Skip to main content

Advertisement

Log in

Phase I study of panobinostat in combination with bevacizumab for recurrent high-grade glioma

  • Clinical Study – Patient Study
  • Published:
Journal of Neuro-Oncology Aims and scope Submit manuscript

Abstract

Bevacizumab is frequently used to treat patients with recurrent high-grade glioma (HGG), but responses are generally not durable. Panobinostat is a histone deacetylase inhibitor with anti-neoplastic and anti-angiogenic effects and may work synergistically with VEGF inhibitors. We performed a phase I study to evaluate the safety and tolerability of the combination of orally administered panobinostat with bevacizumab in patients with recurrent HGG. Patients with recurrent HGG were treated on a 3 + 3 trial design. Patients received bevacizumab 10 mg/kg every other week in combination with oral panobinostat. The starting dose of panobinostat was 20 mg three times per week, weekly (cohort 1). Due to concerns for thrombocytopenia with the weekly dosing regimen, the protocol was amended to examine an every other week regimen. Cohort 2 received panobinostat 20 mg three times per week, every other week, and cohort 3 received 30 mg three times per week, every other week. Dose-limiting toxicity during the first 30 days was used to determine the maximum-tolerated dose. Twelve patients (median age 50, median KPS 90) with recurrent HGG were enrolled. One dose-limiting toxicity (DLT) (Grade 3 thrombocytopenia) was observed in cohort 1. No DLTs were observed in cohorts 2 and 3. The following grade 3 toxicities were seen in one patient each: thrombocytopenia, hypophosphatemia, esophageal hemorrhage, and deep venous thrombosis. There were no grade 4 or 5 toxicities. There were three patients with partial responses and seven with stable disease. The recommended doses for further study are oral panobinostat 30 mg three times per week, every other week, in combination with bevacizumab 10 mg/kg every other week. A phase II clinical trial in recurrent HGG is underway.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. CBTRUS (2009) CBTRUS. Statistical report: primary brain tumors in the United States, 2000-2004. http://www.cbtrus.org/reports/2009-NPCR-04-05/CBTRUS-NPCR2004-2005-Report-.pdf. Accessed October 2009

  2. Wen PY, Kesari S (2008) Malignant gliomas in adults. N Engl J Med 359(5):492–507

    Article  PubMed  CAS  Google Scholar 

  3. Friedman HS, Prados MD, Wen PY et al (2009) Bevacizumab alone and in combination with irinotecan in recurrent glioblastoma. J Clin Oncol 27(28):4733–4740

    Article  PubMed  CAS  Google Scholar 

  4. Kreisl TN, Kim L, Moore K et al (2009) Phase II trial of single-agent bevacizumab followed by bevacizumab plus irinotecan at tumor progression in recurrent glioblastoma. J Clin Oncol 27(5):740–745

    Article  PubMed  CAS  Google Scholar 

  5. Desjardins A, Reardon DA et al (2008) Bevacizumab plus irinotecan in recurrent WHO grade 3 malignant gliomas. Clin Cancer Res 14(21):7068–7073

    Article  PubMed  CAS  Google Scholar 

  6. Vredenburgh JJ, Desjardins A, Herndon JE 2nd et al (2007) Phase II trial of bevacizumab and irinotecan in recurrent malignant glioma. Clin Cancer Res 13(4):1253–1259

    Article  PubMed  CAS  Google Scholar 

  7. Norden AD, Drappatz J, Wen PY (2008) Novel anti-angiogenic therapies for malignant gliomas. Lancet Neurol 7(12):1152–1160

    Article  PubMed  CAS  Google Scholar 

  8. Quant EC, Norden AD, Drappatz J et al (2009) Role of a second chemotherapy in recurrent malignant glioma patients who progress on bevacizumab. Neuro Oncol 11(5):550–555

    Article  PubMed  CAS  Google Scholar 

  9. Atadja P (2009) Development of the pan-DAC inhibitor panobinostat (LBH589): successes and challenges. Cancer Lett 280(2):233–241

    Article  PubMed  CAS  Google Scholar 

  10. Gensert JM, Baranova OV, Weinstein DE, Ratan RR (2007) CD81, a cell cycle regulator, is a novel target for histone deacetylase inhibition in glioma cells. Neurobiol Dis 26(3):671–680

    Article  PubMed  CAS  Google Scholar 

  11. Ugur HC, Ramakrishna N, Bello L et al (2007) Continuous intracranial administration of suberoylanilide hydroxamic acid (SAHA) inhibits tumor growth in an orthotopic glioma model. J Neurooncol 83(3):267–275

    Article  PubMed  CAS  Google Scholar 

  12. Yin D, Ong JM, Hu J et al (2007) Suberoylanilide hydroxamic acid, a histone deacetylase inhibitor: effects on gene expression and growth of glioma cells in vitro and in vivo. Clin Cancer Res 13(3):1045–1052

    Article  PubMed  CAS  Google Scholar 

  13. Sharma V, Koul N, Joseph C, Dixit D, Ghosh S, Sen E (2010) HDAC inhibitor, scriptaid, induces glioma cell apoptosis through JNK activation and inhibits telomerase activity. J Cell Mol Med 14(8):2151–2161

    Article  PubMed  CAS  Google Scholar 

  14. Eyupoglu IY, Hahnen E, Trankle C et al (2006) Experimental therapy of malignant gliomas using the inhibitor of histone deacetylase MS-275. Mol Cancer Ther 5(5):1248–1255

    Article  PubMed  Google Scholar 

  15. Wetzel M, Premkumar DR, Arnold B, Pollack IF (2005) Effect of trichostatin A, a histone deacetylase inhibitor, on glioma proliferation in vitro by inducing cell cycle arrest and apoptosis. J Neurosurg 103(6 Suppl):549–556

    PubMed  Google Scholar 

  16. Eyupoglu IY, Hahnen E, Buslei R et al (2005) Suberoylanilide hydroxamic acid (SAHA) has potent anti-glioma properties in vitro, ex vivo and in vivo. J Neurochem 93(4):992–999

    Article  PubMed  Google Scholar 

  17. Sawa H, Murakami H, Kumagai M et al (2004) Histone deacetylase inhibitor, FK228, induces apoptosis and suppresses cell proliferation of human glioblastoma cells in vitro and in vivo. Acta Neuropathol 107(6):523–531

    Article  PubMed  CAS  Google Scholar 

  18. Galanis E, Jaeckle KA, Maurer MJ et al (2009) Phase II trial of vorinostat in recurrent glioblastoma multiforme: a north central cancer treatment group study. J Clin Oncol 27(12):2052–2058

    Article  PubMed  CAS  Google Scholar 

  19. Deroanne CF, Bonjean K, Servotte S et al (2002) Histone deacetylases inhibitors as anti-angiogenic agents altering vascular endothelial growth factor signaling. Oncogene 21(3):427–436

    Article  PubMed  CAS  Google Scholar 

  20. Qian DZ, Kato Y, Shabbeer S et al (2006) Targeting tumor angiogenesis with histone deacetylase inhibitors: the hydroxamic acid derivative LBH589. Clin Cancer Res 12(2):634–642

    Article  PubMed  CAS  Google Scholar 

  21. Qian DZ, Wang X, Kachhap SK et al (2004) The histone deacetylase inhibitor NVP-LAQ824 inhibits angiogenesis and has a greater antitumor effect in combination with the vascular endothelial growth factor receptor tyrosine kinase inhibitor PTK787/ZK222584. Cancer Res 64(18):6626–6634

    Article  PubMed  CAS  Google Scholar 

  22. Sawa H, Murakami H, Ohshima Y et al (2002) Histone deacetylase inhibitors such as sodium butyrate and trichostatin A inhibit vascular endothelial growth factor (VEGF) secretion from human glioblastoma cells. Brain Tumor Pathol 19(2):77–81

    Article  PubMed  CAS  Google Scholar 

  23. Batchelor TT, Sorensen AG, di Tomaso E et al (2007) AZD2171, a pan-VEGF receptor tyrosine kinase inhibitor, normalizes tumor vasculature and alleviates edema in glioblastoma patients. Cancer Cell 11(1):83–95

    Article  PubMed  CAS  Google Scholar 

  24. Mandawat A, Fiskus W, Buckley KM et al (2010) Pan-histone deacetylase inhibitor panobinostat depletes CXCR4 levels and signaling and exerts synergistic antimyeloid activity in combination with CXCR4 antagonists. Blood 116(24):5306–5315

    Article  PubMed  CAS  Google Scholar 

  25. Kioi M, Vogel H, Schultz G et al (2010) Inhibition of vasculogenesis, but not angiogenesis, prevents the recurrence of glioblastoma after irradiation in mice. J Clin Invest 120(3):694–705

    Article  PubMed  CAS  Google Scholar 

  26. Rubin JB, Kung AL, Klein RS et al (2003) A small-molecule antagonist of CXCR4 inhibits intracranial growth of primary brain tumors. Proc Natl Acad Sci USA 100(23):13513–13518

    Article  PubMed  CAS  Google Scholar 

  27. Lin R, Hu J, Paul S, et al. (2009) Characteristics of thrombocytopenia in patients treated with oral panobinostat (LBH589). Blood (ASH Annual Meeting Abstracts) 114: Abstract 2740

  28. 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(11):1963–1972

    Article  PubMed  Google Scholar 

  29. Novartis (2011) LBH 589 (Panobinostat) Investigator’s Brochure 7th edn, Brochure. Basel, Switzerland

    Google Scholar 

Download references

Acknowledgments

E.Q. Lee has served on the advisory board of Novartis and Genentech/Roche. T. T. Batchelor has served on the advisory board for Genentech/Roche. R. Beroukhim has received research support from Novartis. S.M. Snodgrass is an employee of Novartis. J.J. Raizer has received research support from Novartis and Genentech/Roche, served on the advisory boards of both Novartis and Genentech/Roche and is on the speaker’s bureau of Genentech/Roche. P.Y. Wen has received research support from Novartis and Genentech/Roche and served on the advisory boards of both Novartis and Genentech/Roche.

Conflict of interest

All other authors report no conflicts of interest.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to P. Y. Wen.

Additional information

First three authors contributed equally to this work

Rights and permissions

Reprints and permissions

About this article

Cite this article

Drappatz, J., Lee, E.Q., Hammond, S. et al. Phase I study of panobinostat in combination with bevacizumab for recurrent high-grade glioma. J Neurooncol 107, 133–138 (2012). https://doi.org/10.1007/s11060-011-0717-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11060-011-0717-z

Keywords

Navigation