Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Sep 10:6:349-56.
doi: 10.2147/CMAR.S49494. eCollection 2014.

Treating advanced melanoma: current insights and opportunities

Affiliations
Review

Treating advanced melanoma: current insights and opportunities

Michael Tronnier et al. Cancer Manag Res. .

Abstract

Whereas thin melanomas have an excellent prognosis after sufficient surgical treatment, melanoma disease in advanced stages is still a therapeutic challenge. After decades of frustrating studies, new therapeutic strategies have come up in the past few years. On the one hand, increasing insights into the molecular aberrations in melanoma have led to specific "targeted" therapies to affect only the mutated tumor cells, as in many other types of cancers. Today there are few "targeted" substances which are already approved and successfully used for single or combination therapy, but many others are under development. While on the other hand, nonpersonalized strategy substances have been developed successfully inducing an immunologic tumor response. Both kinds of therapy have been found to result in an improvement not only of the response rate, but also of the overall survival in metastatic disease, which represents a milestone in melanoma therapy. However, using these therapies there is still much to learn regarding the effects, the side effects, and the limitations of these promising substances.

Keywords: BRAF; CTLA-4; immunotherapy; melanoma; targeted therapy; treatment.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Melanoma of superficial spreading type. Notes: Atypical melanocytes are spread within the epidermis and located in the dermis; hematoxylin and eosin stain, ×100.
Figure 2
Figure 2
Immunohistochemistry using antibodies against melanocytic antigen (melan-A). Notes: The atypical melanocytes are stained with antibodies against melan-A; ×100.
Figure 3
Figure 3
Immunohistochemistry using antibodies against mutated BRAF. Notes: The tumor cells are BRAF-mutated as indicated by the immunohistochemical positivity for anti-BRAF V600 antibody; ×100.

Similar articles

Cited by

References

    1. Erickson C, Driscoll MS. Melanoma epidemic: facts and controversies. Clin Dermatol. 2010;28(3):281–286. - PubMed
    1. Tronnier M, Semkova K, Wollina U, Tchernev G. Malignant melanoma: epidemiologic aspects, diagnostic and therapeutic approach. Wien Med Wochenschr. 2013;163(15–16):354–358. - PubMed
    1. Linos E, Swetter SM, Cockburn MG, Colditz GA, Clarke CA. Increasing burden of melanoma in the United States. J Invest Dermatol. 2009;129(7):1666–1674. - PMC - PubMed
    1. Garbe C, Leiter U. Melanoma epidemiology and trends. Clin Dermatol. 2009;27(1):3–9. - PubMed
    1. Volkovova K, Bilanicova D, Bartonova A, Letašiová S, Dusinska M. Associations between environmental factors and incidence of cutaneous melanoma. Environ Health. 2012;11(Suppl 1):S12. - PMC - PubMed