TY - JOUR
T1 - BRAF mutation testing for patients diagnosed with stage III or stage IV melanoma
T2 - practical guidance for the Australian setting
AU - Scolyer, Richard A.
AU - Atkinson, Victoria
AU - Gyorki, David E.
AU - Lambie, Duncan
AU - O'Toole, Sandra
AU - Saw, Robyn P.M.
AU - Amanuel, Benhur
AU - Angel, Christopher M.
AU - Button-Sloan, Alison E.
AU - Carlino, Matteo S.
AU - Ch'ng, Sydney
AU - Colebatch, Andrew J.
AU - Daneshvar, Dariush
AU - Pires da Silva, Inês
AU - Dawson, Tamara
AU - Ferguson, Peter M.
AU - Foster-Smith, Erwin
AU - Fox, Stephen B.
AU - Gill, Anthony J.
AU - Gupta, Ruta
AU - Henderson, Michael A.
AU - Hong, Angela M.
AU - Howle, Julie R.
AU - Jackett, Louise A.
AU - James, Craig
AU - Lee, C. Soon
AU - Lochhead, Alistair
AU - Loh, Daphne
AU - McArthur, Grant A.
AU - McLean, Catriona A.
AU - Menzies, Alexander M.
AU - Nieweg, Omgo E.
AU - O'Brien, Blake H.
AU - Pennington, Thomas E.
AU - Potter, Alison J.
AU - Prakash, Saurabh
AU - Rawson, Robert V.
AU - Read, Rebecca L.
AU - Rtshiladze, Michael A.
AU - Shannon, Kerwin F.
AU - Smithers, B. Mark
AU - Spillane, Andrew J.
AU - Stretch, Jonathan R.
AU - Thompson, John F.
AU - Tucker, Paul
AU - Varey, Alexander H.R.
AU - Vilain, Ricardo E.
AU - Wood, Benjamin A.
AU - Long, Georgina V.
PY - 2022/2
Y1 - 2022/2
N2 - Targeted therapy (BRAF inhibitor plus MEK inhibitor) is now among the possible treatment options for patients with BRAF mutation-positive stage III or stage IV melanoma. This makes prompt BRAF mutation testing an important step in the management of patients diagnosed with stage III or IV melanoma; one that can help better ensure that the optimal choice of systemic treatment is initiated with minimal delay. This article offers guidance about when and how BRAF mutation testing should be conducted when patients are diagnosed with melanoma in Australia. Notably, it recommends that pathologists reflexively order BRAF mutation testing whenever a patient is found to have American Joint Committee on Cancer (AJCC)/Union for International Cancer Control (UICC) stage III or IV melanoma (i.e., any metastatic spread beyond the primary tumour) and that patient's BRAF mutation status is hitherto unknown, even if BRAF mutation testing has not been specifically requested by the treating clinician (in Australia, Medicare-subsidised BRAFV600 mutation testing does not need to be requested by the treating clinician). When performed in centres with appropriate expertise and experience, immunohistochemistry (IHC) using the anti-BRAF V600E monoclonal antibody (VE1) can be a highly sensitive and specific means of detecting BRAFV600E mutations, and may be used as a rapid and relatively inexpensive initial screening test. However, VE1 immunostaining can be technically challenging and difficult to interpret, particularly in heavily pigmented tumours; melanomas with weak, moderate or focal BRAFV600E immunostaining should be regarded as equivocal. It must also be remembered that other activating BRAFV600 mutations (including BRAFV600K), which account for ∼10–20% of BRAFV600 mutations, are not detected with currently available IHC antibodies. For these reasons, if available and practicable, we recommend that DNA-based BRAF mutation testing always be performed, regardless of whether IHC-based testing is also conducted. Advice about tissue/specimen selection for BRAF mutation testing of patients diagnosed with stage III or IV melanoma is also offered in this article; and potential pitfalls when interpreting BRAF mutation tests are highlighted.
AB - Targeted therapy (BRAF inhibitor plus MEK inhibitor) is now among the possible treatment options for patients with BRAF mutation-positive stage III or stage IV melanoma. This makes prompt BRAF mutation testing an important step in the management of patients diagnosed with stage III or IV melanoma; one that can help better ensure that the optimal choice of systemic treatment is initiated with minimal delay. This article offers guidance about when and how BRAF mutation testing should be conducted when patients are diagnosed with melanoma in Australia. Notably, it recommends that pathologists reflexively order BRAF mutation testing whenever a patient is found to have American Joint Committee on Cancer (AJCC)/Union for International Cancer Control (UICC) stage III or IV melanoma (i.e., any metastatic spread beyond the primary tumour) and that patient's BRAF mutation status is hitherto unknown, even if BRAF mutation testing has not been specifically requested by the treating clinician (in Australia, Medicare-subsidised BRAFV600 mutation testing does not need to be requested by the treating clinician). When performed in centres with appropriate expertise and experience, immunohistochemistry (IHC) using the anti-BRAF V600E monoclonal antibody (VE1) can be a highly sensitive and specific means of detecting BRAFV600E mutations, and may be used as a rapid and relatively inexpensive initial screening test. However, VE1 immunostaining can be technically challenging and difficult to interpret, particularly in heavily pigmented tumours; melanomas with weak, moderate or focal BRAFV600E immunostaining should be regarded as equivocal. It must also be remembered that other activating BRAFV600 mutations (including BRAFV600K), which account for ∼10–20% of BRAFV600 mutations, are not detected with currently available IHC antibodies. For these reasons, if available and practicable, we recommend that DNA-based BRAF mutation testing always be performed, regardless of whether IHC-based testing is also conducted. Advice about tissue/specimen selection for BRAF mutation testing of patients diagnosed with stage III or IV melanoma is also offered in this article; and potential pitfalls when interpreting BRAF mutation tests are highlighted.
KW - adjuvant
KW - BRAF mutation testing
KW - BRAF mutation-positive melanoma
KW - diagnosis
KW - melanoma
KW - metastatic melanoma
KW - pathology
KW - stage III melanoma
KW - Stage IV melanoma
KW - targeted therapy
KW - treatment
UR - http://www.scopus.com/inward/record.url?scp=85121516578&partnerID=8YFLogxK
U2 - 10.1016/j.pathol.2021.11.002
DO - 10.1016/j.pathol.2021.11.002
M3 - Review article
C2 - 34937664
AN - SCOPUS:85121516578
SN - 0031-3025
VL - 54
SP - 6
EP - 19
JO - Pathology
JF - Pathology
IS - 1
ER -