Skip to main content
Erschienen in: Current Treatment Options in Oncology 2/2014

01.06.2014 | Skin Cancer (WH Sharfman, Section Editor)

Managing The Skin Toxicities From New Melanoma Drugs

verfasst von: John C. Mavropoulos, MD, MPH, PhD, Timothy S. Wang, MD

Erschienen in: Current Treatment Options in Oncology | Ausgabe 2/2014

Einloggen, um Zugang zu erhalten

Opinion Statement

Patients treated with ipilimumab or targeted inhibitors of the RAF-MEK-ERK pathway (vemurafenib, dabrafenib, and trametinib) for advanced cutaneous melanoma often experience drug-related skin toxicities denoted as dermatologic adverse events (DAEs). Although rarely life-threatening, DAEs may emerge dramatically and potentially compromise oncologic therapy if not managed in a timely and effective manner. Early recognition of DAEs is critical to providing optimal skin care and prompt consultation with a dermatologist should be obtained when a diagnosis is unclear. The expanding utilization of new melanoma drugs compels physicians to maintain a watchful eye for both known and novel DAEs and to adopt a low threshold to biopsy worrisome skin findings. Numerous therapeutic options are available to manage DAEs including topical and systemic agents as well as surgical and destructive modalities. Applying such methods improves overall patient care and optimizes the effectiveness of new therapies for advanced cutaneous melanoma.
Literatur
1.
3.
Zurück zum Zitat Wolchok J, Neyns B, Linette G, et al. Ipilimumab monotherapy in patients with previously treated, advanced melanoma: a randomized, double-blind, multicenter, phase 2, dose-ranging study. Lancet Oncol. 2010;11:155–64.CrossRefPubMed Wolchok J, Neyns B, Linette G, et al. Ipilimumab monotherapy in patients with previously treated, advanced melanoma: a randomized, double-blind, multicenter, phase 2, dose-ranging study. Lancet Oncol. 2010;11:155–64.CrossRefPubMed
4.
Zurück zum Zitat Hodi FS, O’Day SJ, McDermott DF, et al. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med. 2010;363:711–23.PubMedCentralCrossRefPubMed Hodi FS, O’Day SJ, McDermott DF, et al. Improved survival with ipilimumab in patients with metastatic melanoma. N Engl J Med. 2010;363:711–23.PubMedCentralCrossRefPubMed
5.••
Zurück zum Zitat Voskens CJ, Goldinger SM, Loquai C, et al. The price of tumor control: an analysis of rare side effects of anti-CTLA-4 therapy in metastatic melanoma from the ipilimumab network. PLoS One. 2013;8:e53745:1–17. This is an excellent report on rare DAEs associated with ipilimumab and associated treatment recommendations. Voskens CJ, Goldinger SM, Loquai C, et al. The price of tumor control: an analysis of rare side effects of anti-CTLA-4 therapy in metastatic melanoma from the ipilimumab network. PLoS One. 2013;8:e53745:1–17. This is an excellent report on rare DAEs associated with ipilimumab and associated treatment recommendations.
6.
Zurück zum Zitat YERVOY (Ipilimumab) Product insert revised. December, 2013. YERVOY (Ipilimumab) Product insert revised. December, 2013.
7.
Zurück zum Zitat McArthur GA, Ribas A. Targeting oncogenic drivers and the immune system in melanoma. J Clin Oncol. 2013;31:499–506.CrossRefPubMed McArthur GA, Ribas A. Targeting oncogenic drivers and the immune system in melanoma. J Clin Oncol. 2013;31:499–506.CrossRefPubMed
8.
Zurück zum Zitat Ibrahim R, Berman D, de Pril V, et al. Ipilimumab safety profile: summary of findings from completed trials in advanced melanoma. J Clin Oncol. 2011;29: [Abstract no. 8583]. Ibrahim R, Berman D, de Pril V, et al. Ipilimumab safety profile: summary of findings from completed trials in advanced melanoma. J Clin Oncol. 2011;29: [Abstract no. 8583].
9.•
Zurück zum Zitat Choi JN. How to recognize and manage ipilimumab-induced dermatologic adverse events. The ASCO Post. 2013;4. An excellent article offering practical treatment recommendations for ipilimumab-induced DAEs. Choi JN. How to recognize and manage ipilimumab-induced dermatologic adverse events. The ASCO Post. 2013;4. An excellent article offering practical treatment recommendations for ipilimumab-induced DAEs.
10.
Zurück zum Zitat National Cancer Institute, Cancer Therapy Evaluation Program. Common Terminology Criteria for Adverse Events Version 3.0. 2006: p.14–6. Available at: http://ctep.cancer.gov. National Cancer Institute, Cancer Therapy Evaluation Program. Common Terminology Criteria for Adverse Events Version 3.0. 2006: p.14–6. Available at: http://​ctep.​cancer.​gov.
11.
Zurück zum Zitat Bolognia JL, Jorizzo JL, Schaffer JV. Dermatology 3rd Edition. 2012. ISBN-13: 9780723435716. Erythema Multiforme, Stevens-Johnson syndrome, and Toxic Epidermal Necrolysis Elsevier Health Sciences Publisher. 2012; Chapter 20: Bolognia JL, Jorizzo JL, Schaffer JV. Dermatology 3rd Edition. 2012. ISBN-13: 9780723435716. Erythema Multiforme, Stevens-Johnson syndrome, and Toxic Epidermal Necrolysis Elsevier Health Sciences Publisher. 2012; Chapter 20:
12.
Zurück zum Zitat Ensslin CJ, Rosen AC, Wu S, et al. Pruritis in patients treated with targeted cancer therapies: systematic review and meta-analysis. J Am Acad Dermatol. 2013;69:708–20.CrossRefPubMed Ensslin CJ, Rosen AC, Wu S, et al. Pruritis in patients treated with targeted cancer therapies: systematic review and meta-analysis. J Am Acad Dermatol. 2013;69:708–20.CrossRefPubMed
13.
Zurück zum Zitat Pintova S, Sidhu H, Friedlander PA, et al. Sweet’s syndrome in a patient with metastatic melanoma after ipilimumab therapy. Melanoma Res. 2013;23:498–501.CrossRefPubMed Pintova S, Sidhu H, Friedlander PA, et al. Sweet’s syndrome in a patient with metastatic melanoma after ipilimumab therapy. Melanoma Res. 2013;23:498–501.CrossRefPubMed
14.
Zurück zum Zitat Deylon J, Mateus C, Lambert T. Hemophilia A Induced by Ipilimumab. N Engl J Med. 2011;365:1747–8.CrossRef Deylon J, Mateus C, Lambert T. Hemophilia A Induced by Ipilimumab. N Engl J Med. 2011;365:1747–8.CrossRef
15.
Zurück zum Zitat Assi H, Wilson KS. Immune toxicities and long remission duration after ipilimumab therapy for metastatic melanoma: 2 illustrative cases. Curr Oncol. 2013;20:e165–9.PubMedCentralCrossRefPubMed Assi H, Wilson KS. Immune toxicities and long remission duration after ipilimumab therapy for metastatic melanoma: 2 illustrative cases. Curr Oncol. 2013;20:e165–9.PubMedCentralCrossRefPubMed
17.
Zurück zum Zitat Eckert A, Schoeffler A, Dalle S, et al. Anti-CTLA4 monoclonal antibody induced sarcoidosis in a metastatic melanoma patient. Dermatology. 2009;218:69–70.CrossRefPubMed Eckert A, Schoeffler A, Dalle S, et al. Anti-CTLA4 monoclonal antibody induced sarcoidosis in a metastatic melanoma patient. Dermatology. 2009;218:69–70.CrossRefPubMed
18.
Zurück zum Zitat Vogel WV, Guislain A, Kvistborg P, et al. Ipilimumab-induced sarcoidosis in a patient with metastatic melanoma undergoing complete remission. J Clin Oncol. 2012;30:e7–10.CrossRefPubMed Vogel WV, Guislain A, Kvistborg P, et al. Ipilimumab-induced sarcoidosis in a patient with metastatic melanoma undergoing complete remission. J Clin Oncol. 2012;30:e7–10.CrossRefPubMed
19.
Zurück zum Zitat Berthod G, Lazor R, Letovanec I, et al. Pulmonary sarcoid-like granulomatosis induced by ipilimumab. J Clin Oncol. 2012;30:e156–9.CrossRefPubMed Berthod G, Lazor R, Letovanec I, et al. Pulmonary sarcoid-like granulomatosis induced by ipilimumab. J Clin Oncol. 2012;30:e156–9.CrossRefPubMed
20.
Zurück zum Zitat ZELBORAF (Vemurafenib) Product Insert Revised July, 2013. ZELBORAF (Vemurafenib) Product Insert Revised July, 2013.
21.
Zurück zum Zitat Platz A, Egyhazi S, Ringborg U, et al. Human cutaneous melanoma: a review of NRAS and BRAF mutation frequencies in relation to histogenic subclass and body site. Mol Oncol. 2008;1:395–405.CrossRefPubMed Platz A, Egyhazi S, Ringborg U, et al. Human cutaneous melanoma: a review of NRAS and BRAF mutation frequencies in relation to histogenic subclass and body site. Mol Oncol. 2008;1:395–405.CrossRefPubMed
22.
Zurück zum Zitat Chapman PB, Hauschild A, Robert C, et al. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011;364:2507–16.PubMedCentralCrossRefPubMed Chapman PB, Hauschild A, Robert C, et al. Improved survival with vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011;364:2507–16.PubMedCentralCrossRefPubMed
23.••
Zurück zum Zitat Lacouture ME, Duvic M, Hauschild A, et al. Analysis of dermatologic events in vemurafenib-treated patient with melanoma. Oncologist. 2013;18:314–22. An excellent comprehensive analysis of DAEs associated with vemurafenib.PubMedCentralCrossRefPubMed Lacouture ME, Duvic M, Hauschild A, et al. Analysis of dermatologic events in vemurafenib-treated patient with melanoma. Oncologist. 2013;18:314–22. An excellent comprehensive analysis of DAEs associated with vemurafenib.PubMedCentralCrossRefPubMed
24.•
Zurück zum Zitat Boussemart L, Routier E, Mateus C, et al. Prospective study of cutaneous side-effects associated with the BRAF inhibitor vemurafenib: a study of 42 patients. Ann Oncol. 2013;24:1691–7. A well conducted small prospective study on DAEs associated with vemurafenib.CrossRefPubMed Boussemart L, Routier E, Mateus C, et al. Prospective study of cutaneous side-effects associated with the BRAF inhibitor vemurafenib: a study of 42 patients. Ann Oncol. 2013;24:1691–7. A well conducted small prospective study on DAEs associated with vemurafenib.CrossRefPubMed
25.•
Zurück zum Zitat Mattei PL, Alora-Palli MB, Kraft S, et al. Cutaneous effects of BRAF inhibitor therapy: a case series. Ann Oncol. 2013;24:530–7. A thorough and very detailed retrospective analysis of DAEs experienced by 33 patients treated with either vemurafenib or dabrafenib/trametinib combination therapy.CrossRefPubMed Mattei PL, Alora-Palli MB, Kraft S, et al. Cutaneous effects of BRAF inhibitor therapy: a case series. Ann Oncol. 2013;24:530–7. A thorough and very detailed retrospective analysis of DAEs experienced by 33 patients treated with either vemurafenib or dabrafenib/trametinib combination therapy.CrossRefPubMed
26.
27.
Zurück zum Zitat Oberholzer PA, Kee D, Dziunycz P, et al. RAS mutations are associated with the development of cutaneous squamous cell tumors in patients treated with RAF inhibitors. J Clin Oncol. 2012;30:316–21.PubMedCentralCrossRefPubMed Oberholzer PA, Kee D, Dziunycz P, et al. RAS mutations are associated with the development of cutaneous squamous cell tumors in patients treated with RAF inhibitors. J Clin Oncol. 2012;30:316–21.PubMedCentralCrossRefPubMed
28.
29.
Zurück zum Zitat Su F, Viros A, Milagre C, et al. RAS mutations in cutaneous squamous-cell carcinomas in patients treated with BRAF inhibitors. N Engl J Med. 2012;366:207–15.PubMedCentralCrossRefPubMed Su F, Viros A, Milagre C, et al. RAS mutations in cutaneous squamous-cell carcinomas in patients treated with BRAF inhibitors. N Engl J Med. 2012;366:207–15.PubMedCentralCrossRefPubMed
30.
Zurück zum Zitat Sambrano BL, Riddel CE, Chon SY. Eruptive milia secondary to vemurafenib. J Am Acad Dermatol. 2013;69:e258–60.CrossRefPubMed Sambrano BL, Riddel CE, Chon SY. Eruptive milia secondary to vemurafenib. J Am Acad Dermatol. 2013;69:e258–60.CrossRefPubMed
31.
Zurück zum Zitat Hatzivassiliou G, Song K, Yen I, et al. RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. Nature. 2010;464:431–5.CrossRefPubMed Hatzivassiliou G, Song K, Yen I, et al. RAF inhibitors prime wild-type RAF to activate the MAPK pathway and enhance growth. Nature. 2010;464:431–5.CrossRefPubMed
32.
Zurück zum Zitat Heidorn SJ, Milagre C, Whittaker S, et al. Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF. Cell. 2010;140:209–21.PubMedCentralCrossRefPubMed Heidorn SJ, Milagre C, Whittaker S, et al. Kinase-dead BRAF and oncogenic RAS cooperate to drive tumor progression through CRAF. Cell. 2010;140:209–21.PubMedCentralCrossRefPubMed
33.••
Zurück zum Zitat Flaherty KT, Infante JR, Daud A, et al. Combined BRAF and MEK inhibition in melanoma with BRAF V600 mutations. N Engl J Med. 2012;367:1694–703. doi:10.1056/NEJMoa1210093. A landmark clinical trial demonstrating the protective effect of trametinib against new onset KAs/SCCs induced by dabrafenib.PubMedCentralCrossRefPubMed Flaherty KT, Infante JR, Daud A, et al. Combined BRAF and MEK inhibition in melanoma with BRAF V600 mutations. N Engl J Med. 2012;367:1694–703. doi:10.​1056/​NEJMoa1210093. A landmark clinical trial demonstrating the protective effect of trametinib against new onset KAs/SCCs induced by dabrafenib.PubMedCentralCrossRefPubMed
34.
Zurück zum Zitat Flaherty KT, Robert C, Hersey P, et al. Improved survival with MEK inhibition in BRAF-mutated melanoma. N Engl J Med. 2012;367:107–14.CrossRefPubMed Flaherty KT, Robert C, Hersey P, et al. Improved survival with MEK inhibition in BRAF-mutated melanoma. N Engl J Med. 2012;367:107–14.CrossRefPubMed
35.
Zurück zum Zitat Anforth R, Fernandez-Penas P, Long GV. Cutaneous toxicities of RAF inhibitors. Lancet Oncol. 2013;14:e11–8.CrossRefPubMed Anforth R, Fernandez-Penas P, Long GV. Cutaneous toxicities of RAF inhibitors. Lancet Oncol. 2013;14:e11–8.CrossRefPubMed
36.
Zurück zum Zitat Zimmer L, Hillen U, Livingstone E, et al. Atypical melanocytic proliferations and new primary melanomas in patients with advanced melanoma undergoing selective BRAF inhibition. J Clin Oncol. 2012;30:2375–83.PubMedCentralCrossRefPubMed Zimmer L, Hillen U, Livingstone E, et al. Atypical melanocytic proliferations and new primary melanomas in patients with advanced melanoma undergoing selective BRAF inhibition. J Clin Oncol. 2012;30:2375–83.PubMedCentralCrossRefPubMed
37.
Zurück zum Zitat Dalle S, Poulalhon N, Thomas L. Vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011;365:1450.CrossRef Dalle S, Poulalhon N, Thomas L. Vemurafenib in melanoma with BRAF V600E mutation. N Engl J Med. 2011;365:1450.CrossRef
38.••
Zurück zum Zitat Cohen PR, Bedikian AY, Kim KB. Appearance of new vemurafenib-associated melanocytic nevi on normal-appearing skin: case series and a review of changing or new pigmented lesions in patients with metastatic malignant melanoma after initiating treatment with vemurafenib. J Clin Anesth Dermatol. 2013;6:27–37. A comprehensive up-to-date listing of vemurafenib-induced DAEs providing important details regarding evolution of new melanomas in patients treated with vemurafenib. Cohen PR, Bedikian AY, Kim KB. Appearance of new vemurafenib-associated melanocytic nevi on normal-appearing skin: case series and a review of changing or new pigmented lesions in patients with metastatic malignant melanoma after initiating treatment with vemurafenib. J Clin Anesth Dermatol. 2013;6:27–37. A comprehensive up-to-date listing of vemurafenib-induced DAEs providing important details regarding evolution of new melanomas in patients treated with vemurafenib.
39.
Zurück zum Zitat Dalle S, Poulalhon N, Debarbieux S, et al. Tracking of second primary melanomas in vemurafenib-treated patients. JAMA Dermatol. 2013;149:488–90.CrossRefPubMed Dalle S, Poulalhon N, Debarbieux S, et al. Tracking of second primary melanomas in vemurafenib-treated patients. JAMA Dermatol. 2013;149:488–90.CrossRefPubMed
40.
Zurück zum Zitat Boyd KP, Vincent B, Andea A, et al. Nonmalignant cutaneous findings associated with vemurafenib use in patients with metastatic melanoma. J Am Acad Dermatol. 2012;67:1375–9.CrossRefPubMed Boyd KP, Vincent B, Andea A, et al. Nonmalignant cutaneous findings associated with vemurafenib use in patients with metastatic melanoma. J Am Acad Dermatol. 2012;67:1375–9.CrossRefPubMed
41.
Zurück zum Zitat Wang CM, Fleming KF, Hsu S. A case of vemurafenib-induced keratosis pilaris-like eruption. Dermatol Online J. 2012;18:7.PubMed Wang CM, Fleming KF, Hsu S. A case of vemurafenib-induced keratosis pilaris-like eruption. Dermatol Online J. 2012;18:7.PubMed
42.•
Zurück zum Zitat Rinderknecht JD, Goldinger SM, Rozati S, et al. RASopathic Skin Eruptions during Vemurafenib Therapy. PLoS One. 2013;8:e58721:1–11. A very useful article providing excellent clinical photographs and treatment recommendations for common DAEs associated with vemurafenib. Rinderknecht JD, Goldinger SM, Rozati S, et al. RASopathic Skin Eruptions during Vemurafenib Therapy. PLoS One. 2013;8:e58721:1–11. A very useful article providing excellent clinical photographs and treatment recommendations for common DAEs associated with vemurafenib.
43.
Zurück zum Zitat Harding JJ, Pulitzer M, Chapman PB. Vemurafenib sensitivity skin reaction after ipilimumab. N Engl J Med. 2012;366:866–8.CrossRefPubMed Harding JJ, Pulitzer M, Chapman PB. Vemurafenib sensitivity skin reaction after ipilimumab. N Engl J Med. 2012;366:866–8.CrossRefPubMed
44.
Zurück zum Zitat Wenk KS, Pichard DC, Nasabzadeh T, et al. Vemurafenib-Induced DRESS. JAMA Dermatol. 2013;149:1242–3.CrossRefPubMed Wenk KS, Pichard DC, Nasabzadeh T, et al. Vemurafenib-Induced DRESS. JAMA Dermatol. 2013;149:1242–3.CrossRefPubMed
45.
Zurück zum Zitat Sinha R, Lecamwasam K, Purshouse K, et al. Toxic epidermal necrolysis in a patient receiving vemurafenib for treatment of metastatic malignant melanoma. Br J Dermatol. 2013. doi:10.1111/bjd.12796. Sinha R, Lecamwasam K, Purshouse K, et al. Toxic epidermal necrolysis in a patient receiving vemurafenib for treatment of metastatic malignant melanoma. Br J Dermatol. 2013. doi:10.​1111/​bjd.​12796.
46.
Zurück zum Zitat Chu EY, Wanat KA, Miller CJ, et al. Diverse cutaneous side effects associated with BRAF inhibitor therapy: a clinicopathologic study. J Am Acad Dermatol. 2012;67:1265–72.CrossRefPubMed Chu EY, Wanat KA, Miller CJ, et al. Diverse cutaneous side effects associated with BRAF inhibitor therapy: a clinicopathologic study. J Am Acad Dermatol. 2012;67:1265–72.CrossRefPubMed
47.
Zurück zum Zitat Story SG, Beschloss JK, Dolan CK, et al. Eccrine squamous syringometaplasia associated with vemurafenib therapy. J Am Acad Dermatol. 2012;67:e208–10.CrossRefPubMed Story SG, Beschloss JK, Dolan CK, et al. Eccrine squamous syringometaplasia associated with vemurafenib therapy. J Am Acad Dermatol. 2012;67:e208–10.CrossRefPubMed
48.
Zurück zum Zitat Dummer R, Rinderknecht J, Goldinger SM, et al. Ultraviolet A and photosensitivity during vemurafenib therapy. N Engl J Med. 2012;366:480–1.CrossRefPubMed Dummer R, Rinderknecht J, Goldinger SM, et al. Ultraviolet A and photosensitivity during vemurafenib therapy. N Engl J Med. 2012;366:480–1.CrossRefPubMed
49.
Zurück zum Zitat Gelot P, Dutartre H, Khammari A, et al. Vemurafenib: an unusual UVA-induced photosensitivity. Exp Dermatol. 2013;22:297–8.CrossRefPubMed Gelot P, Dutartre H, Khammari A, et al. Vemurafenib: an unusual UVA-induced photosensitivity. Exp Dermatol. 2013;22:297–8.CrossRefPubMed
50.
Zurück zum Zitat Schultze B, Meissner M, Wolter M, et al. Unusual acute and delayed skin reactions during and after whole-brain radiotherapy in combination with the BRAF inhibitor vemurafenib. Strahlenther Onkol. 2013. doi:10.1007/s00066-013-0474-3.PubMed Schultze B, Meissner M, Wolter M, et al. Unusual acute and delayed skin reactions during and after whole-brain radiotherapy in combination with the BRAF inhibitor vemurafenib. Strahlenther Onkol. 2013. doi:10.​1007/​s00066-013-0474-3.PubMed
51.
Zurück zum Zitat Satzger I, Degen A, Asper H, et al. Serious skin toxicity with the combination of BRAF inhibitors and radiotherapy. J Clin Oncol. 2013;31:e220–2.CrossRefPubMed Satzger I, Degen A, Asper H, et al. Serious skin toxicity with the combination of BRAF inhibitors and radiotherapy. J Clin Oncol. 2013;31:e220–2.CrossRefPubMed
52.
Zurück zum Zitat Park JJ, Hawryluk EB, Tahan SR, et al. Cutaneous granulomatous eruption and successful response to potent topical steroids in patients undergoing targeted BRAF inhibitor treatment for metastatic melanoma. JAMA Dermatol. 2013. doi:10.1001/jamadermatol.2013.7919. Park JJ, Hawryluk EB, Tahan SR, et al. Cutaneous granulomatous eruption and successful response to potent topical steroids in patients undergoing targeted BRAF inhibitor treatment for metastatic melanoma. JAMA Dermatol. 2013. doi:10.​1001/​jamadermatol.​2013.​7919.
54.
Zurück zum Zitat Sinha R, Edmonds K, Newton-Bishop J, et al. Erythema nodosum-like panniculitis in patients with melanoma treated with vemurafenib. J Clin Oncol. 2013;31:320–1.CrossRef Sinha R, Edmonds K, Newton-Bishop J, et al. Erythema nodosum-like panniculitis in patients with melanoma treated with vemurafenib. J Clin Oncol. 2013;31:320–1.CrossRef
55.
Zurück zum Zitat Zimmer L, Livingstone E, Hillen U, et al. Panniculitis with arthralgia in patients with melanoma treated with selective BRAF inhibitors and its management. Arch Dermatol. 2012;148:357–61.CrossRefPubMed Zimmer L, Livingstone E, Hillen U, et al. Panniculitis with arthralgia in patients with melanoma treated with selective BRAF inhibitors and its management. Arch Dermatol. 2012;148:357–61.CrossRefPubMed
56.
Zurück zum Zitat Novoa RA, Honda K, Koon HB, et al. Vasculitis and panniculitis associated with vemurafenib. J Am Acad Dermatol. 2012;67:e271–2.CrossRefPubMed Novoa RA, Honda K, Koon HB, et al. Vasculitis and panniculitis associated with vemurafenib. J Am Acad Dermatol. 2012;67:e271–2.CrossRefPubMed
57.
Zurück zum Zitat Maldonado-Seral C, Berros-Fombella JP, Vivanco-Allende B, et al. Vemurafenib-associated neutrophilic panniculitis: an emergent adverse effect of variable severity. Dermatol Online. 2013;19:16. Maldonado-Seral C, Berros-Fombella JP, Vivanco-Allende B, et al. Vemurafenib-associated neutrophilic panniculitis: an emergent adverse effect of variable severity. Dermatol Online. 2013;19:16.
60.
Zurück zum Zitat Falchook GS, Long GV, Kurzrock R, et al. Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet. 2012;379:1893–901.CrossRefPubMed Falchook GS, Long GV, Kurzrock R, et al. Dabrafenib in patients with melanoma, untreated brain metastases, and other solid tumours: a phase 1 dose-escalation trial. Lancet. 2012;379:1893–901.CrossRefPubMed
63.
Zurück zum Zitat Long GV, Trefzer U, Davies MA, et al. 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. 2012;13:1087–95. doi:10.1016/S1470-2045(12)70431-X.CrossRefPubMed Long GV, Trefzer U, Davies MA, et al. 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. 2012;13:1087–95. doi:10.​1016/​S1470-2045(12)70431-X.CrossRefPubMed
64.••
Zurück zum Zitat Anforth RM, Blumetti TC, Kefford RF, et al. Cutaneous manifestations of dabrafenib (GSK2118436): a selective inhibitor of mutant BRAF in patients with metastatic melanoma. Br J Dermatol. 2012;167:1153–60. doi:10.1111/j.1365-2133.2012.11155.x. A useful and comprehensive analysis of common and uncommon DAEs associated with dabrafenib therapy.CrossRefPubMed Anforth RM, Blumetti TC, Kefford RF, et al. Cutaneous manifestations of dabrafenib (GSK2118436): a selective inhibitor of mutant BRAF in patients with metastatic melanoma. Br J Dermatol. 2012;167:1153–60. doi:10.​1111/​j.​1365-2133.​2012.​11155.​x. A useful and comprehensive analysis of common and uncommon DAEs associated with dabrafenib therapy.CrossRefPubMed
65.
Zurück zum Zitat Kim KB, Kefford R, Pavlick AC, et al. Phase II Study of the MEK1/MEK2 inhibitor trametinib in patients with metastatic BRAF-mutant cutaneous melanoma previously treated with or without a BRAF inhibitor. J Clin Oncol. 2013;31:482–9. doi:10.1200/JCO.2012.43.5966.CrossRefPubMed Kim KB, Kefford R, Pavlick AC, et al. Phase II Study of the MEK1/MEK2 inhibitor trametinib in patients with metastatic BRAF-mutant cutaneous melanoma previously treated with or without a BRAF inhibitor. J Clin Oncol. 2013;31:482–9. doi:10.​1200/​JCO.​2012.​43.​5966.CrossRefPubMed
67.
68.
Zurück zum Zitat Tarhini A. Immune-mediated adverse events associated with ipilimumab CTLA-4 blockade therapy: the underlying mechanisms and clinical management. Scientifica (Cairo). 2013;857519. Tarhini A. Immune-mediated adverse events associated with ipilimumab CTLA-4 blockade therapy: the underlying mechanisms and clinical management. Scientifica (Cairo). 2013;857519.
70.
Zurück zum Zitat Sachse MM, Wagner G. Clearance of BRAF inhibitor-associated keratoacanthomas by systemic retinoids. Br J Dermatol. 2013. doi:10.1111/bjd.12659. Sachse MM, Wagner G. Clearance of BRAF inhibitor-associated keratoacanthomas by systemic retinoids. Br J Dermatol. 2013. doi:10.​1111/​bjd.​12659.
71.
Zurück zum Zitat Anforth R, Blumetti TC, Clements A, et al. Systemic retinoids for the chemoprevention of cutaneous squamous cell carcinoma and verrucal keratosis in a cohort of patients on BRAF inhibitors. Br J Dermatol. 2013;169:1310–3.CrossRefPubMed Anforth R, Blumetti TC, Clements A, et al. Systemic retinoids for the chemoprevention of cutaneous squamous cell carcinoma and verrucal keratosis in a cohort of patients on BRAF inhibitors. Br J Dermatol. 2013;169:1310–3.CrossRefPubMed
72.
Zurück zum Zitat Anforth R, Blumetti TC, Mohd Affandi A, et al. Systemic retinoid therapy for chemoprevention of nonmelanoma skin cancer in a patient treated with vemurafenib. J Clin Oncol. 2012;30:e165–7.CrossRefPubMed Anforth R, Blumetti TC, Mohd Affandi A, et al. Systemic retinoid therapy for chemoprevention of nonmelanoma skin cancer in a patient treated with vemurafenib. J Clin Oncol. 2012;30:e165–7.CrossRefPubMed
74.
Zurück zum Zitat Bolognia JL, Jorizzo JL, Schaffer JV. Dermatology 3rd Edition. 2012. ISBN-13: 9780723435716. Cysts. Elsevier Health Sciences Publisher. 2012; Chapter 110. Bolognia JL, Jorizzo JL, Schaffer JV. Dermatology 3rd Edition. 2012. ISBN-13: 9780723435716. Cysts. Elsevier Health Sciences Publisher. 2012; Chapter 110.
75.•
Zurück zum Zitat Fischer A, Rosen AC, Ensslin CJ, et al. Pruritis to anticancer agents targeting the EGFR, BRAF, and CTLA-4. Dermatol Ther. 2013;26:135–48. The authors provide very user-friendly treatment algorithms for rash, xerosis, and pruritis.CrossRefPubMed Fischer A, Rosen AC, Ensslin CJ, et al. Pruritis to anticancer agents targeting the EGFR, BRAF, and CTLA-4. Dermatol Ther. 2013;26:135–48. The authors provide very user-friendly treatment algorithms for rash, xerosis, and pruritis.CrossRefPubMed
76.
Zurück zum Zitat Tsunoda K, Onodera H, Akasaka T. Case of malignant melanoma associated with a sarcoid reaction. J Dermatol. 2011;38:939–42.PubMed Tsunoda K, Onodera H, Akasaka T. Case of malignant melanoma associated with a sarcoid reaction. J Dermatol. 2011;38:939–42.PubMed
77.
Zurück zum Zitat Rochet NM, Chavan RN, Cappel MA, et al. Sweet syndrome: clinical presentation, associations, and response to treatment in 77 patients. J Am Acad Dermatol. 2013;69:557–64.CrossRefPubMed Rochet NM, Chavan RN, Cappel MA, et al. Sweet syndrome: clinical presentation, associations, and response to treatment in 77 patients. J Am Acad Dermatol. 2013;69:557–64.CrossRefPubMed
78.
Zurück zum Zitat Bolognia JL, Jorizzo JL, Schaffer JV. Dermatology 3rd Edition. 2012. ISBN-13: 9780723435716. Neutrophilic Dermatoses. Elsevier Health Sciences Publisher. 2012; Chapter 26. Bolognia JL, Jorizzo JL, Schaffer JV. Dermatology 3rd Edition. 2012. ISBN-13: 9780723435716. Neutrophilic Dermatoses. Elsevier Health Sciences Publisher. 2012; Chapter 26.
Metadaten
Titel
Managing The Skin Toxicities From New Melanoma Drugs
verfasst von
John C. Mavropoulos, MD, MPH, PhD
Timothy S. Wang, MD
Publikationsdatum
01.06.2014
Verlag
Springer US
Erschienen in
Current Treatment Options in Oncology / Ausgabe 2/2014
Print ISSN: 1527-2729
Elektronische ISSN: 1534-6277
DOI
https://doi.org/10.1007/s11864-014-0284-6

Weitere Artikel der Ausgabe 2/2014

Current Treatment Options in Oncology 2/2014 Zur Ausgabe

Lymphoma (A Engert, Section Editor)

Ibrutinib in B-cell Lymphomas

Skin Cancer (WH Sharfman, Section Editor)

Therapy of Advanced Squamous Cell Carcinoma of the Skin

Skin Cancer (WH Sharfman, Section Editor)

Update on Vaccines for High-Risk Melanoma

Lymphoma (A Engert, Section Editor)

Role of PET in Lymphoma

Mehr Brustkrebs, aber weniger andere gynäkologische Tumoren mit Levonorgestrel-IUS

04.06.2024 Levonorgestrel Nachrichten

Unter Frauen, die ein Levonorgestrel-freisetzendes intrauterines System (IUS) verwenden, ist die Brustkrebsrate um 13% erhöht. Dafür kommt es deutlich seltener zu Endometrium-, Zervix- und Ovarialkarzinomen.

Bei seelischem Stress sind Checkpoint-Hemmer weniger wirksam

03.06.2024 NSCLC Nachrichten

Wie stark Menschen mit fortgeschrittenem NSCLC von einer Therapie mit Immun-Checkpoint-Hemmern profitieren, hängt offenbar auch davon ab, wie sehr die Diagnose ihre psychische Verfassung erschüttert

Antikörper mobilisiert Neutrophile gegen Krebs

03.06.2024 Onkologische Immuntherapie Nachrichten

Ein bispezifischer Antikörper formiert gezielt eine Armee neutrophiler Granulozyten gegen Krebszellen. An den Antikörper gekoppeltes TNF-alpha soll die Zellen zudem tief in solide Tumoren hineinführen.

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.