Immunosuppression for ipilimumab-related toxicity can cause pneumocystis pneumonia but spare antitumor immune control
Ipilimumab is a standard therapy for advanced melanoma. Severe immune related adverse events occur in up to 30% of patients and require treatment with immunosuppressants such as steroids or the anti-TNFα antibody, infliximab. We describe two patients with advanced melanoma treated with ipilimumab. B...
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Published in: | Oncoimmunology Vol. 4; no. 10; p. e1040218 |
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03-10-2015
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Abstract | Ipilimumab is a standard therapy for advanced melanoma. Severe immune related adverse events occur in up to 30% of patients and require treatment with immunosuppressants such as steroids or the anti-TNFα antibody, infliximab. We describe two patients with advanced melanoma treated with ipilimumab. Both suffered from severe immune related side effects and required prolonged immunosuppression with steroids and/or infliximab. Both patients recovered and in spite of the immune suppression, demonstrate clinical evidence of tumor control. This argues that distinct immunological effector functions control nosocomial infection and tumor, respectively. To our knowledge, these are also the first two case reports of pneumocystis pneumonia in this setting. |
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AbstractList | Ipilimumab is a standard therapy for advanced melanoma. Severe immune related adverse events occur in up to 30% of patients and require treatment with immunosuppressants such as steroids or the anti-TNFα antibody, infliximab. We describe two patients with advanced melanoma treated with ipilimumab. Both suffered from severe immune related side effects and required prolonged immunosuppression with steroids and/or infliximab. Both patients recovered and in spite of the immune suppression, demonstrate clinical evidence of tumor control. This argues that distinct immunological effector functions control nosocomial infection and tumor, respectively. To our knowledge, these are also the first two case reports of pneumocystis pneumonia in this setting. |
Author | Foria, Vipul Krishnan, Radhika Smart, James Ottensmeier, Christian Wheater, Matthew Arriola, Edurne |
Author_xml | – sequence: 1 givenname: Edurne surname: Arriola fullname: Arriola, Edurne organization: Cancer Sciences Unit; University of Southampton and University Hospital Southampton NHS Foundation Trust ; Southampton, UK ; University Hospital Southampton NHS Foundation Trust ; Southampton, UK ; Southampton Experimental Cancer Medicine Center; University of Southampton and University Hospital Southampton NHS Foundation Trust ; Southampton, UK – sequence: 2 givenname: Matthew surname: Wheater fullname: Wheater, Matthew organization: University Hospital Southampton NHS Foundation Trust ; Southampton, UK ; Southampton Experimental Cancer Medicine Center; University of Southampton and University Hospital Southampton NHS Foundation Trust ; Southampton, UK – sequence: 3 givenname: Radhika surname: Krishnan fullname: Krishnan, Radhika organization: University Hospital Southampton NHS Foundation Trust ; Southampton, UK – sequence: 4 givenname: James surname: Smart fullname: Smart, James organization: University Hospital Southampton NHS Foundation Trust ; Southampton, UK – sequence: 5 givenname: Vipul surname: Foria fullname: Foria, Vipul organization: University Hospital Southampton NHS Foundation Trust ; Southampton, UK – sequence: 6 givenname: Christian surname: Ottensmeier fullname: Ottensmeier, Christian organization: Cancer Sciences Unit; University of Southampton and University Hospital Southampton NHS Foundation Trust ; Southampton, UK ; University Hospital Southampton NHS Foundation Trust ; Southampton, UK ; Southampton Experimental Cancer Medicine Center; University of Southampton and University Hospital Southampton NHS Foundation Trust ; Southampton, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26451305$$D View this record in MEDLINE/PubMed |
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Title | Immunosuppression for ipilimumab-related toxicity can cause pneumocystis pneumonia but spare antitumor immune control |
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