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Poster session 17

1163P - Prognostic value of systemic inflammatory index (SII) in neuroendocrine tumors (NETs) treated with peptide receptor radionuclide therapy (PRRT)

Date

14 Sep 2024

Session

Poster session 17

Topics

Nuclear Medicine and Clinical Molecular Imaging;  Rare Cancers

Tumour Site

Neuroendocrine Neoplasms

Presenters

Eduardo Terán Brage

Citation

Annals of Oncology (2024) 35 (suppl_2): S749-S761. 10.1016/annonc/annonc1598

Authors

E. Terán Brage1, P. Reguera Puertas1, E. Campaña-Díaz2, M. Navarro Martín1, P. Garcia Talavera2, S. Rama Alonso2, Á. López Gutiérrez1, J. Roldan Ruiz1, M.D.C. Garijo Martínez1, D. Morchón Araujo1, L. Posado-Domínguez1, J.C. Redondo González1, P. Díaz Sánchez1, E. Pablo Martín1, L.C. Felix1, R. Lozano Mejorada1, E. Fonseca Sánchez1

Author affiliations

  • 1 Medical Oncology Department, University Hospital of Salamanca, 37007 - Salamanca/ES
  • 2 Nuclear Medicine Department, University Hospital of Salamanca, 37007 - Salamanca/ES

Resources

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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

Conclusions

A SII score ≤2 at baseline or at reassessment could predict better oncological outcomes, although prospective validation is required.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

D. 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.

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