Abstract 91P
Background
Immune Checkpoint inhibitors (ICI) administration at home is considered as a development priority by the French society of cancer immunotherapy and French government with “ma santé 2022” program. The study objective was to analyze the territorial development of ICI infusions at home between 2021 and 2022.
Methods
The national hospital databases from the French statutory health insurance were used to identify all patients treated by ICI and to build a cohort of patients with at least one administration in Hospitalization At Home (HAH). All ICI administrations were collected retrospectively up to 2016. A descriptive analysis was performed to characterize patients, centers and "HAH patients" care pathways (based on treatment sequences clustering algorithms) and administration costs in the French statutory health insurance perspective.
Results
Over 2021 and 2022, 652 ICI (0.6%) patients were treated in HAH. Primary diagnosis among HAH patients were lung cancer with 51% (26%-78% depending on regions), followed by metastatic melanoma with 17%, (1%-18%). The three main regions were Ile de France (IDF), Auvergne Rhône Alpes (AURA) and Nouvelle Aquitaine (NA), with 543 patients (83% of HAH patients). The proportion of HAH patients per region varied from 0.1% to 1.6%. Mean age were similar between regions in main indications, from 65 to 69 years old in lung cancer regions and 68 in metastatic melanoma regions. Men proportion varied in lung cancer (6.6% - 31.8%) and were similar in metastatic melanoma (38.1% - 40.5%). Care pathways’ characteristics and costs per HAH infusion in main indications heavily differed per region (Table). Table: 91P
HAH patients’ and care pathways’ characteristics, and cost of HAH infusion, in the 3 main regions per indication
Regions | N | Mean Duration (±STD) 1st DCU - 1st HAH (days) | Mean Karnofsky Score (±STD) | Cost per infusion (€) | |
Lung | IDF | 80 | 346 (±378) | 57 (±7) | 314 (±213) |
AURA | 101 | 255 (±205) | 74 (±12) | 401 (±1480) | |
NA | 105 | 270 (±337) | 63 (±13) | 325 (±685) | |
France | 330 | 304 (±342) | 64 (±13) | 346 (±901) | |
Metastatic melanoma | IDF | 27 | 351 (±379) | 58 (±4) | 268 (±18) |
AURA | 27 | 513 (±523) | 73 (±8) | 311 (±113) | |
Occitanic | 6* | - | - | - | |
France | 69 | 381 (±433) | 64 (±10) | 290 (±86) |
STD: Standard Deviation * <11 patients : sample results not presented
Conclusions
Patient pathways depended on indication and differed according to regions. Further analyses on healthcare resources will allow to understand how optimizing HAH use for ICI patients in France.
Legal entity responsible for the study
Bristol Myers Squibb.
Funding
Bristol Myers Squibb.
Disclosure
A.C. Toffart, G. Casanova: Financial Interests, Personal, Advisory Board: BMS. M. Pierre, H. Lemasson, V. Moreau-Mallet, M. Chartier: Financial Interests, Personal, Affiliate: BMS. N. Pagès, R. Jolivel, A. Panès: Financial Interests, Personal, Financially compensated role: BMS. M. Pérol: Financial Interests, Personal, Advisory Board, Advisory Board: Roche, AstraZeneca, MSD, BMS, Lilly, Novartis, Takeda, Gritstone, Sanofi, Pfizer, Amgen, Janssen, GSK, Eisai, Ipsen, Novocure, AbbVie, Anheart Therapeutics, Daiichi Sankyo; Financial Interests, Personal, Invited Speaker, Symposium: Roche, AstraZeneca, MSD, BMS, Boehringer Ingelheim, Takeda, Illumina, Pfizer, Medscape; Financial Interests, Personal, Advisory Board, Expert Testimony: AstraZeneca; Financial Interests, Personal, Steering Committee Member, Steering Committee Member: Lilly; Financial Interests, Institutional, Local PI, Local PI: AbbVie, Amgen, Anheart Therapeutics, Apollomics, Arrivent Biopharma, AstraZeneca, Bayer, Boehringer Ingelheim, Daiichi Sankyo, Innate Pharma, Roche; Financial Interests, Institutional, Research Grant, Research Grant: AstraZeneca, Boehringer Ingelheim, Roche, Takeda; Financial Interests, Personal, Trial Chair, Trial Chair: Anheart Therapeutics; Financial Interests, Personal, Steering Committee Member, Idmc Chair: PharmaMar, Sophiagenetics; Financial Interests, Personal, Steering Committee Member, Steering Committee Member: Roche; Financial Interests, Personal, Other, DMSB: Roche.
Resources from the same session
168TiP - A phase I dose escalation/expansion study of GSK5764227 (GSK’227), a B7-homolog 3 (B7-H3) protein targeted antibody-drug conjugate (ADC), in patients with advanced solid tumours
Presenter: Giuseppe Curigliano
Session: Poster Display session
Resources:
Abstract
169TiP - Colorectal carcinoma: Low dose immunotherapy in upfront metastatic d/MMR patients (CLOUD study)
Presenter: Anant Ramaswamy
Session: Poster Display session
Resources:
Abstract
177P - Ubiquitous neoantigens as targets for T cell recognition in a patient with metastatic pancreatic neuroendocrine tumour
Presenter: Jean-Benoit Tanis
Session: Poster Display session
Resources:
Abstract
178P - Comprehensive immunophenotype analysis in anti-PD-1 antibody sensitive and resistant syngeneic mouse model unravels perforin-expressing CD4+T cells dominant cytolytic activity
Presenter: Hiroyuki Inoue
Session: Poster Display session
Resources:
Abstract
179P - Impact of exercise training on tumour-infiltrating T cells in human prostate cancer
Presenter: Louise Lehrskov
Session: Poster Display session
Resources:
Abstract
180P - Chronic circadian disruption promotes melanoma progression by interfering with NK cells
Presenter: Shuwen Xiao
Session: Poster Display session
Resources:
Abstract
181P - Intratumoral heterogeneity of immune infiltrate in leiomyosarcomas
Presenter: Iva Benesova
Session: Poster Display session
Resources:
Abstract
182P - Innovative nano-immunotherapy for modulating tumor-immune interactions and microbiome in pancreatic cancer
Presenter: Liane Moura
Session: Poster Display session
Resources:
Abstract
183P - CAIX negatively modulates inflammatory and anti-tumor immune responses
Presenter: Eliska Svastova
Session: Poster Display session
Resources:
Abstract
184P - Alterations in tumorigenicity and immunogenicity of bladder cancer cells after somatic cell reprogramming
Presenter: Banu Iskender Izgi
Session: Poster Display session
Resources:
Abstract