2018
DOI: 10.1007/s10067-018-4373-y
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Severe necrotizing myositis associated with long term anti-neoplastic efficacy following nivolumab plus ipilimumab combination therapy

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Cited by 17 publications
(8 citation statements)
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“…Ir-Myositis offers some unique insights into traditional autoimmune myositides (AIM). First, if ICI are considered as a class, this "single" exposure can recapitulate a broad spectrum of AIM, including dermatomyositis 29,30,31 , necrotizing myositis 27,32 , and granulomatous myositis 33 . This supports the observation that the same exposure could be responsible for more than 1 traditional AIM.…”
Section: Immune-related Adverse Events Associated With Icimentioning
confidence: 99%
“…Ir-Myositis offers some unique insights into traditional autoimmune myositides (AIM). First, if ICI are considered as a class, this "single" exposure can recapitulate a broad spectrum of AIM, including dermatomyositis 29,30,31 , necrotizing myositis 27,32 , and granulomatous myositis 33 . This supports the observation that the same exposure could be responsible for more than 1 traditional AIM.…”
Section: Immune-related Adverse Events Associated With Icimentioning
confidence: 99%
“…All other reported deaths were caused by disease progression or other causes. Despite the overall excellent tolerability, anecdotally one case of pneumonitis was reported related to pembrolizumab and we found one case report in the literature of a severe necrotizing myositis associated with long term efficacy following nivolumab and ipilimumab combination therapy [24]. Regarding atezolizumab, patients had more grade 3-4 adverse effects when combined with cobimetinib compared to atezolizumab monotherapy, but a similar rate when compared with standard of care regorafenib (61, 31 and 58%, respectively) [22].…”
Section: Safety and Securitymentioning
confidence: 75%
“…12,39 A case report showed a 61-year old woman who received nivolumab + ipilimumab developing rapidly extending proximal muscles weakness with significant muscular oedema, enhancing the possibility of synergy in adverse events when combining ICIs. 44 Most adverse events are noted within 3 − 12 weeks of treatment, 34,45 resolving within 12 weeks of onset. 34 Some of the most common adverse events (skin rash, pruritus) can respond to antihistamines, and topical steroids, 45 which do not appear to interfere with the therapeutic effect of immunotherapy.…”
Section: Possible Adverse Effects Of Treatment With Immunotherapymentioning
confidence: 99%