Melanoma: BRAFi Rechallenge

Author:

Kosmidis Christoforos S.12,Papadopoulou Konstantina3,Mystakidou Chrysi Maria4ORCID,Papadopoulou Evanthia5,Mantalovas Stylianos2,Varsamis Nikolaos1ORCID,Koulouris Charilaos12,Theodorou Vasiliki4,Papadopoulos Konstantinos2,Sevva Christina2ORCID,Miltiadous Petrina4,Petanidis Savvas6,Georgakoudi Eleni1,Papadopoulou Eleni1,Baka Sofia1

Affiliation:

1. European Interbalkan Medical Center, 10 Asklipiou Street, 55535 Pylaia, Greece

2. 3rd Surgical Department, “AHEPA” University Hospital of Thessaloniki, School of Medicine, Aristotle University of Thessaloniki, 1st St. Kiriakidi Street, 54621 Thessaloniki, Greece

3. 1st Department of Internal Medicine, G. Papanikolaou General Hospital of Thessaloniki, 57010 Thessaloniki, Greece

4. Medical School, Faculty of Health Sciences, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece

5. Shakolas Educational Centre for Clinical Medicine, University of Cyprus, Old Road Nicosia-Lemesos 215/6, 2029 Nicosia, Cyprus

6. Laboratory of Medical Biology and Genetics, Department of Medicine, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece

Abstract

Melanoma is the most aggressive type of skin cancer. Half of melanoma cases are characterized by the mutation BRAF V600. The case presented concerns a 41-year-old patient with locally advanced melanoma, being positive in mutation BRAF V600. The patient underwent surgery and received additional targeted therapy as part of a clinical study. In subsequent disease progression, immunotherapy was used. When the disease progressed again while the patient was in a good performance status, targeted therapy was administered again, and a good response was noted, making the patient reach a statistically significant overall survival, exceeding four years. Targeted therapy has proven to be an important tool in the treatment of melanoma. The use of BRAFi targeted therapy does not exclude the option of readministration at subsequent disease progression (BRAFi rechallenge). Preclinical models suggest that the resistance mechanism of cancer cells to BRAFi therapy bends, as these cell clones lose their evolutionary advantage after stopping BRAFi. Cell clones sensitive to BRAFi may then outcompete, making the treatment effective again. Therapeutical dilemmas in the management of patients with locally advanced melanoma that progresses to metastatic cancer are discussed.

Publisher

MDPI AG

Subject

General Medicine

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