Abstract 1163P
Background
PRRT with 177Lu-Dotatate (Lutathera®) (LU) offers an effective approach in gastroenteropancreatic NETs. We know that systemic inflammatory (SI) parameters could show poorer results, however, it remains unknown in patients (p) treated with PRRT. We aim to analyze the prognostic value of SI biomarkers in NETs undergoing LU.
Methods
Retrospective and multicentric study of NETs receiving LU between 2016 and 2024. Clinical features and blood test [at baseline (BL) and after two cycles of PRRT] data were collected to determine SI markers and calculate the following ratios: neutrophil to lymphocyte (NLR), monocyte to lymphocyte (MLR), platelet to lymphocyte (PLR) and albumin to lymphocyte (ALR). The cut-off values were determined as the median of each variable, correlating them with progression-free (PFS) and overall survival (OS).
Results
44 patients (p) with NETs were included with a median age of 57 years and 54.5% males. NETs were of gastrointestinal (n=16), pancreatic (n=15), pulmonary (n=7) and unknown (n=6) origin. Tumor grade (G) was G1 (29.5%) and G2/3 (70.5%). 25p (56.8%) received ≥2 lines of treatment prior to PRRT. We observed significant poorer PFS in p with pulmonary vs pancreatic NETs (16.3m vs 27.7m; p=0.02), and a trend inhigher tumor G (23.6m vs 36.5m; p=0.26) and with ≥2 metastatic sites (23.6m vs 36.5m; p=0.58). We identified as BL values of good prognosis lower ratios of NLR, MLR, PLR and ALR. Also, BL SII (as a set of the parameters analyzed) showed a favorable trend with a score ≤2 in PFS (34.7m vs 12.8m, p=0.07) and in OS (NR vs 29.6m; p=0.09). After2 cycles of LU, SII score ≤2 significantly predicted better OS (NR vs 12.6m; p=0.02).
Table: 1163P
Prognostic value of inflammatory biomarkers in patients with neuroendocrine tumors treated with PRRT
PFS median (months) | Log-rank p-value | OS median (months) | Log-rank p-value | ||
BL NLR | ConclusionsA SII score ≤2 at baseline or at reassessment could predict better oncological outcomes, although prospective validation is required. Clinical trial identificationEditorial acknowledgementLegal entity responsible for the studyThe authors. FundingHas not received any funding. DisclosureD. Morchón Araujo: Financial Interests, Personal, Invited Speaker: Astellas Pharma, PharmaMar. R. Lozano Mejorada: Financial Interests, Personal, Invited Speaker: Janssen, Astellas, Roche, Bayer, Ipsen, AstraZeneca; Financial Interests, Personal, Advisory Board: Janssen, Merck, Pfizer, Orion Pharma, Advanced Accelerator Applications (Novartis); Financial Interests, Personal, Other, Travel/accommodation: MSD, Sanofi; Financial Interests, Personal, Other, Travel/accommodation: BMS; Non-Financial Interests, Member: Sociedad Española de Oncología Médica. All other authors have declared no conflicts of interest. Resources from the same session1407P - Pan-immune-inflammation value predicts the survival of patients with esophageal squamous cell carcinoma receiving immunotherapy and chemoradiotherapy: A pooled-analysis of two phase II trialsPresenter: Xingyuan Cheng Session: Poster session 17 1408P - DVDMS (Sinoporphyrin sodium)-mediated photodynamic therapy (PDT) vs treatment of physician’s choice in patients with advanced esophageal cancer (EC): Preliminary results of DYNA-Esophagus03, a randomized, open-labeled, multicenter phase IIIb studyPresenter: Jun Zhou Session: Poster session 17 1409P - Advancing esophageal cancer radiotherapy: AS-NeSt's 3D predictive proficiency for personalized dose distributionPresenter: Yanhua Duan Session: Poster session 17 Resources: Abstract 1410P - Efficacy of fruquintinib plus paclitaxel (F+PTX) in patients (pts) with prior immunotherapy (prior-IO): Subgroup analysis from FRUTIGA studyPresenter: Lin Shen Session: Poster session 17 1411P - AI-powered immune phenotype predicts favorable outcomes of nivolumab (niv) plus chemotherapy (chemo) in advanced fgastric cancer (AGC): A multi-center real-world data analysisPresenter: Hyung-don Kim Session: Poster session 17 1412P - Intestinal microbiota as a biological marker for pre-neoplastic lesion in gastric cancer in Amazonas, BrazilPresenter: ÁBNER PAZ Session: Poster session 17 Resources: Abstract 1413P - Multi-modal deep-learning model for real-time prediction of recurrence in early-stage esophageal cancer: A multi-modal approachPresenter: Hyun Ae Jung Session: Poster session 17 1414P - Iparomlimab and tuvonralimab (QL1706) with definitive chemoradiotherapy for locally advanced esophageal squamous cell carcinoma: An open-label phase II studyPresenter: Wencheng Zhang Session: Poster session 17 1415P - Real-world data on the use of nivolumab plus chemotherapy for patients with metastatic GC/GEJC/EAC: A Canadian perspectivePresenter: Mustapha Tehfe Session: Poster session 17 1416P - First-line tislelizumab combined with bevacizumab and CAPOX for metastatic gastroesophageal adenocarcinoma (mGEA) with PD-L1 CPS<5: Updated results of a phase II, prospective, single-arm studyPresenter: guanghai dai Session: Poster session 17 This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used. For more detailed information on the cookies we use, please check our Privacy Policy.
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