Abstract 1065P
Background
The nutritional status of patients with advanced cancer seems to affect the immune activity against tumor cells. We investigated the prognostic role of nutritional status in patients with advanced non-small cell lung cancer (NSCLC) and renal cell carcinoma (RCC) treated with immune checkpoint inhibitors (ICIs).
Methods
We prospectively enrolled patients with advanced NSCLC and RCC receiving ICIs from June 2021. Patient nutritional status at baseline and after three months of treatment (T1) was evaluated using the controlling nutritional status (CONUT) score (serum albumin, total cholesterol, and lymphocyte count) and body composition (BC), assessed by trained dietitians through bioelectrical impedance analysis (BIA). Data were correlated to disease control rate (DCR) and progression-free/overall survival (PFS/OS).
Results
Among 69 patients enrolled, 71% (N=49) had NSCLC, 78% (N=54) were treated in first line and 58% (N=40) with ICIs as monotherapy. At a median follow up of 11 months (95%CI 8.2-15.9), patients with a low CONUT score (score value lower than or equal to 4), meaning a good nutritional status, had higher DCR (74% vs 38%, p=0.004), longer PFS (HR: 0.28, 95%CI 0.14-0.55, p<0.001) and longer OS (HR 0.33, 95%CI 0.14-0.80, p=0.01) compared to those with high CONUT score (score value > 4), characterized by poor nutritional status. Among BC parameters, skeletal muscle index (SMI: skeletal muscle mass/height2) predicted clinical outcomes: patients with high SMI (>8.9 for male, > 6.4 for female) showed higher DCR (74% vs 40%, p=0.02), longer PFS (HR: 0.40, 95%CI 0.17-0.92, p=0.03) and longer OS (HR 0.20, 95% CI 0.07-0.56, p=0.002), compared to those with low SMI, defined as sarcopenic patients. Patients with any grade of SMI drop at T1 had shorter PFS (HR 3.04, 95% CI 1.18-7.79, p=0.02) compared to those with stable or increased SMI.
Conclusions
Nutritional status assessed by CONUT score and BC may predict clinical outcomes in patients with advanced NSCLC and RCC treated with ICIs. The study is ongoing to mature follow up and additional translational analyses are planned to disentangle the immunophenotypic features related to patients’ nutritional status.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
R. Berardi: Financial Interests, Personal, Advisory Board: AstraZeneca, BMS, Boehringer Ingelheim, EISAI, Novartis, MSD, Otsuka, Eli Lilly, Roche, Italfarmaco, Seagen. All other authors have declared no conflicts of interest.
Resources from the same session
1353P - Effect of TP53 co-mutation in non-small cell lung cancer (NSCLC) with driver mutations
Presenter: Jamie Feng
Session: Poster session 19
1354P - Beyond the common mutation: Examining chemotherapy success in uncommon EGFR mutations
Presenter: Chien-Chung Lin
Session: Poster session 19
1355P - Evaluation of the role of variant allele frequency in EGFR mutated non-small cell lung cancer treated with first line osimertinib
Presenter: Marta Brambilla
Session: Poster session 19
1356P - 10-year survivors treated with tyrosine kinase inhibitor for advanced non-small cell lung cancer
Presenter: Yu Tanaka
Session: Poster session 19
1357P - Bevacizumab improved prognosis for advanced EGFR mutant lung adenocarcinoma with brain metastasis receiving cerebral radiotherapy
Presenter: YuanLiang Zhou
Session: Poster session 19
1358P - Safety of tepotinib + EGFR TKI (osimertinib or gefitinib) in patients with EGFRm NSCLC
Presenter: Ernest Nadal
Session: Poster session 19
1359P - Relationship between tumor TP53 gene mutation, circulating anti-p53 antibodies and response to first-line osimertinib in EGFR-mutated NSCLC patients
Presenter: Marc Denis
Session: Poster session 19
1361P - Alectinib for treatment-naïve advanced ALK+ NSCLC selected via blood-based NGS: Updated analyses of outcomes, circulating tumour (ct)DNA and biomarker subgroups from BFAST Cohort A
Presenter: Shirish Gadgeel
Session: Poster session 19
1362P - Association of baseline (BL) anaplastic lymphoma kinase (ALK) fusion detected by circulating tumor DNA (ctDNA) with clinical features and outcomes in the phase III ALTA-3 trial
Presenter: Charu Aggarwal
Session: Poster session 19