TY - JOUR
T1 - Systemic therapy for melanoma
T2 - ASCO guideline
AU - Seth, Rahul
AU - Messersmith, Hans
AU - Kaur, Varinder
AU - Kirkwood, John M.
AU - Kudchadkar, Ragini
AU - McQuade, Jennifer Leigh
AU - Provenzano, Anthony
AU - Swami, Umang
AU - Weber, Jeffrey
AU - Alluri, Krishna C.
AU - Agarwala, Sanjiv
AU - Ascierto, Paolo A.
AU - Atkins, Michael B.
AU - Davis, Nancy
AU - Ernstoff, Marc S.
AU - Faries, Mark B.
AU - Gold, Jason S.
AU - Guild, Samantha
AU - Gyorki, David E.
AU - Khushalani, Nikhil I.
AU - Meyers, Michael O.
AU - Robert, Caroline
AU - Santinami, Mario
AU - Sehdev, Amikar
AU - Sondak, Vernon K.
AU - Spurrier, Gilliosa
AU - Tsai, Katy K.
AU - van Akkooi, Alexander
AU - Funchain, Pauline
N1 - Publisher Copyright:
© 2020 by American Society of Clinical Oncology
PY - 2020/11/20
Y1 - 2020/11/20
N2 - PURPOSE To provide guidance to clinicians regarding the use of systemic therapy for melanoma. METHODS ASCO convened an Expert Panel and conducted a systematic review of the literature. RESULTS A systematic review, one meta-analysis, and 34 additional randomized trials were identified. The published studies included a wide range of systemic therapies in cutaneous and noncutaneous melanoma. RECOMMENDATIONS In the adjuvant setting, nivolumab or pembrolizumab should be offered to patients with resected stage IIIA/B/C/D BRAF wild-type cutaneous melanoma, while either of those two agents or the combination of dabrafenib and trametinib should be offered in BRAF-mutant disease. No recommendation could be made for or against the use of neoadjuvant therapy in cutaneous melanoma. In the unresectable/ metastatic setting, ipilimumab plus nivolumab, nivolumab alone, or pembrolizumab alone should be offered to patients with BRAF wild-type cutaneous melanoma, while those three regimens or combination BRAF/MEK inhibitor therapy with dabrafenib/trametinib, encorafenib/binimetinib, or vemurafenib/cobimetinib should be offered in BRAF-mutant disease. Patients with mucosal melanoma may be offered the same therapies recommended for cutaneous melanoma. No recommendation could be made for or against specific therapy for uveal melanoma. Additional information is available at www.asco.org/melanoma-guidelines.
AB - PURPOSE To provide guidance to clinicians regarding the use of systemic therapy for melanoma. METHODS ASCO convened an Expert Panel and conducted a systematic review of the literature. RESULTS A systematic review, one meta-analysis, and 34 additional randomized trials were identified. The published studies included a wide range of systemic therapies in cutaneous and noncutaneous melanoma. RECOMMENDATIONS In the adjuvant setting, nivolumab or pembrolizumab should be offered to patients with resected stage IIIA/B/C/D BRAF wild-type cutaneous melanoma, while either of those two agents or the combination of dabrafenib and trametinib should be offered in BRAF-mutant disease. No recommendation could be made for or against the use of neoadjuvant therapy in cutaneous melanoma. In the unresectable/ metastatic setting, ipilimumab plus nivolumab, nivolumab alone, or pembrolizumab alone should be offered to patients with BRAF wild-type cutaneous melanoma, while those three regimens or combination BRAF/MEK inhibitor therapy with dabrafenib/trametinib, encorafenib/binimetinib, or vemurafenib/cobimetinib should be offered in BRAF-mutant disease. Patients with mucosal melanoma may be offered the same therapies recommended for cutaneous melanoma. No recommendation could be made for or against specific therapy for uveal melanoma. Additional information is available at www.asco.org/melanoma-guidelines.
UR - http://www.scopus.com/inward/record.url?scp=85084057646&partnerID=8YFLogxK
U2 - 10.1200/JCO.20.00198
DO - 10.1200/JCO.20.00198
M3 - Review article
C2 - 32228358
AN - SCOPUS:85084057646
SN - 0732-183X
VL - 38
SP - 3947
EP - 3970
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 33
ER -