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Endocrine Abstracts (2025) 114 P19 | DOI: 10.1530/endoabs.114.P19

1Transforming Cancer Outcomes through Research, King’s College London, London, United Kingdom; 2University Hospitals Sussex NHS Foundation Trust, Sussex, United Kingdom; 3King’s College London, London, United Kingdom; 4Guy’s and St Thomas' NHS Foundation Trust, London, United Kingdom; 5King’s College Hospital, London, United Kingdom


Background: High grade neuroendocrine neoplasms (NENs) are a heterogenous group, including G3 neuroendocrine tumours (NETs), neuroendocrine carcinomas (NECs), and mixed neuroendocrine and non-neuroendocrine neoplasms (MiNENs). There is currently limited evidence for the optimal management of high grade NENs, particularly for MiNENs. This study aims to describe the real-world management and outcomes for patients with high grade NENs at a large NHS cancer centre in London (UK).

Methods: Adults with high grade NENs seen at Guy’s Cancer Centre between 2017-2023 were included. Data was collected using the Research Electronic Data Capture (REDCap) platform. The study received ethical approval from Guy’s Cancer Cohort (Ref 23/NW/0105).

Results: Seventy-six patients were included; comprising 23 G3 NETs, 43 NECs (18 small cell, 10 large cell, 15 not specified), and 10 MiNENs. Gastrointestinal (GI) NENs were most common (72.4%) and most presented with metastatic disease (69.7%). The mean age was 60, the majority male (51.3%), of White ethnicity (64.5%), and performance status 0-1 (60.6%). Amongst G3 NETs (n = 23), the majority were observed in GI sites (73.9%) with Ki67 <55% (82.6%). Palliative chemotherapy was most common in the first line (39.1%), followed by curative surgery (30.4%), and somatostatin analogues (8.7%). Best supportive care (BSC) was received by 13.0%. Median overall survival (mOS) for the G3 NET cohort was 33.4 months (95CI 6.7-65.8). Of the NECs (n = 43), 67.4% affected GI sites. The most frequent first-line treatment was palliative chemotherapy (44.2%), of which most received platinum-etoposide (P-E), and curative surgery (16.3%). BSC occurred in 16.3% of patients. The mOS for the NEC cohort was 8.4 months (95CI 5.2-14.0). Of the MiNENs (n = 10), almost all were GI (90%). All received treatment; 40% receiving palliative chemotherapy (20% P-E, 10% CAPTEM, 10% Other) in the first line. Prognosis was lowest amongst the MiNEN cohort, with mOS of 4.4 months (95CI 1.6-15.3). Finally, molecular profiling data has been collected within this real-world database, with ongoing analyses exploring associations with treatment patterns and outcomes.

Conclusion: This real-world study showed poor survival for NECs and MiNENs compared to G3 NENs. Precise histological categorisation is essential to inform optimal treatment and maximise outcomes.

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