Value of serum calcitonin estimation in clinical oncology
In 132 consecutive patients with carcinoma of various organs, a higher serum immunoreactive calcitonin (ICT) concentration (median level 50 pg/ml) was found than in 68 normal subjects (median level 20 pg/ml). The incidence of hypercalcitoninaemia was 40%. All 9 patients with primary liver-cell carci...
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Veröffentlicht in: | British journal of cancer 1981-06, Vol.43 (6), p.786-792 |
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description | In 132 consecutive patients with carcinoma of various organs, a higher serum immunoreactive calcitonin (ICT) concentration (median level 50 pg/ml) was found than in 68 normal subjects (median level 20 pg/ml). The incidence of hypercalcitoninaemia was 40%. All 9 patients with primary liver-cell carcinoma were hypercalcitoninaemic. On the other hand, none of the 7 patients with a carcinoma of the breast had raised ICT levels. In bronchogenic cancer a relationship between ICT and cell type was found, with a predominance of high ICT in patients with oatcell and other undifferentiated types, whereas in squamous-cell carcinomas and adenocarcinomas of the lung hypercalcitoninaemia was relatively rare. When we divided all our patients according to differentiation of the tumour cell, it was found that the lower the degree of differentiation, the higher the ICT concentration, whereas opposite results were observed for CEA. When ICT and CEA were estimated concurrently, we found at least one marker increased in 70% of our patients. Our results demonstrate that patients with metastases in the liver have more frequently and increased ICT. In addition, we conclude that lifespan can be expected to be lower in patients with high ICT levels. In a longitudinal study of 46 patients, there was a positive correlation between change in serum ICT and tumour mass. |
doi_str_mv | 10.1038/bjc.1981.116 |
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The incidence of hypercalcitoninaemia was 40%. All 9 patients with primary liver-cell carcinoma were hypercalcitoninaemic. On the other hand, none of the 7 patients with a carcinoma of the breast had raised ICT levels. In bronchogenic cancer a relationship between ICT and cell type was found, with a predominance of high ICT in patients with oatcell and other undifferentiated types, whereas in squamous-cell carcinomas and adenocarcinomas of the lung hypercalcitoninaemia was relatively rare. When we divided all our patients according to differentiation of the tumour cell, it was found that the lower the degree of differentiation, the higher the ICT concentration, whereas opposite results were observed for CEA. When ICT and CEA were estimated concurrently, we found at least one marker increased in 70% of our patients. Our results demonstrate that patients with metastases in the liver have more frequently and increased ICT. In addition, we conclude that lifespan can be expected to be lower in patients with high ICT levels. In a longitudinal study of 46 patients, there was a positive correlation between change in serum ICT and tumour mass.</description><identifier>ISSN: 0007-0920</identifier><identifier>EISSN: 1532-1827</identifier><identifier>DOI: 10.1038/bjc.1981.116</identifier><identifier>PMID: 7248159</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>Aged ; Biomedical and Life Sciences ; Biomedicine ; Calcitonin - blood ; Cancer Research ; Carcinoembryonic Antigen - metabolism ; Carcinoma, Bronchogenic - blood ; Drug Resistance ; Epidemiology ; Female ; Humans ; Liver Neoplasms - blood ; Liver Neoplasms - secondary ; Lung Neoplasms - blood ; Male ; Molecular Medicine ; Neoplasms - blood ; Neoplasms - therapy ; Oncology ; original-article ; Prognosis</subject><ispartof>British journal of cancer, 1981-06, Vol.43 (6), p.786-792</ispartof><rights>Cancer Research Campaign 1981</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-703aa8a771472f730df5062c17213e788cd87115f96be0024aaa279dcb24edd53</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010708/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2010708/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27903,27904,41467,42536,51298,53770,53772</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7248159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mulder, H</creatorcontrib><creatorcontrib>Hackeng, W H</creatorcontrib><creatorcontrib>Silberbusch, J</creatorcontrib><creatorcontrib>den Ottolander, G J</creatorcontrib><creatorcontrib>van der Meer, C</creatorcontrib><title>Value of serum calcitonin estimation in clinical oncology</title><title>British journal of cancer</title><addtitle>Br J Cancer</addtitle><addtitle>Br J Cancer</addtitle><description>In 132 consecutive patients with carcinoma of various organs, a higher serum immunoreactive calcitonin (ICT) concentration (median level 50 pg/ml) was found than in 68 normal subjects (median level 20 pg/ml). The incidence of hypercalcitoninaemia was 40%. All 9 patients with primary liver-cell carcinoma were hypercalcitoninaemic. On the other hand, none of the 7 patients with a carcinoma of the breast had raised ICT levels. In bronchogenic cancer a relationship between ICT and cell type was found, with a predominance of high ICT in patients with oatcell and other undifferentiated types, whereas in squamous-cell carcinomas and adenocarcinomas of the lung hypercalcitoninaemia was relatively rare. When we divided all our patients according to differentiation of the tumour cell, it was found that the lower the degree of differentiation, the higher the ICT concentration, whereas opposite results were observed for CEA. When ICT and CEA were estimated concurrently, we found at least one marker increased in 70% of our patients. Our results demonstrate that patients with metastases in the liver have more frequently and increased ICT. In addition, we conclude that lifespan can be expected to be lower in patients with high ICT levels. In a longitudinal study of 46 patients, there was a positive correlation between change in serum ICT and tumour mass.</description><subject>Aged</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Calcitonin - blood</subject><subject>Cancer Research</subject><subject>Carcinoembryonic Antigen - metabolism</subject><subject>Carcinoma, Bronchogenic - blood</subject><subject>Drug Resistance</subject><subject>Epidemiology</subject><subject>Female</subject><subject>Humans</subject><subject>Liver Neoplasms - blood</subject><subject>Liver Neoplasms - secondary</subject><subject>Lung Neoplasms - blood</subject><subject>Male</subject><subject>Molecular Medicine</subject><subject>Neoplasms - blood</subject><subject>Neoplasms - therapy</subject><subject>Oncology</subject><subject>original-article</subject><subject>Prognosis</subject><issn>0007-0920</issn><issn>1532-1827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVJSDZpb70GfMqp3s5IsiVdAiU0HxDope1VyLK81eKVEskO7L-Pwi5LAoWcxPA-vMzoIeQrwhKBye_d2i5RSVwitp_IAhtGa5RUHJEFAIgaFIVTcpbzuowKpDghJ4JyiY1aEPXXjLOr4lBll-ZNZc1o_RSDD5XLk9-YycdQlcmOPviSVjHYOMbV9jM5HsyY3Zf9e07-3Pz8fX1XP_y6vb_-8VBbzuVUC2DGSCMEckEHwaAfGmipRUGROSGl7aVAbAbVdg6AcmMMFaq3HeWu7xt2Tq52vY9zt3G9dWFKZtSPqSyXtjoar98nwf_Tq_isKSAIkKXgcl-Q4tNcrtIbn60bRxNcnLMWrOENp-xDEBveKsXaAn7bgTbFnJMbDtsg6FcnujjRr050cVLwi7cXHOC9hJLXuzyXJKxc0us4p1A-9f99LwqLlqg</recordid><startdate>19810601</startdate><enddate>19810601</enddate><creator>Mulder, H</creator><creator>Hackeng, W H</creator><creator>Silberbusch, J</creator><creator>den Ottolander, G J</creator><creator>van der Meer, C</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19810601</creationdate><title>Value of serum calcitonin estimation in clinical oncology</title><author>Mulder, H ; Hackeng, W H ; Silberbusch, J ; den Ottolander, G J ; van der Meer, C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-703aa8a771472f730df5062c17213e788cd87115f96be0024aaa279dcb24edd53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><topic>Aged</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Calcitonin - blood</topic><topic>Cancer Research</topic><topic>Carcinoembryonic Antigen - metabolism</topic><topic>Carcinoma, Bronchogenic - blood</topic><topic>Drug Resistance</topic><topic>Epidemiology</topic><topic>Female</topic><topic>Humans</topic><topic>Liver Neoplasms - blood</topic><topic>Liver Neoplasms - secondary</topic><topic>Lung Neoplasms - blood</topic><topic>Male</topic><topic>Molecular Medicine</topic><topic>Neoplasms - blood</topic><topic>Neoplasms - therapy</topic><topic>Oncology</topic><topic>original-article</topic><topic>Prognosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mulder, H</creatorcontrib><creatorcontrib>Hackeng, W H</creatorcontrib><creatorcontrib>Silberbusch, J</creatorcontrib><creatorcontrib>den Ottolander, G J</creatorcontrib><creatorcontrib>van der Meer, C</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>British journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mulder, H</au><au>Hackeng, W H</au><au>Silberbusch, J</au><au>den Ottolander, G J</au><au>van der Meer, C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Value of serum calcitonin estimation in clinical oncology</atitle><jtitle>British journal of cancer</jtitle><stitle>Br J Cancer</stitle><addtitle>Br J Cancer</addtitle><date>1981-06-01</date><risdate>1981</risdate><volume>43</volume><issue>6</issue><spage>786</spage><epage>792</epage><pages>786-792</pages><issn>0007-0920</issn><eissn>1532-1827</eissn><abstract>In 132 consecutive patients with carcinoma of various organs, a higher serum immunoreactive calcitonin (ICT) concentration (median level 50 pg/ml) was found than in 68 normal subjects (median level 20 pg/ml). The incidence of hypercalcitoninaemia was 40%. All 9 patients with primary liver-cell carcinoma were hypercalcitoninaemic. On the other hand, none of the 7 patients with a carcinoma of the breast had raised ICT levels. In bronchogenic cancer a relationship between ICT and cell type was found, with a predominance of high ICT in patients with oatcell and other undifferentiated types, whereas in squamous-cell carcinomas and adenocarcinomas of the lung hypercalcitoninaemia was relatively rare. When we divided all our patients according to differentiation of the tumour cell, it was found that the lower the degree of differentiation, the higher the ICT concentration, whereas opposite results were observed for CEA. When ICT and CEA were estimated concurrently, we found at least one marker increased in 70% of our patients. Our results demonstrate that patients with metastases in the liver have more frequently and increased ICT. In addition, we conclude that lifespan can be expected to be lower in patients with high ICT levels. In a longitudinal study of 46 patients, there was a positive correlation between change in serum ICT and tumour mass.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>7248159</pmid><doi>10.1038/bjc.1981.116</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Biomedical and Life Sciences Biomedicine Calcitonin - blood Cancer Research Carcinoembryonic Antigen - metabolism Carcinoma, Bronchogenic - blood Drug Resistance Epidemiology Female Humans Liver Neoplasms - blood Liver Neoplasms - secondary Lung Neoplasms - blood Male Molecular Medicine Neoplasms - blood Neoplasms - therapy Oncology original-article Prognosis |
title | Value of serum calcitonin estimation in clinical oncology |
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