Wb. Jones et al., MANAGEMENT OF HIGH-RISK GESTATIONAL TROPHOBLASTIC DISEASE - THE MEMORIAL HOSPITAL EXPERIENCE, International journal of gynecological cancer, 7(1), 1997, pp. 27-33
Thirty-two patients with high-risk gestational trophoblastic disease (
GTD), defined as metastases to the brain or liver (regardless of hCG l
evel or duration of disease) or prior unsuccessful chemotherapy are re
viewed. In this classification, an antecedent term pregnancy is not co
nsidered to be an independent high-risk factor. Initial chemotherapy i
n 15 (46.8%) patients consisted of methotrexate, actinomycin D, and ch
lorambucil (MAC), actinomycin D alone in seven (21.8%), etoposide, met
hotrexate, actinomycin D, cytoxan on covin (EMACO) EMACO in three (9.4
%), ITMA (hydroxyurea, vincristine, methotrexate, folinic acid, cyclop
hosphamide, actinomycin D, adriamycin, and melphalan) in three (9.4%).
The remaining patients were treated with actinomycin D and 6-mercapto
purine (1), CHAMOCA (1), carboplatin and Taxol (1), and methotrexate (
1). All patients with brain metastases were treated with cranial radio
therapy. Overall complete remission was achieved in 14 of 32 (43.7%) p
atients. Five of 9 (55.5%) patients whose disease followed a term preg
nancy survived compared to nine of 23 (39.1%) patients whose disease f
ollowed other types of pregnancies. The data analyzed according to the
clinical classification of 'high-risk' indicates that an overall surv
ival rate of 70% was achieved. The Memorial Hospital classification th
erefore identifies patients who need primary chemotherapy more aggress
ive than MAC and similar to the WHO scoring system is a better predict
or of survival than the clinical classification.