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Small vessel vasculitis and dry gangrene secondary to combined CTLA-4 and PD-1 blockade in malignant mesothelioma.
Kefas, Joanna; Harwood, Catherine; Lewis, Myles J; Szlosarek, Peter.
Afiliação
  • Kefas J; Department of Medicine, St Bartholomew's Hospital, London, UK. Joannakefas@nhs.net.
  • Harwood C; Department of Dermatology, Royal London Hospital, London, UK.
  • Lewis MJ; Department of Rheumatology, Barts and the London, London, UK.
  • Szlosarek P; Barts Cancer Institute, Queen Mary University of London, London, UK.
BMC Rheumatol ; 6(1): 10, 2022 Feb 08.
Article em En | MEDLINE | ID: mdl-35130961
BACKGROUND: Malignant pleural mesothelioma (MPM) is a rare and aggressive tumour with an overall poor prognosis. In October 2020, first line treatment with the PD-1 antagonist nivolumab and the CTLA-4 antagonist ipilimumab for unresectable disease was FDA approved-the first approved treatment regime since 2004. Interim analyses from the phase 3 CHECKMATE-743 study shows improvements in overall survival. Skin-related toxicities are the most commonly reported any-grade treatment-related adverse event from combined nivolumab and ipilimumab therapy. CASE PRESENTATION: Here we report a case of a 35-year-old white male who developed digital ischaemia secondary to small vessel vasculitis after receiving PD-1 and CTLA-4 blockade therapy for MPM. His progressive ischaemia became gangrenous, and he required multi-speciality input and treatment with prednisolone, prostacyclin, mycophenolate mofetil and hydroxychloroquine. CONCLUSIONS: Our case highlights the importance of early detection, intervention, and a multispecialty approach to managing such complications in order to minimise the associated morbidity and mortality.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: BMC Rheumatol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: BMC Rheumatol Ano de publicação: 2022 Tipo de documento: Article