Abstract 1860P
Background
Limited knowledge currently exists on NCF in advanced cancer survivors treated with ICB. Here, we present the baseline data of an ongoing prospective trial regarding objective and subjective NCF.
Methods
Patients (pts) followed-up at a single center, diagnosed with stage III/IV cancer of any type, who initiated ICB at least one year prior to and were in complete remission (CR) at time of inclusion, were invited to participate. Objective NCF was assessed using the test battery COGBAT®. Neurocognitive impairment (NCI) was defined by the International Cancer and Cognition Taskforce guidelines and deficits per subtest as 1.5 standard deviation below the normative mean. Subjective NCF, anxiety, depression and fatigue were assessed respectively through the Cognitive Failures Questionnaire, Hospital Anxiety and Depression Scale, and Fatigue Severity Scale.
Results
From July 2022 to April 2023, 58 pts were enrolled (48 melanoma, 6 non-small cell lung carcinoma, 2 colon cancer, 1 renal cell carcinoma, 1 bladder cancer), median age was 64 y [34-92]); 34 male; 55 pts (95%) had stage IV disease; 12 pts (21%) had a history of brain metastasis. Median time since CR was 3.0 y [0.1-14.1]; median time since last ICB administration was 3.6 y [0.0-11.4]. We found objective NCI in 34 pts (59%), with deficits predominantly in memory (33%) and attention (31%) and in a lesser amount in executive functioning (16%). Moderate to severe subjective cognitive complaints were found in 12 pts (21%). Objective NCF only correlated significantly with age (r = -.782, p < .001) but not with subjective NCF, fatigue, anxiety, depression or a history of brain metastasis. Subjective NCF correlated significantly with anxiety, depression and fatigue (respectively r = .694, r = .454, r = .447, all p-values < .001).
Conclusions
A majority of the advanced cancer survivors treated with ICB had objective NCI. A noteworthy lesser proportion had subjective cognitive complaints, indicating the need of neuropsychological assessment. Moderate to strong associations exist between subjective NCF and psychological distress, indicating the value of an integrative approach, including NCF remediation and psychosocial support when treating cognitive complaints.
Clinical trial identification
NCT05667857.
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Fonds Wetenschappelijk Onderzoek Vlaanderen.
Disclosure
S. Aspeslagh: Financial Interests, Institutional, Advisory Board: MSD, Sanofi, Roche, BMS, Pfizer, Ipsen, Galapagos. L. Decoster: Financial Interests, Institutional, Advisory Board: AstraZeneca, BMS, MSD; Financial Interests, Institutional, Invited Speaker: BMS, MSD, Roche, Servier, Sanofi; Financial Interests, Institutional, Research Grant, conduct of academic trial: Boehringer Ingelheim; Non-Financial Interests, Leadership Role, member of board: European Cancer Organisation; Non-Financial Interests, Leadership Role, Board member: International Society of Geriatric Oncology (SIOG). A. Rogiers: Financial Interests, Institutional, Advisory Role: BMS, MSD. B. Neyns: Financial Interests, Institutional, Advisory Board: Novartis, BMS, Pierre-Fabre, MSD (Merck Sharp & Dohme); Financial Interests, Institutional, Research Grant: Novartis, Pfizer; Non-Financial Interests, Institutional, Product Samples: Bayer. All other authors have declared no conflicts of interest.
Resources from the same session
2008P - Brazilian real-world data of immunotherapy (IO) in extensive disease small cell lung cancer (ES-SCLC)
Presenter: Flávia Duarte
Session: Poster session 05
2009P - CNS efficacy of immune checkpoint inhibitors when combined to stereotactic radiosurgery in extensive stage small cell lung cancer
Presenter: Muhammad Awidi
Session: Poster session 05
2010P - Non-invasive radiomics signature predicts response to combination chemoimmunotherapy in extensive-stage small cell lung cancer (ES SCLC)
Presenter: Stuthi Perimbeti
Session: Poster session 05
2011P - Machine-derived features of tumor infiltrating lymphocytes (TILs) as biomarkers of clinical outcomes to platinum chemotherapy in small cell lung cancer (SCLC)
Presenter: Prantesh Jain
Session: Poster session 05
2012P - Spatially resolved transcriptomics deciphers inter- and intra-tumor heterogeneity of small cell lung cancer
Presenter: xujie Sun
Session: Poster session 05
2013P - Investigating the clinical relevance of immune checkpoint expression in the peripheral blood of patients with small cell lung cancer (SCLC)
Presenter: Dimitrios Mavroudis
Session: Poster session 05
2014P - ATR inhibition upregulates PD-L1 and potentiates the antitumor immune response to chemoimmunotherapy in small cell lung cancer
Presenter: Triparna Sen
Session: Poster session 05
2015P - Association between gene characteristics and mutation abundance with the prognosis of small cell lung cancer
Presenter: Lian Yu
Session: Poster session 05
2016P - The role of galectin-1 in SCLC: Prognostic significance and therapeutic implications
Presenter: Arancha Cebrian
Session: Poster session 05
2017P - Comprehensive molecular profiling of small cell lung cancer patients treated with chemo-immunotherapy or chemotherapy alone
Presenter: Milena Urbini
Session: Poster session 05