Abstract 2160P
Background
The dawn of immunotherapies and tyrosine kinase inhibitors (TKI) for patients with metastatic non-small cell lung cancer (NSCLC) has brought about improved survival. As a consequence, there is now a rapidly growing population of lung cancer survivors (LCS), even in the metastatic setting. Little is known about patient reported outcomes such as financial toxicity during the survivorship period. We evaluated sociodemographic and clinical factors in LCS with metastatic disease at the time of diagnosis and whether these factors are associated with financial toxicity (FT) in a survivorship period.
Methods
We performed a survey study of 176 patients with stage IV NSCLC at diagnosis from December 2020 to March 2023. Surveys with 80% or more of self-reported demographic data completed and 100% of COST tool, a validated 11-part Likert-scale-based questionnaire measuring FT, were analyzed. Final analysis included 129 surveys. Descriptive statistics were used to categorize sociodemographic and clinical features of participants. The Kruskal-Wallis one-way analysis of variance was used to identify sociodemographic or clinical factors associated with FT.
Results
Females were significantly more likely to have completed survey data (p=0.0057). 56% of participants were female, 50% were above the age of sixty-five years, 74% Caucasian, 54% current/former smokers and 91% had an ECOG 0-1. Sixty percent were more than 2 years since diagnosis, 81% on active systemic therapy at the time of the survey, 48% received immunotherapy, and 60% received targeted therapies. Additionally, 76% had private insurance, 86% employed or retired, 20% had a change in employment after the diagnosis, 60% reported annual household income >$75,000 and 82% reported some college level or higher education. We identified that lower household income (p=0.001), unemployment status (p=0.02), and lower education levels (p=0.005) were significantly associated with worsened FT.
Conclusions
Sociodemographic factors are associated with disparities in financial toxicity in LCS with metastatic disease. Future work to identify high-risk populations and potential interventions, such as financial counseling, may improve disparities in patient reported outcomes.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
M.L. Hsu: Financial Interests, Personal, Advisory Board: Regeneron. J. Feliciano: Financial Interests, Personal, Advisory Board, one time advisory board: Genentech, Takeda; Financial Interests, Personal, Advisory Board, one time advisory groups, and one time advisory board leader: AstraZeneca; Financial Interests, Personal, Other, consultant: Merck; Financial Interests, Personal, Advisory Board, one time consultant: Bristol Myers Squibb; Financial Interests, Personal, Advisory Board, Advisory Board member to address disparities in clinical trials: Eli Lilly; Financial Interests, Personal, Advisory Board, advisory board group: Coherus; Financial Interests, Institutional, Local PI, Local PI support for clinical trial: Bristol Myers Squibb; Financial Interests, Institutional, Funding, Research support for health outcomes research project in delays in diagnosis for NSCLC: AstraZeneca; Financial Interests, Institutional, Funding, Research Support for NSCLC survivorship survey of needs - health outcomes research group: AstraZeneca; Financial Interests, Institutional, Research Grant, Co-primary investigator for research grant awarded to Northwestern University and Johns Hopkins for care delivery project in patients with targetable mutations in lung cancer: Pfizer. All other authors have declared no conflicts of interest.
Resources from the same session
2237P - Avelumab (AVE), cetuximab (CET) and irinotecan (IRI) for treatment refractory microsatellite stable (MSS) metastatic colorectal cancer (mCRC): Translational analyses of the AVETUXIRI phase II trial
Presenter: Nicolas Huyghe
Session: Poster session 07
2238P - Tebentafusp reprograms immunosuppressive tumor-associated M2 macrophages towards anti-tumoral M1 macrophages
Presenter: Josep M. Piulats
Session: Poster session 07
2239P - Gene expression profiling in tumors with and without tertiary lymphoid structures across cancer-types
Presenter: Elia Segui Solis
Session: Poster session 07
2240P - Novel genetic markers associated with immune checkpoint inhibitor induced immune-related adverse events
Presenter: Ik Shin Chin
Session: Poster session 07
2241P - A novel 89Zr-anti-PD-1 immuno-PET-CT may predict response to PD-1 inhibitors and improve response assessment in a lung cancer murine model receiving immunotherapy
Presenter: Ander Puyalto
Session: Poster session 07
2242P - Engineering immune-cell targeting nanoparticles for precise delivery of loaded-cargo and enhanced immunotherapy efficacy
Presenter: Na Kyeong Lee
Session: Poster session 07
2243P - Immune-modulating magnetic nanoparticles to enhance the immune response for the treatment of breast cancer metastasis and recurrence
Presenter: Jaesung Lim
Session: Poster session 07
2244P - Anti CTLA-4 and PD-1 monoclonal antibodies increases systemic SDF-1 and galectin-3 levels through NLRP3 and MyD-88 pathways in preclinical models
Presenter: Vincenzo Quagliariello
Session: Poster session 07
2245P - Graphene oxide: A promising platform for delivery of cancer immunotherapy
Presenter: Sorayut Chattrakarn
Session: Poster session 07
2246P - Tumor-infiltrating lymphocites and gene expression across multiple cancer-types: A translational analysis from the SOLTI-1904-ACROPOLI study
Presenter: Elia Segui Solis
Session: Poster session 07