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Lower risk of severe checkpoint inhibitor toxicity in more advanced disease
- Source :
- ESMO OPEN, 5(6):000945. BMJ Publishing Group, Esmo Open, 5, 6, Esmo Open, 5, ESMO Open, 5(6):e000945. BMJ Publishing Group, ESMO Open, Vol 5, Iss 6 (2020), ESMO Open, 5(6):000945. BMJ Publishing Group, ESMO Open, 5(6):000945. BMJ PUBLISHING GROUP, Verheijden, R J, May, A M, Blank, C U, van der Veldt, A A M, Boers-Sonderen, M J, Aarts, M J B, van den Berkmortel, F W P J, van den Eertwegh, A J M, de Groot, J W B, van der Hoeven, J J M, Hospers, G A P, Piersma, D, van Rijn, R S, ten Tije, A J, Vreugdenhil, G, van Zeijl, M C T, Wouters, M W J M, Haanen, J B A G, Kapiteijn, E & Suijkerbuijk, K P M 2020, ' Lower risk of severe checkpoint inhibitor toxicity in more advanced disease ', ESMO OPEN, vol. 5, no. 6, 000945 . https://doi.org/10.1136/esmoopen-2020-000945, ESMO Open, 5(6). BMJ PUBLISHING GROUP, ESMO Open
- Publication Year :
- 2020
-
Abstract
- Contains fulltext : 229623.pdf (Publisher’s version ) (Open Access) BACKGROUND: Immune checkpoint inhibitor (ICI) can cause severe and sometimes fatal immune-related adverse events (irAEs). Since these irAEs mimick immunological disease, a female predominance has been speculated on. Nevertheless, no demographic or tumour-related factors associated with an increased risk of irAEs have been identified until now. METHODS: Risk ratios of severe (grade ≥3) irAEs for age, sex, WHO performance status, number of comorbidities, stage of disease, number of metastases and serum lactate dehydrogenases (LDH) were estimated using data from anti-PD1-treated patients with advanced melanoma in the prospective nationwide Dutch Melanoma Treatment Registry. RESULTS: 111 (11%) out of 819 anti-programmed cell death 1 treated patients experienced severe irAEs. Patients with non-lung visceral metastases (stage IV M1c or higher) less often experienced severe irAEs (11%) compared with patients with only lung and/or lymph node/soft tissue involvement (stage IV M1b or lower; 19%; adjusted risk ratio (RR(adj)) 0.63; 95% CI 0.41 to 0.94). Patients with LDH of more than two times upper limit of normal had a non-significantly lower risk of developing severe irAEs than those with normal LDH (RR(adj) 0.65; 95% CI 0.20 to 2.13). None of the other variables were associated with severe irAEs. CONCLUSION: In patients with melanoma, more advanced disease is associated with a lower rate of severe irAEs. No association with sex was found.
- Subjects :
- Cancer Research
medicine.medical_specialty
Programmed Cell Death 1 Receptor
MONOTHERAPY
Disease
Lower risk
lcsh:RC254-282
Gastroenterology
Healthcare improvement science Radboud Institute for Health Sciences [Radboudumc 18]
Antineoplastic Agents, Immunological
Internal medicine
checkpoint inhibition
medicine
melanoma
Humans
immune-related adverse event (irAE)
Prospective Studies
Stage (cooking)
IMMUNOTHERAPY
anti-PD1
Adverse effect
Lymph node
Original Research
Retrospective Studies
DMTR
Performance status
IMMUNE CHECKPOINTS
business.industry
Melanoma
IPILIMUMAB
NIVOLUMAB
ASSOCIATION
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
medicine.disease
CANCER
medicine.anatomical_structure
Oncology
Relative risk
SURVIVAL
Female
ADVERSE EVENTS
business
Rare cancers Radboud Institute for Health Sciences [Radboudumc 9]
Subjects
Details
- Language :
- English
- ISSN :
- 20597029
- Database :
- OpenAIRE
- Journal :
- ESMO OPEN, 5(6):000945. BMJ Publishing Group, Esmo Open, 5, 6, Esmo Open, 5, ESMO Open, 5(6):e000945. BMJ Publishing Group, ESMO Open, Vol 5, Iss 6 (2020), ESMO Open, 5(6):000945. BMJ Publishing Group, ESMO Open, 5(6):000945. BMJ PUBLISHING GROUP, Verheijden, R J, May, A M, Blank, C U, van der Veldt, A A M, Boers-Sonderen, M J, Aarts, M J B, van den Berkmortel, F W P J, van den Eertwegh, A J M, de Groot, J W B, van der Hoeven, J J M, Hospers, G A P, Piersma, D, van Rijn, R S, ten Tije, A J, Vreugdenhil, G, van Zeijl, M C T, Wouters, M W J M, Haanen, J B A G, Kapiteijn, E & Suijkerbuijk, K P M 2020, ' Lower risk of severe checkpoint inhibitor toxicity in more advanced disease ', ESMO OPEN, vol. 5, no. 6, 000945 . https://doi.org/10.1136/esmoopen-2020-000945, ESMO Open, 5(6). BMJ PUBLISHING GROUP, ESMO Open
- Accession number :
- edsair.doi.dedup.....a6b2810a24d327b462bf0cdb07832e35