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首页> 外文期刊>Clinical Chemistry >National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines for Use of Tumor Markers in Liver, Bladder, Cervical, and Gastric Cancers
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National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines for Use of Tumor Markers in Liver, Bladder, Cervical, and Gastric Cancers

机译:美国国家生物化学临床化学实验室医学实践指南在肝癌,膀胱癌,宫颈癌和胃癌中使用肿瘤标志物

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摘要

Updated National Academy of Clinical Biochemistry Laboratory Medicine Practice Guidelines for the use of tumor markers in the clinic have been developed. Published reports relevant to use of tumor markers for 4 cancer sites-liver, bladder, cervical, and gastric-were critically reviewed. α-Fetoprotein (AFP) may be used in conjunction with abdominal ultrasound for early detection of hepatocellular carcinoma (HCC) in patients with chronic hepatitis or cirrhosis associated with hepatitis B or C virus infection. AFP concentrations >200 µg/L in cirrhotic patients with typical hypervascular lesions >2 cmin size are consistent with HCC. After a diagnosis of HCC, posttreatment monitoring with AFP is recommended as an adjunct to imaging, especially in the absence of measurable disease. Although several urine markers have been proposed for bladder cancer, none at present can replace routine cystoscopy and cytology in the management of patients with this malignancy. Some may, however, be used as complementary adjuncts to direct more effective use of clinical procedures. Although carcinoembryonic antigen and CA 19-9 have been proposed for use gastric cancer and squamous cell carcinoma antigen for use in cervical cancer, none of these markers can currently be recommended for routine clinical use. Implementation of these recommendations should encourage optimal use of tumor markers for patients with liver, bladder, cervical, or gastric cancers.
机译:已经制定了有关临床中使用肿瘤标志物的最新的《国家临床生物化学临床医学实验医学实践指南》。严格审查了已发表的有关在四个癌症部位(肝脏,膀胱癌,宫颈癌和胃癌)使用肿瘤标志物的报道。 α-甲胎蛋白(AFP)可与腹部超声结合使用,以早期发现患有乙型或丙型肝炎病毒感染的慢性肝炎或肝硬化患者的肝细胞癌(HCC)。典型肝血管病变大于2 cmin的肝硬化患者中AFP浓度> 200 µg / L与HCC一致。在诊断出肝癌后,建议使用AFP进行治疗后监测作为影像学的辅助手段,尤其是在没有可测量的疾病的情况下。尽管已经提出了几种用于膀胱癌的尿液标记物,但是在治疗这种恶性肿瘤的患者中,目前没有一种可以代替常规的膀胱镜检查和细胞学检查。但是,有些可以用作辅助手段,以指导更有效地使用临床程序。尽管已提出癌胚抗原和CA 19-9用于胃癌和鳞状细胞癌抗原用于宫颈癌,但目前尚不推荐将这些标记物推荐用于常规临床。这些建议的实施应鼓励肝癌,膀胱癌,宫颈癌或胃癌患者最佳使用肿瘤标志物。

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    《Clinical Chemistry》 |2010年第6期|p.1-49|共49页
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    Catharine M. Sturgeon,1* Michael J. Duffy,2 Barry R. Hofmann,3 Rolf Lamerz,4 Herbert A. Fritsche,5 Katja Gaarenstroom,6 Johannes Bonfrer,7 Thorsten H. Ecke,8 H. Barton Grossman,9 Peter Hayes,10 Ralf-Thorsten Hoffmann,11 Seth P. Lerner,12 Florian Löhe,13 Johanna Louhimo,14 Ihor Sawczuk,15 Kazuhisa Taketa,16 and Eleftherios P. Diamandis3NACB SUB-COMMITTEE MEMBERSLiver Cancer: Rolf Lamerz, Chair, Peter Hayes, Ralf-Thorsten Hoffmann, Florian Löhe, and Kazuhisa Taketa, Bladder Cancer: Herbert A. Fritsche, Chair, Thorsten H. Ecke, H. Barton Grossman, Seth P. Lerner, and Ihor Sawczuk, Cervical Cancer: Katja Gaarenstroom, Chair, Johannes Bonfrer, Gastric Cancer: Johannes Bonfrer, Chair, and Johanna Louhimo1 Department of Clinical Biochemistry, Royal Infirmary of Edinburgh, Edinburgh, UK, 2 Department of Pathology and Laboratory Medicine, St Vincent's University Hospital and UCD School of Medicine and Medical Science, Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland, 3 Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, and Department of Laboratory Medicine and Pathobiology, University of Toronto, Ontario, Canada, 4 Department of Medicine, LMU-Klinikum- Grosshadern, University of Munich, Germany, 5 Department of Laboratory Medicine, the University of Texas M. D. Anderson Cancer Center, Houston, TX, 6 Department of Gynecology, Leiden University Medical Center, Leiden, the Netherlands, 7 Department of Clinical Chemistry, Netherlands Cancer Institute, Amsterdam, the Netherlands, 8 Department of Urology, Helios Hospital, Bad Saarow, Germany, 9 Department of Urology, the University of Texas M. D. Anderson Cancer Center, Houston, TX, 10 Scottish Liver Transplant Unit, Department of Medicine, Royal Infirmary of Edinburgh, Edinburgh, UK, 11 Department of Clinical Radiology, LMU-Klinikum-Grosshadern, University of Munich, Germany, 12 Department of Surgery, LMU-Klinikum-Grosshadern, University of Munich, Germany, 13 Department of Urology, Baylor College of Medicine, Houston, Texas, 14 Department of Clinical Chemistry, Helsinki University Central Hospital, Finland, 15 Department of Urology, Hackensack University Medical Center, Hackensack, New Jersey,16 Clinical Trial Center, Brain Attack Center, Oota Memorial Hospital, Fukuyama, Japan.* Address correspondence to this author at: the Department of Clinical Biochemistry, Royal Infirmary, Edinburgh EH16 4SA, UK. Fax µ44-1311-242-6882, e-mail C.Sturgeon@ed.ac.uk.Received July 3, 2009, accepted December 11, 2009.Previously published online at DOI: 10.1373/clinchem.2009.133124Author Contributions: All authors confirmed they have contributed to the intellectual content of this paper and have met the following 3 requirements: (a) significant contributions to the conception and design, acquisition of data, or analysis and interpretation of data, (b) drafting or revising the article for intellectual content, and (c) final approval of the published article.Authors' Disclosures of Potential Conflicts of Interest: Upon manuscript submission, all authors completed the Disclosures of Potential Conflict of Interest form. Potential conflicts of interest:Employment or Leadership: H.A. Fritsche, MD Anderson Cancer Center.Consultant or Advisory Role: H.A. Fritsche, Tosoh, Gen Probe, Cepheid, OncImmune, and Health Discovery Corp, J. Bonfrer, Dia- Genic ASA, H.B. Grossman, Abbott Molecular.Stock Ownership: H.A. Fritsche, Health Discovery Corp and Third Nerve.Honoraria: C.M. Sturgeon, Abbott Diagnostics, Beckman Coulter Diagnostics, Becton Dickinson Diagnostics, DAKO, Roche Diagnostics, Siemens Diagnostics, Tosoh Biosciences, and Wallac Oy, M.J. Duffy, Abbott Diagnostics, H.B. Grossman, Abbott Molecular.Research Funding: M.J. Duffy, Randox Laboratories, H.A. Fritsche, Roche, Tosoh, Veridex, and Oncovista, S. Lerner, Pfizer, Eli Lilly.Expert Testimony: None declared.Role of Sponsor: The funding organizations played no role in the design of study, choice of enrolled patients, review and interpretation of data, or preparation or approval of manuscript.,;

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