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Lower risk of severe checkpoint inhibitor toxicity in more advanced disease.

Rik J Verheijden ,
Anne M May ,
Christian U Blank ,
Astrid A M van der Veldt ,
Marye J Boers-Sonderen ,
Maureen J B Aarts ,
Franchette W P J van den Berkmortel ,
Alfonsus J M van den Eertwegh ,
Jan Willem B de Groot ,
Jacobus J M van der Hoeven ,
Geke A P Hospers ,
Djura Piersma ,
Rozemarijn S van Rijn ,
Albert J Ten Tije ,
Gerard Vreugdenhil ,
Michiel C T van Zeijl ,
Michel W J M Wouters ,
John B A G Haanen ,
Ellen Kapiteijn ,
Karijn P M Suijkerbuijk

Abstract

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.

CONCLUSION

In patients with melanoma, more advanced disease is associated with a lower rate of severe irAEs. No association with sex was found.

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 (RRadj) 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 (RRadj 0.65; 95% CI 0.20 to 2.13). None of the other variables were associated with severe irAEs.

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.

More about this publication

ESMO open

Volume 5
Issue nr. 6
Pages e000945
Publication date 01-11-2020

Full text links

Publisher website (DOI) 10.1136/esmoopen-2020-000945
Europe PubMed Central 33199288
Pubmed 33199288

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