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Conference Paper: Prediction of treatment response following transarterial chemoembolization in patients with HCC using dualtracer positron emission tomography
Title | Prediction of treatment response following transarterial chemoembolization in patients with HCC using dualtracer positron emission tomography |
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Authors | |
Issue Date | 2019 |
Publisher | SpringerOpen. The Journal's web site is located at http://www.springer.com/medicine/radiology/journal/13244 |
Citation | 30th European Society of Gastrointestinal and Abdominal Radiology Annual Meeting (ESGAR 2019), Rome, Italy, 5-8 June 2019. In Insights into Imaging, 2019, v. 10 n. Suppl. 2, p. 20, article no. SS 5.6 How to Cite? |
Abstract | Purpose: While dual-tracer positron emission tomography (DT-PET) with 18F-FDG and 11C-acetate is highly sensitive in detecting HCC, its ability to prognosticate outcomes has not been previously explored. This study aims to evaluate whether DT-PET can predict treatment response in patients with HCC undergoing transarterial chemoembolization (TACE). Material and methods: Patients with HCC who had undergone DT-PET prior to TACE were retrospectively identified. Patient demographics, radiotracer uptake patterns, treatment response as per modified Response Evaluation Criteria In Solid Tumours (mRECIST), progression-free (PFS) and overall (OS) survival were analysed. Results: Between 2015 and 2018, 28 patients (M:F 22:6, median age 64) with 38 target lesions were included. Ten patients had multifocal while 18 had a solitary HCC (median size 19mm). 18F-FDG and 11C-acetate avidities were seen in 37% and 79% of HCC, respectively. Patients who responded to treatment had significantly longer OS (median 47.3 vs 20.9 months, p=0.022) while FDG uptake was associated with shorter PFS (median 2.7 vs 20.8 months, p=0.013) and OS (median 22.3 vs 44.7 months, p=0.008). Baseline raised AFP and multifocal disease were also associated with poorer OS. Lesion-based analysis showed acetate uptake (defined as tumour-to-liver ratio <2 for low or >2 for high) was predictive of treatment response (78% vs 47%, p=0.045). Conclusion: Our study shows that HCC with high acetate uptake is associated with less favourable response to TACE on a per lesion basis while FDG uptake in HCC is associated with shorter PFS and OS. DT-PET can potentially be a novel prognostic biomarker in the era of precision medicine. |
Description | Presentation Number - SS 5.6 V. 10, suppl. 2 has special title: ESGAR 2019 Book of Abstracts |
Persistent Identifier | http://hdl.handle.net/10722/275243 |
ISSN | 2023 Impact Factor: 4.1 2023 SCImago Journal Rankings: 1.240 |
DC Field | Value | Language |
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dc.contributor.author | Chiu, WHK | - |
dc.contributor.author | Yuan, H | - |
dc.contributor.author | Van Lunenburg, JTJ | - |
dc.contributor.author | Vardhanabhuti, V | - |
dc.contributor.author | Tse, D | - |
dc.contributor.author | Lee, EYP | - |
dc.date.accessioned | 2019-09-10T02:38:34Z | - |
dc.date.available | 2019-09-10T02:38:34Z | - |
dc.date.issued | 2019 | - |
dc.identifier.citation | 30th European Society of Gastrointestinal and Abdominal Radiology Annual Meeting (ESGAR 2019), Rome, Italy, 5-8 June 2019. In Insights into Imaging, 2019, v. 10 n. Suppl. 2, p. 20, article no. SS 5.6 | - |
dc.identifier.issn | 1869-4101 | - |
dc.identifier.uri | http://hdl.handle.net/10722/275243 | - |
dc.description | Presentation Number - SS 5.6 | - |
dc.description | V. 10, suppl. 2 has special title: ESGAR 2019 Book of Abstracts | - |
dc.description.abstract | Purpose: While dual-tracer positron emission tomography (DT-PET) with 18F-FDG and 11C-acetate is highly sensitive in detecting HCC, its ability to prognosticate outcomes has not been previously explored. This study aims to evaluate whether DT-PET can predict treatment response in patients with HCC undergoing transarterial chemoembolization (TACE). Material and methods: Patients with HCC who had undergone DT-PET prior to TACE were retrospectively identified. Patient demographics, radiotracer uptake patterns, treatment response as per modified Response Evaluation Criteria In Solid Tumours (mRECIST), progression-free (PFS) and overall (OS) survival were analysed. Results: Between 2015 and 2018, 28 patients (M:F 22:6, median age 64) with 38 target lesions were included. Ten patients had multifocal while 18 had a solitary HCC (median size 19mm). 18F-FDG and 11C-acetate avidities were seen in 37% and 79% of HCC, respectively. Patients who responded to treatment had significantly longer OS (median 47.3 vs 20.9 months, p=0.022) while FDG uptake was associated with shorter PFS (median 2.7 vs 20.8 months, p=0.013) and OS (median 22.3 vs 44.7 months, p=0.008). Baseline raised AFP and multifocal disease were also associated with poorer OS. Lesion-based analysis showed acetate uptake (defined as tumour-to-liver ratio <2 for low or >2 for high) was predictive of treatment response (78% vs 47%, p=0.045). Conclusion: Our study shows that HCC with high acetate uptake is associated with less favourable response to TACE on a per lesion basis while FDG uptake in HCC is associated with shorter PFS and OS. DT-PET can potentially be a novel prognostic biomarker in the era of precision medicine. | - |
dc.language | eng | - |
dc.publisher | SpringerOpen. The Journal's web site is located at http://www.springer.com/medicine/radiology/journal/13244 | - |
dc.relation.ispartof | Insights into Imaging | - |
dc.relation.ispartof | European Society of Gastrointestinal and Abdominal Radiology (ESGAR) Annual Meeting, 2019 | - |
dc.title | Prediction of treatment response following transarterial chemoembolization in patients with HCC using dualtracer positron emission tomography | - |
dc.type | Conference_Paper | - |
dc.identifier.email | Chiu, WHK: kwhchiu@hku.hk | - |
dc.identifier.email | Yuan, H: oliveryh@HKUCC-COM.hku.hk | - |
dc.identifier.email | Vardhanabhuti, V: varv@hku.hk | - |
dc.identifier.email | Lee, EYP: eyplee77@hku.hk | - |
dc.identifier.authority | Chiu, WHK=rp02074 | - |
dc.identifier.authority | Vardhanabhuti, V=rp01900 | - |
dc.identifier.authority | Lee, EYP=rp01456 | - |
dc.identifier.hkuros | 303947 | - |
dc.identifier.volume | 10 | - |
dc.identifier.issue | Suppl. 2 | - |
dc.identifier.spage | 20, article no. SS 5.6 | - |
dc.identifier.epage | 20, article no. SS 5.6 | - |
dc.publisher.place | Germany | - |
dc.identifier.issnl | 1869-4101 | - |