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The depth of post-treatment perirectal tissue invasion is a predictor of outcome in patients with clinical T3N1M0 rectal cancer treated with neoadjuvant chemoradiation followed by surgical resection
Abstract Background To determine if patients with clinical stage III rectal cancer treated with neoadjuvant chemoradiotherapy (CRT) and surgery have an improved survival when the response to treatment results in a pathologic T3 tumor with a microscopic focus (≤5 mm) compared with a larger (>5 mm)...
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Published in: | The American journal of surgery 2014-03, Vol.207 (3), p.357-360 |
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creator | Brandt, Whitney S., B.S Yong, Sherri, M.D Abood, Gerard, M.D., M.S Micetich, Kenneth, M.D Walther, Ashley, M.D Shoup, Margo, M.D., F.A.C.S |
description | Abstract Background To determine if patients with clinical stage III rectal cancer treated with neoadjuvant chemoradiotherapy (CRT) and surgery have an improved survival when the response to treatment results in a pathologic T3 tumor with a microscopic focus (≤5 mm) compared with a larger (>5 mm) invasion of the perirectal tissue. Methods A retrospective review was conducted of 56 consecutive patients clinically diagnosed as T3N1M0 rectal cancer before treatment, who completed neoadjuvant CRT followed by surgical resection. Those with residual pathologic T3 disease ( n = 28) were analyzed separately. Clinicopathologic data including T stage, lymph node status, k-ras status, and differentiation were reviewed. Results Among all 56 patients, there was no identified predictor of survival following neoadjuvant CRT and surgery. Among those with residual T3 disease, tumors extending >5 mm invasion into the perirectal tissue were associated with a higher risk of recurrence (50% vs 17%) and worse overall survival (4.3 vs 6.8 years, P = .015) when compared to tumors with ≤5 mm invasion into the perirectal tissue. Conclusion The depth of residual T3 tumor invasion into the perirectal tissue correlates with recurrence and overall survival in patients who underwent neoadjuvant therapy followed by surgical resection for clinically staged T3N1M0 rectal cancer. |
doi_str_mv | 10.1016/j.amjsurg.2013.09.011 |
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Methods A retrospective review was conducted of 56 consecutive patients clinically diagnosed as T3N1M0 rectal cancer before treatment, who completed neoadjuvant CRT followed by surgical resection. Those with residual pathologic T3 disease ( n = 28) were analyzed separately. Clinicopathologic data including T stage, lymph node status, k-ras status, and differentiation were reviewed. Results Among all 56 patients, there was no identified predictor of survival following neoadjuvant CRT and surgery. Among those with residual T3 disease, tumors extending >5 mm invasion into the perirectal tissue were associated with a higher risk of recurrence (50% vs 17%) and worse overall survival (4.3 vs 6.8 years, P = .015) when compared to tumors with ≤5 mm invasion into the perirectal tissue. Conclusion The depth of residual T3 tumor invasion into the perirectal tissue correlates with recurrence and overall survival in patients who underwent neoadjuvant therapy followed by surgical resection for clinically staged T3N1M0 rectal cancer.</description><identifier>ISSN: 0002-9610</identifier><identifier>EISSN: 1879-1883</identifier><identifier>DOI: 10.1016/j.amjsurg.2013.09.011</identifier><identifier>PMID: 24456833</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Abdomen ; Adult ; Aged ; Aged, 80 and over ; Cancer therapies ; Chemoradiotherapy, Adjuvant ; Chemotherapy ; Colorectal cancer ; Confidence intervals ; Female ; Humans ; Male ; Medical prognosis ; Metastasis ; Middle Aged ; Neoadjuvant therapy ; Neoplasm Invasiveness ; Neoplasm Recurrence, Local - mortality ; Neoplasm Recurrence, Local - pathology ; Neoplasm Staging ; Postoperative period ; Prognosis ; Rectal cancer ; Rectal Neoplasms - mortality ; Rectal Neoplasms - pathology ; Rectal Neoplasms - surgery ; Rectal Neoplasms - therapy ; Rectal surgery ; Retrospective Studies ; Statistical analysis ; Surgery ; Survival Analysis ; Treatment Outcome ; Tumors</subject><ispartof>The American journal of surgery, 2014-03, Vol.207 (3), p.357-360</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Limited Mar 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-dfb783a3c895cfcfd2b99b685d4e46e8bec926656132f6ef6d163fdf7d70d5a13</citedby><cites>FETCH-LOGICAL-c448t-dfb783a3c895cfcfd2b99b685d4e46e8bec926656132f6ef6d163fdf7d70d5a13</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/24456833$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Brandt, Whitney S., B.S</creatorcontrib><creatorcontrib>Yong, Sherri, M.D</creatorcontrib><creatorcontrib>Abood, Gerard, M.D., M.S</creatorcontrib><creatorcontrib>Micetich, Kenneth, M.D</creatorcontrib><creatorcontrib>Walther, Ashley, M.D</creatorcontrib><creatorcontrib>Shoup, Margo, M.D., F.A.C.S</creatorcontrib><title>The depth of post-treatment perirectal tissue invasion is a predictor of outcome in patients with clinical T3N1M0 rectal cancer treated with neoadjuvant chemoradiation followed by surgical resection</title><title>The American journal of surgery</title><addtitle>Am J Surg</addtitle><description>Abstract Background To determine if patients with clinical stage III rectal cancer treated with neoadjuvant chemoradiotherapy (CRT) and surgery have an improved survival when the response to treatment results in a pathologic T3 tumor with a microscopic focus (≤5 mm) compared with a larger (>5 mm) invasion of the perirectal tissue. Methods A retrospective review was conducted of 56 consecutive patients clinically diagnosed as T3N1M0 rectal cancer before treatment, who completed neoadjuvant CRT followed by surgical resection. Those with residual pathologic T3 disease ( n = 28) were analyzed separately. Clinicopathologic data including T stage, lymph node status, k-ras status, and differentiation were reviewed. Results Among all 56 patients, there was no identified predictor of survival following neoadjuvant CRT and surgery. Among those with residual T3 disease, tumors extending >5 mm invasion into the perirectal tissue were associated with a higher risk of recurrence (50% vs 17%) and worse overall survival (4.3 vs 6.8 years, P = .015) when compared to tumors with ≤5 mm invasion into the perirectal tissue. Conclusion The depth of residual T3 tumor invasion into the perirectal tissue correlates with recurrence and overall survival in patients who underwent neoadjuvant therapy followed by surgical resection for clinically staged T3N1M0 rectal cancer.</description><subject>Abdomen</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Cancer therapies</subject><subject>Chemoradiotherapy, Adjuvant</subject><subject>Chemotherapy</subject><subject>Colorectal cancer</subject><subject>Confidence intervals</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Neoadjuvant therapy</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Recurrence, Local - mortality</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Staging</subject><subject>Postoperative period</subject><subject>Prognosis</subject><subject>Rectal cancer</subject><subject>Rectal Neoplasms - mortality</subject><subject>Rectal Neoplasms - pathology</subject><subject>Rectal Neoplasms - surgery</subject><subject>Rectal Neoplasms - therapy</subject><subject>Rectal surgery</subject><subject>Retrospective Studies</subject><subject>Statistical analysis</subject><subject>Surgery</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><issn>0002-9610</issn><issn>1879-1883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFksFu1DAQhiMEotvCI4AsceGSxY4db3IBVRUUpAIHlrPl2BPWIYmD7Wy1L8hzMeluQeqFk2X5m3_G_pxlLxhdM8rkm26thy7O4ce6oIyvab2mjD3KVqza1DmrKv44W1FKi7yWjJ5l5zF2uGVM8KfZWSFEKSvOV9nv7Q6IhSntiG_J5GPKUwCdBhgTmSC4ACbpniQX4wzEjXsdnR-Ji0STKYB1Jvmw1Po5GT8sCJl0clgfya3DXNO70RnM2PIv7DMlp0SjRwOB3HUDe0RH8Np2815jc7ODwQdtHYZhw9b3vb9FsDmQ5dp3iQEihuHxs-xJq_sIz0_rRfb9w_vt1cf85uv1p6vLm9wIUaXcts2m4pqbqi5Na1pbNHXdyKq0AoSEqgFTF1KWkvGildBKyyRvbbuxG2pLzfhF9vqYOwX_a4aY1OCigb7XOPocFSupYAIVcERfPUA7P4cRp0OKC85LJkqkyiNlgo8xQKum4AYdDopRtYhWnTqJVotoRWuFFrHu5Sl9bgawf6vuzSLw7ggAPsfeQVDRoBSDxhYBynr33xZvHyTcm_wJB4j_bqNioaj6tvy25bMxTummwIf7Aw-D1mM</recordid><startdate>20140301</startdate><enddate>20140301</enddate><creator>Brandt, Whitney S., B.S</creator><creator>Yong, Sherri, M.D</creator><creator>Abood, Gerard, M.D., M.S</creator><creator>Micetich, Kenneth, M.D</creator><creator>Walther, Ashley, M.D</creator><creator>Shoup, Margo, M.D., F.A.C.S</creator><general>Elsevier Inc</general><general>Elsevier Limited</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>7QO</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20140301</creationdate><title>The depth of post-treatment perirectal tissue invasion is a predictor of outcome in patients with clinical T3N1M0 rectal cancer treated with neoadjuvant chemoradiation followed by surgical resection</title><author>Brandt, Whitney S., B.S ; Yong, Sherri, M.D ; Abood, Gerard, M.D., M.S ; Micetich, Kenneth, M.D ; Walther, Ashley, M.D ; Shoup, Margo, M.D., F.A.C.S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-dfb783a3c895cfcfd2b99b685d4e46e8bec926656132f6ef6d163fdf7d70d5a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Abdomen</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Cancer therapies</topic><topic>Chemoradiotherapy, Adjuvant</topic><topic>Chemotherapy</topic><topic>Colorectal cancer</topic><topic>Confidence intervals</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Neoadjuvant therapy</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Recurrence, Local - mortality</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Staging</topic><topic>Postoperative period</topic><topic>Prognosis</topic><topic>Rectal cancer</topic><topic>Rectal Neoplasms - mortality</topic><topic>Rectal Neoplasms - pathology</topic><topic>Rectal Neoplasms - surgery</topic><topic>Rectal Neoplasms - therapy</topic><topic>Rectal surgery</topic><topic>Retrospective Studies</topic><topic>Statistical analysis</topic><topic>Surgery</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Brandt, Whitney S., B.S</creatorcontrib><creatorcontrib>Yong, Sherri, M.D</creatorcontrib><creatorcontrib>Abood, Gerard, M.D., M.S</creatorcontrib><creatorcontrib>Micetich, Kenneth, M.D</creatorcontrib><creatorcontrib>Walther, Ashley, M.D</creatorcontrib><creatorcontrib>Shoup, Margo, M.D., F.A.C.S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>ProQuest Health and Medical</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Research Library</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Brandt, Whitney S., B.S</au><au>Yong, Sherri, M.D</au><au>Abood, Gerard, M.D., M.S</au><au>Micetich, Kenneth, M.D</au><au>Walther, Ashley, M.D</au><au>Shoup, Margo, M.D., F.A.C.S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The depth of post-treatment perirectal tissue invasion is a predictor of outcome in patients with clinical T3N1M0 rectal cancer treated with neoadjuvant chemoradiation followed by surgical resection</atitle><jtitle>The American journal of surgery</jtitle><addtitle>Am J Surg</addtitle><date>2014-03-01</date><risdate>2014</risdate><volume>207</volume><issue>3</issue><spage>357</spage><epage>360</epage><pages>357-360</pages><issn>0002-9610</issn><eissn>1879-1883</eissn><abstract>Abstract Background To determine if patients with clinical stage III rectal cancer treated with neoadjuvant chemoradiotherapy (CRT) and surgery have an improved survival when the response to treatment results in a pathologic T3 tumor with a microscopic focus (≤5 mm) compared with a larger (>5 mm) invasion of the perirectal tissue. Methods A retrospective review was conducted of 56 consecutive patients clinically diagnosed as T3N1M0 rectal cancer before treatment, who completed neoadjuvant CRT followed by surgical resection. Those with residual pathologic T3 disease ( n = 28) were analyzed separately. Clinicopathologic data including T stage, lymph node status, k-ras status, and differentiation were reviewed. Results Among all 56 patients, there was no identified predictor of survival following neoadjuvant CRT and surgery. Among those with residual T3 disease, tumors extending >5 mm invasion into the perirectal tissue were associated with a higher risk of recurrence (50% vs 17%) and worse overall survival (4.3 vs 6.8 years, P = .015) when compared to tumors with ≤5 mm invasion into the perirectal tissue. Conclusion The depth of residual T3 tumor invasion into the perirectal tissue correlates with recurrence and overall survival in patients who underwent neoadjuvant therapy followed by surgical resection for clinically staged T3N1M0 rectal cancer.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24456833</pmid><doi>10.1016/j.amjsurg.2013.09.011</doi><tpages>4</tpages></addata></record> |
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subjects | Abdomen Adult Aged Aged, 80 and over Cancer therapies Chemoradiotherapy, Adjuvant Chemotherapy Colorectal cancer Confidence intervals Female Humans Male Medical prognosis Metastasis Middle Aged Neoadjuvant therapy Neoplasm Invasiveness Neoplasm Recurrence, Local - mortality Neoplasm Recurrence, Local - pathology Neoplasm Staging Postoperative period Prognosis Rectal cancer Rectal Neoplasms - mortality Rectal Neoplasms - pathology Rectal Neoplasms - surgery Rectal Neoplasms - therapy Rectal surgery Retrospective Studies Statistical analysis Surgery Survival Analysis Treatment Outcome Tumors |
title | The depth of post-treatment perirectal tissue invasion is a predictor of outcome in patients with clinical T3N1M0 rectal cancer treated with neoadjuvant chemoradiation followed by surgical resection |
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