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  • American Association for Cancer Research (AACR)  (2)
  • Wu, Min-Hsien  (2)
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  • American Association for Cancer Research (AACR)  (2)
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  • 1
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2017
    In:  Cancer Research Vol. 77, No. 13_Supplement ( 2017-07-01), p. 3790-3790
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 77, No. 13_Supplement ( 2017-07-01), p. 3790-3790
    Abstract: Background: Circulating tumor cell (CTC) has been prognostic and predictive in numerous types of cancer; however, its role in early diagnosis of relapse remains unclear. Methods: Eighty-six patients were prospectively enrolled between March 2015 and June 2016. Among these patients, 51 head and neck squamous cell carcinoma (HNSCC) patients had suspicious recurrent lesion(s), whilst 35 HNSCC patients were newly diagnosed. CTC test was performed by negative selection strategy and CD45-negative and EpCAM-positive cells were identified as CTCs. Biopsy on suspicious lesion(s) and CTC analysis were performed simultaneously. We analyzed the differences of CTC numbers among HNSCC patients with true recurrence, biopsy-negative and newly-diagnosed. Results: Mean±standard deviation(SD) of CTC numbers in baseline at diagnosis (n=35), true recurrence (n=40) and biopsy-negative (n=11) groups were 41.98±32.02, 81.75±64.91 and 16.55±6.82 cells/mL, respectively. The difference of CTC numbers among three groups was significant (P & lt;0.001). CTCs (mean±SD) among different failure types were 110.89±84.69, 105.67±50.77, 73.31±37.82 and 59.11±54.09 in lung metastasis, second primary tumor, extrapulmonary metastasis and locoregional recurrence respectively and significantly different (P = 0.049). Also, CTC numbers between first cancer (baseline at diagnosis) and second primary tumor were different (P = 0.004). Conclusion: CTCs numbers are significantly higher in true recurrence than the biopsy-negative group when a patient had a lesion suspected to be a recurrence. CTC test may be useful to help distinguish true recurrence in HNSCC patients after curative therapy. Citation Format: Jason Chia-Hsun Hsieh, Ting-Hsiuan Yeh, Hung-Ming Wang, Yung-Chang Lin, Nina Ming-Jung Lin, Siou-Ru Ye, Jane Ying-Chieh Lee, Min-Hsien Wu. Circulating tumor cells at disease recurrence in patients with head and neck cancer after curative therapy [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 3790. doi:10.1158/1538-7445.AM2017-3790
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2017
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
    Location Call Number Limitation Availability
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  • 2
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2012
    In:  Cancer Research Vol. 72, No. 8_Supplement ( 2012-04-15), p. 2383-2383
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 72, No. 8_Supplement ( 2012-04-15), p. 2383-2383
    Abstract: The number of circulating tumor cells (CTCs) has been demonstrated as a good indicator for cancer progression and for monitoring treatment response of cancer patients. Most of the current methods for detecting CTCs were based on positive selection using the antibody specific to epithelial cell surface marker. In this study, we established a novel PowerMag system for negative selection and enrichment of CTCs by depletion of CD45+ cells. The efficacy of PowerMag system in CTCs isolation was first analyzed by spiking prostatic PC3 cancer cells into the peripheral blood from healthy volunteers. Our data revealed that, when compared with the methods that have been reported, the PowerMag system had high sensitivity (6-7 log10 enrichment), comparable recovery rate (50-60%), broad detection range (more than 3 log10), and stable and reproducible experimental results (r2=0.999). Notably, the cancer cells obtained from PowerMag system were label-free and viable with the capability for proliferation. To validate the feasibility of PowerMag system in clinical application, the numbers and characteristics of CTCs from 38 metastatic cancer patients with a total of 175 blood samples were determined. At least two populations of CTCs with the surface markers of EpCAM+CD45−CD146− and EpCAM−CD45−CD146− were identified. The detection rate reached 100% for the patients in the baseline level before treatment. The change in CTCs numbers for both cell populations appears to correlate with patient clinical outcomes after chemotherapy. As a whole, the PowerMag system is proven to be capable of isolating CTCs from whole blood effectively and economically, by which time- consuming sample pretreatment and costly equipments are not required. PowerMag has paved an alternation rout to monitor the progression and treatment response of cancer patients. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 2383. doi:1538-7445.AM2012-2383
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2012
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
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