Immune checkpoint inhibitor-related colitis assessment and prognosis: can IBD scoring point the way?
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Published:2020-05-18
Issue:2
Volume:123
Page:207-215
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ISSN:0007-0920
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Container-title:British Journal of Cancer
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language:en
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Short-container-title:Br J Cancer
Author:
Cheung Vincent Ting FungORCID, Gupta Tarun, Olsson-Brown Anna, Subramanian Sreedhar, Sasson Sarah Christina, Heseltine Jonathan, Fryer Eve, Collantes Elena, Sacco Joseph J., Pirmohamed Munir, Simmons Alison, Klenerman Paul, Tuthill Mark, Protheroe Andrew S., Chitnis Meenali, Fairfax Benjamin Peter, Payne Miranda Jane, Middleton Mark Ross, Brain Oliver
Abstract
Abstract
Background
Immune checkpoint inhibitors (ICI) improve survival but cause immune-related adverse events (irAE). We sought to determine if CTCAE classification, IBD biomarkers/endoscopic/histological scores correlate with irAE colitis outcomes.
Methods
A dual-centre retrospective study was performed on patients receiving ICI for melanoma, NSCLC or urothelial cancer from 2012 to 2018. Demographics, clinical data, endoscopies (reanalysed using Mayo/Ulcerative Colitis Endoscopic Index of Severity (UCEIS) scores), histology (scored with Nancy Index) and treatment outcomes were analysed.
Results
In all, 1074 patients were analysed. Twelve percent (134) developed irAE colitis. Median patient age was 66, 59% were male. CTCAE diarrhoea grade does not correlate with steroid/ infliximab use. G3/4 colitis patients are more likely to need infliximab (p < 0.0001) but colitis grade does not correlate with steroid duration. CRP, albumin and haemoglobin do not correlate with severity. The UCEIS (p = 0.008) and Mayo (p = 0.016) scores correlate with severity/infliximab requirement. Patients with higher Nancy indices (3/4) are more likely to require infliximab (p = 0.03).
Conclusions
CTCAE assessment does not accurately reflect colitis severity and our data do not support its use in isolation, as this may negatively impact timely management. Our data support utilising endoscopic scoring for patients with >grade 1 CTCAE disease, and demonstrate the potential prognostic utility of objective histologic scoring.
Funder
Norman Collisson Foundation Lee Placito Fellowship RCUK | Medical Research Council Celgene Wellcome Trust
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Oncology
Reference30 articles.
1. Wolchok, J., Kluger, H., Callahan, M., Postow, M., Rizvi, N., Lesokhin, A. et al. Nivolumab plus ipilimumab in advanced melanoma. N. Engl. J. Med. 369, 122–133 (2013). 2. Hodi, F., O’Day, S., McDermott, D., Weber, R., Sosman, J., Haanen, J. et al. Improved survival with ipilimumab in patients with metastatic melanoma. N. Engl. J. Med. 363, 711–723 (2010). 3. Garon, E., Rizvi, N., Hui, R., Leighl, N., Balmanoukian, A., Eder, J. et al. Pembrolizumab for the treatment of non-small-cell lung cancer. N. Engl. J. Med. 372, 2018–2028 (2015). 4. Motzer, R., Escudier, B., McDermott, D., George, S., Hammers, H., Srinivas, S. et al. Nivolumab versus everolimus in advanced renal-cell carcinoma. N. Engl. J. Med. 373, 1803–1813 (2015). 5. Herbst, R., Soria, J.-C., Kowanetz, M., Fine, G., Hamid, O., Gordon, M. et al. Predictive correlates of response to the anti-PD-L1 antibody MPDL3280A in cancer patients. Nature 515, 563–567 (2014).
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