TY - CHAP
T1 - Dermatological Complications of Systemic Therapies for Melanoma
AU - Ramelyte, Egle
AU - Dummer, Reinhard
AU - Libenciuc, Cristina
AU - Phillips, Gregory S.
AU - Lacouture, Mario E.
AU - Robert, Caroline
N1 - Publisher Copyright:
© Springer Nature Switzerland AG 2020.
PY - 2020/1/1
Y1 - 2020/1/1
N2 - Modern melanoma therapies, such as targeted therapy (TT) and immunotherapy (IT), proved to significantly prolong progression free and overall survival in patients with advanced melanoma. Since their approval for metastatic disease, these drugs have also been tested and met with success in the adjuvant setting. As the list of indications for systemic melanoma therapies expands, increasing numbers of patients are exposed to systemic therapies and placed at risk of developing adverse events. The skin is the organ that is most commonly affected by modern melanoma therapies. Cutaneous adverse events occur in over 95% of patients treated with BRAF inhibitors, over 90% of those treated with MEK inhibitors, and less frequently in patients undergoing combination therapy. With immune checkpointbased immunotherapy the incidence rates vary between 43.5% and 58.7% with anti- TLA-4 antibodies, 37.4–41.9% in thosereceiving anti-PD-1, and up to 70% in those receiving combination immunotherapy.is dermatologic adverse events can causesignificant morbidity, patient education, prophylaxis, timely recognition, and early intervention of adverse events are crucial in management of patients receiving modern systemic therapies.
AB - Modern melanoma therapies, such as targeted therapy (TT) and immunotherapy (IT), proved to significantly prolong progression free and overall survival in patients with advanced melanoma. Since their approval for metastatic disease, these drugs have also been tested and met with success in the adjuvant setting. As the list of indications for systemic melanoma therapies expands, increasing numbers of patients are exposed to systemic therapies and placed at risk of developing adverse events. The skin is the organ that is most commonly affected by modern melanoma therapies. Cutaneous adverse events occur in over 95% of patients treated with BRAF inhibitors, over 90% of those treated with MEK inhibitors, and less frequently in patients undergoing combination therapy. With immune checkpointbased immunotherapy the incidence rates vary between 43.5% and 58.7% with anti- TLA-4 antibodies, 37.4–41.9% in thosereceiving anti-PD-1, and up to 70% in those receiving combination immunotherapy.is dermatologic adverse events can causesignificant morbidity, patient education, prophylaxis, timely recognition, and early intervention of adverse events are crucial in management of patients receiving modern systemic therapies.
UR - http://www.scopus.com/inward/record.url?scp=85150577851&partnerID=8YFLogxK
U2 - 10.1007/978-3-030-05070-2_63
DO - 10.1007/978-3-030-05070-2_63
M3 - Chapter
AN - SCOPUS:85150577851
SN - 9783030050689
VL - 2
SP - 1337
EP - 1358
BT - Cutaneous Melanoma, Sixth Edition
PB - Springer International Publishing
ER -