Skip to main content
Erschienen in: Cancer Chemotherapy and Pharmacology 1/2016

01.01.2016 | Original Article

Hydroxyurea with or without imatinib in the treatment of recurrent or progressive meningiomas: a randomized phase II trial by Gruppo Italiano Cooperativo di Neuro-Oncologia (GICNO)

verfasst von: Elena Mazza, Alba Brandes, Silvia Zanon, Marika Eoli, Giuseppe Lombardi, Marina Faedi, Enrico Franceschi, Michele Reni

Erschienen in: Cancer Chemotherapy and Pharmacology | Ausgabe 1/2016

Einloggen, um Zugang zu erhalten

Abstract

Purpose

Hydroxyurea (HU) is among the most widely used salvage therapies in progressive meningiomas. Platelet-derived growth factor receptors are expressed in virtually all meningiomas. Imatinib sensitizes transformed cells to the cytotoxic effects of chemotherapeutic agents that interfere with DNA metabolism. The combination of HU with imatinib yielded intriguing results in recurrent malignant glioma. The current trial addressed the activity of this association against meningioma.

Methods

Patients with recurrent or progressive WHO grade I–III meningioma, without therapeutic indication for surgery, radiotherapy, or stereotactic radiosurgery, aged 18–75 years, ECOG performance status 0–2, and not on enzyme-inducing anti-epileptic drugs were randomized to receive HU 500 mg BID ± imatinib 400 mg QD until progression, unacceptable toxicity, or patient’s refusal. The primary endpoint was progression-free survival rate at 9 months (PFS-9).

Results

Between September 2009 and February 2012, 15 patients were randomized to receive HU + imatinib (N = 7; Arm A) or HU alone (N = 8; Arm B). Afterward the trial was prematurely closed due to slow enrollment rate. PFS-9 (A/B) was 0/75 %, and median PFS was 4/19.5 months. Median and 2-year overall survival (A/B) rates were: 6/27.5 months; 28.5/75 %, respectively. Main G3-4 toxicities were: G3 neutropenia in 1/0, G4 headache in 1/1, and G3 vomiting in 1/0.

Conclusion

The conduction of a study in recurrent or progressive meningioma remains a challenge. Given the limited number of patients enrolled, no firm conclusions can be drawn about the combination of imatinib and HU. The optimal systemic therapy for meningioma failing surgery and radiation has yet to be identified.
Literatur
3.
Zurück zum Zitat Kaley T, Barani I, Chamberlain M et al (2014) Historical benchmarks for medical therapy trials in surgery- and radiation-refractory meningioma: a RANO review. Neuro-Oncology 16:829–840PubMedPubMedCentralCrossRef Kaley T, Barani I, Chamberlain M et al (2014) Historical benchmarks for medical therapy trials in surgery- and radiation-refractory meningioma: a RANO review. Neuro-Oncology 16:829–840PubMedPubMedCentralCrossRef
4.
Zurück zum Zitat Schrell UM, Rittig MG, Anders M et al (1997) Hydroxyurea for treatment of unresectable and recurrent meningiomas. I. Inhibition of primary human meningioma cells in culture and in meningioma transplants by induction of the apoptotic pathway. J Neurosurg 86(5):845–852PubMedCrossRef Schrell UM, Rittig MG, Anders M et al (1997) Hydroxyurea for treatment of unresectable and recurrent meningiomas. I. Inhibition of primary human meningioma cells in culture and in meningioma transplants by induction of the apoptotic pathway. J Neurosurg 86(5):845–852PubMedCrossRef
5.
Zurück zum Zitat Schrell UM, Rittig MG, Anders M et al (1997) Hydroxyurea for treatment of unresectable and recurrent meningiomas. II. Decrease in the size of meningiomas in patients treated with hydroxyurea. J Neurosurg 86:840–844PubMedCrossRef Schrell UM, Rittig MG, Anders M et al (1997) Hydroxyurea for treatment of unresectable and recurrent meningiomas. II. Decrease in the size of meningiomas in patients treated with hydroxyurea. J Neurosurg 86:840–844PubMedCrossRef
6.
Zurück zum Zitat Newton HB, Slivka MA, Stevens C (2000) Hydroxyurea chemotherapy for unresectable or residual meningioma. J Neurooncol 49:165–170PubMedCrossRef Newton HB, Slivka MA, Stevens C (2000) Hydroxyurea chemotherapy for unresectable or residual meningioma. J Neurooncol 49:165–170PubMedCrossRef
7.
Zurück zum Zitat Mason WP, Gentili F, Macdonald DR, Hariharan S, Cruz CR, Abrey LE (2002) Stabilization of disease progression by hydroxyurea in patients with recurrent or unresectable meningioma. J Neurosurg 97:341–346PubMedCrossRef Mason WP, Gentili F, Macdonald DR, Hariharan S, Cruz CR, Abrey LE (2002) Stabilization of disease progression by hydroxyurea in patients with recurrent or unresectable meningioma. J Neurosurg 97:341–346PubMedCrossRef
8.
Zurück zum Zitat Rosenthal MA, Ashley DL, Cher L (2002) Treatment of high risk or recurrent meningiomas with hydroxyurea. J Clin Neurosci 9:156–158PubMedCrossRef Rosenthal MA, Ashley DL, Cher L (2002) Treatment of high risk or recurrent meningiomas with hydroxyurea. J Clin Neurosci 9:156–158PubMedCrossRef
9.
Zurück zum Zitat Paus S, Klockgether T, Urbach H, Schlegel U (2003) Meningioma of the optic nerve sheath: treatment with hydroxyurea. J Neurol Neurosurg Psychiatry 74:1348–1350PubMedPubMedCentralCrossRef Paus S, Klockgether T, Urbach H, Schlegel U (2003) Meningioma of the optic nerve sheath: treatment with hydroxyurea. J Neurol Neurosurg Psychiatry 74:1348–1350PubMedPubMedCentralCrossRef
10.
Zurück zum Zitat Loven D, Hardoff R, Sever ZB et al (2004) Non-resectable slow-growing meningiomas treated by hydroxyurea. J Neurooncol 67:221–226PubMedCrossRef Loven D, Hardoff R, Sever ZB et al (2004) Non-resectable slow-growing meningiomas treated by hydroxyurea. J Neurooncol 67:221–226PubMedCrossRef
11.
Zurück zum Zitat Hahn BM, Schrell UM, Sauer R, Fahlbusch R, Ganslandt O, Grabenbauer GG (2005) Prolonged oral hydroxyurea and concurrent 3D-conformal radiation in patients with progressive or recurrent meningioma: results of a pilot study. J Neurooncol 74:157–165PubMedCrossRef Hahn BM, Schrell UM, Sauer R, Fahlbusch R, Ganslandt O, Grabenbauer GG (2005) Prolonged oral hydroxyurea and concurrent 3D-conformal radiation in patients with progressive or recurrent meningioma: results of a pilot study. J Neurooncol 74:157–165PubMedCrossRef
12.
Zurück zum Zitat Wen PY, Yung WK, Lamborn KR et al (2009) Phase II study of imatinib mesylate for recurrent meningiomas (North American Brain Tumor Consortium study 01-08). Neuro Oncol 11:853–860PubMedPubMedCentralCrossRef Wen PY, Yung WK, Lamborn KR et al (2009) Phase II study of imatinib mesylate for recurrent meningiomas (North American Brain Tumor Consortium study 01-08). Neuro Oncol 11:853–860PubMedPubMedCentralCrossRef
13.
Zurück zum Zitat Swinnen, LJ, Rankin C, Rushing EJ, Laura HF, Damek DM, Barger GR (2009) Phase II study of hydroxyurea for unresectable meningioma (Southwest Oncology Group S9811). In: Journal of Clinical Oncology, ASCO annual meeting proceedings (Post-Meeting Edition), vol 27, No 15S (May 20 Supplement):2063 Swinnen, LJ, Rankin C, Rushing EJ, Laura HF, Damek DM, Barger GR (2009) Phase II study of hydroxyurea for unresectable meningioma (Southwest Oncology Group S9811). In: Journal of Clinical Oncology, ASCO annual meeting proceedings (Post-Meeting Edition), vol 27, No 15S (May 20 Supplement):2063
14.
Zurück zum Zitat Chamberlain MC, Johnston SK (2011) Hydroxyurea for recurrent surgery and radiation refractory meningioma: a retrospective case series. J Neurooncol 104:765–771PubMedCrossRef Chamberlain MC, Johnston SK (2011) Hydroxyurea for recurrent surgery and radiation refractory meningioma: a retrospective case series. J Neurooncol 104:765–771PubMedCrossRef
15.
Zurück zum Zitat Chamberlain MC (2012) Hydroxyurea for recurrent surgery and radiation refractory high-grade meningioma. J Neurooncol 107:315–321PubMedCrossRef Chamberlain MC (2012) Hydroxyurea for recurrent surgery and radiation refractory high-grade meningioma. J Neurooncol 107:315–321PubMedCrossRef
16.
Zurück zum Zitat Holdhoff M, Kreuzer KA, Appett C et al (2005) Imatinib mesylate radiosensitizes human glioblastoma cells through inhibition of platelet-derived growth factor receptor. Blood Cells Mol Dis 34:181–185PubMedCrossRef Holdhoff M, Kreuzer KA, Appett C et al (2005) Imatinib mesylate radiosensitizes human glioblastoma cells through inhibition of platelet-derived growth factor receptor. Blood Cells Mol Dis 34:181–185PubMedCrossRef
17.
Zurück zum Zitat O’Reilly T, Wartmann M, Maira SM et al (2004) Patupilone (epothilone B, EPO906) and imatinib (STI571, Imatinib) in combination display enhanced antitumour activity in vivo against experimental rat C6 glioma. Cancer Chemother Pharmacol 55:307–317PubMedCrossRef O’Reilly T, Wartmann M, Maira SM et al (2004) Patupilone (epothilone B, EPO906) and imatinib (STI571, Imatinib) in combination display enhanced antitumour activity in vivo against experimental rat C6 glioma. Cancer Chemother Pharmacol 55:307–317PubMedCrossRef
18.
Zurück zum Zitat Katayama R, Huelsmeyer MK, Marr AK et al (2004) Imatinib mesylate inhibits platelet-derived growth factor activity and increases chemosensitivity in feline vaccine-associated sarcoma. Cancer Chemother Pharmacol 54:25–33PubMedCrossRef Katayama R, Huelsmeyer MK, Marr AK et al (2004) Imatinib mesylate inhibits platelet-derived growth factor activity and increases chemosensitivity in feline vaccine-associated sarcoma. Cancer Chemother Pharmacol 54:25–33PubMedCrossRef
19.
Zurück zum Zitat Aloyz R, Grzywacz K, Xu ZY et al (2004) Imatinib sensitizes CLL lymphocytes to chlorambucil. Leukemia 18:409–414PubMedCrossRef Aloyz R, Grzywacz K, Xu ZY et al (2004) Imatinib sensitizes CLL lymphocytes to chlorambucil. Leukemia 18:409–414PubMedCrossRef
20.
Zurück zum Zitat Kano Y, Akutsu M, Tsunoda S et al (2001) In vitro cytotoxic effects of a tyrosine kinase inhibitor STI571 in combination with commonly used antileukemic agents. Blood 97:1999–2007PubMedCrossRef Kano Y, Akutsu M, Tsunoda S et al (2001) In vitro cytotoxic effects of a tyrosine kinase inhibitor STI571 in combination with commonly used antileukemic agents. Blood 97:1999–2007PubMedCrossRef
21.
Zurück zum Zitat Dogruel M, Gibbs JE, Thomas SA (2003) Hydroxyurea transport across the blood–brain and blood–cerebrospinal fluid barriers of the guinea-pig. J Neurochem 87:76–84PubMedCrossRef Dogruel M, Gibbs JE, Thomas SA (2003) Hydroxyurea transport across the blood–brain and blood–cerebrospinal fluid barriers of the guinea-pig. J Neurochem 87:76–84PubMedCrossRef
22.
Zurück zum Zitat Reardon DA et al (2012) Phase II study of Gleveec® plus hydroxyurea (HU) in adults with progressive or recurrent meningioma. J Neuroncol 106(2):409–415CrossRef Reardon DA et al (2012) Phase II study of Gleveec® plus hydroxyurea (HU) in adults with progressive or recurrent meningioma. J Neuroncol 106(2):409–415CrossRef
23.
Zurück zum Zitat Chamberlain MC, Blumenthal DT (2004) Intracranial meningiomas: diagnosis and treatment. Expert Rev Neurother 4(4):641–648PubMedCrossRef Chamberlain MC, Blumenthal DT (2004) Intracranial meningiomas: diagnosis and treatment. Expert Rev Neurother 4(4):641–648PubMedCrossRef
25.
Zurück zum Zitat Chamberlain MC, Tsao-Wei DD, Groshen S (2004) Temozolomide for treatment-resistant recurrent meningioma. Neurology 62(7):1210–1212PubMedCrossRef Chamberlain MC, Tsao-Wei DD, Groshen S (2004) Temozolomide for treatment-resistant recurrent meningioma. Neurology 62(7):1210–1212PubMedCrossRef
26.
Zurück zum Zitat Chamberlain MC, Tsao-Wei DD, Groshen S (2006) Salvage chemotherapy with CPT-11 for recurrent meningioma. J Neurooncol 78(3):271–276PubMedCrossRef Chamberlain MC, Tsao-Wei DD, Groshen S (2006) Salvage chemotherapy with CPT-11 for recurrent meningioma. J Neurooncol 78(3):271–276PubMedCrossRef
27.
Zurück zum Zitat Newton HB, Scott SR, Volpi C (2004) Hydroxyurea chemotherapy for meningiomas: enlarged cohort with extended follow-up. Br J Neurosurg 18(5):495–499PubMedCrossRef Newton HB, Scott SR, Volpi C (2004) Hydroxyurea chemotherapy for meningiomas: enlarged cohort with extended follow-up. Br J Neurosurg 18(5):495–499PubMedCrossRef
28.
Zurück zum Zitat Ragel BT, Jensen RL (2010) Aberrant signaling pathways in meningiomas. J Neurooncol 99(3):315–324PubMedCrossRef Ragel BT, Jensen RL (2010) Aberrant signaling pathways in meningiomas. J Neurooncol 99(3):315–324PubMedCrossRef
29.
Zurück zum Zitat Choy W, Kim W, Nagasawa D et al (2011) The molecular genetics and tumor pathogenesis of meningiomas and the future directions of meningioma treatments. Neurosurg Focus 30(5):E6PubMed Choy W, Kim W, Nagasawa D et al (2011) The molecular genetics and tumor pathogenesis of meningiomas and the future directions of meningioma treatments. Neurosurg Focus 30(5):E6PubMed
30.
Zurück zum Zitat Johnson MD, O’Connell M, Pilcher W (2011) Lopinavir inhibits meningioma cell proliferation by Akt independent mechanism. J Neurooncol 101(3):441–448PubMedCrossRef Johnson MD, O’Connell M, Pilcher W (2011) Lopinavir inhibits meningioma cell proliferation by Akt independent mechanism. J Neurooncol 101(3):441–448PubMedCrossRef
31.
Zurück zum Zitat Norden AD, Raizer JJ, Abrey LE et al (2010) Phase II trials of erlotinib or gefitinib in patients with recurrent meningioma. J Neurooncol 96(2):211–217PubMedPubMedCentralCrossRef Norden AD, Raizer JJ, Abrey LE et al (2010) Phase II trials of erlotinib or gefitinib in patients with recurrent meningioma. J Neurooncol 96(2):211–217PubMedPubMedCentralCrossRef
32.
Zurück zum Zitat Nayak L, Iwamoto FM, Rudnick JD et al (2012) Atypical and anaplastic meningiomas treated with bevacizumab. J Neurooncol 109(1):187–193PubMedCrossRef Nayak L, Iwamoto FM, Rudnick JD et al (2012) Atypical and anaplastic meningiomas treated with bevacizumab. J Neurooncol 109(1):187–193PubMedCrossRef
33.
Zurück zum Zitat Lou E, Sumrall AL, Turner S et al (2012) Bevacizumab therapy for adults with recurrent/progressive meningioma: a retrospective series. J Neurooncol 109(1):63–70PubMedPubMedCentralCrossRef Lou E, Sumrall AL, Turner S et al (2012) Bevacizumab therapy for adults with recurrent/progressive meningioma: a retrospective series. J Neurooncol 109(1):63–70PubMedPubMedCentralCrossRef
34.
Zurück zum Zitat Raizer JJ, Grimm SA, Rademaker A et al (2014) A phase II trial of PTK787/ZK 222584 in recurrent or progressive radiation and surgery refractory meningiomas. J Neurooncol 117(1):93–101PubMedCrossRef Raizer JJ, Grimm SA, Rademaker A et al (2014) A phase II trial of PTK787/ZK 222584 in recurrent or progressive radiation and surgery refractory meningiomas. J Neurooncol 117(1):93–101PubMedCrossRef
35.
Zurück zum Zitat Kaley TJ, Wen P, Schiff D et al (2015) Phase II trial of sunitinib for recurrent and progressive atypical and anaplastic meningioma. Neuro Oncol 17(1):116–121PubMedPubMedCentralCrossRef Kaley TJ, Wen P, Schiff D et al (2015) Phase II trial of sunitinib for recurrent and progressive atypical and anaplastic meningioma. Neuro Oncol 17(1):116–121PubMedPubMedCentralCrossRef
36.
Zurück zum Zitat Preusser M, Spiegl-Kreinecker S, Lötsch D et al (2012) Trabectedin has promising antineoplastic activity in high-grade meningioma. Cancer 118(20):5038–5049PubMedCrossRef Preusser M, Spiegl-Kreinecker S, Lötsch D et al (2012) Trabectedin has promising antineoplastic activity in high-grade meningioma. Cancer 118(20):5038–5049PubMedCrossRef
Metadaten
Titel
Hydroxyurea with or without imatinib in the treatment of recurrent or progressive meningiomas: a randomized phase II trial by Gruppo Italiano Cooperativo di Neuro-Oncologia (GICNO)
verfasst von
Elena Mazza
Alba Brandes
Silvia Zanon
Marika Eoli
Giuseppe Lombardi
Marina Faedi
Enrico Franceschi
Michele Reni
Publikationsdatum
01.01.2016
Verlag
Springer Berlin Heidelberg
Erschienen in
Cancer Chemotherapy and Pharmacology / Ausgabe 1/2016
Print ISSN: 0344-5704
Elektronische ISSN: 1432-0843
DOI
https://doi.org/10.1007/s00280-015-2927-0

Weitere Artikel der Ausgabe 1/2016

Cancer Chemotherapy and Pharmacology 1/2016 Zur Ausgabe

Alphablocker schützt vor Miktionsproblemen nach der Biopsie

16.05.2024 alpha-1-Rezeptorantagonisten Nachrichten

Nach einer Prostatabiopsie treten häufig Probleme beim Wasserlassen auf. Ob sich das durch den periinterventionellen Einsatz von Alphablockern verhindern lässt, haben australische Mediziner im Zuge einer Metaanalyse untersucht.

Mammakarzinom: Senken Statine das krebsbedingte Sterberisiko?

15.05.2024 Mammakarzinom Nachrichten

Frauen mit lokalem oder metastasiertem Brustkrebs, die Statine einnehmen, haben eine niedrigere krebsspezifische Mortalität als Patientinnen, die dies nicht tun, legen neue Daten aus den USA nahe.

Labor, CT-Anthropometrie zeigen Risiko für Pankreaskrebs

13.05.2024 Pankreaskarzinom Nachrichten

Gerade bei aggressiven Malignomen wie dem duktalen Adenokarzinom des Pankreas könnte Früherkennung die Therapiechancen verbessern. Noch jedoch klafft hier eine Lücke. Ein Studienteam hat einen Weg gesucht, sie zu schließen.

Viel pflanzliche Nahrung, seltener Prostata-Ca.-Progression

12.05.2024 Prostatakarzinom Nachrichten

Ein hoher Anteil pflanzlicher Nahrung trägt möglicherweise dazu bei, das Progressionsrisiko von Männern mit Prostatakarzinomen zu senken. In einer US-Studie war das Risiko bei ausgeprägter pflanzlicher Ernährung in etwa halbiert.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.