An integrated disease-specific graded prognostic assessment scale for melanoma: contributions of KPS, CITV, number of metastases, and BRAF mutation status.

BRAF CITV brain metastasis ds-GPA melanoma

Journal

Neuro-oncology advances
ISSN: 2632-2498
Titre abrégé: Neurooncol Adv
Pays: England
ID NLM: 101755003

Informations de publication

Date de publication:
Historique:
entrez: 28 1 2021
pubmed: 29 1 2021
medline: 29 1 2021
Statut: epublish

Résumé

Stereotactic radiosurgery (SRS) remains a mainstay therapy in the treatment of melanoma brain metastases (BM). While prognostic scales have been developed for melanoma patients who underwent SRS treatment for BM, the pertinence of these scales in the context of molecularly targeted therapies remains unclear. Through a multi-institutional collaboration, we collated the survival patterns of 331 melanoma BM patients with known BRAF mutation status treated with SRS. We established a prognostic scale that was validated in an independent cohort of 174 patients. All patients with BRAF mutations in this series were treated with BRAF inhibitors. Prognostic utility was assessed using Net Reclassification Index (NRI > 0) and integrated discrimination improvement (IDI) metrics. In a multivariate Cox proportional hazards model, BRAF mutation status, KPS, number of metastases, and cumulative intracranial tumor volume (CITV) independently contributed to survival prognostication for melanoma patients with SRS-treated BM ( Optimal survival prognostication for SRS-treated patients with melanoma BM requires an integrated assessment of patient characteristics (KPS), tumor characteristics (CITV and number of metastases), and the mutational profile of the melanoma (BRAF mutation status).

Sections du résumé

BACKGROUND BACKGROUND
Stereotactic radiosurgery (SRS) remains a mainstay therapy in the treatment of melanoma brain metastases (BM). While prognostic scales have been developed for melanoma patients who underwent SRS treatment for BM, the pertinence of these scales in the context of molecularly targeted therapies remains unclear.
METHODS METHODS
Through a multi-institutional collaboration, we collated the survival patterns of 331 melanoma BM patients with known BRAF mutation status treated with SRS. We established a prognostic scale that was validated in an independent cohort of 174 patients. All patients with BRAF mutations in this series were treated with BRAF inhibitors. Prognostic utility was assessed using Net Reclassification Index (NRI > 0) and integrated discrimination improvement (IDI) metrics.
RESULTS RESULTS
In a multivariate Cox proportional hazards model, BRAF mutation status, KPS, number of metastases, and cumulative intracranial tumor volume (CITV) independently contributed to survival prognostication for melanoma patients with SRS-treated BM (
CONCLUSIONS CONCLUSIONS
Optimal survival prognostication for SRS-treated patients with melanoma BM requires an integrated assessment of patient characteristics (KPS), tumor characteristics (CITV and number of metastases), and the mutational profile of the melanoma (BRAF mutation status).

Identifiants

pubmed: 33506199
doi: 10.1093/noajnl/vdaa152
pii: vdaa152
pmc: PMC7810198
doi:

Types de publication

Journal Article

Langues

eng

Pagination

vdaa152

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001863
Pays : United States

Informations de copyright

© The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology.

Références

Cancer. 2009 Jul 1;115(13):2930-8
pubmed: 19441110
Nat Rev Clin Oncol. 2015 Sep;12(9):527-40
pubmed: 26122185
Cancer. 2018 Jan 15;124(2):297-305
pubmed: 29023643
World Neurosurg. 2017 Feb;98:761-767.e1
pubmed: 27867125
Int J Radiat Oncol Biol Phys. 2013 Mar 1;85(3):656-61
pubmed: 22898384
BMC Cancer. 2018 Apr 27;18(1):490
pubmed: 29703161
Surg Oncol Clin N Am. 2011 Jan;20(1):1-17
pubmed: 21111956
World Neurosurg. 2017 Dec;108:151-156
pubmed: 28754641
World Neurosurg. 2017 Nov;107:944-951.e1
pubmed: 28735121
Neurosurgery. 2016 Aug;79(2):246-52
pubmed: 26579964
Lancet Oncol. 2012 Nov;13(11):1087-95
pubmed: 23051966
World Neurosurg. 2017 Oct;106:666-675
pubmed: 28735139
J Invest Dermatol. 2011 Oct;131(10):2139-42
pubmed: 21697891
J Neurosurg. 2013 Nov;119(5):1139-44
pubmed: 23971958
Adv Radiat Oncol. 2017 Nov 24;3(2):146-153
pubmed: 29904739
Int J Radiat Oncol Biol Phys. 2000 May 1;47(2):291-8
pubmed: 10802351
N Engl J Med. 2019 Aug 15;381(7):626-636
pubmed: 31166680
Front Oncol. 2016 May 02;6:107
pubmed: 27200295
World Neurosurg. 2019 Jan;121:e747-e754
pubmed: 30308343
J Neurooncol. 2016 May;128(1):119-128
pubmed: 26948673
J Neurosurg. 2015 Aug;123(2):395-401
pubmed: 25768829
Lancet. 2004 May 22;363(9422):1665-72
pubmed: 15158627
J Clin Oncol. 2015 Jun 10;33(17):1889-94
pubmed: 25667295
Int J Ayurveda Res. 2010 Oct;1(4):274-8
pubmed: 21455458
Melanoma Manag. 2016 Mar;3(1):33-45
pubmed: 30190871
J Neurosurg. 2017 Mar;126(3):726-734
pubmed: 27203149
Ann Gastroenterol Surg. 2018 Jul 04;2(5):332-338
pubmed: 30238073
Am J Surg. 1978 Jun;135(6):807-10
pubmed: 665907
J Neurosurg. 1998 Jan;88(1):11-20
pubmed: 9420067
Nat Rev Genet. 2019 Jul;20(7):404-416
pubmed: 30918367
Int J Radiat Oncol Biol Phys. 2017 Nov 15;99(4):812-816
pubmed: 29063850
J Radiosurg SBRT. 2016;4(3):181-190
pubmed: 29296443
Cancer Treat Rev. 2014 Feb;40(1):48-59
pubmed: 23810288
Am J Epidemiol. 2012 Sep 15;176(6):473-81
pubmed: 22875755
J Clin Oncol. 2012 Feb 1;30(4):419-25
pubmed: 22203767
Eur J Cancer. 2014 Apr;50(6):1148-58
pubmed: 24529832
Neurosurgery. 2018 Aug 1;83(2):237-244
pubmed: 28973506
Surg Neurol Int. 2015 Aug 20;6(Suppl 12):S355-65
pubmed: 26392919
J Neurosurg. 2016 Jul;125(1):17-23
pubmed: 26544782
Perspect Clin Res. 2010 Apr;1(2):67-9
pubmed: 21829786
Annu Rev Clin Psychol. 2010;6:109-38
pubmed: 20192788
Int J Radiat Oncol Biol Phys. 1998 Oct 1;42(3):581-9
pubmed: 9806518
BMC Cancer. 2014 Dec 11;14:931
pubmed: 25496194
Int J Radiat Oncol Biol Phys. 2017 Aug 1;98(5):1069-1077
pubmed: 28721890
Med Sci Monit. 2012 Jul;18(7):CR450-5
pubmed: 22739735
J Oncol Pract. 2016 Jun;12(6):536-42
pubmed: 27288470
Ann Emerg Med. 1990 Dec;19(12):1462-8
pubmed: 2240762
N Engl J Med. 2018 Aug 23;379(8):722-730
pubmed: 30134131
Cancer Med. 2018 Mar;7(3):757-764
pubmed: 29441722
Int J Radiat Oncol Biol Phys. 2012 May 1;83(1):303-9
pubmed: 22079723

Auteurs

Manmeet Ahluwalia (M)

Brain Tumor and Neuro-Oncology Center, Cleveland Clinic, Cleveland, Ohio, USA.

Mir A Ali (MA)

Department of Neurosurgery, Vanderbilt University Medical Center, Nashville, Tennessee, USA.

Rushikesh S Joshi (RS)

School of Medicine, University of California San Diego, San Diego, California, USA.

Eun Suk Park (ES)

Department of Neurosurgery, University of Minnesota, Minneapolis, Minnesota, USA.

Birra Taha (B)

Department of Neurosurgery, University of Minnesota, Minneapolis, Minnesota, USA.

Ian McCutcheon (I)

Department of Neurosurgery, MD Anderson Cancer Center, Houston, Texas, USA.

Veronica Chiang (V)

Department of Neurosurgery, Yale University School of Medicine, and Yale Cancer Center, New Haven, Connecticut, USA.

Angela Hong (A)

Melanoma Institute Australia, Wollstonecraft, NSW, Australia.

Georges Sinclair (G)

Department of Oncology, James Cook University Hospital, Middlesbrough, UK.
Department of Neurosurgery, Karolinska University Hospital, Stockholm, Sweden.

Jiri Bartek (J)

Department of Neurosurgery, Karolinska University Hospital, Stockholm, Sweden.

Clark C Chen (CC)

Department of Neurosurgery, University of Minnesota, Minneapolis, Minnesota, USA.

Classifications MeSH