Machine-Learning Algorithms Using Systemic Inflammatory Markers to Predict the Oncologic Outcomes of Colorectal Cancer After Surgery

Background This study aimed to investigate the clinical significance of machine-learning (ML) algorithms based on serum inflammatory markers to predict survival outcomes for patients with colorectal cancer (CRC). Methods The study included 941 patients with stages I to III CRC. Based on random fores...

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Veröffentlicht in:Annals of surgical oncology 2023-12, Vol.30 (13), p.8717-8726
Hauptverfasser: Yang, Songsoo, Jang, Hyosoon, Park, In Kyu, Lee, Hye Sun, Lee, Kang Young, Oh, Ga Eul, Park, Chihyun, Kang, Jeonghyun
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container_end_page 8726
container_issue 13
container_start_page 8717
container_title Annals of surgical oncology
container_volume 30
creator Yang, Songsoo
Jang, Hyosoon
Park, In Kyu
Lee, Hye Sun
Lee, Kang Young
Oh, Ga Eul
Park, Chihyun
Kang, Jeonghyun
description Background This study aimed to investigate the clinical significance of machine-learning (ML) algorithms based on serum inflammatory markers to predict survival outcomes for patients with colorectal cancer (CRC). Methods The study included 941 patients with stages I to III CRC. Based on random forest algorithms using 15 compositions of inflammatory markers, four different prediction scores (DFS score-1, DFS score-2, DFS score-3, and DFS score-4) were developed for the Yonsei cohort (training set, n = 803) and tested in the Ulsan cohort (test set, n = 138). The Cox proportional hazards model was used to determine correlation between prediction scores and disease-free survival (DFS). Harrell’s concordance index (C-index) was used to compare the predictive ability of prediction scores for each composition. Results The multivariable analysis showed the DFS score-4 to be an independent prognostic factor after adjustment for clinicopathologic factors in both the training and test sets (hazard ratio [HR], 8.98; 95% confidence interval [CI] 6.7–12.04; P < 0.001 for the training set and HR, 2.55; 95% CI 1.1–5.89; P = 0.028 for the test set]. With regard to DFS, the highest C-index among single compositions was observed in the lymphocyte-to-C-reactive protein ratio (LCR) (0.659; 95% CI 0.656–0.662), and the C-index of DFS score-4 (0.727; 95% CI 0.724–0.729) was significantly higher than that of LCR in the test set. The C-index of DFS score-3 (0.725; 95% CI 0.723–0.728) was similar to that of DFS score-4, but higher than that of DFS score-2 (0.680; 95% CI 0.676–0.683). Conclusions The ML-based approaches showed prognostic utility in predicting DFS. They could enhance clinical use of inflammatory markers in patients with CRC.
doi_str_mv 10.1245/s10434-023-14136-5
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Methods The study included 941 patients with stages I to III CRC. Based on random forest algorithms using 15 compositions of inflammatory markers, four different prediction scores (DFS score-1, DFS score-2, DFS score-3, and DFS score-4) were developed for the Yonsei cohort (training set, n = 803) and tested in the Ulsan cohort (test set, n = 138). The Cox proportional hazards model was used to determine correlation between prediction scores and disease-free survival (DFS). Harrell’s concordance index (C-index) was used to compare the predictive ability of prediction scores for each composition. Results The multivariable analysis showed the DFS score-4 to be an independent prognostic factor after adjustment for clinicopathologic factors in both the training and test sets (hazard ratio [HR], 8.98; 95% confidence interval [CI] 6.7–12.04; P &lt; 0.001 for the training set and HR, 2.55; 95% CI 1.1–5.89; P = 0.028 for the test set]. With regard to DFS, the highest C-index among single compositions was observed in the lymphocyte-to-C-reactive protein ratio (LCR) (0.659; 95% CI 0.656–0.662), and the C-index of DFS score-4 (0.727; 95% CI 0.724–0.729) was significantly higher than that of LCR in the test set. The C-index of DFS score-3 (0.725; 95% CI 0.723–0.728) was similar to that of DFS score-4, but higher than that of DFS score-2 (0.680; 95% CI 0.676–0.683). Conclusions The ML-based approaches showed prognostic utility in predicting DFS. They could enhance clinical use of inflammatory markers in patients with CRC.</description><identifier>ISSN: 1068-9265</identifier><identifier>EISSN: 1534-4681</identifier><identifier>DOI: 10.1245/s10434-023-14136-5</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Algorithms ; C-reactive protein ; Colorectal cancer ; Colorectal carcinoma ; Inflammation ; Learning algorithms ; Lymphocytes ; Machine learning ; Medicine ; Medicine &amp; Public Health ; Oncology ; Patients ; Predictions ; Surgery ; Surgical Oncology ; Translational Research</subject><ispartof>Annals of surgical oncology, 2023-12, Vol.30 (13), p.8717-8726</ispartof><rights>Society of Surgical Oncology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c303t-718f094b13546215789dba2036c73a759ae1bbe79890e5c16931f8f8ab8987883</cites><orcidid>0000-0001-7311-6053</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1245/s10434-023-14136-5$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1245/s10434-023-14136-5$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids></links><search><creatorcontrib>Yang, Songsoo</creatorcontrib><creatorcontrib>Jang, Hyosoon</creatorcontrib><creatorcontrib>Park, In Kyu</creatorcontrib><creatorcontrib>Lee, Hye Sun</creatorcontrib><creatorcontrib>Lee, Kang Young</creatorcontrib><creatorcontrib>Oh, Ga Eul</creatorcontrib><creatorcontrib>Park, Chihyun</creatorcontrib><creatorcontrib>Kang, Jeonghyun</creatorcontrib><title>Machine-Learning Algorithms Using Systemic Inflammatory Markers to Predict the Oncologic Outcomes of Colorectal Cancer After Surgery</title><title>Annals of surgical oncology</title><addtitle>Ann Surg Oncol</addtitle><description>Background This study aimed to investigate the clinical significance of machine-learning (ML) algorithms based on serum inflammatory markers to predict survival outcomes for patients with colorectal cancer (CRC). Methods The study included 941 patients with stages I to III CRC. Based on random forest algorithms using 15 compositions of inflammatory markers, four different prediction scores (DFS score-1, DFS score-2, DFS score-3, and DFS score-4) were developed for the Yonsei cohort (training set, n = 803) and tested in the Ulsan cohort (test set, n = 138). The Cox proportional hazards model was used to determine correlation between prediction scores and disease-free survival (DFS). Harrell’s concordance index (C-index) was used to compare the predictive ability of prediction scores for each composition. Results The multivariable analysis showed the DFS score-4 to be an independent prognostic factor after adjustment for clinicopathologic factors in both the training and test sets (hazard ratio [HR], 8.98; 95% confidence interval [CI] 6.7–12.04; P &lt; 0.001 for the training set and HR, 2.55; 95% CI 1.1–5.89; P = 0.028 for the test set]. With regard to DFS, the highest C-index among single compositions was observed in the lymphocyte-to-C-reactive protein ratio (LCR) (0.659; 95% CI 0.656–0.662), and the C-index of DFS score-4 (0.727; 95% CI 0.724–0.729) was significantly higher than that of LCR in the test set. The C-index of DFS score-3 (0.725; 95% CI 0.723–0.728) was similar to that of DFS score-4, but higher than that of DFS score-2 (0.680; 95% CI 0.676–0.683). Conclusions The ML-based approaches showed prognostic utility in predicting DFS. They could enhance clinical use of inflammatory markers in patients with CRC.</description><subject>Algorithms</subject><subject>C-reactive protein</subject><subject>Colorectal cancer</subject><subject>Colorectal carcinoma</subject><subject>Inflammation</subject><subject>Learning algorithms</subject><subject>Lymphocytes</subject><subject>Machine learning</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Oncology</subject><subject>Patients</subject><subject>Predictions</subject><subject>Surgery</subject><subject>Surgical Oncology</subject><subject>Translational Research</subject><issn>1068-9265</issn><issn>1534-4681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kU9LJDEQxZvFBXV2v4CngBcvveZ_J8dhUHdgZAR3ziEdq2fa7U40SR_m7gc3OoLgwUtV8fi9oopXVWcE_yGUi8tEMGe8xpTVhBMma_GjOiGiSFwqclRmLFWtqRTH1WlKjxiThmFxUr3cWrfrPdQrsNH3fovmwzbEPu_GhDbpTbjfpwxj79DSd4MdR5tD3KNbG_9DTCgHdBfhoXcZ5R2gtXdhCNtCr6fswggJhQ4tihbBZTughfUOIpp3udT7KW4h7n9VPzs7JPj90WfV5vrq3-JvvVrfLBfzVe0YZrluiOqw5i1hgktKRKP0Q2spZtI1zDZCWyBtC41WGoNwRGpGOtUp2yqtGqXYrLo47H2K4XmClM3YJwfDYD2EKRmqBNeyoQIX9PwL-him6Mt1hVKSCMolKxQ9UC6GlCJ05in2o417Q7B5C8YcgjElGPMejBHFxA6mVGBf_v9c_Y3rFYTEkPM</recordid><startdate>20231201</startdate><enddate>20231201</enddate><creator>Yang, Songsoo</creator><creator>Jang, Hyosoon</creator><creator>Park, In Kyu</creator><creator>Lee, Hye Sun</creator><creator>Lee, Kang Young</creator><creator>Oh, Ga Eul</creator><creator>Park, Chihyun</creator><creator>Kang, Jeonghyun</creator><general>Springer International Publishing</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-7311-6053</orcidid></search><sort><creationdate>20231201</creationdate><title>Machine-Learning Algorithms Using Systemic Inflammatory Markers to Predict the Oncologic Outcomes of Colorectal Cancer After Surgery</title><author>Yang, Songsoo ; Jang, Hyosoon ; Park, In Kyu ; Lee, Hye Sun ; Lee, Kang Young ; Oh, Ga Eul ; Park, Chihyun ; Kang, Jeonghyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c303t-718f094b13546215789dba2036c73a759ae1bbe79890e5c16931f8f8ab8987883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Algorithms</topic><topic>C-reactive protein</topic><topic>Colorectal cancer</topic><topic>Colorectal carcinoma</topic><topic>Inflammation</topic><topic>Learning algorithms</topic><topic>Lymphocytes</topic><topic>Machine learning</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Oncology</topic><topic>Patients</topic><topic>Predictions</topic><topic>Surgery</topic><topic>Surgical Oncology</topic><topic>Translational Research</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Songsoo</creatorcontrib><creatorcontrib>Jang, Hyosoon</creatorcontrib><creatorcontrib>Park, In Kyu</creatorcontrib><creatorcontrib>Lee, Hye Sun</creatorcontrib><creatorcontrib>Lee, Kang Young</creatorcontrib><creatorcontrib>Oh, Ga Eul</creatorcontrib><creatorcontrib>Park, Chihyun</creatorcontrib><creatorcontrib>Kang, Jeonghyun</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Health &amp; 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Methods The study included 941 patients with stages I to III CRC. Based on random forest algorithms using 15 compositions of inflammatory markers, four different prediction scores (DFS score-1, DFS score-2, DFS score-3, and DFS score-4) were developed for the Yonsei cohort (training set, n = 803) and tested in the Ulsan cohort (test set, n = 138). The Cox proportional hazards model was used to determine correlation between prediction scores and disease-free survival (DFS). Harrell’s concordance index (C-index) was used to compare the predictive ability of prediction scores for each composition. Results The multivariable analysis showed the DFS score-4 to be an independent prognostic factor after adjustment for clinicopathologic factors in both the training and test sets (hazard ratio [HR], 8.98; 95% confidence interval [CI] 6.7–12.04; P &lt; 0.001 for the training set and HR, 2.55; 95% CI 1.1–5.89; P = 0.028 for the test set]. With regard to DFS, the highest C-index among single compositions was observed in the lymphocyte-to-C-reactive protein ratio (LCR) (0.659; 95% CI 0.656–0.662), and the C-index of DFS score-4 (0.727; 95% CI 0.724–0.729) was significantly higher than that of LCR in the test set. The C-index of DFS score-3 (0.725; 95% CI 0.723–0.728) was similar to that of DFS score-4, but higher than that of DFS score-2 (0.680; 95% CI 0.676–0.683). Conclusions The ML-based approaches showed prognostic utility in predicting DFS. They could enhance clinical use of inflammatory markers in patients with CRC.</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><doi>10.1245/s10434-023-14136-5</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-7311-6053</orcidid></addata></record>
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subjects Algorithms
C-reactive protein
Colorectal cancer
Colorectal carcinoma
Inflammation
Learning algorithms
Lymphocytes
Machine learning
Medicine
Medicine & Public Health
Oncology
Patients
Predictions
Surgery
Surgical Oncology
Translational Research
title Machine-Learning Algorithms Using Systemic Inflammatory Markers to Predict the Oncologic Outcomes of Colorectal Cancer After Surgery
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