Recurrent gestational trophoblastic disease after hCG normalization following hydatidiform mole in The Netherlands

被引:24
作者
Kerkmeijer, Linda G. W.
Wielsma, Sabien
Massuger, Leon F. A. G.
Sweep, Fred C. G. J.
Thomas, Chris M. G.
机构
[1] Radboud Univ Nijmegen Med Ctr, Dept Chem Endocrinol, ACE 479, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen Med Ctr, Dept Obstet & Gynaecol, NL-6500 HB Nijmegen, Netherlands
关键词
human chorionic gonadotropin; hydatidiform mole; persistent trophoblastic disease; recurrent trophoblastic disease;
D O I
10.1016/j.ygyno.2007.03.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives. To determine the risk for recurrent trophoblastic disease after spontaneous nonualization of human chorionic gonadotropin (hCG) levels in patients with hydatidiform mole and to determine the risk for tumor relapse after apparent remission following chemotherapy in patients with low- and high-risk persistent trophoblastic disease. Methods. From 1994 until 2004, 355 patients with hydatidiform mole were registered at the Dutch Central Registry of Hydatidiform Mole and were monitored by sequential hCG assays in serum at the department of Chemical Endocrinology of the Radboud University Nijmegen Medical Centre. HCG regression curves were analyzed together with clinical information collected from the Hydatidifonn Mole Database. Results. Among the 355 registered hydatidiform mole patients, 265 patients attained spontaneous normalization following evacuation. Of the 265 patients, one patient (0.38%) subsequently required chemotherapeutic treatment for recurrent trophoblastic disease (95% confidence interval 0.0% to 2.1%). HCG levels did not decline to normal (<2.0 ng/ml) spontaneously in 90 patients; those patients were subsequently treated. Relapse rates were 8.1% (6/74) and 6.3% (1/16) for the low- and high-risk category respectively. Conclusion. Our analysis indicates that relapse risk in hydatidifon-n mole patients with spontaneous normalization is extremely low (one in 265 patients) after two normal hCG levels (<2.0 ng/ml) are achieved. Our results support the suggestion that two subsequent normal hCG levels may be sufficient to ensure sustained remission after hydatidiform mole evacuation. In contrary, in order to assure sustained remission, the relapse rates after chemotherapy in the current study emphasize the need for surveillance of trophoblastic tumor patients even after complete remission has apparently been achieved. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:142 / 146
页数:5
相关论文
共 26 条
[1]  
BAGSHAWE KD, 1986, LANCET, V2, P673
[2]   How long should patients be followed after molar pregnancy? Analysis of serum hCG follow-up data [J].
Batorfi, J ;
Vegh, G ;
Szepesi, J ;
Szigetvari, I ;
Doszpod, J ;
Fulop, V .
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 2004, 112 (01) :95-97
[3]  
Benedet JL, 2000, INT J GYNECOL OBSTET, V70, P209
[4]   The effect of early pregnancy following chemotherapy on disease relapse and foetal outcome in women treated for gestational trophoblastic tumours [J].
Blagden, SP ;
Foskett, MA ;
Fisher, RA ;
Short, D ;
Fuller, S ;
Newlands, ES ;
Seckl, MJ .
BRITISH JOURNAL OF CANCER, 2002, 86 (01) :26-30
[5]   EMA/CO for high-risk gestational trophoblastic tumors: Results from a cohort of 272 patients [J].
Bower, M ;
Newlands, ES ;
Holden, L ;
Short, D ;
Brock, C ;
Rustin, GJS ;
Begent, RHJ ;
Bagshawe, KD .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (07) :2636-2643
[6]  
DELFS E, 1957, OBSTET GYNECOL, V9, P1
[7]   Human chorionic gonadotropin follow-up in patients with molar pregnancy: A time for reevaluation [J].
Feltmate, CM ;
Batorfi, J ;
Fulop, V ;
Goldstein, DP ;
Doszpod, J ;
Berkowitz, RS .
OBSTETRICS AND GYNECOLOGY, 2003, 101 (04) :732-736
[8]  
FINE C, 1989, OBSTET GYNECOL, V73, P414
[9]   Immunohistochemical characterization of p57KIP2 expression in early hydatidiform moles [J].
Fukunaga, M .
HUMAN PATHOLOGY, 2002, 33 (12) :1188-1192
[10]   Duration of human chorionic gonadotropin surveillance for partial hydatidiform moles [J].
Lavie, I ;
Rao, GG ;
Castrillon, DH ;
Miller, DS ;
Schorge, JO .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2005, 192 (05) :1362-1364