TY - JOUR
T1 - Early prediction of post-molar gestational trophoblastic neoplasia and resistance to methotrexate, based on a single serum human chorionic gonadotropin measurement
AU - Hoeijmakers, Yvonne M.
AU - Eysbouts, Yalck K.
AU - Massuger, Leon F.A.G.
AU - Dandis, Rana
AU - Inthout, Joanna
AU - van Trommel, N. E.
AU - Ottevanger, Petronella B.
AU - Thomas, Chris M.G.
AU - Sweep, Fred C.G.J.
N1 - Publisher Copyright:
© 2021 The Authors
PY - 2021/12
Y1 - 2021/12
N2 - Background: Clinicians are unable to provide individualized counseling regarding risk of progression for patients with a complete hydatidiform mole (CHM). We developed nomograms enabling early prediction of post-molar gestational trophoblastic neoplasia (GTN) and resistance to methotrexate (MTX) based on a single serum human chorion gonadotropin (hCG) measurement. Methods: We generated two nomograms with logistic regression: to predict post-molar GTN, and MTX resistance. For patients with high probability to progress to post-molar GTN or MTX resistance, we determined hCG cut-offs at 97.5% specificity to select patients for additional- or adjustments in current treatment. Results: The nomograms had a good to excellent ability to distinguish either between patients with uneventful hCG regression versus progression to post molar GTN, or between patients cured by MTX versus patients in whom resistance would occur. At 97.5% specificity, we identified 66% (95%CI 56–75) of the 149 patients who would progress to post-molar GTN, four weeks after initial curettage. For patients treated with MTX, we identified 55% (95%CI 23–83) of the 43 patients who would become resistant, preceding their third course at 97.5% specificity. Conclusion: The nomograms and cut-off levels can be used to assist in counseling for patients diagnosed with CHM.
AB - Background: Clinicians are unable to provide individualized counseling regarding risk of progression for patients with a complete hydatidiform mole (CHM). We developed nomograms enabling early prediction of post-molar gestational trophoblastic neoplasia (GTN) and resistance to methotrexate (MTX) based on a single serum human chorion gonadotropin (hCG) measurement. Methods: We generated two nomograms with logistic regression: to predict post-molar GTN, and MTX resistance. For patients with high probability to progress to post-molar GTN or MTX resistance, we determined hCG cut-offs at 97.5% specificity to select patients for additional- or adjustments in current treatment. Results: The nomograms had a good to excellent ability to distinguish either between patients with uneventful hCG regression versus progression to post molar GTN, or between patients cured by MTX versus patients in whom resistance would occur. At 97.5% specificity, we identified 66% (95%CI 56–75) of the 149 patients who would progress to post-molar GTN, four weeks after initial curettage. For patients treated with MTX, we identified 55% (95%CI 23–83) of the 43 patients who would become resistant, preceding their third course at 97.5% specificity. Conclusion: The nomograms and cut-off levels can be used to assist in counseling for patients diagnosed with CHM.
KW - Complete hydatidiform mole
KW - Gestational trophoblastic disease
KW - Human chorionic gonadotropin
KW - Methotrexate
KW - Nomogram
KW - Resistance
UR - http://www.scopus.com/inward/record.url?scp=85116102061&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2021.09.016
DO - 10.1016/j.ygyno.2021.09.016
M3 - Article
C2 - 34602288
AN - SCOPUS:85116102061
SN - 0090-8258
VL - 163
SP - 531
EP - 537
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 3
ER -