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

Chang Chang Ting, Chen Yen Tzu, Tai Li Yiu, Ching Wu Yen, Cheng Chang Yu, Kwan Ng Koon, Ming Jung Shih, I. Wu Tzu, Huey Lai Chyong*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

29 Scopus citations

Abstract

Purpose: We conducted a pilot trial to evaluate the value of 18F-fluorodeoxyglucose (18F-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 β-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 18F-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 18F-FDG PET in GTT.

Original languageEnglish
Pages (from-to)156-163
Number of pages8
JournalEuropean Journal of Nuclear Medicine and Molecular Imaging
Volume33
Issue number2
DOIs
StatePublished - 02 2006

Keywords

  • Chemoresistant
  • F-FDG
  • Gestational trophoblastic tumour
  • PET
  • β-hCG

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