Abstract 2138P
Background
Older adults with cancer undergoing cytotoxic chemotherapy (CTx) are at increased risk of treatment-associated toxicity. Data supporting the efficacy of systemic anticancer therapy (SACT) in this patient population are sometimes limited. The concept of time toxicity has emerged to describe the time commitments and opportunity cost involved in undertaking SACT, particularly when the magnitude of clinical benefit is expected to be modest.
Methods
We conducted a retrospective review of patients attending the multidisciplinary Geriatric Oncology Assessment and Liaison (GOAL) clinic of University Hospital Waterford, Ireland over a 3.5-year period. We included patients for whom an initial or subsequent line of palliative CTx was commenced in the last 6 months of life. We recorded ambulatory physical healthcare contact days related to the delivery of CTx as well as treatment-related inpatient admissions as a measure of time toxicity.
Results
Of 304 patients assessed, 64 patients commenced SACT with palliative intent. A total of 26 patients met inclusion criteria for the study. The median age of patients was 78 (67-86). At initial GOAL clinic review, 15 patients (58%) had an ECOG performance status of 1, and 10 patients (38%) had a performance status of 2. Most patients received single agent cytotoxic CTx (17/26; 65%) and 85% of patients received only 1 line of treatment. 23 patients (88%) required hospital admission during treatment and 11 patients (42%) required more than one admission. 5 patients (19%) were admitted due to treatment-associated toxicity. The median number of physical healthcare contact days related to CTx (including hospital admissions directly due to treatment toxicity) was 14 (5-37). Median survival from initiation of CTx was 119 days (15-170). 9 patients (35%) received treatment in the last month of life.
Conclusions
High rates of hospitalisation were noted in our study, reflecting the challenges in delivering CTx to an older adult population. Physical healthcare contact days represented a substantial proportion of days alive from commencing systemic treatment. Consideration of the time toxicity of CTx in this population may help to better align palliative-intent treatment with patient goals.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
2184TiP - Extensive cardiovascular characterization and follow-up of patients receiving immune checkpoint inhibitors: A prospective multicenter study
Presenter: Danielle Delombaerde
Session: Poster session 07
2185TiP - Belgian FORX trial: FOod interventions to Reduce immunotherapy toXicity
Presenter: Marthe Verhaert
Session: Poster session 07
2186P - KN046 in patients with thymic carcinoma: A prospective, single-arm, multi-centre, phase II study
Presenter: Wentao Fang
Session: Poster session 07
2187P - Efficacy and safety of gemcitabine as maintenance treatment in unresectable malignant pleural mesothelioma: A phase II randomized study
Presenter: Mohamed Emam Sobeih
Session: Poster session 07
2188P - First-line combination of toripalimab and chemotherapy in advanced thymic carcinoma: A prospective, single-arm, phase II trial
Presenter: hui'yang shi
Session: Poster session 07
2189P - Combining SBRT with GM-CSF and Peg-IFNα to induce abscopal effects in previously treated patients with stage IV thymic tumors
Presenter: Boyan Wang
Session: Poster session 07
2190P - First-line atezolizumab in combination with platinum etoposide in patients with metastatic lung large cell neuroendocrine carcinoma (LCNEC)
Presenter: Georgios Evangelou
Session: Poster session 07
2191P - Real-world outcomes of patients with malignant pleural mesothelioma (MPM) treated with combination nivolumab and ipilimumab in the first- or later line setting
Presenter: Sabine Schmid
Session: Poster session 07
2192P - Quality of life (QoL) of patients (pts) with advanced malignant pleural mesothelioma (aMPM) treated in a real-world setting
Presenter: Abhenil Mittal
Session: Poster session 07
2193P - Real-world evidence of the impact of immunotherapy (IT) on overall survival (OS) of patients (p) with malignant pleural mesothelioma (MPM) adjusted for tumor histology
Presenter: Susana Cedres Perez
Session: Poster session 07