Validated Pretreatment Prediction Models for Response to Neoadjuvant Therapy in Patients with Rectal Cancer: A Systematic Review and Critical Appraisal
Pretreatment response prediction is crucial to select those patients with rectal cancer who will benefit from organ preservation strategies following (intensified) neoadjuvant therapy and to avoid unnecessary toxicity in those who will not. The combination of individual predictors in multivariable p...
Gespeichert in:
Veröffentlicht in: | Cancers 2023-08, Vol.15 (15), p.3945 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 15 |
container_start_page | 3945 |
container_title | Cancers |
container_volume | 15 |
creator | Tanaka, Max D Geubels, Barbara M Grotenhuis, Brechtje A Marijnen, Corrie A M Peters, Femke P van der Mierden, Stevie Maas, Monique Couwenberg, Alice M |
description | Pretreatment response prediction is crucial to select those patients with rectal cancer who will benefit from organ preservation strategies following (intensified) neoadjuvant therapy and to avoid unnecessary toxicity in those who will not. The combination of individual predictors in multivariable prediction models might improve predictive accuracy. The aim of this systematic review was to summarize and critically appraise validated pretreatment prediction models (other than radiomics-based models or image-based deep learning models) for response to neoadjuvant therapy in patients with rectal cancer and provide evidence-based recommendations for future research. MEDLINE via Ovid, Embase.com, and Scopus were searched for eligible studies published up to November 2022. A total of 5006 studies were screened and 16 were included for data extraction and risk of bias assessment using Prediction model Risk Of Bias Assessment Tool (PROBAST). All selected models were unique and grouped into five predictor categories: clinical, combined, genetics, metabolites, and pathology. Studies generally included patients with intermediate or advanced tumor stages who were treated with neoadjuvant chemoradiotherapy. Evaluated outcomes were pathological complete response and pathological tumor response. All studies were considered to have a high risk of bias and none of the models were externally validated in an independent study. Discriminative performances, estimated with the area under the curve (AUC), ranged per predictor category from 0.60 to 0.70 (clinical), 0.78 to 0.81 (combined), 0.66 to 0.91 (genetics), 0.54 to 0.80 (metabolites), and 0.71 to 0.91 (pathology). Model calibration outcomes were reported in five studies. Two collagen feature-based models showed the best predictive performance (AUCs 0.83-0.91 and good calibration). In conclusion, some pretreatment models for response prediction in rectal cancer show encouraging predictive potential but, given the high risk of bias in these studies, their value should be evaluated in future, well-designed studies. |
doi_str_mv | 10.3390/cancers15153945 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10417363</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A760514269</galeid><sourcerecordid>A760514269</sourcerecordid><originalsourceid>FETCH-LOGICAL-c489t-7cb5a473eaaeb1d186ecc66d5bf6ff54a18360dafec9a38a9aca9483f42f7fef3</originalsourceid><addsrcrecordid>eNptkk1vEzEQhlcIRKvSMzdkiQuXtOv1x-5yQVHEl1SggsLVmtjjxtGuvdhOqvwS_i4OLaWtsA-2Z555PWNPVT2n9QljfX2qwWuMiQoqWM_Fo-qwqdtmJmXPH9_ZH1THKa3rMhijrWyfVgesFbJrZX1Y_foBgzOQ0ZDziDki5BF93h-M09kFTz4Fg0MiNkTyFdMUfEKSA_mMAcx6s4VCX6wwwrQjzpNzyK4IJHLl8qoE6AwDWfzJ9DWZk2-7lHEsjC6-rcMrAt6QRXTFUsD5NEVwCYZn1RMLQ8Ljm_Wo-v7u7cXiw-zsy_uPi_nZTPOuz7NWLwXwliEALqmhnUStpTRiaaW1ggPtmKwNWNQ9sA560NDzjlne2NaiZUfVm2vdabMc0eiSeoRBTdGNEHcqgFP3Pd6t1GXYKlpz2jLJisKrG4UYfm4wZTW6pHEYwGPYJNV0oma0axte0JcP0HXYRF_qK1Spp_yJ6P9RlzCgct6GcrHei6p5-TNBeSP31Ml_qDINjk4Hj9YV-72A0-sAHUNKEe1tkbRW-35SD_qpRLy4-za3_N_uYb8B-VDKgQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2848968759</pqid></control><display><type>article</type><title>Validated Pretreatment Prediction Models for Response to Neoadjuvant Therapy in Patients with Rectal Cancer: A Systematic Review and Critical Appraisal</title><source>PubMed Central Open Access</source><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Tanaka, Max D ; Geubels, Barbara M ; Grotenhuis, Brechtje A ; Marijnen, Corrie A M ; Peters, Femke P ; van der Mierden, Stevie ; Maas, Monique ; Couwenberg, Alice M</creator><creatorcontrib>Tanaka, Max D ; Geubels, Barbara M ; Grotenhuis, Brechtje A ; Marijnen, Corrie A M ; Peters, Femke P ; van der Mierden, Stevie ; Maas, Monique ; Couwenberg, Alice M</creatorcontrib><description>Pretreatment response prediction is crucial to select those patients with rectal cancer who will benefit from organ preservation strategies following (intensified) neoadjuvant therapy and to avoid unnecessary toxicity in those who will not. The combination of individual predictors in multivariable prediction models might improve predictive accuracy. The aim of this systematic review was to summarize and critically appraise validated pretreatment prediction models (other than radiomics-based models or image-based deep learning models) for response to neoadjuvant therapy in patients with rectal cancer and provide evidence-based recommendations for future research. MEDLINE via Ovid, Embase.com, and Scopus were searched for eligible studies published up to November 2022. A total of 5006 studies were screened and 16 were included for data extraction and risk of bias assessment using Prediction model Risk Of Bias Assessment Tool (PROBAST). All selected models were unique and grouped into five predictor categories: clinical, combined, genetics, metabolites, and pathology. Studies generally included patients with intermediate or advanced tumor stages who were treated with neoadjuvant chemoradiotherapy. Evaluated outcomes were pathological complete response and pathological tumor response. All studies were considered to have a high risk of bias and none of the models were externally validated in an independent study. Discriminative performances, estimated with the area under the curve (AUC), ranged per predictor category from 0.60 to 0.70 (clinical), 0.78 to 0.81 (combined), 0.66 to 0.91 (genetics), 0.54 to 0.80 (metabolites), and 0.71 to 0.91 (pathology). Model calibration outcomes were reported in five studies. Two collagen feature-based models showed the best predictive performance (AUCs 0.83-0.91 and good calibration). In conclusion, some pretreatment models for response prediction in rectal cancer show encouraging predictive potential but, given the high risk of bias in these studies, their value should be evaluated in future, well-designed studies.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers15153945</identifier><identifier>PMID: 37568760</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adjuvant treatment ; Analysis ; Cancer ; Cancer patients ; Cancer therapies ; Care and treatment ; Chemoradiotherapy ; Colorectal cancer ; Content analysis ; Deep learning ; Evidence-based medicine ; Metastasis ; Multiple database searches ; Neoadjuvant therapy ; Oncology, Experimental ; Pathology ; Patients ; Prediction models ; Preservation ; Quality of life ; Radiation therapy ; Radiomics ; Rectum ; Surgery ; Systematic Review ; Toxicity ; Tumors ; Validation studies</subject><ispartof>Cancers, 2023-08, Vol.15 (15), p.3945</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c489t-7cb5a473eaaeb1d186ecc66d5bf6ff54a18360dafec9a38a9aca9483f42f7fef3</citedby><cites>FETCH-LOGICAL-c489t-7cb5a473eaaeb1d186ecc66d5bf6ff54a18360dafec9a38a9aca9483f42f7fef3</cites><orcidid>0000-0001-7080-1872 ; 0000-0003-4318-6688 ; 0000-0001-7721-2341</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417363/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10417363/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37568760$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tanaka, Max D</creatorcontrib><creatorcontrib>Geubels, Barbara M</creatorcontrib><creatorcontrib>Grotenhuis, Brechtje A</creatorcontrib><creatorcontrib>Marijnen, Corrie A M</creatorcontrib><creatorcontrib>Peters, Femke P</creatorcontrib><creatorcontrib>van der Mierden, Stevie</creatorcontrib><creatorcontrib>Maas, Monique</creatorcontrib><creatorcontrib>Couwenberg, Alice M</creatorcontrib><title>Validated Pretreatment Prediction Models for Response to Neoadjuvant Therapy in Patients with Rectal Cancer: A Systematic Review and Critical Appraisal</title><title>Cancers</title><addtitle>Cancers (Basel)</addtitle><description>Pretreatment response prediction is crucial to select those patients with rectal cancer who will benefit from organ preservation strategies following (intensified) neoadjuvant therapy and to avoid unnecessary toxicity in those who will not. The combination of individual predictors in multivariable prediction models might improve predictive accuracy. The aim of this systematic review was to summarize and critically appraise validated pretreatment prediction models (other than radiomics-based models or image-based deep learning models) for response to neoadjuvant therapy in patients with rectal cancer and provide evidence-based recommendations for future research. MEDLINE via Ovid, Embase.com, and Scopus were searched for eligible studies published up to November 2022. A total of 5006 studies were screened and 16 were included for data extraction and risk of bias assessment using Prediction model Risk Of Bias Assessment Tool (PROBAST). All selected models were unique and grouped into five predictor categories: clinical, combined, genetics, metabolites, and pathology. Studies generally included patients with intermediate or advanced tumor stages who were treated with neoadjuvant chemoradiotherapy. Evaluated outcomes were pathological complete response and pathological tumor response. All studies were considered to have a high risk of bias and none of the models were externally validated in an independent study. Discriminative performances, estimated with the area under the curve (AUC), ranged per predictor category from 0.60 to 0.70 (clinical), 0.78 to 0.81 (combined), 0.66 to 0.91 (genetics), 0.54 to 0.80 (metabolites), and 0.71 to 0.91 (pathology). Model calibration outcomes were reported in five studies. Two collagen feature-based models showed the best predictive performance (AUCs 0.83-0.91 and good calibration). In conclusion, some pretreatment models for response prediction in rectal cancer show encouraging predictive potential but, given the high risk of bias in these studies, their value should be evaluated in future, well-designed studies.</description><subject>Adjuvant treatment</subject><subject>Analysis</subject><subject>Cancer</subject><subject>Cancer patients</subject><subject>Cancer therapies</subject><subject>Care and treatment</subject><subject>Chemoradiotherapy</subject><subject>Colorectal cancer</subject><subject>Content analysis</subject><subject>Deep learning</subject><subject>Evidence-based medicine</subject><subject>Metastasis</subject><subject>Multiple database searches</subject><subject>Neoadjuvant therapy</subject><subject>Oncology, Experimental</subject><subject>Pathology</subject><subject>Patients</subject><subject>Prediction models</subject><subject>Preservation</subject><subject>Quality of life</subject><subject>Radiation therapy</subject><subject>Radiomics</subject><subject>Rectum</subject><subject>Surgery</subject><subject>Systematic Review</subject><subject>Toxicity</subject><subject>Tumors</subject><subject>Validation studies</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkk1vEzEQhlcIRKvSMzdkiQuXtOv1x-5yQVHEl1SggsLVmtjjxtGuvdhOqvwS_i4OLaWtsA-2Z555PWNPVT2n9QljfX2qwWuMiQoqWM_Fo-qwqdtmJmXPH9_ZH1THKa3rMhijrWyfVgesFbJrZX1Y_foBgzOQ0ZDziDki5BF93h-M09kFTz4Fg0MiNkTyFdMUfEKSA_mMAcx6s4VCX6wwwrQjzpNzyK4IJHLl8qoE6AwDWfzJ9DWZk2-7lHEsjC6-rcMrAt6QRXTFUsD5NEVwCYZn1RMLQ8Ljm_Wo-v7u7cXiw-zsy_uPi_nZTPOuz7NWLwXwliEALqmhnUStpTRiaaW1ggPtmKwNWNQ9sA560NDzjlne2NaiZUfVm2vdabMc0eiSeoRBTdGNEHcqgFP3Pd6t1GXYKlpz2jLJisKrG4UYfm4wZTW6pHEYwGPYJNV0oma0axte0JcP0HXYRF_qK1Spp_yJ6P9RlzCgct6GcrHei6p5-TNBeSP31Ml_qDINjk4Hj9YV-72A0-sAHUNKEe1tkbRW-35SD_qpRLy4-za3_N_uYb8B-VDKgQ</recordid><startdate>20230803</startdate><enddate>20230803</enddate><creator>Tanaka, Max D</creator><creator>Geubels, Barbara M</creator><creator>Grotenhuis, Brechtje A</creator><creator>Marijnen, Corrie A M</creator><creator>Peters, Femke P</creator><creator>van der Mierden, Stevie</creator><creator>Maas, Monique</creator><creator>Couwenberg, Alice M</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7080-1872</orcidid><orcidid>https://orcid.org/0000-0003-4318-6688</orcidid><orcidid>https://orcid.org/0000-0001-7721-2341</orcidid></search><sort><creationdate>20230803</creationdate><title>Validated Pretreatment Prediction Models for Response to Neoadjuvant Therapy in Patients with Rectal Cancer: A Systematic Review and Critical Appraisal</title><author>Tanaka, Max D ; Geubels, Barbara M ; Grotenhuis, Brechtje A ; Marijnen, Corrie A M ; Peters, Femke P ; van der Mierden, Stevie ; Maas, Monique ; Couwenberg, Alice M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c489t-7cb5a473eaaeb1d186ecc66d5bf6ff54a18360dafec9a38a9aca9483f42f7fef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adjuvant treatment</topic><topic>Analysis</topic><topic>Cancer</topic><topic>Cancer patients</topic><topic>Cancer therapies</topic><topic>Care and treatment</topic><topic>Chemoradiotherapy</topic><topic>Colorectal cancer</topic><topic>Content analysis</topic><topic>Deep learning</topic><topic>Evidence-based medicine</topic><topic>Metastasis</topic><topic>Multiple database searches</topic><topic>Neoadjuvant therapy</topic><topic>Oncology, Experimental</topic><topic>Pathology</topic><topic>Patients</topic><topic>Prediction models</topic><topic>Preservation</topic><topic>Quality of life</topic><topic>Radiation therapy</topic><topic>Radiomics</topic><topic>Rectum</topic><topic>Surgery</topic><topic>Systematic Review</topic><topic>Toxicity</topic><topic>Tumors</topic><topic>Validation studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tanaka, Max D</creatorcontrib><creatorcontrib>Geubels, Barbara M</creatorcontrib><creatorcontrib>Grotenhuis, Brechtje A</creatorcontrib><creatorcontrib>Marijnen, Corrie A M</creatorcontrib><creatorcontrib>Peters, Femke P</creatorcontrib><creatorcontrib>van der Mierden, Stevie</creatorcontrib><creatorcontrib>Maas, Monique</creatorcontrib><creatorcontrib>Couwenberg, Alice M</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tanaka, Max D</au><au>Geubels, Barbara M</au><au>Grotenhuis, Brechtje A</au><au>Marijnen, Corrie A M</au><au>Peters, Femke P</au><au>van der Mierden, Stevie</au><au>Maas, Monique</au><au>Couwenberg, Alice M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Validated Pretreatment Prediction Models for Response to Neoadjuvant Therapy in Patients with Rectal Cancer: A Systematic Review and Critical Appraisal</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2023-08-03</date><risdate>2023</risdate><volume>15</volume><issue>15</issue><spage>3945</spage><pages>3945-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>Pretreatment response prediction is crucial to select those patients with rectal cancer who will benefit from organ preservation strategies following (intensified) neoadjuvant therapy and to avoid unnecessary toxicity in those who will not. The combination of individual predictors in multivariable prediction models might improve predictive accuracy. The aim of this systematic review was to summarize and critically appraise validated pretreatment prediction models (other than radiomics-based models or image-based deep learning models) for response to neoadjuvant therapy in patients with rectal cancer and provide evidence-based recommendations for future research. MEDLINE via Ovid, Embase.com, and Scopus were searched for eligible studies published up to November 2022. A total of 5006 studies were screened and 16 were included for data extraction and risk of bias assessment using Prediction model Risk Of Bias Assessment Tool (PROBAST). All selected models were unique and grouped into five predictor categories: clinical, combined, genetics, metabolites, and pathology. Studies generally included patients with intermediate or advanced tumor stages who were treated with neoadjuvant chemoradiotherapy. Evaluated outcomes were pathological complete response and pathological tumor response. All studies were considered to have a high risk of bias and none of the models were externally validated in an independent study. Discriminative performances, estimated with the area under the curve (AUC), ranged per predictor category from 0.60 to 0.70 (clinical), 0.78 to 0.81 (combined), 0.66 to 0.91 (genetics), 0.54 to 0.80 (metabolites), and 0.71 to 0.91 (pathology). Model calibration outcomes were reported in five studies. Two collagen feature-based models showed the best predictive performance (AUCs 0.83-0.91 and good calibration). In conclusion, some pretreatment models for response prediction in rectal cancer show encouraging predictive potential but, given the high risk of bias in these studies, their value should be evaluated in future, well-designed studies.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>37568760</pmid><doi>10.3390/cancers15153945</doi><orcidid>https://orcid.org/0000-0001-7080-1872</orcidid><orcidid>https://orcid.org/0000-0003-4318-6688</orcidid><orcidid>https://orcid.org/0000-0001-7721-2341</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2072-6694 |
ispartof | Cancers, 2023-08, Vol.15 (15), p.3945 |
issn | 2072-6694 2072-6694 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10417363 |
source | PubMed Central Open Access; MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals; PubMed Central |
subjects | Adjuvant treatment Analysis Cancer Cancer patients Cancer therapies Care and treatment Chemoradiotherapy Colorectal cancer Content analysis Deep learning Evidence-based medicine Metastasis Multiple database searches Neoadjuvant therapy Oncology, Experimental Pathology Patients Prediction models Preservation Quality of life Radiation therapy Radiomics Rectum Surgery Systematic Review Toxicity Tumors Validation studies |
title | Validated Pretreatment Prediction Models for Response to Neoadjuvant Therapy in Patients with Rectal Cancer: A Systematic Review and Critical Appraisal |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T08%3A19%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Validated%20Pretreatment%20Prediction%20Models%20for%20Response%20to%20Neoadjuvant%20Therapy%20in%20Patients%20with%20Rectal%20Cancer:%20A%20Systematic%20Review%20and%20Critical%20Appraisal&rft.jtitle=Cancers&rft.au=Tanaka,%20Max%20D&rft.date=2023-08-03&rft.volume=15&rft.issue=15&rft.spage=3945&rft.pages=3945-&rft.issn=2072-6694&rft.eissn=2072-6694&rft_id=info:doi/10.3390/cancers15153945&rft_dat=%3Cgale_pubme%3EA760514269%3C/gale_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2848968759&rft_id=info:pmid/37568760&rft_galeid=A760514269&rfr_iscdi=true |