Abstract 115P
Background
Immune checkpoint inhibitors (ICIs), a standard in the treatment of various cancer types, induce immune-related adverse events (irAEs) that can potentially impact any organ. This can lead to discontinuation of ICI therapy, immunosuppression, hospital admissions, and even long-term sequelae. This study assessed irAE incidence among German ICI therapy patients using a German payers’ database.
Methods
Patients aged ≥ 12 years with hepatic or hepatocellular cancer (HCC), non-small cell lung cancer (NSCLC), renal, urothelial, or skin cancer initiating ICI therapy from 2017-2020 were included. Claims were analyzed for irAE diagnoses (ICD-10 codes; International Statistical Classification of Diseases and Related Health Problems, 10th version) within half a year after treatment initiation and grouped by affected organ. Incident cases were defined as patients with irAE diagnoses and no pre-existing irAE diagnoses / autoimmune disease the year before. Number of patients hospitalized due to an irAE was analyzed.
Results
Of 5,805,407 enrollees, 307,141 had one of the defined cancer types, and 6,350 started ICI therapy. Of these, 4,237 (66.7%) were male, with a mean (SD) age of 66.8 (10.7) years. 75.5% of the cohort had NSCLC, 19.9% skin cancer, 19.7% HCC, 18.6% renal, 10.3% urothelial cancer (including double counts for multiple cancers). Every second patient (n=3,163, 49.8%) was hospitalized with an irAE diagnosis within half a year after treatment initiation. Of the study population, a total of 1,996 patients (31.4% [95% CI: 30.3 – 32.6%] had incident irAEs. The most common irAEs detected by this analysis were respiratory (n=744, 11.7% [11.0 – 12.5%] and gastroenterological ones (n=493, 7.8% [7.1 – 8.5%]). In patients with HCC, 33.9% (95% CI: 31.4% - 36.6%, n=424) experienced irAEs, while in those with skin cancer, the incidence was 30.0% (95% CI: 27.6% - 32.6%, n=380).
Conclusions
This German population-based analysis demonstrates that every second patient treated with ICI needed inpatient treatment due to irAE diagnosis within half a year after ICI start. The incidence of irAEs varied across different types of cancer. irAE should be assigned ICD-10 codes to improve the data quality.
Legal entity responsible for the study
The authors.
Funding
Mallinckrodt Pharmaceuticals.
Disclosure
L. Heinzerling: Other, Institutional, Advisory Role: Mallinckrodt Pharmaceuticals. T. Vogelmann: Financial Interests, Institutional, Advisory Role: Mallinckrodt Pharmaceuticals. I.T. Seemann, A. Ingram: Financial Interests, Personal, Full or part-time Employment: Mallinckrodt Pharmaceuticals. T. Schubert: Financial Interests, Institutional, Advisory Role: Mallinckrodt Pharmaceuticals.
Resources from the same session
53P - Novel ex-vivo manufacturing of transiently expressed armoured CAR T cells for glioblastoma
Presenter: Saket Srivastava
Session: Poster Display session
Resources:
Abstract
54P - Superior antitumor activities of fourth-generation CAR-T cells containing three costimulatory domains targeting GD2-positive tumors
Presenter: Jatuporn Sujjitjoon
Session: Poster Display session
Resources:
Abstract
55P - Engineering of chimeric cytokine receptors (CCR) to induce IL-7 signaling to CAR-T cells for solid tumor treatment
Presenter: Marta Soria Castellano
Session: Poster Display session
Resources:
Abstract
56P - Potent antitumor efficiency of CD19-CAR T cells self-secreting PD-L1 x CD3 BiTE against aggressive B-cell lymphoma
Presenter: Jatuporn Sujjitjoon
Session: Poster Display session
Resources:
Abstract
57P - SENDER™ Directed LNP Delivery of mRNA for In Situ generation of highly potent CAR T Cells
Presenter: Biao Ma
Session: Poster Display session
Resources:
Abstract
58P - Cardiovascular outcomes of novel CAR-T cell therapies: A meta-analysis of incidence, risk factors, and management of cardiotoxicity
Presenter: Hashim Talib Hashim
Session: Poster Display session
Resources:
Abstract
59P - Long term survival data from all recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC) patients treated with MVX-ONCO-1 during open-labelled phase I and phase IIa clinical trials
Presenter: Nicolas Mach
Session: Poster Display session
Resources:
Abstract
60P - Innovative applications of neoantigens in dendritic cell-derived exosome (DEX) therapy and their impact on personalized cancer treatment
Presenter: Ramon Gutierrez
Session: Poster Display session
Resources:
Abstract
61P - Optimized protocol for the accelerated production of dendritic cell-derived exosomes (DEXs): Achieving speed without compromising efficacy
Presenter: Ramon Gutierrez
Session: Poster Display session
Resources:
Abstract
62P - Ecto-CRT induction of NKp46 surface expression increases osimertinib-resistant lung cancer’s sensitivity to NK cells
Presenter: Sumei Chen
Session: Poster Display session
Resources:
Abstract