18F-FDG PET/CT Is an Early Predictor of Pathologic Tumor Response and Survival After Preoperative Radiochemotherapy with Bevacizumab in High-Risk Locally Advanced Rectal Cancer
There is an unmet need for predictive biomarkers of the clinical benefit of antiangiogenic drugs. The aim of the present study was to prospectively evaluate the value of 18F-FDG PET/CT performed during and after preoperative chemoradiotherapy with bevacizumab for the prediction of complete pathologi...
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Veröffentlicht in: | The Journal of nuclear medicine (1978) 2019-11, Vol.60 (11), p.1560-1568 |
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creator | Avallone, Antonio Aloj, Luigi Pecori, Biagio Caracò, Corradina De Stefano, Alfonso Tatangelo, Fabiana Silvestro, Lucrezia Granata, Vincenza Bianco, Francesco Romano, Carmela Di Gennaro, Francesca Budillon, Alfredo Petrillo, Antonella Muto, Paolo Botti, Gerardo Delrio, Paolo Lastoria, Secondo |
description | There is an unmet need for predictive biomarkers of the clinical benefit of antiangiogenic drugs. The aim of the present study was to prospectively evaluate the value of 18F-FDG PET/CT performed during and after preoperative chemoradiotherapy with bevacizumab for the prediction of complete pathologic tumor regression and survival in patients with MRI-defined high-risk locally advanced rectal cancer. Methods: Sixty-one patients treated in a nonrandomized phase II study (BRANCH) with concomitant or sequential (4 d before chemoradiotherapy) administration of bevacizumab with preoperative chemoradiotherapy were included. 18F-FDG PET/CT was performed at baseline, 11 d after the beginning of chemoradiotherapy (early), and before surgery (late). Metabolic changes were compared with pathologic complete tumor regression (TRG1) versus incomplete tumor regression (TRG2–TRG5), progression-free survival, cancer-specific survival, and overall survival. Receiver-operating-characteristic curves were calculated for those 18F-FDG PET/CT parameters that significantly correlated with TRG1. Results: Early total-lesion glycolysis and its percentage change compared with baseline (ΔTLG-early) could discriminate TRG1 from TRG2–TRG5. Only receiver-operating-characteristic analysis of ΔTLG-early showed an area under the curve greater than 0.7 (0.76), with an optimal cutoff at 59.5% (80% sensitivity, 71.4% specificity), for identifying TRG1. Late metabolic assessment could not discriminate between the 2 groups. After a median follow-up of 98 mo (range, 77–132 mo), metabolic responders (ΔTLG-early ≥ 59.5%) demonstrated a significantly higher 10-y progression-free survival (89.3% vs. 63.6%, P = 0.02) and cancer-specific survival (92.9% vs. 72.6%, P = 0.04) than incomplete metabolic responders. Conclusion: Our results suggest that early metabolic response can act as a surrogate marker of the benefit of antiangiogenic therapy. The findings provide further support for the use of early 18F-FDG PET/CT evaluation to predict pathologic response and survival in the preoperative treatment of patients with locally advanced rectal cancer. ΔTLG-early showed the best accuracy in predicting tumor regression and may be particularly useful in guiding treatment-modifying decisions during preoperative chemoradiotherapy based on expected response. |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6836863</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2312781120</sourcerecordid><originalsourceid>FETCH-LOGICAL-p1594-2d41e28a4b4551afb22f4818fc383d3975167624110253e2ccc0b0b8ac6771f3</originalsourceid><addsrcrecordid>eNpdkMGO0zAQhi0EYsvCA3CzxIVLuh47dpwLUint7kqVqErukeM4jUsSBzsJKk_FI-IVe4HTaGb--X7Nj9B7IGuai-zuMsy9qdcAck0pFSR9gVbAGU-4ENlLtCIgIOGc8Bv0JoQLIURIKV-jG0ZklkHGV-g3yH2y_3KPj7viblvgx4DVgHfKd1d89Ka2enIeuwYf1dS6zp2txsXcx9nJhNENwUR9jb_NfrGL6vCmmYx_unSj8Wqyi8EnVVunW9O7qY2z8Yp_2qnFn82itP0196rCdsAP9twmJxu-44PTqov2m3pRgzZ1dNJTRG-fOv8WvWpUF8y753qLiv2u2D4kh6_3j9vNIRmB52lC6xQMlSqtUs5BNRWlTSpBNppJVrM84yAyQVMAQjkzVGtNKlJJpUVMpmG36NNf7DhXMWNthsmrrhy97ZW_lk7Z8t_NYNvy7JZSSCakYBHw8Rng3Y_ZhKnsbdCm69Rg3BxKCjkDwdKcR-mH_6QXN_shfldSBjSTAJSwP-78mUc</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2312781120</pqid></control><display><type>article</type><title>18F-FDG PET/CT Is an Early Predictor of Pathologic Tumor Response and Survival After Preoperative Radiochemotherapy with Bevacizumab in High-Risk Locally Advanced Rectal Cancer</title><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Avallone, Antonio ; Aloj, Luigi ; Pecori, Biagio ; Caracò, Corradina ; De Stefano, Alfonso ; Tatangelo, Fabiana ; Silvestro, Lucrezia ; Granata, Vincenza ; Bianco, Francesco ; Romano, Carmela ; Di Gennaro, Francesca ; Budillon, Alfredo ; Petrillo, Antonella ; Muto, Paolo ; Botti, Gerardo ; Delrio, Paolo ; Lastoria, Secondo</creator><creatorcontrib>Avallone, Antonio ; Aloj, Luigi ; Pecori, Biagio ; Caracò, Corradina ; De Stefano, Alfonso ; Tatangelo, Fabiana ; Silvestro, Lucrezia ; Granata, Vincenza ; Bianco, Francesco ; Romano, Carmela ; Di Gennaro, Francesca ; Budillon, Alfredo ; Petrillo, Antonella ; Muto, Paolo ; Botti, Gerardo ; Delrio, Paolo ; Lastoria, Secondo</creatorcontrib><description>There is an unmet need for predictive biomarkers of the clinical benefit of antiangiogenic drugs. The aim of the present study was to prospectively evaluate the value of 18F-FDG PET/CT performed during and after preoperative chemoradiotherapy with bevacizumab for the prediction of complete pathologic tumor regression and survival in patients with MRI-defined high-risk locally advanced rectal cancer. Methods: Sixty-one patients treated in a nonrandomized phase II study (BRANCH) with concomitant or sequential (4 d before chemoradiotherapy) administration of bevacizumab with preoperative chemoradiotherapy were included. 18F-FDG PET/CT was performed at baseline, 11 d after the beginning of chemoradiotherapy (early), and before surgery (late). Metabolic changes were compared with pathologic complete tumor regression (TRG1) versus incomplete tumor regression (TRG2–TRG5), progression-free survival, cancer-specific survival, and overall survival. Receiver-operating-characteristic curves were calculated for those 18F-FDG PET/CT parameters that significantly correlated with TRG1. Results: Early total-lesion glycolysis and its percentage change compared with baseline (ΔTLG-early) could discriminate TRG1 from TRG2–TRG5. Only receiver-operating-characteristic analysis of ΔTLG-early showed an area under the curve greater than 0.7 (0.76), with an optimal cutoff at 59.5% (80% sensitivity, 71.4% specificity), for identifying TRG1. Late metabolic assessment could not discriminate between the 2 groups. After a median follow-up of 98 mo (range, 77–132 mo), metabolic responders (ΔTLG-early ≥ 59.5%) demonstrated a significantly higher 10-y progression-free survival (89.3% vs. 63.6%, P = 0.02) and cancer-specific survival (92.9% vs. 72.6%, P = 0.04) than incomplete metabolic responders. Conclusion: Our results suggest that early metabolic response can act as a surrogate marker of the benefit of antiangiogenic therapy. The findings provide further support for the use of early 18F-FDG PET/CT evaluation to predict pathologic response and survival in the preoperative treatment of patients with locally advanced rectal cancer. ΔTLG-early showed the best accuracy in predicting tumor regression and may be particularly useful in guiding treatment-modifying decisions during preoperative chemoradiotherapy based on expected response.</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><identifier>DOI: 10.2967/jnumed.118.222604</identifier><identifier>PMID: 30877175</identifier><language>eng</language><publisher>New York: Society of Nuclear Medicine</publisher><subject>Antiangiogenic agents ; Antiangiogenics ; Bevacizumab ; Biomarkers ; Cancer ; Chemoradiotherapy ; Colorectal cancer ; Evaluation ; Fluorine isotopes ; Glycolysis ; Health risks ; Immunotherapy ; Magnetic resonance imaging ; Metabolic response ; Metabolism ; Monoclonal antibodies ; Oncology ; Patients ; Positron emission tomography ; Predictions ; Rectum ; Regression analysis ; Sensitivity analysis ; Surgery ; Survival ; Targeted cancer therapy ; Tumors</subject><ispartof>The Journal of nuclear medicine (1978), 2019-11, Vol.60 (11), p.1560-1568</ispartof><rights>Copyright Society of Nuclear Medicine Nov 1, 2019</rights><rights>2019 by the Society of Nuclear Medicine and Molecular Imaging. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids></links><search><creatorcontrib>Avallone, Antonio</creatorcontrib><creatorcontrib>Aloj, Luigi</creatorcontrib><creatorcontrib>Pecori, Biagio</creatorcontrib><creatorcontrib>Caracò, Corradina</creatorcontrib><creatorcontrib>De Stefano, Alfonso</creatorcontrib><creatorcontrib>Tatangelo, Fabiana</creatorcontrib><creatorcontrib>Silvestro, Lucrezia</creatorcontrib><creatorcontrib>Granata, Vincenza</creatorcontrib><creatorcontrib>Bianco, Francesco</creatorcontrib><creatorcontrib>Romano, Carmela</creatorcontrib><creatorcontrib>Di Gennaro, Francesca</creatorcontrib><creatorcontrib>Budillon, Alfredo</creatorcontrib><creatorcontrib>Petrillo, Antonella</creatorcontrib><creatorcontrib>Muto, Paolo</creatorcontrib><creatorcontrib>Botti, Gerardo</creatorcontrib><creatorcontrib>Delrio, Paolo</creatorcontrib><creatorcontrib>Lastoria, Secondo</creatorcontrib><title>18F-FDG PET/CT Is an Early Predictor of Pathologic Tumor Response and Survival After Preoperative Radiochemotherapy with Bevacizumab in High-Risk Locally Advanced Rectal Cancer</title><title>The Journal of nuclear medicine (1978)</title><description>There is an unmet need for predictive biomarkers of the clinical benefit of antiangiogenic drugs. The aim of the present study was to prospectively evaluate the value of 18F-FDG PET/CT performed during and after preoperative chemoradiotherapy with bevacizumab for the prediction of complete pathologic tumor regression and survival in patients with MRI-defined high-risk locally advanced rectal cancer. Methods: Sixty-one patients treated in a nonrandomized phase II study (BRANCH) with concomitant or sequential (4 d before chemoradiotherapy) administration of bevacizumab with preoperative chemoradiotherapy were included. 18F-FDG PET/CT was performed at baseline, 11 d after the beginning of chemoradiotherapy (early), and before surgery (late). Metabolic changes were compared with pathologic complete tumor regression (TRG1) versus incomplete tumor regression (TRG2–TRG5), progression-free survival, cancer-specific survival, and overall survival. Receiver-operating-characteristic curves were calculated for those 18F-FDG PET/CT parameters that significantly correlated with TRG1. Results: Early total-lesion glycolysis and its percentage change compared with baseline (ΔTLG-early) could discriminate TRG1 from TRG2–TRG5. Only receiver-operating-characteristic analysis of ΔTLG-early showed an area under the curve greater than 0.7 (0.76), with an optimal cutoff at 59.5% (80% sensitivity, 71.4% specificity), for identifying TRG1. Late metabolic assessment could not discriminate between the 2 groups. After a median follow-up of 98 mo (range, 77–132 mo), metabolic responders (ΔTLG-early ≥ 59.5%) demonstrated a significantly higher 10-y progression-free survival (89.3% vs. 63.6%, P = 0.02) and cancer-specific survival (92.9% vs. 72.6%, P = 0.04) than incomplete metabolic responders. Conclusion: Our results suggest that early metabolic response can act as a surrogate marker of the benefit of antiangiogenic therapy. The findings provide further support for the use of early 18F-FDG PET/CT evaluation to predict pathologic response and survival in the preoperative treatment of patients with locally advanced rectal cancer. ΔTLG-early showed the best accuracy in predicting tumor regression and may be particularly useful in guiding treatment-modifying decisions during preoperative chemoradiotherapy based on expected response.</description><subject>Antiangiogenic agents</subject><subject>Antiangiogenics</subject><subject>Bevacizumab</subject><subject>Biomarkers</subject><subject>Cancer</subject><subject>Chemoradiotherapy</subject><subject>Colorectal cancer</subject><subject>Evaluation</subject><subject>Fluorine isotopes</subject><subject>Glycolysis</subject><subject>Health risks</subject><subject>Immunotherapy</subject><subject>Magnetic resonance imaging</subject><subject>Metabolic response</subject><subject>Metabolism</subject><subject>Monoclonal antibodies</subject><subject>Oncology</subject><subject>Patients</subject><subject>Positron emission tomography</subject><subject>Predictions</subject><subject>Rectum</subject><subject>Regression analysis</subject><subject>Sensitivity analysis</subject><subject>Surgery</subject><subject>Survival</subject><subject>Targeted cancer therapy</subject><subject>Tumors</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNpdkMGO0zAQhi0EYsvCA3CzxIVLuh47dpwLUint7kqVqErukeM4jUsSBzsJKk_FI-IVe4HTaGb--X7Nj9B7IGuai-zuMsy9qdcAck0pFSR9gVbAGU-4ENlLtCIgIOGc8Bv0JoQLIURIKV-jG0ZklkHGV-g3yH2y_3KPj7viblvgx4DVgHfKd1d89Ka2enIeuwYf1dS6zp2txsXcx9nJhNENwUR9jb_NfrGL6vCmmYx_unSj8Wqyi8EnVVunW9O7qY2z8Yp_2qnFn82itP0196rCdsAP9twmJxu-44PTqov2m3pRgzZ1dNJTRG-fOv8WvWpUF8y753qLiv2u2D4kh6_3j9vNIRmB52lC6xQMlSqtUs5BNRWlTSpBNppJVrM84yAyQVMAQjkzVGtNKlJJpUVMpmG36NNf7DhXMWNthsmrrhy97ZW_lk7Z8t_NYNvy7JZSSCakYBHw8Rng3Y_ZhKnsbdCm69Rg3BxKCjkDwdKcR-mH_6QXN_shfldSBjSTAJSwP-78mUc</recordid><startdate>20191101</startdate><enddate>20191101</enddate><creator>Avallone, Antonio</creator><creator>Aloj, Luigi</creator><creator>Pecori, Biagio</creator><creator>Caracò, Corradina</creator><creator>De Stefano, Alfonso</creator><creator>Tatangelo, Fabiana</creator><creator>Silvestro, Lucrezia</creator><creator>Granata, Vincenza</creator><creator>Bianco, Francesco</creator><creator>Romano, Carmela</creator><creator>Di Gennaro, Francesca</creator><creator>Budillon, Alfredo</creator><creator>Petrillo, Antonella</creator><creator>Muto, Paolo</creator><creator>Botti, Gerardo</creator><creator>Delrio, Paolo</creator><creator>Lastoria, Secondo</creator><general>Society of Nuclear Medicine</general><scope>4T-</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20191101</creationdate><title>18F-FDG PET/CT Is an Early Predictor of Pathologic Tumor Response and Survival After Preoperative Radiochemotherapy with Bevacizumab in High-Risk Locally Advanced Rectal Cancer</title><author>Avallone, Antonio ; Aloj, Luigi ; Pecori, Biagio ; Caracò, Corradina ; De Stefano, Alfonso ; Tatangelo, Fabiana ; Silvestro, Lucrezia ; Granata, Vincenza ; Bianco, Francesco ; Romano, Carmela ; Di Gennaro, Francesca ; Budillon, Alfredo ; Petrillo, Antonella ; Muto, Paolo ; Botti, Gerardo ; Delrio, Paolo ; Lastoria, Secondo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p1594-2d41e28a4b4551afb22f4818fc383d3975167624110253e2ccc0b0b8ac6771f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Antiangiogenic agents</topic><topic>Antiangiogenics</topic><topic>Bevacizumab</topic><topic>Biomarkers</topic><topic>Cancer</topic><topic>Chemoradiotherapy</topic><topic>Colorectal cancer</topic><topic>Evaluation</topic><topic>Fluorine isotopes</topic><topic>Glycolysis</topic><topic>Health risks</topic><topic>Immunotherapy</topic><topic>Magnetic resonance imaging</topic><topic>Metabolic response</topic><topic>Metabolism</topic><topic>Monoclonal antibodies</topic><topic>Oncology</topic><topic>Patients</topic><topic>Positron emission tomography</topic><topic>Predictions</topic><topic>Rectum</topic><topic>Regression analysis</topic><topic>Sensitivity analysis</topic><topic>Surgery</topic><topic>Survival</topic><topic>Targeted cancer therapy</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Avallone, Antonio</creatorcontrib><creatorcontrib>Aloj, Luigi</creatorcontrib><creatorcontrib>Pecori, Biagio</creatorcontrib><creatorcontrib>Caracò, Corradina</creatorcontrib><creatorcontrib>De Stefano, Alfonso</creatorcontrib><creatorcontrib>Tatangelo, Fabiana</creatorcontrib><creatorcontrib>Silvestro, Lucrezia</creatorcontrib><creatorcontrib>Granata, Vincenza</creatorcontrib><creatorcontrib>Bianco, Francesco</creatorcontrib><creatorcontrib>Romano, Carmela</creatorcontrib><creatorcontrib>Di Gennaro, Francesca</creatorcontrib><creatorcontrib>Budillon, Alfredo</creatorcontrib><creatorcontrib>Petrillo, Antonella</creatorcontrib><creatorcontrib>Muto, Paolo</creatorcontrib><creatorcontrib>Botti, Gerardo</creatorcontrib><creatorcontrib>Delrio, Paolo</creatorcontrib><creatorcontrib>Lastoria, Secondo</creatorcontrib><collection>Docstoc</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing & Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Avallone, Antonio</au><au>Aloj, Luigi</au><au>Pecori, Biagio</au><au>Caracò, Corradina</au><au>De Stefano, Alfonso</au><au>Tatangelo, Fabiana</au><au>Silvestro, Lucrezia</au><au>Granata, Vincenza</au><au>Bianco, Francesco</au><au>Romano, Carmela</au><au>Di Gennaro, Francesca</au><au>Budillon, Alfredo</au><au>Petrillo, Antonella</au><au>Muto, Paolo</au><au>Botti, Gerardo</au><au>Delrio, Paolo</au><au>Lastoria, Secondo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>18F-FDG PET/CT Is an Early Predictor of Pathologic Tumor Response and Survival After Preoperative Radiochemotherapy with Bevacizumab in High-Risk Locally Advanced Rectal Cancer</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><date>2019-11-01</date><risdate>2019</risdate><volume>60</volume><issue>11</issue><spage>1560</spage><epage>1568</epage><pages>1560-1568</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><abstract>There is an unmet need for predictive biomarkers of the clinical benefit of antiangiogenic drugs. The aim of the present study was to prospectively evaluate the value of 18F-FDG PET/CT performed during and after preoperative chemoradiotherapy with bevacizumab for the prediction of complete pathologic tumor regression and survival in patients with MRI-defined high-risk locally advanced rectal cancer. Methods: Sixty-one patients treated in a nonrandomized phase II study (BRANCH) with concomitant or sequential (4 d before chemoradiotherapy) administration of bevacizumab with preoperative chemoradiotherapy were included. 18F-FDG PET/CT was performed at baseline, 11 d after the beginning of chemoradiotherapy (early), and before surgery (late). Metabolic changes were compared with pathologic complete tumor regression (TRG1) versus incomplete tumor regression (TRG2–TRG5), progression-free survival, cancer-specific survival, and overall survival. Receiver-operating-characteristic curves were calculated for those 18F-FDG PET/CT parameters that significantly correlated with TRG1. Results: Early total-lesion glycolysis and its percentage change compared with baseline (ΔTLG-early) could discriminate TRG1 from TRG2–TRG5. Only receiver-operating-characteristic analysis of ΔTLG-early showed an area under the curve greater than 0.7 (0.76), with an optimal cutoff at 59.5% (80% sensitivity, 71.4% specificity), for identifying TRG1. Late metabolic assessment could not discriminate between the 2 groups. After a median follow-up of 98 mo (range, 77–132 mo), metabolic responders (ΔTLG-early ≥ 59.5%) demonstrated a significantly higher 10-y progression-free survival (89.3% vs. 63.6%, P = 0.02) and cancer-specific survival (92.9% vs. 72.6%, P = 0.04) than incomplete metabolic responders. Conclusion: Our results suggest that early metabolic response can act as a surrogate marker of the benefit of antiangiogenic therapy. The findings provide further support for the use of early 18F-FDG PET/CT evaluation to predict pathologic response and survival in the preoperative treatment of patients with locally advanced rectal cancer. ΔTLG-early showed the best accuracy in predicting tumor regression and may be particularly useful in guiding treatment-modifying decisions during preoperative chemoradiotherapy based on expected response.</abstract><cop>New York</cop><pub>Society of Nuclear Medicine</pub><pmid>30877175</pmid><doi>10.2967/jnumed.118.222604</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antiangiogenic agents Antiangiogenics Bevacizumab Biomarkers Cancer Chemoradiotherapy Colorectal cancer Evaluation Fluorine isotopes Glycolysis Health risks Immunotherapy Magnetic resonance imaging Metabolic response Metabolism Monoclonal antibodies Oncology Patients Positron emission tomography Predictions Rectum Regression analysis Sensitivity analysis Surgery Survival Targeted cancer therapy Tumors |
title | 18F-FDG PET/CT Is an Early Predictor of Pathologic Tumor Response and Survival After Preoperative Radiochemotherapy with Bevacizumab in High-Risk Locally Advanced Rectal Cancer |
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