Neoadjuvant BRAF‐targeted therapy in regionally advanced and oligometastatic melanoma
Current management of locoregional and oligometastatic melanoma is typically with surgery; however, some patients are unable to undergo resection due to location/size of their tumors and/or the anticipated morbidity of the surgery. While there are currently no established guidelines for neoadjuvant...
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Published in | Pigment cell and melanoma research Vol. 33; no. 1; pp. 86 - 95 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.01.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Current management of locoregional and oligometastatic melanoma is typically with surgery; however, some patients are unable to undergo resection due to location/size of their tumors and/or the anticipated morbidity of the surgery. While there are currently no established guidelines for neoadjuvant therapy in melanoma, neoadjuvant BRAF‐targeted therapy may make resection more feasible. A retrospective analysis was conducted of 23 patients with BRAFV600‐mutant, stage III/IV melanoma treated with BRAF‐targeted therapy prior to surgery, with no adjuvant treatment. Surgical specimens, preoperative imaging, and clinical outcomes were evaluated. Results: Ten of 23 patients (44%) attained a pathologic complete response (pCR), with no correlation between RECIST response based on preoperative imaging and pathologic response. After a median of 43‐month follow‐up, only 1 patient (10%) with a pCR recurred, while 8 of 13 (62%) patients without a pCR recurred. Patients with a pCR had significantly improved relapse‐free (RFS) and overall survival (OS) compared to patients with residual tumor. Neoadjuvant BRAF‐targeted therapy is associated with a high pCR rate in patients with stage III‐IV melanoma, which may correlate with improved RFS and OS. |
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Bibliography: | Funding information This work has been supported in part by NCI Skin SPORE P50CA168536‐01A1 and the Tissue Core Facility (P30‐CA076292) at the H. Lee Moffitt Cancer Center & Research Institute ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Study concept and design: Zeynep Eroglu, Jane Messina, Vernon Sondak, Nikhil Khushalani Drafting of the manuscript: Zeynep Eroglu, Jennifer Eatrides Critical revision of the manuscript for important intellectual content: All authors. Statistical analysis: Syeda Mahrukh Hussnain Naqvi, Youngchul Kim Acquisition, analysis, or interpretation of data: Zeynep Eroglu, Jennifer Eatrides, Jeani Rich, Nalan Akgul Babacan, Vernon Sondak, Jane Messina These authors contributed equally |
ISSN: | 1755-1471 1755-148X |
DOI: | 10.1111/pcmr.12813 |