EpigenOMic Determinants of the Neuroendocrine Phenotype As Biomarkers for Neuroendocrine Neoplasms

EpigenOMic Determinants of the Neuroendocrine Phenotype As Biomarkers for Noninvasive Diagnosis of Neuroendocrine Neoplasms

For GEP mixed neuroendocrine (NE) non-neuroendocrine neoplasms (MiNENs) a key issue affecting prognosis is sometimes the difficulty in obtaining a timely diagnosis, as the NE component is often localized in deeper anatomical locations and/or becomes prevalent over time. The tissue material of biopsies may be not enough to define the NE component when this is particularly small and this could impact on therapeutic decision. Furthermore GEP NENs need to be characterized for potentially druggable biomarkers and liquid biopsy has clear advantage to the solid one to this aim. Here, we will exploit epigenetic differences characterizing NE tumors to build a DNA methylation-based liquid biopsy assay able to detect circulating tumor DNA of NE derivation, to enable the non-invasive diagnosis and monitoring of GEP-MiNENs.

Study Overview

• Status: Recruiting
• Conditions: Neuroendocrine Neoplasm; Mixed Neuroendocrine-Non Neuroendocrine Neoplasm

Detailed Description

GEP-NENs are a heterogeneous group of diseases that encompasses relatively indolent and more aggressive tumors, sometimes with mixed exocrine/endocrine components (MINENs). Due to persistent uncertainties in diagnosis and treatment, prognosis of the mixed and more aggressive forms remains poor. Non-invasive tests would enable timely identification and monitoring over time. A better understanding of their biology and of the phenotypic differentiation process may pave the way for novel therapies. Differentiation follows, and can be inferred from, changes in the epigenetic landscape that shape transcriptional programs. Among epigenetic markers, DNA methylation is particularly well suited for non-invasive detection as it can be measured in circulating tumor DNA (ctDNA). New technologies like Oxford Nanopore Technologies (ONT) enable simultaneous analysis of DNA sequence and methylation, as we recently showed by Magi et al Nat Comms Biol 2022. Previous studies identified distinct neuroendocrine epi-transcriptomic landscapes but were conducted on tumor specimens (Yachida et al Cancer Discov 2022), impeding the discrimination of signals specifically generated within neuroendocrine tumor cells from the noise due to surrounding nontumoral or exocrine tumoral cells. This is now potentially solved by methods allowing single-cell sequencing directly from frozen or paraffin-embedded patient samples.

The main expected outcome is the development of a novel liquid biopsy assay for the detection and monitoring of GEP-NENs and MiNENs. To this end, we will exploit the ability of Oxford Nanopore Technologies (ONT) sequencing to simultaneously yield sequencing and methylated DNA profiles. Importantly, assessment of cell of origin from ctDNA requires the comparison of methylation and fragmentomics signals with previously generated maps of reference cells and tissues (Katsman et al 2022 Genome Biology). For rare tumors like NENs, these maps are not available in the literature; the few studies that have characterized the epigenomic features of NENs are likely contaminated by the surrounding stroma, so epigenetic signals (including both DNA methylation and tumor-specific transcription factor binding sites, essential for fragmentomics) may be uninformative for detection in the blood.

• Study Type: Observational
• Enrollment (Estimated): 130

Contacts and Locations

• Study Contact: Name: Nicola Fazio, MD; Phone Number: 0257489258; Email: divisione.gastrointestinale@ieo.it
• Study Contact Backup: Name: Francesca Spada, MD; Phone Number: 0257489258; Email: divisione.gastrointestinale@ieo.it

Study Locations

• Italy
  • Milan, Italy, 20141
    • Recruiting
    • European Institute of Oncology
    • Contact: Giuseppe Badalamenti, MD
    • Contact: Chiara Maria Grana, MD
    • Contact: Lorenzo Gervaso, MD
    • Contact: Chiara Alessandra Cella, MD
    • Contact: Nicola Fazio, MD,PhD; Phone Number: 0257489258; Email: divisione.gastrointestinale@ieo.it
    • Contact: Nicola Fazio, MD,PhD
    • Contact: Francesca Spada, MD
    • Contact: Luca Mazzarella, MD
    • Contact: Elenora Pisa, MD
    • Contact: Emilio Bertani, MD
    • Contact: Laura Algeri, MD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

• Sampling Method: Probability Sample

Study Population

Patients with GEP-NENs, aiming to collect adequate material and for a formal clinical to establish sensitivity and specificity of the assay in a clinically meaningful scenario.

Due to the relative rarity of the disease compared to non-NENs we will not enroll a consecutive population, but we will set up a case-control study:

• Cases: patients with resectable, histologically confirmed NENs
• Controls: patients with resectable, histologically confirmed non-neuroendocrine gastrointestinal tumors (including gastric, pancreatic, colorectal, small intestine).

Patients will be enrolled as cases or controls based on their pre-surgical diagnostic biopsy but will be definitively allocated in the case or control group based on their post-surgery full histological examination.

Description

Inclusion Criteria:

• Patient with histologically confirmed diagnosis of NEC/MINEN amenable to surgery with radical intent
• Patient with histologically confirmed diagnosis of NET amenable to surgery with radical intent
• Patient with metastatic NET/NEC, amenable to biopsy or surgery, including palliative intent

• Patient histologically confirmed non-NEN histotype:

  1. Colorectal carcinoma
  2. Small intestine carcinoma
  3. Gastric or oesophageal carcinoma
  4. Pancreatic ductal adenocarcinoma
  5. Metastasectomy from any non-NEN GI carcinoma

Exclusion Criteria:

• Grading G1 and G2 <=10% Ki67
• Presence of concomitant neoplasm (within 3 years)
• Concomitant major haematological alteration
• Concomitant major organ dysfunction (e.g. G3/4 liver or kidney failure)
• Ongoing chemotherapy

Study Plan

How is the study designed?

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort
Neuroendocrine neoplasm case; patient with histologically confirmed neuroendocrine neoplasm and onfirmed Mixed Neuroendocrine-non neuroendocrine neoplasm with each component > 30%) and high-grade Neuroendocrine Carcinomas
Non-neuroendocrine neoplasm control; patient with histologically confirmed non-neuroendocrine gastrointestinal tumors (including gastric, pancreatic, colorectal, small intestine).

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Develop a circulating methDNA/fragmentomics diagnostic assay	Epigenetic differences characterizing neuroendocrine tumors will be exploited to build a DNA methylation-based liquid biopsy assay able to detect circulating tumor DNA of neuroendocrine derivation, to enable the non-invasive diagnosis and monitoring of GEP-MiNENs.	2 years

Collaborators and Investigators

• Sponsor: European Institute of Oncology
• Collaborators: Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo
• Investigators: Principal Investigator: Nicola Fazio, MD, European Institute of Oncology

Study record dates

Study Major Dates

• Study Start (Actual): October 21, 2024
• Primary Completion (Estimated): October 21, 2026
• Study Completion (Estimated): October 21, 2026

Study Registration Dates

• First Submitted: January 15, 2025
• First Submitted That Met QC Criteria: January 15, 2025
• First Posted (Actual): March 25, 2025

Study Record Updates

• Last Update Posted (Actual): March 25, 2025
• Last Update Submitted That Met QC Criteria: January 15, 2025
• Last Verified: August 1, 2024

More Information

Terms related to this study

• Keywords: biomarker; global molecular profiling; neuroendocrine phenotype; epigenomic determinant
• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms, Nerve Tissue; Neoplasms; Neuroendocrine Tumors
• Other Study ID Numbers: L2-154

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No