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 session961P - Sodium-glucose co-transporter 2 inhibitors (SGLT2i) improve oncologic outcomes in diabetic patients with hepatocellular carcinoma (HCC): A nationwide database studyPresenter: Chien-Huai Chuang Session: Poster session 17 962P - Best practices and impact of multi-disciplinary teams on hepatocellular carcinoma treatment: Insights from a global effortPresenter: Pablo Azcue Session: Poster session 17 963P - Quality-adjusted time without symptoms or toxicity (Q-TWiST) analysis to assess the impact of treatment with camrelizumab + rivoceranib (cam+rivo) on quality of life vs sorafenib (sora) in patients (pts) with unresectable hepatocellular carcinoma (uHCC): Study CARES-310Presenter: Andrew Moon Session: Poster session 17 964P - Lenvatinib (L) and sorafenib (S) in patients (pts) with advanced or unresectable hepatocellular carcinoma (uHCC): An international, multicenter, phase IV study (STELLAR)Presenter: Markus Peck Radosavljevic Session: Poster session 17 967P - Lenvatinib (L) versus sorafenib (S) second-line therapy in hepatocellular carcinoma (HCC) patients (P) progressed to atezolizumab plus bevacizumab (AB)Presenter: Mara Persano Session: Poster session 17 968P - HAIC combined with lenvatinib and PD-1 inhibitors versus lenvatinib plus PD-1 inhibitors for advanced HCC with portal vein tumor thrombosis: A prospective controlled trialPresenter: Xiaodong Wang Session: Poster session 17 969P - Lenvatinib versus sorafenib as a second-line option in patients with unresectable hepatocellular carcinoma previously treated with atezolizumab plus bevacizumab: An observational studyPresenter: Pasquale Lombardi Session: Poster session 17 970P - Comparing clinical outcomes between PD-1 and PD-L1 inhibitors plus bevacizumab combined with hepatic arterial interventional therapies in unresectable hepatocellular carcinoma: A single-center, real-world studyPresenter: Yangxun Pan Session: Poster session 17 Resources: Abstract 971P - Chemotherapy combined with lenvatinib and PD-1 may be a potential better alternative optionfor advanced unresectable intrahepatic cholangiocarcinoma: A retrospective real-world studyPresenter: binghua 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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