88P Utilisation of the ESMO-MCBS in prioritising immune-checkpoint inhibitors for a WHO model list of essential medicines application

Results: Of the patients with irAEs, 26% (31/116) needed inpatient treatment.Hospitalization was associated with severe (grade III to IV) toxicities (p<0.001).The mOS of patients hospitalized due to an irAE was 12.9 months, while that of outpatients with irAEs was 26.9 months (p0.006).The mOS was especially poor if hospital stay exceeded 6 days (7.0 months vs. 19.1 months, p0.015).Systemic glucocorticoid therapy was administered to 90.3% of hospitalized and 35.3% of non-hospitalized patients (p<0.05).At disease progression after an irAE, palliative care instead of active oncological therapies was more often provided for hospitalized patients (35.4% vs. 17.6%, p0.041).At the initiation of salvage systemic therapy after an irAE, hospitalized patients tended to be in poorer physical condition than outpatients (WHO performance status >2 in 35.7% vs. 14.6% of patients, p0.089).Conclusions: Hospital admission due to an irAE appeared to significantly deteriorate the survival of ICI treated metastatic cancer patients.This may be attributed to decreased physical fitness due to long admissions and high-dose, long-term glucocorticoid treatments of severe irAEs.Early rehabilitation and effective tapering of corticosteroid, if possible, should be provided for patients hospitalized due to an irAE.

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Publication Details

Journal
Immuno-Oncology Technology
Published
2024-12-01
DOI
https://doi.org/10.1016/j.iotech.2024.100831
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
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article

88P Utilisation of the ESMO-MCBS in prioritising immune-checkpoint inhibitors for a WHO model list of essential medicines application

Lorenzo Moja, Marius Goldkuhle, M. Csenar, Nicole Skoetz et al.
Immuno-Oncology Technology
Cancer Immunotherapy and Biomarkers
article

88P Utilisation of the ESMO-MCBS in prioritising immune-checkpoint inhibitors for a WHO model list of essential medicines application

Lorenzo Moja, Marius Goldkuhle, M. Csenar, Nicole Skoetz, Julia Schroer
article en

Abstract

Results: Of the patients with irAEs, 26% (31/116) needed inpatient treatment.Hospitalization was associated with severe (grade III to IV) toxicities (p<0.001).The mOS of patients hospitalized due to an irAE was 12.9 months, while that of outpatients with irAEs was 26.9 months (p0.006).The mOS was especially poor if hospital stay exceeded 6 days (7.0 months vs. 19.1 months, p0.015).Systemic glucocorticoid therapy was administered to 90.3% of hospitalized and 35.3% of non-hospitalized patients (p<0.05).At disease progression after an irAE, palliative care instead of active oncological therapies was more often provided for hospitalized patients (35.4% vs. 17.6%, p0.041).At the initiation of salvage systemic therapy after an irAE, hospitalized patients tended to be in poorer physical condition than outpatients (WHO performance status >2 in 35.7% vs. 14.6% of patients, p0.089).Conclusions: Hospital admission due to an irAE appeared to significantly deteriorate the survival of ICI treated metastatic cancer patients.This may be attributed to decreased physical fitness due to long admissions and high-dose, long-term glucocorticoid treatments of severe irAEs.Early rehabilitation and effective tapering of corticosteroid, if possible, should be provided for patients hospitalized due to an irAE.

Immuno-Oncology TechnologyVol. 24
University of Cologne (DE), World Health Organization (CH), University Hospital Cologne (DE)
Zero hunger
Openalex Percentile: Top 60%
Cancer Immunotherapy and Biomarkers
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88P Utilisation of the ESMO-MCBS in prioritising immune-checkpoint inhibitors for a WHO model list of essential medicines application — Lorenzo Moja, Marius Goldkuhle, et al. · Immuno-Oncology Technology (2024) | TGRS Research Map | TGRS