The role of 18F-fluorodeoxyglucose positron emission tomography in gestational trophoblastic tumours:: a pilot study

被引:30
作者
Chang, TC
Yen, TC
Li, YT
Wu, YC
Chang, YC
Ng, KK
Jung, SM
Wu, TI
Lai, CH
机构
[1] Chang Gung Mem Hosp, Linkou Med Ctr, Dept Obstet & Gynecol, Taoyuan 333, Taiwan
[2] Chang Gung Mem Hosp, Dept Obstet & Gynecol, Div Gynecol Oncol, Taoyuan 333, Taiwan
[3] Chang Gung Univ, Coll Med, Dept Diagnost Radiol, Taoyuan, Taiwan
[4] Chang Gung Mem Hosp, Dept Nucl Med, Taoyuan 333, Taiwan
[5] Kuo Gen Hosp, Dept Obstet & Gynecol, Tainan, Taiwan
[6] Chang Gung Mem Hosp, Dept Diagnost Radiol, Taoyuan 333, Taiwan
关键词
F-18-FDG; PET; gestational trophoblastic tumour; beta-hCG; chemoresistant;
D O I
10.1007/s00259-005-1873-1
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose: We conducted a pilot trial to evaluate the value of F-18-fluorodeoxyglucose (F-18-FDG) positron emission tomography ( PET) in gestational trophoblastic tumours (GTTs). Methods: Patients with placental site trophoblastic tumour (PSTT), high-risk GTT ( World Health Organisation score >= 8, disease onset at postpartum or greater than 6 months after antecedent pregnancy), metastatic GTT, recurrent/resistant GTT after chemotherapy, or post-molar GTT with unexplained abnormal beta-hCG regression and patients undergoing re-evaluation after salvage treatment were enrolled. PET was undertaken within 1 week after computed tomography (CT). Clinical impacts of additional PET were determined on a scan basis. Results: A total of 14 patients were recruited. Sixteen PET scans were performed, with one patient having three serial studies. Benefits of additional PET were seen in 7 of 16 (43.8%) scans; these benefits included disclosure of chemotherapy-resistant lesions (n= 2), exclusion of false-positive CT lesions ( n= 1), detection of an additional lesion not found by conventional imaging ( n= 1) in high-risk GTT at the start of primary chemotherapy, and confirmation of complete response to treatment for PSTT or to salvage therapy for recurrent/resistant GTT ( n= 3). On the other hand, in two instances there were false-negative PET findings, six scans yielded no benefit, and one showed an indeterminate lesion. Conclusion: Our preliminary results suggest that F-18-FDG PET is potentially useful in selected patients with GTT by providing precise mapping of metastases and tumour extent upfront, by monitoring treatment response and by localising viable tumours after chemotherapy. A larger study is necessary to further define the role of F-18-FDG PET in GTT.
引用
收藏
页码:156 / 163
页数:8
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