18F-FDG PET for assessment of therapy response and preoperative re-evaluation after neoadjuvant radio-chemotherapy in stage III non-small cell lung cancer
The aim of this study was to evaluate FDG-PET for assessment of therapy response and for prediction of patient outcome after neo-adjuvant radio-chemotherapy (NARCT) of advanced non-small cell lung cancer (NSCLC). Seventy patients with histologically proven stage III NSCLC underwent FDG-PET investiga...
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Veröffentlicht in: | European journal of nuclear medicine and molecular imaging 2007-04, Vol.34 (4), p.463-471 |
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creator | Eschmann, Susanne Martina Friedel, Godehard Paulsen, Frank Reimold, Matthias Hehr, Thomas Budach, Wilfried Langen, Heinz-Jakob Bares, Roland |
description | The aim of this study was to evaluate FDG-PET for assessment of therapy response and for prediction of patient outcome after neo-adjuvant radio-chemotherapy (NARCT) of advanced non-small cell lung cancer (NSCLC).
Seventy patients with histologically proven stage III NSCLC underwent FDG-PET investigations before and after NARCT. Changes in FDG uptake and PET findings after completion of NARCT were compared with (1) the histology of tumour samples obtained at surgery or repeat mediastinoscopy, and (2) treatment results in terms of achieved operability and long-term survival.
The mean average FDG uptake of the primary tumours in the patient group decreased significantly during NARCT (p = 0.004). Sensitivity, specificity and overall accuracy of FDG-PET were 94.5%, 80% and 91%, respectively, for the detection of residual viable primary tumour, and 77%, 68% and 73%, respectively, for the presence of lymph node metastases. A negative PET scan or a reduction in the standardised uptake value (SUV) of more than 80% was the best predictive factor for a favourable outcome of further treatment. Progressive disease according to PET (new tumour manifestations or increasing SUV) was significantly correlated with an unfavourable outcome (p = 0.005). In this subgroup, survival of patients who underwent surgery was not significantly different from survival among those who did not undergo surgery, whereas for the whole patient group, complete tumour resection had a significant influence on outcome.
FDG-PET is suitable to assess response to NARCT in patients with stage III NSCLC accurately. It was highly predictive for treatment outcome and patient survival. PET may be helpful in improving restaging after NARCT by allowing reliable assessment of residual tumour viability. |
doi_str_mv | 10.1007/s00259-006-0273-5 |
format | Article |
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Seventy patients with histologically proven stage III NSCLC underwent FDG-PET investigations before and after NARCT. Changes in FDG uptake and PET findings after completion of NARCT were compared with (1) the histology of tumour samples obtained at surgery or repeat mediastinoscopy, and (2) treatment results in terms of achieved operability and long-term survival.
The mean average FDG uptake of the primary tumours in the patient group decreased significantly during NARCT (p = 0.004). Sensitivity, specificity and overall accuracy of FDG-PET were 94.5%, 80% and 91%, respectively, for the detection of residual viable primary tumour, and 77%, 68% and 73%, respectively, for the presence of lymph node metastases. A negative PET scan or a reduction in the standardised uptake value (SUV) of more than 80% was the best predictive factor for a favourable outcome of further treatment. Progressive disease according to PET (new tumour manifestations or increasing SUV) was significantly correlated with an unfavourable outcome (p = 0.005). In this subgroup, survival of patients who underwent surgery was not significantly different from survival among those who did not undergo surgery, whereas for the whole patient group, complete tumour resection had a significant influence on outcome.
FDG-PET is suitable to assess response to NARCT in patients with stage III NSCLC accurately. It was highly predictive for treatment outcome and patient survival. PET may be helpful in improving restaging after NARCT by allowing reliable assessment of residual tumour viability.</description><identifier>ISSN: 1619-7070</identifier><identifier>EISSN: 1619-7089</identifier><identifier>DOI: 10.1007/s00259-006-0273-5</identifier><identifier>PMID: 17103167</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Adult ; Aged ; Carcinoma, Non-Small-Cell Lung - diagnostic imaging ; Carcinoma, Non-Small-Cell Lung - mortality ; Carcinoma, Non-Small-Cell Lung - therapy ; Chemotherapy ; Chemotherapy, Adjuvant - mortality ; Diagnostics ; Female ; Fluorodeoxyglucose F18 ; Germany - epidemiology ; Humans ; Lung cancer ; Lung Neoplasms - diagnostic imaging ; Lung Neoplasms - mortality ; Lung Neoplasms - secondary ; Lung Neoplasms - therapy ; Lymphatic Metastasis ; Male ; Medical imaging ; Middle Aged ; Neoadjuvant Therapy ; Neoplasm Staging - methods ; Positron-Emission Tomography - statistics & numerical data ; Preoperative Care - statistics & numerical data ; Prevalence ; Prognosis ; Radiopharmaceuticals ; Radiotherapy, Adjuvant - mortality ; Risk Assessment - methods ; Risk Factors ; Survival Analysis ; Survival Rate ; Tomography ; Treatment Outcome</subject><ispartof>European journal of nuclear medicine and molecular imaging, 2007-04, Vol.34 (4), p.463-471</ispartof><rights>Springer-Verlag 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2377-b7f9dbffbf1f4ee0e8f4a48ca5d7c0dae2ab3c06f3e31ccea77b153fc15bc5e3</citedby><cites>FETCH-LOGICAL-c2377-b7f9dbffbf1f4ee0e8f4a48ca5d7c0dae2ab3c06f3e31ccea77b153fc15bc5e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17103167$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Eschmann, Susanne Martina</creatorcontrib><creatorcontrib>Friedel, Godehard</creatorcontrib><creatorcontrib>Paulsen, Frank</creatorcontrib><creatorcontrib>Reimold, Matthias</creatorcontrib><creatorcontrib>Hehr, Thomas</creatorcontrib><creatorcontrib>Budach, Wilfried</creatorcontrib><creatorcontrib>Langen, Heinz-Jakob</creatorcontrib><creatorcontrib>Bares, Roland</creatorcontrib><title>18F-FDG PET for assessment of therapy response and preoperative re-evaluation after neoadjuvant radio-chemotherapy in stage III non-small cell lung cancer</title><title>European journal of nuclear medicine and molecular imaging</title><addtitle>Eur J Nucl Med Mol Imaging</addtitle><description>The aim of this study was to evaluate FDG-PET for assessment of therapy response and for prediction of patient outcome after neo-adjuvant radio-chemotherapy (NARCT) of advanced non-small cell lung cancer (NSCLC).
Seventy patients with histologically proven stage III NSCLC underwent FDG-PET investigations before and after NARCT. Changes in FDG uptake and PET findings after completion of NARCT were compared with (1) the histology of tumour samples obtained at surgery or repeat mediastinoscopy, and (2) treatment results in terms of achieved operability and long-term survival.
The mean average FDG uptake of the primary tumours in the patient group decreased significantly during NARCT (p = 0.004). Sensitivity, specificity and overall accuracy of FDG-PET were 94.5%, 80% and 91%, respectively, for the detection of residual viable primary tumour, and 77%, 68% and 73%, respectively, for the presence of lymph node metastases. A negative PET scan or a reduction in the standardised uptake value (SUV) of more than 80% was the best predictive factor for a favourable outcome of further treatment. Progressive disease according to PET (new tumour manifestations or increasing SUV) was significantly correlated with an unfavourable outcome (p = 0.005). In this subgroup, survival of patients who underwent surgery was not significantly different from survival among those who did not undergo surgery, whereas for the whole patient group, complete tumour resection had a significant influence on outcome.
FDG-PET is suitable to assess response to NARCT in patients with stage III NSCLC accurately. It was highly predictive for treatment outcome and patient survival. PET may be helpful in improving restaging after NARCT by allowing reliable assessment of residual tumour viability.</description><subject>Adult</subject><subject>Aged</subject><subject>Carcinoma, Non-Small-Cell Lung - diagnostic imaging</subject><subject>Carcinoma, Non-Small-Cell Lung - mortality</subject><subject>Carcinoma, Non-Small-Cell Lung - therapy</subject><subject>Chemotherapy</subject><subject>Chemotherapy, Adjuvant - mortality</subject><subject>Diagnostics</subject><subject>Female</subject><subject>Fluorodeoxyglucose F18</subject><subject>Germany - epidemiology</subject><subject>Humans</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - diagnostic imaging</subject><subject>Lung Neoplasms - mortality</subject><subject>Lung Neoplasms - secondary</subject><subject>Lung Neoplasms - therapy</subject><subject>Lymphatic Metastasis</subject><subject>Male</subject><subject>Medical imaging</subject><subject>Middle Aged</subject><subject>Neoadjuvant Therapy</subject><subject>Neoplasm Staging - methods</subject><subject>Positron-Emission Tomography - statistics & numerical data</subject><subject>Preoperative Care - statistics & numerical data</subject><subject>Prevalence</subject><subject>Prognosis</subject><subject>Radiopharmaceuticals</subject><subject>Radiotherapy, Adjuvant - mortality</subject><subject>Risk Assessment - methods</subject><subject>Risk Factors</subject><subject>Survival Analysis</subject><subject>Survival Rate</subject><subject>Tomography</subject><subject>Treatment Outcome</subject><issn>1619-7070</issn><issn>1619-7089</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpdkcFu1DAQhi0EoqXwAFyQxYGbYRwncXJEbbddqRIc9m5NnHGbVWIHO1mpr9KnxatdQOIynrH__9dYH2MfJXyVAPpbAiiqVgDUAgqtRPWKXcpatkJD077-22u4YO9S2gPIpmjat-xCaglK1vqSvchmIzY3d_zn7Y67EDmmRClN5BceHF-eKOL8zCOlOfhEHH3P50hhzvfLcKD8IuiA45qn4Dm6hSL3FLDfrwfMIRH7IQj7RFP4EzZ4nhZ8JL7dbrkPXqQJx5FbymVc_SO36C3F9-yNwzHRh_N5xXab2931vXj4cbe9_v4gbKG0Fp12bd851znpSiKgxpVYNharXlvokQrslIXaKVLSWkKtO1kpZ2XV2YrUFftyip1j-LVSWsw0pOMumL-xJqOhqAtVlVn4-T_hPqzR59VMIcu6BqVVFsmTyMaQUiRn5jhMGJ-NBHOEZk7QTIZmjtBMlT2fzsFrN1H_z3GmpH4DWP-VmA</recordid><startdate>200704</startdate><enddate>200704</enddate><creator>Eschmann, Susanne Martina</creator><creator>Friedel, Godehard</creator><creator>Paulsen, Frank</creator><creator>Reimold, Matthias</creator><creator>Hehr, Thomas</creator><creator>Budach, Wilfried</creator><creator>Langen, Heinz-Jakob</creator><creator>Bares, Roland</creator><general>Springer Nature B.V</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>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>200704</creationdate><title>18F-FDG PET for assessment of therapy response and preoperative re-evaluation after neoadjuvant radio-chemotherapy in stage III non-small cell lung cancer</title><author>Eschmann, Susanne Martina ; Friedel, Godehard ; Paulsen, Frank ; Reimold, Matthias ; Hehr, Thomas ; Budach, Wilfried ; Langen, Heinz-Jakob ; Bares, Roland</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2377-b7f9dbffbf1f4ee0e8f4a48ca5d7c0dae2ab3c06f3e31ccea77b153fc15bc5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Carcinoma, Non-Small-Cell Lung - diagnostic imaging</topic><topic>Carcinoma, Non-Small-Cell Lung - mortality</topic><topic>Carcinoma, Non-Small-Cell Lung - therapy</topic><topic>Chemotherapy</topic><topic>Chemotherapy, Adjuvant - mortality</topic><topic>Diagnostics</topic><topic>Female</topic><topic>Fluorodeoxyglucose F18</topic><topic>Germany - epidemiology</topic><topic>Humans</topic><topic>Lung cancer</topic><topic>Lung Neoplasms - diagnostic imaging</topic><topic>Lung Neoplasms - mortality</topic><topic>Lung Neoplasms - secondary</topic><topic>Lung Neoplasms - therapy</topic><topic>Lymphatic Metastasis</topic><topic>Male</topic><topic>Medical imaging</topic><topic>Middle Aged</topic><topic>Neoadjuvant Therapy</topic><topic>Neoplasm Staging - methods</topic><topic>Positron-Emission Tomography - statistics & numerical data</topic><topic>Preoperative Care - statistics & numerical data</topic><topic>Prevalence</topic><topic>Prognosis</topic><topic>Radiopharmaceuticals</topic><topic>Radiotherapy, Adjuvant - mortality</topic><topic>Risk Assessment - 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Academic</collection><jtitle>European journal of nuclear medicine and molecular imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Eschmann, Susanne Martina</au><au>Friedel, Godehard</au><au>Paulsen, Frank</au><au>Reimold, Matthias</au><au>Hehr, Thomas</au><au>Budach, Wilfried</au><au>Langen, Heinz-Jakob</au><au>Bares, Roland</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>18F-FDG PET for assessment of therapy response and preoperative re-evaluation after neoadjuvant radio-chemotherapy in stage III non-small cell lung cancer</atitle><jtitle>European journal of nuclear medicine and molecular imaging</jtitle><addtitle>Eur J Nucl Med Mol Imaging</addtitle><date>2007-04</date><risdate>2007</risdate><volume>34</volume><issue>4</issue><spage>463</spage><epage>471</epage><pages>463-471</pages><issn>1619-7070</issn><eissn>1619-7089</eissn><abstract>The aim of this study was to evaluate FDG-PET for assessment of therapy response and for prediction of patient outcome after neo-adjuvant radio-chemotherapy (NARCT) of advanced non-small cell lung cancer (NSCLC).
Seventy patients with histologically proven stage III NSCLC underwent FDG-PET investigations before and after NARCT. Changes in FDG uptake and PET findings after completion of NARCT were compared with (1) the histology of tumour samples obtained at surgery or repeat mediastinoscopy, and (2) treatment results in terms of achieved operability and long-term survival.
The mean average FDG uptake of the primary tumours in the patient group decreased significantly during NARCT (p = 0.004). Sensitivity, specificity and overall accuracy of FDG-PET were 94.5%, 80% and 91%, respectively, for the detection of residual viable primary tumour, and 77%, 68% and 73%, respectively, for the presence of lymph node metastases. A negative PET scan or a reduction in the standardised uptake value (SUV) of more than 80% was the best predictive factor for a favourable outcome of further treatment. Progressive disease according to PET (new tumour manifestations or increasing SUV) was significantly correlated with an unfavourable outcome (p = 0.005). In this subgroup, survival of patients who underwent surgery was not significantly different from survival among those who did not undergo surgery, whereas for the whole patient group, complete tumour resection had a significant influence on outcome.
FDG-PET is suitable to assess response to NARCT in patients with stage III NSCLC accurately. It was highly predictive for treatment outcome and patient survival. PET may be helpful in improving restaging after NARCT by allowing reliable assessment of residual tumour viability.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>17103167</pmid><doi>10.1007/s00259-006-0273-5</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Aged Carcinoma, Non-Small-Cell Lung - diagnostic imaging Carcinoma, Non-Small-Cell Lung - mortality Carcinoma, Non-Small-Cell Lung - therapy Chemotherapy Chemotherapy, Adjuvant - mortality Diagnostics Female Fluorodeoxyglucose F18 Germany - epidemiology Humans Lung cancer Lung Neoplasms - diagnostic imaging Lung Neoplasms - mortality Lung Neoplasms - secondary Lung Neoplasms - therapy Lymphatic Metastasis Male Medical imaging Middle Aged Neoadjuvant Therapy Neoplasm Staging - methods Positron-Emission Tomography - statistics & numerical data Preoperative Care - statistics & numerical data Prevalence Prognosis Radiopharmaceuticals Radiotherapy, Adjuvant - mortality Risk Assessment - methods Risk Factors Survival Analysis Survival Rate Tomography Treatment Outcome |
title | 18F-FDG PET for assessment of therapy response and preoperative re-evaluation after neoadjuvant radio-chemotherapy in stage III non-small cell lung cancer |
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