# A new, machine learning‐based approach to metastatic neuroendocrine tumors of unknown origin

**Authors:** Jiaxi Lü, Tania Amin, Till Clauditz, Kira Steinkraus, Oliver Buchstab, Samuel Huber, Jakob Izbicki, Thorben Fründt, Jörg Schrader, René Werner, Rüdiger Schmitz

PMC · DOI: 10.1111/jne.70134 · Journal of Neuroendocrinology · 2026-02-06

## TL;DR

A machine learning tool helps identify the origin of metastatic neuroendocrine tumors using liver biopsy slides, improving treatment decisions.

## Contribution

A novel machine learning model predicts primary tumor origin from H&E-stained liver metastases with high accuracy and public availability.

## Key findings

- The model identifies small intestine NETs with 71.4% sensitivity at 100% specificity and PPV.
- It detects pancreatic NETs with 33.3% sensitivity and 94.1% specificity.
- The tool is validated on external datasets and made publicly available for research and clinical use.

## Abstract

Neuroendocrine tumors (NETs) frequently present at a metastatic stage, particularly with liver metastases. Identifying the site of the primary tumor is critical for guiding therapy but often proves difficult. Small intestine NETs are especially distinct in their prognosis and treatment. To address this challenge, we developed a novel, machine learning‐based tool to predict the site of origin—specifically small intestine or pancreas—using routine hematoxylin and eosin (H&E)‐stained slides from hepatic metastases. To avoid mislabeling in the clinically relevant scenario of any possible tumor origin, the method applies a two‐step approach with optional abstention for uncertain classifications or non‐small intestine/non‐pancreas cases. In a retrospective, clinically realistic cohort with unrestricted tumor origin, the model identified small intestine NETs with a sensitivity of 71.4% at 100% specificity and positive predictive value (PPV), and high negative predictive value. A relevant subset of pancreatic NETs can also be reliably detected (sensitivity 33.3%, specificity 94.1%, PPV 85.7%). Generalizability and robustness were rigorously validated on an external dataset using different scanners, institutions, and resection techniques. The tool is intended as an additional method where other diagnostic modalities remain inconclusive regarding the location of the primary tumor. To facilitate further research and clinical translation, all models and extracted features are publicly released.

From HE‐stained tissue of NET hepatic metastases, a machine learning‐based tool identifies most cases with small intestine and many with pancreatic origin, while flagging all others as “uncertain” to prevent misdiagnosis. The model is validated thoroughly and made publicly available. It may impact management of metastatic NET of unknown primary.

## Full-text entities

- **Genes:** CDX2 (caudal type homeobox 2) [NCBI Gene 1045] {aka CDX-3, CDX2/AS, CDX3}, TTF1 (transcription termination factor 1) [NCBI Gene 7270] {aka TTF-1, TTF-I}, PAX8 (paired box 8) [NCBI Gene 7849] {aka PAX-8}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}, ISL1 (ISL LIM homeobox 1) [NCBI Gene 3670] {aka ISLET1, Isl-1}
- **Diseases:** colorectal cancer (MESH:D015179), pancreatic-like (MESH:D010195), Liver metastases (MESH:D009362), Small intestine NETs (MESH:D018358), pancreatic and small intestine NETs (MESH:D007414), Tumor (MESH:D009369), gastroenteropancreatic NETs (MESH:C535650), liver (MESH:D017093), pancreatic origin tumors (MESH:D010190)
- **Chemicals:** 5-FU (MESH:D005472), hematoxylin (MESH:D006416), H&amp;E (MESH:D006371), Temozolomide (MESH:D000077204), Streptozotocin (MESH:D013311), eosin (MESH:D004801), Capecitabine (MESH:D000069287), H&amp;E (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12881840/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC12881840/full.md

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Source: https://tomesphere.com/paper/PMC12881840