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Published in: Pediatric Drugs 1/2012

01-02-2012 | Adis Drug Profile

Everolimus

In Patients with Subependymal Giant Cell Astrocytoma Associated with Tuberous Sclerosis Complex

Author: Monique P. Curran

Published in: Pediatric Drugs | Issue 1/2012

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Abstract

Everolimus is an orally administered inhibitor of the mammalian target of rapamycin (mTOR).
Everolimus (starting dosage 3.0 mg/m2) was associated with a significant reduction in the volume of the largest subependymal giant cell astrocytoma (SEGA) in 28 patients aged ≥3 years with tuberous sclerosis complex (TSC) in a phase II trial (C2485). At 6 months, 32% of patients treated with everolimus had a ≥50% reduction in the volume of their largest SEGA lesion (assessed via an independent central radiology review); 75% had a ≥30% reduction. No patients developed new lesions. During the extension phase of this trial (median duration 34 months), the reduction in SEGA volume was maintained, with no everolimus recipient requiring surgery or other therapy for SEGA or hydrocephalus.
In a phase III trial (EXIST-1) in 117 patients with SEGA associated with TSC, 35% of everolimus recipients (starting dosage 4.5mg/m2) versus none of the placebo recipients (p< 0.0001) had an overall response (a reduction in the sum of all target SEGA volumes of ≥50% relative to baseline, nonworsening of non-target SEGA lesions, no new SEGA lesions, and no new/worsening hydrocephalus).
Everolimus was generally well tolerated in patients with SEGA associated with TSC; most drug-related adverse reactions were mild to moderate in severity.
Literature
1.
go back to reference Krueger DA, Franz DN. Current management of tuberous sclerosis complex. Pediatr Drugs 2008; 10(5): 299–313CrossRef Krueger DA, Franz DN. Current management of tuberous sclerosis complex. Pediatr Drugs 2008; 10(5): 299–313CrossRef
2.
4.
7.
go back to reference Novartis Pharmaceuticals Canada, Inc. Afinitor® (everolimus): Canadian prescribing information. Dorval (QC): Novartis Pharmaceuticals, 2011 Novartis Pharmaceuticals Canada, Inc. Afinitor® (everolimus): Canadian prescribing information. Dorval (QC): Novartis Pharmaceuticals, 2011
8.
go back to reference Dunn C, Croom KF. Everolimus: a review of its use in renal and cardiac transplantation. Drugs 2006; 66(4): 547–70PubMedCrossRef Dunn C, Croom KF. Everolimus: a review of its use in renal and cardiac transplantation. Drugs 2006; 66(4): 547–70PubMedCrossRef
10.
go back to reference Garnock-Jones KP, Keating GM. Everolimus: in advanced renal cell carcinoma. Drugs 2009 Oct 22; 69(15): 2115–24PubMedCrossRef Garnock-Jones KP, Keating GM. Everolimus: in advanced renal cell carcinoma. Drugs 2009 Oct 22; 69(15): 2115–24PubMedCrossRef
12.
go back to reference Abraham RT, Gibbons JJ. The mammalian target of rapamycin signaling pathway: twists and turns in the road to cancer therapy. Clin Cancer Res 2007 Jun 1; 13(11): 3109–14PubMedCrossRef Abraham RT, Gibbons JJ. The mammalian target of rapamycin signaling pathway: twists and turns in the road to cancer therapy. Clin Cancer Res 2007 Jun 1; 13(11): 3109–14PubMedCrossRef
13.
go back to reference Mabuchi S, Altomare DA, Cheung M, et al. RAD001 inhibits human ovarian cancer cell proliferation, enhances cisplatin-induced apoptosis, and prolongs survival in an ovarian cancer model. Clin Cancer Res 2007 Jul 15; 13(14): 4261–70PubMedCrossRef Mabuchi S, Altomare DA, Cheung M, et al. RAD001 inhibits human ovarian cancer cell proliferation, enhances cisplatin-induced apoptosis, and prolongs survival in an ovarian cancer model. Clin Cancer Res 2007 Jul 15; 13(14): 4261–70PubMedCrossRef
14.
go back to reference Beuvink I, Boulay A, Fumagalli S, et al. The mTOR inhibitor RAD001 sensitizes tumor cells to DNA-damaged induced apoptosis through inhibition of p21 translation. Cell 2005 Mar 25; 120(6): 747–59PubMedCrossRef Beuvink I, Boulay A, Fumagalli S, et al. The mTOR inhibitor RAD001 sensitizes tumor cells to DNA-damaged induced apoptosis through inhibition of p21 translation. Cell 2005 Mar 25; 120(6): 747–59PubMedCrossRef
15.
go back to reference Lane HA, Wood JM, McSheehy PM, et al. mTOR inhibitor RAD001 (everolimus) has antiangiogenic/vascular properties distinct from a VEGFR tyrosine kinase inhibitor. Clin Cancer Res 2009 Mar 1; 15(5): 1612–22PubMedCrossRef Lane HA, Wood JM, McSheehy PM, et al. mTOR inhibitor RAD001 (everolimus) has antiangiogenic/vascular properties distinct from a VEGFR tyrosine kinase inhibitor. Clin Cancer Res 2009 Mar 1; 15(5): 1612–22PubMedCrossRef
16.
go back to reference Boulay A, Zumstein-Mecker S, Stephan C, et al. Antitumor efficacy of intermittent treatment schedules with the rapamycin derivative RAD001 correlates with prolonged inactivation of ribosomal protein S6 kinase 1 in peripheral blood mononuclear cells. Cancer Res 2004 Jan 1; 64(1): 252–61PubMedCrossRef Boulay A, Zumstein-Mecker S, Stephan C, et al. Antitumor efficacy of intermittent treatment schedules with the rapamycin derivative RAD001 correlates with prolonged inactivation of ribosomal protein S6 kinase 1 in peripheral blood mononuclear cells. Cancer Res 2004 Jan 1; 64(1): 252–61PubMedCrossRef
17.
go back to reference Tabernero J, Rojo F, Calvo E, et al. Dose- and schedule-dependent inhibition of the mammalian target of rapamycin pathway with everolimus: a phase I tumor pharmacodynamic study in patients with advanced solid tumors. J Clin Oncol 2008 Apr 1; 26(10): 1603–10PubMedCrossRef Tabernero J, Rojo F, Calvo E, et al. Dose- and schedule-dependent inhibition of the mammalian target of rapamycin pathway with everolimus: a phase I tumor pharmacodynamic study in patients with advanced solid tumors. J Clin Oncol 2008 Apr 1; 26(10): 1603–10PubMedCrossRef
18.
go back to reference Meikle L, Pollizzi K, Egnor A, et al. Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: effects on mTORC1 and Akt signaling lead to improved survival and function. J Neurosci 2008 May 21; 28(21): 5422–32PubMedCrossRef Meikle L, Pollizzi K, Egnor A, et al. Response of a neuronal model of tuberous sclerosis to mammalian target of rapamycin (mTOR) inhibitors: effects on mTORC1 and Akt signaling lead to improved survival and function. J Neurosci 2008 May 21; 28(21): 5422–32PubMedCrossRef
19.
go back to reference Pollizzi K, Malinowska-Kolodziej I, Stumm M, et al. Equivalent benefit of mTORC1 blockade and combined PI3K-mTOR blockade in a mouse model of tuberous sclerosis. Mol Cancer 2009; 8: 38PubMedCrossRef Pollizzi K, Malinowska-Kolodziej I, Stumm M, et al. Equivalent benefit of mTORC1 blockade and combined PI3K-mTOR blockade in a mouse model of tuberous sclerosis. Mol Cancer 2009; 8: 38PubMedCrossRef
20.
go back to reference Torres-Arzayus MI, Yuan J, DellaGatta JL, et al. Targeting the AIB1 oncogene through mammalian target of rapamycin inhibition in the mammary gland. Cancer Res 2006 Dec 1; 66(23): 11381–8PubMedCrossRef Torres-Arzayus MI, Yuan J, DellaGatta JL, et al. Targeting the AIB1 oncogene through mammalian target of rapamycin inhibition in the mammary gland. Cancer Res 2006 Dec 1; 66(23): 11381–8PubMedCrossRef
21.
go back to reference Boulay A, Rudloff J, Ye J, et al. Dual inhibition of mTOR and estrogen receptor signaling in vitro induces cell death in models of breast cancer. Clin Cancer Res 2005 Jul 15; 11(14): 5319–28PubMedCrossRef Boulay A, Rudloff J, Ye J, et al. Dual inhibition of mTOR and estrogen receptor signaling in vitro induces cell death in models of breast cancer. Clin Cancer Res 2005 Jul 15; 11(14): 5319–28PubMedCrossRef
22.
go back to reference Treeck O, Wackwitz B, Haus U, et al. Effects of a combined treatment with mTOR inhibitor RAD001 and tamoxifen in vitro on growth and apoptosis of human cancer cells. Gynecol Oncol 2006 Aug; 102(2): 292–9PubMedCrossRef Treeck O, Wackwitz B, Haus U, et al. Effects of a combined treatment with mTOR inhibitor RAD001 and tamoxifen in vitro on growth and apoptosis of human cancer cells. Gynecol Oncol 2006 Aug; 102(2): 292–9PubMedCrossRef
23.
go back to reference Ma BB, Lui VW, Hui EP, et al. The activity of mTOR inhibitor RAD001 (everolimus) in nasopharyngeal carcinoma and cisplatin-resistant cell lines. Invest New Drugs 2010 Aug; 28(4): 413–20PubMedCrossRef Ma BB, Lui VW, Hui EP, et al. The activity of mTOR inhibitor RAD001 (everolimus) in nasopharyngeal carcinoma and cisplatin-resistant cell lines. Invest New Drugs 2010 Aug; 28(4): 413–20PubMedCrossRef
24.
go back to reference O’Reilly T, McSheehy PM, Wartmann M, et al. Evaluation of the mTOR inhibitor, everolimus, in combination with cytotoxic antitumor agents using human tumor models in vitro and in vivo. Anticancer Drugs 2011 Jan; 22(1): 58–78PubMedCrossRef O’Reilly T, McSheehy PM, Wartmann M, et al. Evaluation of the mTOR inhibitor, everolimus, in combination with cytotoxic antitumor agents using human tumor models in vitro and in vivo. Anticancer Drugs 2011 Jan; 22(1): 58–78PubMedCrossRef
25.
go back to reference Haritunians T, Mori A, O’Kelly J, et al. Antiproliferative activity of RAD001 (everolimus) as a single agent and combined with other agents in mantle cell lymphoma. Leukemia 2007 Feb; 21(2): 333–9PubMedCrossRef Haritunians T, Mori A, O’Kelly J, et al. Antiproliferative activity of RAD001 (everolimus) as a single agent and combined with other agents in mantle cell lymphoma. Leukemia 2007 Feb; 21(2): 333–9PubMedCrossRef
26.
go back to reference Shinohara ET, Cao C, Niermann K, et al. Enhanced radiation damage of tumor vasculature by mTOR inhibitors. Oncogene 2005 Aug 18; 24(35): 5414–22PubMedCrossRef Shinohara ET, Cao C, Niermann K, et al. Enhanced radiation damage of tumor vasculature by mTOR inhibitors. Oncogene 2005 Aug 18; 24(35): 5414–22PubMedCrossRef
27.
go back to reference O’Donnell A, Faivre S, Burris 3rd HA, et al. Phase I pharmacokinetic and pharmacodynamic study of the oral mammalian target of rapamycin inhibitor everolimus in patients with advanced solid tumors. J Clin Oncol 2008 Apr 1; 26(10): 1588–95PubMedCrossRef O’Donnell A, Faivre S, Burris 3rd HA, et al. Phase I pharmacokinetic and pharmacodynamic study of the oral mammalian target of rapamycin inhibitor everolimus in patients with advanced solid tumors. J Clin Oncol 2008 Apr 1; 26(10): 1588–95PubMedCrossRef
28.
go back to reference Fouladi M, Laningham F, Wu J, et al. Phase I study of everolimus in pediatric patients with refractory solid tumors. J Clin Oncol 2007 Oct 20; 25(30): 4806–12PubMedCrossRef Fouladi M, Laningham F, Wu J, et al. Phase I study of everolimus in pediatric patients with refractory solid tumors. J Clin Oncol 2007 Oct 20; 25(30): 4806–12PubMedCrossRef
29.
go back to reference Krueger DA, Care MM, Holland K, et al. Everolimus for subependymal giant cell astrocytomas in tuberous sclerosis. N Engl J Med 2010 Nov 4; 363(19): 1801–11PubMedCrossRef Krueger DA, Care MM, Holland K, et al. Everolimus for subependymal giant cell astrocytomas in tuberous sclerosis. N Engl J Med 2010 Nov 4; 363(19): 1801–11PubMedCrossRef
30.
go back to reference Kovarik JM, Sabia HD, Figueiredo J, et al. Influence of hepatic impairment on everolimus pharmacokinetics: implications for dose adjustment. Clin Pharmacol Ther 2001 Nov; 70(5): 425–30PubMed Kovarik JM, Sabia HD, Figueiredo J, et al. Influence of hepatic impairment on everolimus pharmacokinetics: implications for dose adjustment. Clin Pharmacol Ther 2001 Nov; 70(5): 425–30PubMed
31.
go back to reference Kirchner GI, Meier-Wiedenbach I, Manns MP. Clinical pharmacokinetics of everolimus. Clin Pharmacokinet 2004; 43(2): 83–95PubMedCrossRef Kirchner GI, Meier-Wiedenbach I, Manns MP. Clinical pharmacokinetics of everolimus. Clin Pharmacokinet 2004; 43(2): 83–95PubMedCrossRef
32.
go back to reference Kovarik JM, Kahan BD, Kaplan B, et al. Longitudinal assessment of everolimus in de novo renal transplant recipients over the first post-transplant year: pharmacokinetics, exposure-response relationships, and influence on cyclosporine. Clin Pharmacol Ther 2001 Jan; 69(1): 48–56PubMedCrossRef Kovarik JM, Kahan BD, Kaplan B, et al. Longitudinal assessment of everolimus in de novo renal transplant recipients over the first post-transplant year: pharmacokinetics, exposure-response relationships, and influence on cyclosporine. Clin Pharmacol Ther 2001 Jan; 69(1): 48–56PubMedCrossRef
33.
go back to reference Xu B, Wu Y, Shen L, et al. Two-dose-level confirmatory study of the pharmacokinetics and tolerability of everolimus in Chinese patients with advanced solid tumors. J Hematol Oncol 2011; 4: 3PubMedCrossRef Xu B, Wu Y, Shen L, et al. Two-dose-level confirmatory study of the pharmacokinetics and tolerability of everolimus in Chinese patients with advanced solid tumors. J Hematol Oncol 2011; 4: 3PubMedCrossRef
34.
go back to reference Okamoto I, Doi T, Ohtsu A, et al. Phase I clinical and pharmacokinetic study of RAD001 (everolimus) administered daily to Japanese patients with advanced solid tumors. Jpn J Clin Oncol 2010 Jan; 40(1): 17–23PubMedCrossRef Okamoto I, Doi T, Ohtsu A, et al. Phase I clinical and pharmacokinetic study of RAD001 (everolimus) administered daily to Japanese patients with advanced solid tumors. Jpn J Clin Oncol 2010 Jan; 40(1): 17–23PubMedCrossRef
35.
go back to reference Kovarik JM, Beyer D, Bizot MN, et al. Blood concentrations of everolimus are markedly increased by ketoconazole. J Clin Pharmacol 2005 May; 45(5): 514–8PubMedCrossRef Kovarik JM, Beyer D, Bizot MN, et al. Blood concentrations of everolimus are markedly increased by ketoconazole. J Clin Pharmacol 2005 May; 45(5): 514–8PubMedCrossRef
36.
go back to reference Kovarik JM, Beyer D, Schmouder RL. Everolimus drug interactions: application of a classification system for clinical decision making. Biopharm Drug Dispos 2006 Dec; 27(9): 421–6PubMedCrossRef Kovarik JM, Beyer D, Schmouder RL. Everolimus drug interactions: application of a classification system for clinical decision making. Biopharm Drug Dispos 2006 Dec; 27(9): 421–6PubMedCrossRef
37.
go back to reference Kovarik JM, Beyer D, Bizot MN, et al. Effect of multiple-dose erythromycin on everolimus pharmacokinetics. Eur J Clin Pharmacol 2005 Mar; 61(1): 35–8PubMedCrossRef Kovarik JM, Beyer D, Bizot MN, et al. Effect of multiple-dose erythromycin on everolimus pharmacokinetics. Eur J Clin Pharmacol 2005 Mar; 61(1): 35–8PubMedCrossRef
38.
go back to reference Kovarik JM, Hartmann S, Figueiredo J, et al. Effect of rifampin on apparent clearance of everolimus. Ann Pharmacother 2002 Jun; 36(6): 981–5PubMedCrossRef Kovarik JM, Hartmann S, Figueiredo J, et al. Effect of rifampin on apparent clearance of everolimus. Ann Pharmacother 2002 Jun; 36(6): 981–5PubMedCrossRef
39.
go back to reference Roach ES, Gomez MR, Northrup H. Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria. J Child Neurol 1998 Dec; 13(12): 624–8PubMedCrossRef Roach ES, Gomez MR, Northrup H. Tuberous sclerosis complex consensus conference: revised clinical diagnostic criteria. J Child Neurol 1998 Dec; 13(12): 624–8PubMedCrossRef
40.
go back to reference Mehrotra N, Pfuma E, Garnett Q, et al. Exposure-response analysis as evidence for anti-tumour activity of everolimus in the treatment of patients with subependymal giant-cell astrocytoma (SEGA) associated with tuberous scleroisis (TS) [abstract no. 9550]. J Clin Oncol 2011; 29 Suppl Mehrotra N, Pfuma E, Garnett Q, et al. Exposure-response analysis as evidence for anti-tumour activity of everolimus in the treatment of patients with subependymal giant-cell astrocytoma (SEGA) associated with tuberous scleroisis (TS) [abstract no. 9550]. J Clin Oncol 2011; 29 Suppl
41.
go back to reference Krueger DA, Care MM, Holland K, et al. Long-term safety and efficacy results from an extension phase of an open-label, prospective, phase 1/2 trial of oral everolimus in patients with subependymal giant-cell astrocytomas in tuberous sclerosis complex [abstract plus poster]. Summit on Drug Discovery in TSC and Related Disorders: International TSC Research Conference; 2011 Jul 6–9; Washington, DC Krueger DA, Care MM, Holland K, et al. Long-term safety and efficacy results from an extension phase of an open-label, prospective, phase 1/2 trial of oral everolimus in patients with subependymal giant-cell astrocytomas in tuberous sclerosis complex [abstract plus poster]. Summit on Drug Discovery in TSC and Related Disorders: International TSC Research Conference; 2011 Jul 6–9; Washington, DC
42.
go back to reference Bebin M, Franz DN, Sahmoud T, et al. Everolimus in subependymal giant cell astrocytomas (SEGA) associated with tuberous sclerosis complex (TSC): results of EXIST-1, a double-blind placebo-controlled phase 3 trial [abstract]. 2011 European Multidisciplinary Cancer Congress; 2011 Sep 23–27; Stockholm Bebin M, Franz DN, Sahmoud T, et al. Everolimus in subependymal giant cell astrocytomas (SEGA) associated with tuberous sclerosis complex (TSC): results of EXIST-1, a double-blind placebo-controlled phase 3 trial [abstract]. 2011 European Multidisciplinary Cancer Congress; 2011 Sep 23–27; Stockholm
43.
go back to reference Franz DN, Belousova E, Curatolo P, et al. Results from a double-blind, placebo-controlled, phase 3 trial of everolimus in subependymal giant cell astrocytomas associated with tuberous sclerosis complex [abstract plus poster]. 29th International Epilepsy Congress (IEC); 2011 28 Aug-1 Sep; Rome Franz DN, Belousova E, Curatolo P, et al. Results from a double-blind, placebo-controlled, phase 3 trial of everolimus in subependymal giant cell astrocytomas associated with tuberous sclerosis complex [abstract plus poster]. 29th International Epilepsy Congress (IEC); 2011 28 Aug-1 Sep; Rome
44.
go back to reference Franz D. Clinical trials in the USA for TSC and related disorders [abstract]. Summit on Drug Discovery in TSC and Related Disorders: International TSC Research Conference; 2011 Jul 6–9; Washington, DC Franz D. Clinical trials in the USA for TSC and related disorders [abstract]. Summit on Drug Discovery in TSC and Related Disorders: International TSC Research Conference; 2011 Jul 6–9; Washington, DC
45.
go back to reference US National Institutes of Health. Efficacy and safety study of RAD001 in patients aged 18 or over with angiomyolipoma associated with tuberous sclerosis complex (TSC) or lymphangioleiomyomatosis (LAM) (EXIST-2) [ClinicalTrials.gov identifier NCT00790400]. US National Institutes of Health, ClinicalTrials.gov [online]. Available from URL: http://www.clinicaltrials.gov [Accessed 2011 Aug 23] US National Institutes of Health. Efficacy and safety study of RAD001 in patients aged 18 or over with angiomyolipoma associated with tuberous sclerosis complex (TSC) or lymphangioleiomyomatosis (LAM) (EXIST-2) [ClinicalTrials.gov identifier NCT00790400]. US National Institutes of Health, ClinicalTrials.gov [online]. Available from URL: http://​www.​clinicaltrials.​gov [Accessed 2011 Aug 23]
Metadata
Title
Everolimus
In Patients with Subependymal Giant Cell Astrocytoma Associated with Tuberous Sclerosis Complex
Author
Monique P. Curran
Publication date
01-02-2012
Publisher
Springer International Publishing
Published in
Pediatric Drugs / Issue 1/2012
Print ISSN: 1174-5878
Electronic ISSN: 1179-2019
DOI
https://doi.org/10.2165/11207730-000000000-00000

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