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Erschienen in: Journal of Neuro-Oncology 3/2016

11.07.2016 | Topic Review

Rapid progression of intracranial melanoma metastases controlled with combined BRAF/MEK inhibition after discontinuation of therapy: a clinical challenge

verfasst von: Daniel N. Cagney, Brian M. Alexander, F. Stephen Hodi, Elizabeth I. Buchbinder, Patrick A. Ott, Ayal A. Aizer

Erschienen in: Journal of Neuro-Oncology | Ausgabe 3/2016

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Abstract

Novel systemic therapies with anti-tumor activity in the brain including small molecules targeting BRAF and MEK, and immune checkpoint inhibition, offer the possibility of improved control of intracranial disease. A number of prospective trials support the judicious use of modern systemic therapies in patients with melanoma and limited brain metastases .The intracranial clinical course of patients who progress extracranially on BRAF/MEK inhibition remains poorly described in the literature. In this report, we highlight a series of clinical cases, with rapid progression of intracranial disease following discontinuation of dabrafenib/trametinib for extracranial disease progression or toxicity, a previously unreported finding in the medical literature with significant implications for patient care.
Literatur
1.
Zurück zum Zitat Chiarion-Sileni V, Murr R, Pigozzo J (2001) Brain metastases from malignant melanoma. Int Soc Cell 13:170–185 Chiarion-Sileni V, Murr R, Pigozzo J (2001) Brain metastases from malignant melanoma. Int Soc Cell 13:170–185
2.
Zurück zum Zitat Tarhini AA, Agarwala SS (2004) Management of brain metastases in patients with melanoma. Curr Opin Oncol 16:61–166CrossRef Tarhini AA, Agarwala SS (2004) Management of brain metastases in patients with melanoma. Curr Opin Oncol 16:61–166CrossRef
3.
Zurück zum Zitat Ott PA, Hodi FS (2013) Treatment for advanced melanoma: new drugs, new opportunities, new challenges. Oncology (Williston Park) 27(5):381–392 Ott PA, Hodi FS (2013) Treatment for advanced melanoma: new drugs, new opportunities, new challenges. Oncology (Williston Park) 27(5):381–392
4.
Zurück zum Zitat Korn EL, Liu PY, Lee SJ, Chapman JA, Niedzwiecki D, Suman VJ et al (2008) Metaanalysis of phase II cooperative group trials in metastatic stage IV melanoma to determine progression-free and overall survival benchmarks for future phase II trials. J Clin Oncol 26:527–534CrossRefPubMed Korn EL, Liu PY, Lee SJ, Chapman JA, Niedzwiecki D, Suman VJ et al (2008) Metaanalysis of phase II cooperative group trials in metastatic stage IV melanoma to determine progression-free and overall survival benchmarks for future phase II trials. J Clin Oncol 26:527–534CrossRefPubMed
5.
Zurück zum Zitat Schmittel A, Proebstle T, Engenhart-Cabillic R (2003) Brain metastases following interleukin-2 plus interferon-alpha-2a therapy: a follow-up study in 94 stage IV melanoma patients. Eur J Cancer 39:476–480CrossRefPubMed Schmittel A, Proebstle T, Engenhart-Cabillic R (2003) Brain metastases following interleukin-2 plus interferon-alpha-2a therapy: a follow-up study in 94 stage IV melanoma patients. Eur J Cancer 39:476–480CrossRefPubMed
6.
Zurück zum Zitat Chang EL et al (2009) Neurocognition in patients with brain metastases treated with radiosurgery or radiosurgery plus whole-brain irradiation: a randomised controlled trial. Lancet Oncol 10(11):1037–1044CrossRefPubMed Chang EL et al (2009) Neurocognition in patients with brain metastases treated with radiosurgery or radiosurgery plus whole-brain irradiation: a randomised controlled trial. Lancet Oncol 10(11):1037–1044CrossRefPubMed
7.
Zurück zum Zitat Kocher M et al (2011) Adjuvant whole-brain radiotherapy versus observation after radiosurgery or surgical resection of one to three cerebral metastases: results of the EORTC 22952-26001 study. J Clin Oncol 29(2):134–141CrossRefPubMed Kocher M et al (2011) Adjuvant whole-brain radiotherapy versus observation after radiosurgery or surgical resection of one to three cerebral metastases: results of the EORTC 22952-26001 study. J Clin Oncol 29(2):134–141CrossRefPubMed
8.
Zurück zum Zitat Soffietti R et al (2013) A European Organisation for Research and Treatment of Cancer phase III trial of adjuvant whole-brain radiotherapy versus observation in patients with one to three brain metastases from solid tumors after surgical resection or radiosurgery: quality-of-life results. J Clin Oncol 31(1):65–72CrossRefPubMed Soffietti R et al (2013) A European Organisation for Research and Treatment of Cancer phase III trial of adjuvant whole-brain radiotherapy versus observation in patients with one to three brain metastases from solid tumors after surgical resection or radiosurgery: quality-of-life results. J Clin Oncol 31(1):65–72CrossRefPubMed
9.
Zurück zum Zitat Kolar GR et al (2013) Neoadjuvant treatment of a solitary melanoma brain metastasis with vemurafenib. J Clin Oncol 31(3):e40–e43CrossRefPubMed Kolar GR et al (2013) Neoadjuvant treatment of a solitary melanoma brain metastasis with vemurafenib. J Clin Oncol 31(3):e40–e43CrossRefPubMed
10.
Zurück zum Zitat Schäfer N et al (2013) Vemurafenib for leptomeningeal melanomatosis. J Clin Oncol 31(11):e173–e174CrossRefPubMed Schäfer N et al (2013) Vemurafenib for leptomeningeal melanomatosis. J Clin Oncol 31(11):e173–e174CrossRefPubMed
11.
Zurück zum Zitat Falchook GS et al (2012) Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet 379(9829):1893–1901CrossRefPubMedPubMedCentral Falchook GS et al (2012) Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet 379(9829):1893–1901CrossRefPubMedPubMedCentral
12.
Zurück zum Zitat Long V et al (2012) Dabrafenib in patients with Val600Glu or Val600Lys BRAF-mutant melanoma metastatic to the brain (BREAK-MB): a multicentre, open-label, phase 2 trial. Lancet Oncol 13(11):1087–1095CrossRefPubMed Long V et al (2012) Dabrafenib in patients with Val600Glu or Val600Lys BRAF-mutant melanoma metastatic to the brain (BREAK-MB): a multicentre, open-label, phase 2 trial. Lancet Oncol 13(11):1087–1095CrossRefPubMed
17.
Zurück zum Zitat Long GV et al (2014) Combined BRAF and MEK inhibition versus BRAF inhibition alone in melanoma. N Engl J Med 37(120):1877–1888CrossRef Long GV et al (2014) Combined BRAF and MEK inhibition versus BRAF inhibition alone in melanoma. N Engl J Med 37(120):1877–1888CrossRef
18.
Zurück zum Zitat Robert C et al (2015) Improved overall survival in melanoma with combined dabrafenib and trametinib. N Engl J Med 372(1):30–39CrossRefPubMed Robert C et al (2015) Improved overall survival in melanoma with combined dabrafenib and trametinib. N Engl J Med 372(1):30–39CrossRefPubMed
19.
Zurück zum Zitat Carlino MS, Gowrishankar K, Saunders CA et al (2013) Antiproliferative effects of continued mitogen-activated protein kinase pathway inhibition following acquired resistance to BRAF and/or MEK inhibition in melanoma. Mol Cancer Ther 12:1332CrossRefPubMed Carlino MS, Gowrishankar K, Saunders CA et al (2013) Antiproliferative effects of continued mitogen-activated protein kinase pathway inhibition following acquired resistance to BRAF and/or MEK inhibition in melanoma. Mol Cancer Ther 12:1332CrossRefPubMed
20.
Zurück zum Zitat Menzies AM, Long GV (2014) Systemic treatment for BRAF-mutant melanoma: where do we go next? Lancet Oncol 15:e371CrossRefPubMed Menzies AM, Long GV (2014) Systemic treatment for BRAF-mutant melanoma: where do we go next? Lancet Oncol 15:e371CrossRefPubMed
21.
Zurück zum Zitat Jakob JA et al (2012) NRAS mutation status is an independent prognostic factor in metastatic melanoma. Cancer 118(16):4014–4023CrossRefPubMed Jakob JA et al (2012) NRAS mutation status is an independent prognostic factor in metastatic melanoma. Cancer 118(16):4014–4023CrossRefPubMed
22.
Zurück zum Zitat Kumar R et al (2003) BRAF Mutations in metastatic melanoma: a possible association with clinical outcome. Clin Cancer Res 9(9):3362–3368PubMed Kumar R et al (2003) BRAF Mutations in metastatic melanoma: a possible association with clinical outcome. Clin Cancer Res 9(9):3362–3368PubMed
23.
Zurück zum Zitat Scholtens A, Geukes Foppen MH, Blank CU, van Thienen JV, van Tinteren H, Haanen JB (2015) Vemurafenib for BRAF V600 mutated advanced melanoma: Results of treatment beyond progression. Eur J Cancer 51:642–652CrossRefPubMed Scholtens A, Geukes Foppen MH, Blank CU, van Thienen JV, van Tinteren H, Haanen JB (2015) Vemurafenib for BRAF V600 mutated advanced melanoma: Results of treatment beyond progression. Eur J Cancer 51:642–652CrossRefPubMed
24.
Zurück zum Zitat Cancello G, Montagna E, D’Agostino D, Giuliano M, Giordano A, Di Lorenzo G et al (2008) Continuing trastuzumab beyond disease progression: outcomes analysis in patients with metastatic breast cancer. Breast Cancer Res 10(4):R60.CrossRefPubMedPubMedCentral Cancello G, Montagna E, D’Agostino D, Giuliano M, Giordano A, Di Lorenzo G et al (2008) Continuing trastuzumab beyond disease progression: outcomes analysis in patients with metastatic breast cancer. Breast Cancer Res 10(4):R60.CrossRefPubMedPubMedCentral
25.
Zurück zum Zitat Faehling M, Eckert R, Kamp T, Kuom S, Griese U, Strater J et al (2013) EGFR-tyrosine kinase inhibitor treatment beyond progression in long-term Caucasian responders to erlotinib in advanced non-small cell lung cancer: a case-control study of overall survival. Lung Cancer 80(3):306–312CrossRefPubMed Faehling M, Eckert R, Kamp T, Kuom S, Griese U, Strater J et al (2013) EGFR-tyrosine kinase inhibitor treatment beyond progression in long-term Caucasian responders to erlotinib in advanced non-small cell lung cancer: a case-control study of overall survival. Lung Cancer 80(3):306–312CrossRefPubMed
26.
Zurück zum Zitat Grothey A, Sugrue MM, Purdie DM, Dong W, Sargent D, Hedrick E et al (2008) Bevacizumab beyond first progression is associated with prolonged overall survival in metastatic colorectal cancer: results from a large observational cohort study (BRiTE). J Clin Oncol 26(33):5326–5334CrossRefPubMed Grothey A, Sugrue MM, Purdie DM, Dong W, Sargent D, Hedrick E et al (2008) Bevacizumab beyond first progression is associated with prolonged overall survival in metastatic colorectal cancer: results from a large observational cohort study (BRiTE). J Clin Oncol 26(33):5326–5334CrossRefPubMed
Metadaten
Titel
Rapid progression of intracranial melanoma metastases controlled with combined BRAF/MEK inhibition after discontinuation of therapy: a clinical challenge
verfasst von
Daniel N. Cagney
Brian M. Alexander
F. Stephen Hodi
Elizabeth I. Buchbinder
Patrick A. Ott
Ayal A. Aizer
Publikationsdatum
11.07.2016
Verlag
Springer US
Erschienen in
Journal of Neuro-Oncology / Ausgabe 3/2016
Print ISSN: 0167-594X
Elektronische ISSN: 1573-7373
DOI
https://doi.org/10.1007/s11060-016-2196-8

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