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 session498P - Report of 9 cases of embryonal tumours of the central nervous system with multilayered rosettes (ETMR)Presenter: Ruyu Ai Session: Poster session 17 Resources: Abstract 499TiP - A phase II study of BPM31510 (a lipid nanodispersion of oxidized CoQ10) with vitamin K in combination with standard of care (SOC) RT and TMZ in glioblastoma multiforme (GBM) patients without prior therapyPresenter: Brian Stockdale Session: Poster session 17 500TiP - Update on GBM AGILE: A global, phase II/III adaptive platform trial to evaluate multiple regimens in newly diagnosed and recurrent glioblastomaPresenter: Michael Weller Session: Poster session 17 501TiP - Clinical performance evaluation of a brain cancer liquid biopsyPresenter: James Cameron Session: Poster session 17 692P - Role of adjunctive surgery after platinum-based chemotherapy in management patients with adrenocortical carcinoma: Observation studyPresenter: Yaroslav Zhulikov Session: Poster session 17 693P - Causes of death in patients with malignant adrenal tumors: A population-based analysisPresenter: Shangqing Ren Session: Poster session 17 946P - Ipilimumab and nivolumab in advanced hepatocellular carcinoma after failure of prior atezolizumab and bevacizumab treatment: A multicenter retrospective studyPresenter: Jung Sun Kim Session: Poster session 17 948P - Drug type and duration of adjuvant immune checkpoint inhibitors in hepatocellular carcinoma with high-risk recurrence factors (PREVENT): An update analysis of a prospective, multicentric cohort studyPresenter: Jia-Yong Su Session: Poster session 17 Resources: Abstract 949P - Update results of ALTER-H006: A phase II study of TQB2450 plus anlotinib as adjuvant therapy in hepatocellular carcinoma (HCC) with high risk of recurrence after surgical resectionPresenter: Xianhai Mao Session: Poster session 17 950P - Outcomes by baseline tumour burden in EMERALD-1: A phase III, randomised, placebo (PBO)-controlled study of durvalumab (D) ± bevacizumab (B) with transarterial chemoembolisation (TACE) in participants (pts) with embolisation-eligible unresectable hepatocellular carcinoma (uHCC)Presenter: Masatoshi Kudo 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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