DOI: 10.1097/as9.0000000000000700 ISSN: 2691-3593

Clinical Value of a 51-Neuroendocrine Tumor–Specific Gene Signature (NETest 2.0) for Management of Pancreatic and Small Bowel Neuroendocrine Tumors: A Prospective Study in a Consecutive Cohort of 82 Patients Considered for Surgery

Andrea Frilling, Ashley Clift, Duncan Spalding, Panagiotis Drymousis, Alexander von Roon, Robert Goldin, Jamshed Bomanji, Harpreet Wasa, Abdel B. Halim, Mark Kidd

Objectives:

To prospectively evaluate the clinical utility of NETest2.0, a 51-neuroendocrine tumor (NET)–specific gene whole blood assay (NETest2.0) for monitoring surgical patients with gastroenteropancreatic NETs (GEPNET).

Background:

GEPNETs are challenging regarding postoperative surveillance and monitoring for recurrence or progression.

Methods:

Blood samples were collected at baseline and during follow-up, and NETest2.0 was measured (scored 0–100; cutoff normal: <50) in 82 consecutive patients with GEPNET. Scores were correlated with follow-up and disease status, including no evidence of disease, stable disease, recurrent disease, and progressive disease.

Results:

Pancreatic NET (n = 29): median age, 57 (26–81) years, M:F (17:12), G1: 19, G2: 8, G3: 2, stages I to III (n = 18), and stage IV (n = 11). Median follow-up, 122 (4–163) months; 7 (24%) died. NETest2.0 correlated with outcomes and was significantly higher in those who died ( P = 0.0215). Small bowel NET (n = 53): median age, 66 (36–86) years, M:F (22:31), G1: 45, G2: 8, G3: 0, stages I to III (n = 25), and stage IV (n = 28). Median follow-up, 83 (12–157) months; thirteen (25%) died. NETest2.0 correlated with outcomes and was significantly higher in those who died ( P = 0.0011). Scores ≥50 were significantly associated with recurrent disease ( P = 0.0013). Scores ≥65 were associated with progression and poorer overall survival.

Conclusions:

NETest2.0 accurately identified disease status and correlated with clinical outcomes. Patients were stratified into molecular remission, stable disease, and high-risk progression states. Low scores (<50) identified surgical patients unlikely to recur; scores ≥65 identified individuals at increased risk for progression.

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