TY - JOUR
T1 - Severe pyrexia from nivolumab-resistant advanced melanoma after successful combined therapy with encorafenib plus binimetinib
AU - Amagai, Ryo
AU - Fujimura, Taku
AU - Kambayashi, Yumi
AU - Sato, Yota
AU - Tanita, Kayo
AU - Ohuchi, Kentaro
AU - Hashimoto, Akira
AU - Aiba, Setsuya
N1 - Funding Information:
This study was supported in part by the Japan Agency for Medical Research and Development (19cm0106434h0002). Author contributions are as follows T. F. designed the research study; R. A., T. F., Y. S., K. T. and K. O. collected and analyzed the enzyme‐linked immunosorbent assay data; R. A., T. F., Y. K., Y. S. and A. H. treated the patients and collected the clinical data and samples; T. F. wrote the manuscript; and T. F. and S. A. supervised the study.
Publisher Copyright:
© 2020 Japanese Dermatological Association
Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - Various serious adverse events (AE) have been reported to occur at a high rate in patients treated with BRAF plus mitogen-activated protein kinase kinase (MEK) inhibitor combination therapy, but their subtypes differ among the BRAF/MEK inhibitors. Pyrexia or a spike of fever are well-known AE of BRAF inhibitors, with or without MEK inhibitors, and have been reported to have a high incidence after dabrafenib/trametinib, but not after encorafenib/binimetinib. In this report, we describe three cases of severe pyrexia in nivolumab-resistant advanced melanoma after successful combined therapy with encorafenib plus binimetinib. Interestingly, in all cases, the serum levels of soluble CD163 C-X-C motif chemokine (CXCL)9, CXCL10 and CXCL11, which are known biomarkers for adult-onset Still’s disease (AOSD), increased in parallel with the development of pyrexia. Our present cases suggest that pyrexia caused by BRAF/MEK inhibitors may possess a similar pathophysiology as that of AOSD.
AB - Various serious adverse events (AE) have been reported to occur at a high rate in patients treated with BRAF plus mitogen-activated protein kinase kinase (MEK) inhibitor combination therapy, but their subtypes differ among the BRAF/MEK inhibitors. Pyrexia or a spike of fever are well-known AE of BRAF inhibitors, with or without MEK inhibitors, and have been reported to have a high incidence after dabrafenib/trametinib, but not after encorafenib/binimetinib. In this report, we describe three cases of severe pyrexia in nivolumab-resistant advanced melanoma after successful combined therapy with encorafenib plus binimetinib. Interestingly, in all cases, the serum levels of soluble CD163 C-X-C motif chemokine (CXCL)9, CXCL10 and CXCL11, which are known biomarkers for adult-onset Still’s disease (AOSD), increased in parallel with the development of pyrexia. Our present cases suggest that pyrexia caused by BRAF/MEK inhibitors may possess a similar pathophysiology as that of AOSD.
KW - adult-onset Still’s disease
KW - adverse events
KW - encorafenib plus binimetinib combined therapy
KW - nivolumab
KW - pyrexia
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U2 - 10.1111/1346-8138.15346
DO - 10.1111/1346-8138.15346
M3 - Article
C2 - 32293049
AN - SCOPUS:85083447289
SN - 0385-2407
VL - 47
SP - 654
EP - 657
JO - Journal of Dermatology
JF - Journal of Dermatology
IS - 6
ER -