Ovarian adult-type
granulosa cell tumors (AGCTs) require prolonged follow-up, but evidence regarding the optimal follow-up marker is lacking. The objective of our study was to validate the clinical usefulness of serum anti-Müllerian
hormone (AMH) and the current marker
inhibin B as single and combined markers of AGCTs. We conducted a longitudinal, partially prospective cohort study of 123 premenopausal and postmenopausal AGCT patients with a median follow-up time of 10.5 years (range 0.3-50.0 years). Serum AMH and
inhibin B levels were measured from 560 pretreatment and follow-up serum samples by using immunoenzymometric assays. We found that serum AMH and
inhibin B levels were significantly elevated in patients with primary or recurrent AGCTs. The levels of both markers positively correlated to
tumor size (p < 0.05). AMH and
inhibin B performed similarly in receiving operator characteristic analyses; area under the curve (AUC) values were 0.92 [95% confidence interval (CI) 0.88-0.95] for AMH, and 0.94 (95% CI 0.90-0.96) for
inhibin B. AMH was highly sensitive (92%) and specific (81%) in detecting a macroscopic AGCT. However, in AUC comparison analyses, the combination of the markers was superior to
inhibin B alone. In conclusion, serum AMH is a sensitive and specific marker of AGCT, and either AMH or
inhibin B can be monitored during follow-up. However, combining AMH and
inhibin B in AGCT patient follow-up improves the detection of recurrent disease.