TY - JOUR
T1 - Postmolar choriocarcinoma
T2 - An independent risk factor for chemotherapy resistance in low-risk gestational trophoblastic neoplasia
AU - Strohl, Anna E.
AU - Lurain, John R.
N1 - Publisher Copyright:
© 2016 Elsevier Inc. All rights reserved.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - Objective To evaluate the effect of a clinicopathologic diagnosis of choriocarcinoma (CCA) on clinical characteristics, extent of disease, and response to chemotherapy in low-risk gestational trophoblastic neoplasia (GTN). Methods We reviewed the records of 678 patients with low-risk GTN (FIGO stage I and stages II-III, score < 7) treated from 1962 to 2009. Patient and disease characteristics, treatment course, as well as clinical response and survival were analyzed retrospectively. Patients with a clinicopathologic diagnosis of CCA were compared to those with a clinical diagnosis of postmolar GTN. Results Of 678 women with low-risk GTN, 129 (19.0%) had a clinicopathologic diagnosis of CCA. Patients with CCA had higher parity (median 1 vs. 0, p = 0.003), more pretreatment human chorionic gonadotropin (hCG) levels at > 100,000 mIU/mL (12.7% vs. 5.9%, p = 0.009), longer duration of disease (19.6 vs. 9.9 weeks, p < 0.001), and higher FIGO scores (median 2 vs. 1, p < 0.001) compared with those with other histology; however, patients with CCA and postmolar GTN presented with similar stage of disease (stage I, 83.1% vs 88.2%, p = 0.126). Although there was no difference in survival between groups, increased resistance to first-line methotrexate chemotherapy was significantly associated with a diagnosis of postmolar CCA (OR 2.67, p = 0.007)), pretreatment hCG level at > 10,000 mIU/mL (OR 2.62, p = 0.002), and higher FIGO score (3-4: OR 2.02, p = 0.027; 5-6: OR 5.56, p < 0.001) on multivariate analysis. Conclusions Clinicopathologic diagnosis of postmolar CCA in patients with low-risk GTN is associated with higher pretreatment hCG levels, higher FIGO scores, and increased resistance to first-line single-agent methotrexate chemotherapy.
AB - Objective To evaluate the effect of a clinicopathologic diagnosis of choriocarcinoma (CCA) on clinical characteristics, extent of disease, and response to chemotherapy in low-risk gestational trophoblastic neoplasia (GTN). Methods We reviewed the records of 678 patients with low-risk GTN (FIGO stage I and stages II-III, score < 7) treated from 1962 to 2009. Patient and disease characteristics, treatment course, as well as clinical response and survival were analyzed retrospectively. Patients with a clinicopathologic diagnosis of CCA were compared to those with a clinical diagnosis of postmolar GTN. Results Of 678 women with low-risk GTN, 129 (19.0%) had a clinicopathologic diagnosis of CCA. Patients with CCA had higher parity (median 1 vs. 0, p = 0.003), more pretreatment human chorionic gonadotropin (hCG) levels at > 100,000 mIU/mL (12.7% vs. 5.9%, p = 0.009), longer duration of disease (19.6 vs. 9.9 weeks, p < 0.001), and higher FIGO scores (median 2 vs. 1, p < 0.001) compared with those with other histology; however, patients with CCA and postmolar GTN presented with similar stage of disease (stage I, 83.1% vs 88.2%, p = 0.126). Although there was no difference in survival between groups, increased resistance to first-line methotrexate chemotherapy was significantly associated with a diagnosis of postmolar CCA (OR 2.67, p = 0.007)), pretreatment hCG level at > 10,000 mIU/mL (OR 2.62, p = 0.002), and higher FIGO score (3-4: OR 2.02, p = 0.027; 5-6: OR 5.56, p < 0.001) on multivariate analysis. Conclusions Clinicopathologic diagnosis of postmolar CCA in patients with low-risk GTN is associated with higher pretreatment hCG levels, higher FIGO scores, and increased resistance to first-line single-agent methotrexate chemotherapy.
KW - Choriocarcinoma
KW - Gestational trophoblastic neoplasia
KW - Low-risk
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U2 - 10.1016/j.ygyno.2016.02.014
DO - 10.1016/j.ygyno.2016.02.014
M3 - Article
C2 - 26896825
AN - SCOPUS:84959264032
SN - 0090-8258
VL - 141
SP - 276
EP - 280
JO - Gynecologic Oncology
JF - Gynecologic Oncology
IS - 2
ER -