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- Publisher Website: 10.1038/s41416-020-0871-1
- Scopus: eid_2-s2.0-85085152859
- PMID: 32372027
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Article: Clinical utility of serial analysis of circulating tumour cells for detection of minimal residual disease of metastatic nasopharyngeal carcinoma
Title | Clinical utility of serial analysis of circulating tumour cells for detection of minimal residual disease of metastatic nasopharyngeal carcinoma |
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Authors | |
Keywords | Circulating Neoplastic Cell Liquid Biopsy Circulating Tumor DNA |
Issue Date | 2020 |
Publisher | Springer Nature, published in association with Cancer Research UK. The Journal's web site is located at http://www.nature.com/bjc |
Citation | British Journal of Cancer, 2020, v. 123 n. 1, p. 114-125 How to Cite? |
Abstract | Background: Nasopharyngeal carcinoma (NPC) is an important cancer in Hong Kong. We aim to utilise liquid biopsies for serial monitoring of disseminated NPC in patients to compare with PET-CT imaging in detection of minimal residual disease.
Method: Prospective serial monitoring of liquid biopsies was performed for 21 metastatic patients. Circulating tumour cell (CTC) enrichment and characterisation was performed using a sized-based microfluidics CTC chip, enumerating by immunofluorescence staining, and using target-capture sequencing to determine blood mutation load. PET-CT scans were used to monitor NPC patients throughout their treatment according to EORTC guidelines.
Results: The longitudinal molecular analysis of CTCs by enumeration or NGS mutational profiling findings provide supplementary information to the plasma EBV assay for disease progression for good responders. Strikingly, post-treatment CTC findings detected positive findings in 75% (6/8) of metastatic NPC patients showing complete response by imaging, thereby demonstrating more sensitive CTC detection of minimal residual disease. Positive baseline, post-treatment CTC, and longitudinal change of CTCs significantly associated with poorer progression-free survival by the Kaplan–Meier analysis.
Conclusions: We show the potential usefulness of application of serial analysis in metastatic NPC of liquid biopsy CTCs, as a novel more sensitive biomarker for minimal residual disease, when compared with imaging. |
Persistent Identifier | http://hdl.handle.net/10722/284044 |
ISSN | 2023 Impact Factor: 6.4 2023 SCImago Journal Rankings: 3.000 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Ko, JMY | - |
dc.contributor.author | Vardhanabhuti, V | - |
dc.contributor.author | Ng, WT | - |
dc.contributor.author | Lam, KO | - |
dc.contributor.author | Ngan, RKC | - |
dc.contributor.author | Kwong, DLW | - |
dc.contributor.author | Lee, VHF | - |
dc.contributor.author | Lui, YH | - |
dc.contributor.author | Yau, CC | - |
dc.contributor.author | Kwan, CK | - |
dc.contributor.author | Li, WS | - |
dc.contributor.author | Yau, S | - |
dc.contributor.author | Guo, C | - |
dc.contributor.author | Choi, SSA | - |
dc.contributor.author | Lei, LC | - |
dc.contributor.author | Chan, KCH | - |
dc.contributor.author | Lam, CCS | - |
dc.contributor.author | Chan, CKC | - |
dc.contributor.author | Dai, W | - |
dc.contributor.author | Khong, PL | - |
dc.contributor.author | Lung, ML | - |
dc.date.accessioned | 2020-07-20T05:55:39Z | - |
dc.date.available | 2020-07-20T05:55:39Z | - |
dc.date.issued | 2020 | - |
dc.identifier.citation | British Journal of Cancer, 2020, v. 123 n. 1, p. 114-125 | - |
dc.identifier.issn | 0007-0920 | - |
dc.identifier.uri | http://hdl.handle.net/10722/284044 | - |
dc.description.abstract | Background: Nasopharyngeal carcinoma (NPC) is an important cancer in Hong Kong. We aim to utilise liquid biopsies for serial monitoring of disseminated NPC in patients to compare with PET-CT imaging in detection of minimal residual disease. Method: Prospective serial monitoring of liquid biopsies was performed for 21 metastatic patients. Circulating tumour cell (CTC) enrichment and characterisation was performed using a sized-based microfluidics CTC chip, enumerating by immunofluorescence staining, and using target-capture sequencing to determine blood mutation load. PET-CT scans were used to monitor NPC patients throughout their treatment according to EORTC guidelines. Results: The longitudinal molecular analysis of CTCs by enumeration or NGS mutational profiling findings provide supplementary information to the plasma EBV assay for disease progression for good responders. Strikingly, post-treatment CTC findings detected positive findings in 75% (6/8) of metastatic NPC patients showing complete response by imaging, thereby demonstrating more sensitive CTC detection of minimal residual disease. Positive baseline, post-treatment CTC, and longitudinal change of CTCs significantly associated with poorer progression-free survival by the Kaplan–Meier analysis. Conclusions: We show the potential usefulness of application of serial analysis in metastatic NPC of liquid biopsy CTCs, as a novel more sensitive biomarker for minimal residual disease, when compared with imaging. | - |
dc.language | eng | - |
dc.publisher | Springer Nature, published in association with Cancer Research UK. The Journal's web site is located at http://www.nature.com/bjc | - |
dc.relation.ispartof | British Journal of Cancer | - |
dc.subject | Circulating Neoplastic Cell | - |
dc.subject | Liquid Biopsy | - |
dc.subject | Circulating Tumor DNA | - |
dc.title | Clinical utility of serial analysis of circulating tumour cells for detection of minimal residual disease of metastatic nasopharyngeal carcinoma | - |
dc.type | Article | - |
dc.identifier.email | Ko, JMY: joko@hku.hk | - |
dc.identifier.email | Vardhanabhuti, V: varv@hku.hk | - |
dc.identifier.email | Lam, KO: lamkaon@hku.hk | - |
dc.identifier.email | Kwong, DLW: dlwkwong@hku.hk | - |
dc.identifier.email | Lee, VHF: vhflee@hku.hk | - |
dc.identifier.email | Choi, SSA: ssachoi@HKUCC-COM.hku.hk | - |
dc.identifier.email | Lei, LC: clei@HKUCC-COM.hku.hk | - |
dc.identifier.email | Lam, CCS: lamcandy@hku.hk | - |
dc.identifier.email | Chan, CKC: biocandy@hku.hk | - |
dc.identifier.email | Dai, W: weidai2@hku.hk | - |
dc.identifier.email | Khong, PL: plkhong@hku.hk | - |
dc.identifier.email | Lung, ML: mlilung@hku.hk | - |
dc.identifier.authority | Ko, JMY=rp02011 | - |
dc.identifier.authority | Vardhanabhuti, V=rp01900 | - |
dc.identifier.authority | Lam, KO=rp01501 | - |
dc.identifier.authority | Kwong, DLW=rp00414 | - |
dc.identifier.authority | Lee, VHF=rp00264 | - |
dc.identifier.authority | Dai, W=rp02146 | - |
dc.identifier.authority | Khong, PL=rp00467 | - |
dc.identifier.authority | Lung, ML=rp00300 | - |
dc.description.nature | postprint | - |
dc.identifier.doi | 10.1038/s41416-020-0871-1 | - |
dc.identifier.pmid | 32372027 | - |
dc.identifier.pmcid | PMC7341819 | - |
dc.identifier.scopus | eid_2-s2.0-85085152859 | - |
dc.identifier.hkuros | 311248 | - |
dc.identifier.volume | 123 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 114 | - |
dc.identifier.epage | 125 | - |
dc.identifier.isi | WOS:000531499700001 | - |
dc.publisher.place | United Kingdom | - |
dc.identifier.issnl | 0007-0920 | - |