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Schwabe, Andrej

0009-0003-0983-7333

Mayo Clinic

Thermo Fisher Scientific (Germany)

Citations 1

Circulating Chromogranin A as a Surveillance Biomarker in Patients with Carcinoids—The CASPAR Study
Meng, Qing H. , Hálfdánarson, Þorvarður R. , Bornhorst, Joshua A. , Jann, Henning , Shaheen, Shagufta , Shi, Run‐Zhang , Schwabe, Andrej , Stade, Katrin , Halperin, Daniel M. , Halfdanarson, Thorvardur R , Bornhorst, Joshua

Clinical Cancer Research | October 25, 2024 | Volume: 30 | Issue: 24 | Pages: 5559-5567

10.1158/1078-0432.ccr-24-1875 Get It

Abstract Purpose: Gastroenteropancreatic neuroendocrine tumors (GEP-NET) are relatively indolent but can be more aggressive. The current recommendations for using serum chromogranin A (CgA) for patients with GEP-NET are equivocal. This study was designed to validate an automated CgA immunofluorescence assay for monitoring disease progression in patients with GEP-NET. Patients and Methods: A prospective, multicenter, blinded observational study was designed to validate an automated CgA immunofluorescence assay for monitoring disease progression in patients with GEP-NET. Tumor progression was evaluated with RECIST 1.1 by CT/MRI. An increase ≥50% above the prior CgA concentration to a value >100 ng/mL in the following CgA concentration was considered positive. Results: A total of 153 patients with GEP-NET were enrolled. Using the prespecified cut-off of CgA change for tumor progression, specificity was 93.4% (95% confidence interval, 90.4%–95.5%; P < 0.001), sensitivity 34.4% (25.6%–44.3%), positive predictive value 57.9% (45.0–69.8), negative predictive value 84.3% (80.5–87.6), and AUC 0.73 (0.67–0.79). Conclusions: Changes in serial measurements of serum CgA had a favorable specificity and negative predictive value, making this test a useful adjunct to routine radiographic monitoring.