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Please use this identifier to cite or link to this item: https://wslhd.intersearch.com.au/wslhdjspui/handle/1/9506
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dc.contributor.authorMcNamee, Nicholas-
dc.contributor.authorHarvey, Catriona-
dc.contributor.authorGray, Lauren-
dc.contributor.authorKhoo, T.-
dc.contributor.authorLingam, L.-
dc.contributor.authorZhang, B.-
dc.contributor.authorNindra, U.-
dc.contributor.authorYip, P. Y.-
dc.contributor.authorPal, A.-
dc.contributor.authorClay, T.-
dc.contributor.authorArulananda, S.-
dc.contributor.authorItchins, M.-
dc.contributor.authorPavlakis, N.-
dc.contributor.authorKao, S.-
dc.contributor.authorBowyer, S.-
dc.contributor.authorChin, V.-
dc.contributor.authorWarburton, L.-
dc.contributor.authorPires da Silva, Ines-
dc.contributor.authorJohn, T.-
dc.contributor.authorSolomon, B.-
dc.contributor.authorAlexander, M.-
dc.contributor.authorNagrial, Adnan M.-
dc.date.accessioned2024-04-26T04:08:07Z-
dc.date.available2024-04-26T04:08:07Z-
dc.date.issued2024-
dc.identifier.citationJournal of Thoracic Oncology 19(4):636-642, 2024-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9506-
dc.description.abstractBACKGROUND: Australia has one of the highest rates of asbestos-associated diseases. Mesothelioma remains an area of unmet need with a 5-year overall survival of 10%. First-line immunotherapy with ipilimumab and nivolumab is now a standard of care for unresectable pleural mesothelioma following the CheckMate 743 trial, with supportive data from the later line single-arm MAPS2 trial. RIOMeso evaluates survival and toxicity of this regimen in real-world practice. METHODS: Demographic and clinicopathologic data of Australian patients treated with ipilimumab and nivolumab in first- and subsequent-line settings for pleural mesothelioma were collected retrospectively. Survival was reported using the Kaplan-Meier method and compared between subgroups with the log-rank test. Toxicity was investigator assessed using Common Terminology Criteria for Adverse Events version 5.0. RESULTS: A total of 119 patients were identified from 11 centers. The median age was 72 years, 83% were male, 92% had Eastern Cooperative Oncology Group less than or equal to 1, 50% were past or current smokers, and 78% had known asbestos exposure. In addition, 50% were epithelioid, 19% sarcomatoid, 14% biphasic, and 17% unavailable. Ipilimumab and nivolumab were used first line in 75% of patients. Median overall survival (mOS) was 14.5 months (95% confidence interval [CI]: 13.0-not reached [NR]) for the entire cohort. For patients treated first line, mOS was 14.5 months (95% CI: 12.5-NR) and in second- or later-line patients was 15.4 months (95% CI: 11.2-NR). There was no statistically significant difference in mOS for epithelioid patients compared with nonepithelioid (19.1 mo [95% CI: 15.4-NR] versus 13.0 mo [95% CI: 9.7-NR], respectively, p = 0.064). Furthermore, 24% of the patients had a Common Terminology Criteria for Adverse Events grade greater than or equal to 3 adverse events, including three treatment-related deaths. Colitis was the most frequent adverse event. CONCLUSIONS: Combination immunotherapy in real-world practice has poorer survival outcomes and seems more toxic compared with clinical trial data. This is the first detailed report of real-world survival and toxicity outcomes using ipilimumab and nivolumab treatment of pleural mesothelioma.-
dc.subjectOncology-
dc.titleBrief Report: Real-world toxicity and survival of combination immunotherapy in pleural mesothelioma-RIOMeso-
dc.typeJournal Article-
dc.identifier.doihttps://dx.doi.org/10.1016/j.jtho.2023.11.014-
dc.subject.keywordsimmunotherapy-
dc.subject.keywordslung neoplasms-
dc.subject.keywordsmesothelioma-
dc.subject.keywordspleura neoplasms-
dc.subject.keywordsasbestos-
dc.subject.keywordsipilimumab-
dc.subject.keywordsnivolumab-
dc.identifier.journaltitleJournal of Thoracic Oncology-
dc.identifier.departmentOncology-
dc.contributor.wslhdMcNamee, Nicholas-
dc.contributor.wslhdHarvey, Catriona-
dc.contributor.wslhdGray, Lauren-
dc.contributor.wslhdPires da Silva, Ines-
dc.contributor.wslhdNagrial, Adnan M.-
dc.type.studyortrialClinical Trial-
dc.type.studyortrialControlled Study-
dc.type.studyortrialMajor Clinical Study-
dc.type.studyortrialRetrospective Study-
dc.identifier.pmid38036250-
dc.identifier.affiliationThe Kinghorn Cancer Centre, St. Vincent's Hospital, Sydney, Australia-
dc.identifier.affiliationCrown Princess Mary Cancer Centre, Westmead Hospital, Sydney, Australia-
dc.identifier.affiliationGarvan Institute of Medical Research, Sydney, Australia-
dc.identifier.affiliationSir Charles Gairdner Hospital, Perth, Australia-
dc.identifier.affiliationFiona Stanley Hospital, Perth, Australia-
dc.identifier.affiliationChris O'Brien Lifehouse, Sydney, Australia-
dc.identifier.affiliationLiverpool Hospital, Sydney, Australia-
dc.identifier.affiliationCampbelltown Hospital, Sydney, Australia-
dc.identifier.affiliationSt. John of God Subiaco Hospital, Perth, Australia-
dc.identifier.affiliationEdith Cowan University, Perth, Australia-
dc.identifier.affiliationMonash Health, Melbourne, Australia-
dc.identifier.affiliationMonash University, Melbourne, Australia-
dc.identifier.affiliationRoyal North Shore Hospital, Sydney, Australia-
dc.identifier.affiliationUniversity of Sydney, Sydney, Australia-
dc.identifier.affiliationUniversity of Western Australia, Perth, Australia-
dc.identifier.affiliationUniversity of New South Wales, Sydney, Australia-
dc.identifier.affiliationBlacktown Hospital, Sydney, Australia-
dc.identifier.affiliationPeter MacCallum Cancer Centre, Melbourne, Australia-
dc.identifier.affiliationUniversity of Melbourne, Melbourne, Australia-
dc.identifier.facilityBlacktown-
dc.identifier.facilityWestmead-
Appears in Collections:Blacktown Mount Druitt Hospital

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