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Ixazomib-induced cutaneous necrotizing vasculitis.
Alloo, A; Khosravi, H; Granter, S R; Jadeja, S M; Richardson, P G; Castillo, J J; LeBoeuf, N R.
Afiliação
  • Alloo A; Department of Dermatology, Northwell Health, Hofstra Northwell School of Medicine, Hempstead, NY, USA.
  • Khosravi H; Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Granter SR; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Jadeja SM; Department of Pathology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
  • Richardson PG; Dana-Farber Cancer Institute, Jerome Lipper Multiple Myeloma Center, Harvard Medical School, Boston, MA, USA.
  • Castillo JJ; The Center for Hematologic Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
  • LeBoeuf NR; Department of Dermatology, The Center for Cutaneous Oncology, Dana-Farber Cancer Institute and Brigham and Women's Hospital, Boston, MA, USA. nleboeuf@partners.org.
Support Care Cancer ; 26(7): 2247-2250, 2018 Jul.
Article em En | MEDLINE | ID: mdl-29392482
ABSTRACT
Ixazomib is a second-generation proteasome inhibitor that has been approved in the combination treatment of multiple myeloma and is currently under clinical investigation for the management of Waldenstrom's macroglobulinemia. While cutaneous adverse events secondary to proteasome inhibitors have been reported, the side effect profile of ixazomib remains to be documented. We report two patients, one with multiple myeloma and one with Waldenstrom's macroglobulinemia, who developed cutaneous necrotizing vasculitis after the initiation of ixazomib. Both patients exhibited no signs of systemic vasculitis and completed their anti-cancer regimens with resolution of their respective eruptions following dose reductions in ixazomib and initiation of low-dose prednisone. A collaborative effort towards the characterization of such cutaneous toxicities facilitates early intervention, maintenance of life-preserving anti-cancer therapy, and allows clinicians opportunity to better understand the pathophysiology of vasculitis. Moreover, appropriate identification and characterization of cutaneous toxicities from novel therapies allows providers to accurately identify safety concerns, treat toxicity, and improve patient quality of life.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vasculite / Compostos de Boro / Inibidores de Proteassoma / Glicina Tipo de estudo: Prognostic_studies Limite: Aged80 / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Vasculite / Compostos de Boro / Inibidores de Proteassoma / Glicina Tipo de estudo: Prognostic_studies Limite: Aged80 / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article