Characterizing indeterminate liver lesions in patients with localized pancreatic cancer at the time of diagnosis

Background In patients with newly diagnosed pancreatic cancer, the classification of indeterminate liver lesions is an unanswered clinical dilemma as misclassification of these lesions can impact the assignment of clinical stage and subsequent treatment planning. Our objective was to design a standa...

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Veröffentlicht in:Abdominal imaging 2018-02, Vol.43 (2), p.351-363
Hauptverfasser: Bhalla, Manav, Aldakkak, Mohammed, Kulkarni, Naveen M., O’Connor, Stacy D., Griffin, Michael O., Christians, Kathleen K., Evans, Douglas B., Tsai, Susan, Tolat, Parag P.
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container_end_page 363
container_issue 2
container_start_page 351
container_title Abdominal imaging
container_volume 43
creator Bhalla, Manav
Aldakkak, Mohammed
Kulkarni, Naveen M.
O’Connor, Stacy D.
Griffin, Michael O.
Christians, Kathleen K.
Evans, Douglas B.
Tsai, Susan
Tolat, Parag P.
description Background In patients with newly diagnosed pancreatic cancer, the classification of indeterminate liver lesions is an unanswered clinical dilemma as misclassification of these lesions can impact the assignment of clinical stage and subsequent treatment planning. Our objective was to design a standardized classification system to more accurately define the risk of malignancy in indeterminate liver lesions. Methods In this retrospective study, patients with localized, non-metastatic pancreatic cancer were identified and pre-treatment computed tomography (CT) scans were evaluated for the presence or absence of liver lesions. Liver lesions were defined as definitely benign (1) or indeterminate (2). Indeterminate lesions were further sub-classified as either indeterminate probably benign (2B) or indeterminate possibly malignant (2M). The index liver lesion was evaluated on follow-up imaging for stability or unequivocal disease progression. Results From 2008 to 2015, 304 patients with localized, non-metastatic pancreatic cancer were identified and 125 (41%) patients had liver lesions. Of the 125 patients, the liver lesions in 35 (28%) were classified as definitely benign and in 90 (72%) patients they were classified as indeterminate. The 90 patients with indeterminate lesions included 80 (89%) classified as indeterminate probably benign (2B) and 10 (11%) classified as indeterminate possibly malignant (2M). After a median follow-up of 56 weeks, no patient with a definitely benign lesion had metastatic disease progression of the index lesion. Of the 90 patients with indeterminate liver lesions, the index lesion progressed to unequivocal liver metastasis in 8 (9%) patients; 5 (6%) of the 80 lesions classified as indeterminate probably benign (2B), and 3 (30%) of the ten lesions classified as indeterminate possibly malignant (2M). The sensitivity of the classification system was 38% and the specificity was 91%. The positive predictive value was 30% and the negative predictive value was 94%. Conclusions A significant proportion of patients with localized pancreatic cancer will have liver lesions identified at the time of diagnosis and most of these lesions will have indeterminate characteristics. A classification system which further stratifies indeterminate liver lesions by malignant potential can assist clinicians in determining optimal treatment plan and is associated with a high negative predictive value.
doi_str_mv 10.1007/s00261-017-1404-0
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Our objective was to design a standardized classification system to more accurately define the risk of malignancy in indeterminate liver lesions. Methods In this retrospective study, patients with localized, non-metastatic pancreatic cancer were identified and pre-treatment computed tomography (CT) scans were evaluated for the presence or absence of liver lesions. Liver lesions were defined as definitely benign (1) or indeterminate (2). Indeterminate lesions were further sub-classified as either indeterminate probably benign (2B) or indeterminate possibly malignant (2M). The index liver lesion was evaluated on follow-up imaging for stability or unequivocal disease progression. Results From 2008 to 2015, 304 patients with localized, non-metastatic pancreatic cancer were identified and 125 (41%) patients had liver lesions. Of the 125 patients, the liver lesions in 35 (28%) were classified as definitely benign and in 90 (72%) patients they were classified as indeterminate. The 90 patients with indeterminate lesions included 80 (89%) classified as indeterminate probably benign (2B) and 10 (11%) classified as indeterminate possibly malignant (2M). After a median follow-up of 56 weeks, no patient with a definitely benign lesion had metastatic disease progression of the index lesion. Of the 90 patients with indeterminate liver lesions, the index lesion progressed to unequivocal liver metastasis in 8 (9%) patients; 5 (6%) of the 80 lesions classified as indeterminate probably benign (2B), and 3 (30%) of the ten lesions classified as indeterminate possibly malignant (2M). The sensitivity of the classification system was 38% and the specificity was 91%. The positive predictive value was 30% and the negative predictive value was 94%. Conclusions A significant proportion of patients with localized pancreatic cancer will have liver lesions identified at the time of diagnosis and most of these lesions will have indeterminate characteristics. A classification system which further stratifies indeterminate liver lesions by malignant potential can assist clinicians in determining optimal treatment plan and is associated with a high negative predictive value.</description><identifier>ISSN: 2366-004X</identifier><identifier>EISSN: 2366-0058</identifier><identifier>DOI: 10.1007/s00261-017-1404-0</identifier><identifier>PMID: 29185014</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Benign ; Cancer ; Classification ; Computed tomography ; Design standards ; Diagnosis ; Gastroenterology ; Hepatology ; Imaging ; Lesions ; Liver ; Liver cancer ; Malignancy ; Medical diagnosis ; Medicine ; Medicine &amp; Public Health ; Metastases ; Metastasis ; Pancreatic cancer ; Patients ; Radiology ; Stability analysis</subject><ispartof>Abdominal imaging, 2018-02, Vol.43 (2), p.351-363</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2017</rights><rights>Abdominal Radiology is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-91d202c0b72fc18a3ef2b24a7dbae47b6b9d66abdcb5f74ddc655bf4f1b5241e3</citedby><cites>FETCH-LOGICAL-c372t-91d202c0b72fc18a3ef2b24a7dbae47b6b9d66abdcb5f74ddc655bf4f1b5241e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00261-017-1404-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00261-017-1404-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29185014$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bhalla, Manav</creatorcontrib><creatorcontrib>Aldakkak, Mohammed</creatorcontrib><creatorcontrib>Kulkarni, Naveen M.</creatorcontrib><creatorcontrib>O’Connor, Stacy D.</creatorcontrib><creatorcontrib>Griffin, Michael O.</creatorcontrib><creatorcontrib>Christians, Kathleen K.</creatorcontrib><creatorcontrib>Evans, Douglas B.</creatorcontrib><creatorcontrib>Tsai, Susan</creatorcontrib><creatorcontrib>Tolat, Parag P.</creatorcontrib><title>Characterizing indeterminate liver lesions in patients with localized pancreatic cancer at the time of diagnosis</title><title>Abdominal imaging</title><addtitle>Abdom Radiol</addtitle><addtitle>Abdom Radiol (NY)</addtitle><description>Background In patients with newly diagnosed pancreatic cancer, the classification of indeterminate liver lesions is an unanswered clinical dilemma as misclassification of these lesions can impact the assignment of clinical stage and subsequent treatment planning. Our objective was to design a standardized classification system to more accurately define the risk of malignancy in indeterminate liver lesions. Methods In this retrospective study, patients with localized, non-metastatic pancreatic cancer were identified and pre-treatment computed tomography (CT) scans were evaluated for the presence or absence of liver lesions. Liver lesions were defined as definitely benign (1) or indeterminate (2). Indeterminate lesions were further sub-classified as either indeterminate probably benign (2B) or indeterminate possibly malignant (2M). The index liver lesion was evaluated on follow-up imaging for stability or unequivocal disease progression. Results From 2008 to 2015, 304 patients with localized, non-metastatic pancreatic cancer were identified and 125 (41%) patients had liver lesions. Of the 125 patients, the liver lesions in 35 (28%) were classified as definitely benign and in 90 (72%) patients they were classified as indeterminate. The 90 patients with indeterminate lesions included 80 (89%) classified as indeterminate probably benign (2B) and 10 (11%) classified as indeterminate possibly malignant (2M). After a median follow-up of 56 weeks, no patient with a definitely benign lesion had metastatic disease progression of the index lesion. Of the 90 patients with indeterminate liver lesions, the index lesion progressed to unequivocal liver metastasis in 8 (9%) patients; 5 (6%) of the 80 lesions classified as indeterminate probably benign (2B), and 3 (30%) of the ten lesions classified as indeterminate possibly malignant (2M). The sensitivity of the classification system was 38% and the specificity was 91%. The positive predictive value was 30% and the negative predictive value was 94%. Conclusions A significant proportion of patients with localized pancreatic cancer will have liver lesions identified at the time of diagnosis and most of these lesions will have indeterminate characteristics. A classification system which further stratifies indeterminate liver lesions by malignant potential can assist clinicians in determining optimal treatment plan and is associated with a high negative predictive value.</description><subject>Benign</subject><subject>Cancer</subject><subject>Classification</subject><subject>Computed tomography</subject><subject>Design standards</subject><subject>Diagnosis</subject><subject>Gastroenterology</subject><subject>Hepatology</subject><subject>Imaging</subject><subject>Lesions</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Malignancy</subject><subject>Medical diagnosis</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Pancreatic cancer</subject><subject>Patients</subject><subject>Radiology</subject><subject>Stability analysis</subject><issn>2366-004X</issn><issn>2366-0058</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp1kctqHDEUREVwiI3jD8gmCLzxpp0rtR7TyzDkYTBkk0B2Qo_bMzLd6omkcbC_PjJjm2DwSleqUyWhIuQDg0sGoD8VAK5YB0x3TIDo4A054b1SHYBcHT3P4vcxOSvlBgCYkoxx-Y4c84GtJDBxQnbrrc3WV8zxPqYNjSlg28wx2Yp0ireY6YQlLqk0je5sjZhqoX9j3dJp8XaK9xjaefIZm-ipb2Mz2UrrFmmNM9JlpCHaTVpKLO_J29FOBc8e11Py6-uXn-vv3fWPb1frz9ed7zWv3cACB-7BaT56trI9jtxxYXVwFoV2yg1BKeuCd3LUIgSvpHSjGJmTXDDsT8nFIXeXlz97LNXMsXicJptw2RfDBg1ccyVkQ89foDfLPqf2ukapQfR8AN4odqB8XkrJOJpdjrPNd4aBeWjEHBoxrRHz0IiB5vn4mLx3M4Znx9P_N4AfgNKktMH839Wvpv4Df0yX9A</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Bhalla, Manav</creator><creator>Aldakkak, Mohammed</creator><creator>Kulkarni, Naveen M.</creator><creator>O’Connor, Stacy D.</creator><creator>Griffin, Michael O.</creator><creator>Christians, Kathleen K.</creator><creator>Evans, Douglas B.</creator><creator>Tsai, Susan</creator><creator>Tolat, Parag P.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</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>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K7-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20180201</creationdate><title>Characterizing indeterminate liver lesions in patients with localized pancreatic cancer at the time of diagnosis</title><author>Bhalla, Manav ; 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Our objective was to design a standardized classification system to more accurately define the risk of malignancy in indeterminate liver lesions. Methods In this retrospective study, patients with localized, non-metastatic pancreatic cancer were identified and pre-treatment computed tomography (CT) scans were evaluated for the presence or absence of liver lesions. Liver lesions were defined as definitely benign (1) or indeterminate (2). Indeterminate lesions were further sub-classified as either indeterminate probably benign (2B) or indeterminate possibly malignant (2M). The index liver lesion was evaluated on follow-up imaging for stability or unequivocal disease progression. Results From 2008 to 2015, 304 patients with localized, non-metastatic pancreatic cancer were identified and 125 (41%) patients had liver lesions. Of the 125 patients, the liver lesions in 35 (28%) were classified as definitely benign and in 90 (72%) patients they were classified as indeterminate. The 90 patients with indeterminate lesions included 80 (89%) classified as indeterminate probably benign (2B) and 10 (11%) classified as indeterminate possibly malignant (2M). After a median follow-up of 56 weeks, no patient with a definitely benign lesion had metastatic disease progression of the index lesion. Of the 90 patients with indeterminate liver lesions, the index lesion progressed to unequivocal liver metastasis in 8 (9%) patients; 5 (6%) of the 80 lesions classified as indeterminate probably benign (2B), and 3 (30%) of the ten lesions classified as indeterminate possibly malignant (2M). The sensitivity of the classification system was 38% and the specificity was 91%. The positive predictive value was 30% and the negative predictive value was 94%. Conclusions A significant proportion of patients with localized pancreatic cancer will have liver lesions identified at the time of diagnosis and most of these lesions will have indeterminate characteristics. A classification system which further stratifies indeterminate liver lesions by malignant potential can assist clinicians in determining optimal treatment plan and is associated with a high negative predictive value.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29185014</pmid><doi>10.1007/s00261-017-1404-0</doi><tpages>13</tpages></addata></record>
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subjects Benign
Cancer
Classification
Computed tomography
Design standards
Diagnosis
Gastroenterology
Hepatology
Imaging
Lesions
Liver
Liver cancer
Malignancy
Medical diagnosis
Medicine
Medicine & Public Health
Metastases
Metastasis
Pancreatic cancer
Patients
Radiology
Stability analysis
title Characterizing indeterminate liver lesions in patients with localized pancreatic cancer at the time of diagnosis
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