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 inPigment cell and melanoma research Vol. 33; no. 1; pp. 86 - 95
Main Authors Eroglu, Zeynep, Eatrides, Jennifer, Naqvi, Syeda Mahrukh Hussnain, Kim, Youngchul, Rich, Jeani, Babacan, Nalan Akgul, Brohl, Andrew S., Markowitz, Joseph, Sarnaik, Amod, Zager, Jonathan, Khushalani, Nikhil I., Sondak, Vernon K., Messina, Jane
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.01.2020
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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.
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
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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