.unil.ch/?id=serval:BIB_5C7C06CCCD40

isbn:1527-7755[electronic], 0732-183X[linking]

pmid:20439646

doi:10.1200/JCO.2009.26.6650

isiid:000278108800010

Idioma(s)

en

Fonte

Journal of Clinical Oncology, vol. 28, no. 16, pp. 2712-2718

Palavras-Chave #MGMT Promoter Methylation; Integrin Inhibitors; Malignant Glioma; Alpha(V)Beta(3); Alpha-V-Beta-3; Angiogenesis; Expression; Growth; Tumors
Tipo

info:eu-repo/semantics/article

article