Preoperative Chemoradiation Therapy in Combination With Panitumumab for Patients With Resectable Esophageal Cancer: The PACT Study

Purpose Preoperative chemoradiation therapy (CRT) has become the standard treatment strategy for patients with resectable esophageal cancer. This multicenter phase 2 study investigated the efficacy of the addition of the epidermal growth factor receptor (EGFR) inhibitor panitumumab to a preoperative...

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Veröffentlicht in:International journal of radiation oncology, biology, physics biology, physics, 2014-09, Vol.90 (1), p.190-196
Hauptverfasser: Kordes, Sil, MD, van Berge Henegouwen, Mark I., MD, PhD, Hulshof, Maarten C., MD, PhD, Bergman, Jacques J.G.H.M., MD, PhD, van der Vliet, Hans J., MD, PhD, Kapiteijn, Ellen, MD, PhD, van Laarhoven, Hanneke W.M., MD, PhD, Richel, Dick J., MD, PhD, Klinkenbijl, Jean H.G., MD, PhD, Meijer, Sybren L., MD, PhD, Wilmink, Johanna W., MD, PhD
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container_issue 1
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container_title International journal of radiation oncology, biology, physics
container_volume 90
creator Kordes, Sil, MD
van Berge Henegouwen, Mark I., MD, PhD
Hulshof, Maarten C., MD, PhD
Bergman, Jacques J.G.H.M., MD, PhD
van der Vliet, Hans J., MD, PhD
Kapiteijn, Ellen, MD, PhD
van Laarhoven, Hanneke W.M., MD, PhD
Richel, Dick J., MD, PhD
Klinkenbijl, Jean H.G., MD, PhD
Meijer, Sybren L., MD, PhD
Wilmink, Johanna W., MD, PhD
description Purpose Preoperative chemoradiation therapy (CRT) has become the standard treatment strategy for patients with resectable esophageal cancer. This multicenter phase 2 study investigated the efficacy of the addition of the epidermal growth factor receptor (EGFR) inhibitor panitumumab to a preoperative CRT regimen with carboplatin, paclitaxel, and radiation therapy in patients with resectable esophageal cancer. Methods and Materials Patients with resectable cT1N1M0 or cT2-3N0 to -2M0 tumors received preoperative CRT consisting of panitumumab (6 mg/kg) on days 1, 15, and 29, weekly administrations of carboplatin (area under the curve [AUC] = 2), and paclitaxel (50 mg/m2 ) for 5 weeks and concurrent radiation therapy (41.4 Gy in 23 fractions, 5 days per week), followed by surgery. Primary endpoint was pathologic complete response (pCR) rate. We aimed at a pCR rate of more than 40%. Furthermore, we explored the predictive value of biomarkers (EGFR, HER 2, and P53) for pCR. Results From January 2010 until December 2011, 90 patients were enrolled. Patients were diagnosed predominantly with adenocarcinoma (AC) (80%), T3 disease (89%), and were node positive (81%). Three patients were not resected due to progressive disease. The primary aim was unmet, with a pCR rate of 22%. Patients with AC and squamous cell carcinoma reached a pCR of 14% and 47%, respectively. R0 resection was achieved in 95% of the patients. Main grade 3 toxicities were rash (12%), fatigue (11%), and nonfebrile neutropenia (11%). None of the biomarkers was predictive for response. Conclusions The addition of panitumumab to CRT with carboplatin and paclitaxel was safe and well tolerated but could not improve pCR rate to the preset criterion of 40%.
doi_str_mv 10.1016/j.ijrobp.2014.05.022
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This multicenter phase 2 study investigated the efficacy of the addition of the epidermal growth factor receptor (EGFR) inhibitor panitumumab to a preoperative CRT regimen with carboplatin, paclitaxel, and radiation therapy in patients with resectable esophageal cancer. Methods and Materials Patients with resectable cT1N1M0 or cT2-3N0 to -2M0 tumors received preoperative CRT consisting of panitumumab (6 mg/kg) on days 1, 15, and 29, weekly administrations of carboplatin (area under the curve [AUC] = 2), and paclitaxel (50 mg/m2 ) for 5 weeks and concurrent radiation therapy (41.4 Gy in 23 fractions, 5 days per week), followed by surgery. Primary endpoint was pathologic complete response (pCR) rate. We aimed at a pCR rate of more than 40%. Furthermore, we explored the predictive value of biomarkers (EGFR, HER 2, and P53) for pCR. Results From January 2010 until December 2011, 90 patients were enrolled. Patients were diagnosed predominantly with adenocarcinoma (AC) (80%), T3 disease (89%), and were node positive (81%). Three patients were not resected due to progressive disease. The primary aim was unmet, with a pCR rate of 22%. Patients with AC and squamous cell carcinoma reached a pCR of 14% and 47%, respectively. R0 resection was achieved in 95% of the patients. Main grade 3 toxicities were rash (12%), fatigue (11%), and nonfebrile neutropenia (11%). None of the biomarkers was predictive for response. Conclusions The addition of panitumumab to CRT with carboplatin and paclitaxel was safe and well tolerated but could not improve pCR rate to the preset criterion of 40%.</description><identifier>ISSN: 0360-3016</identifier><identifier>EISSN: 1879-355X</identifier><identifier>DOI: 10.1016/j.ijrobp.2014.05.022</identifier><identifier>PMID: 25195993</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject><![CDATA[Adenocarcinoma - chemistry ; Adenocarcinoma - mortality ; Adenocarcinoma - pathology ; Adenocarcinoma - therapy ; Adult ; Aged ; Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal - adverse effects ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - adverse effects ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - adverse effects ; Area Under Curve ; BIOLOGICAL MARKERS ; Biomarkers, Tumor - analysis ; Carboplatin - administration & dosage ; Carcinoma, Squamous Cell - chemistry ; Carcinoma, Squamous Cell - mortality ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - therapy ; CARCINOMAS ; Chemoradiotherapy - methods ; CHEMOTHERAPY ; DIAGNOSIS ; Dose Fractionation ; Drug Administration Schedule ; Esophageal Neoplasms - chemistry ; Esophageal Neoplasms - mortality ; Esophageal Neoplasms - pathology ; Esophageal Neoplasms - therapy ; ESOPHAGUS ; FATIGUE ; Feasibility Studies ; Female ; GROWTH FACTORS ; Hematology, Oncology and Palliative Medicine ; Humans ; Male ; Middle Aged ; Neoplasm Staging ; Paclitaxel - administration & dosage ; PATIENTS ; Preoperative Care - methods ; Radiology ; RADIOLOGY AND NUCLEAR MEDICINE ; RADIOTHERAPY ; Receptor, Epidermal Growth Factor - antagonists & inhibitors ; RECEPTORS ; SURGERY ; TOXICITY]]></subject><ispartof>International journal of radiation oncology, biology, physics, 2014-09, Vol.90 (1), p.190-196</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-b2b64f8b92e1313bd8d9d392a70729cebe2ab299045b539713c8284d55a14b2d3</citedby><cites>FETCH-LOGICAL-c445t-b2b64f8b92e1313bd8d9d392a70729cebe2ab299045b539713c8284d55a14b2d3</cites><orcidid>0000-0002-9796-1734</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijrobp.2014.05.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25195993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/22420425$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Kordes, Sil, MD</creatorcontrib><creatorcontrib>van Berge Henegouwen, Mark I., MD, PhD</creatorcontrib><creatorcontrib>Hulshof, Maarten C., MD, PhD</creatorcontrib><creatorcontrib>Bergman, Jacques J.G.H.M., MD, PhD</creatorcontrib><creatorcontrib>van der Vliet, Hans J., MD, PhD</creatorcontrib><creatorcontrib>Kapiteijn, Ellen, MD, PhD</creatorcontrib><creatorcontrib>van Laarhoven, Hanneke W.M., MD, PhD</creatorcontrib><creatorcontrib>Richel, Dick J., MD, PhD</creatorcontrib><creatorcontrib>Klinkenbijl, Jean H.G., MD, PhD</creatorcontrib><creatorcontrib>Meijer, Sybren L., MD, PhD</creatorcontrib><creatorcontrib>Wilmink, Johanna W., MD, PhD</creatorcontrib><title>Preoperative Chemoradiation Therapy in Combination With Panitumumab for Patients With Resectable Esophageal Cancer: The PACT Study</title><title>International journal of radiation oncology, biology, physics</title><addtitle>Int J Radiat Oncol Biol Phys</addtitle><description>Purpose Preoperative chemoradiation therapy (CRT) has become the standard treatment strategy for patients with resectable esophageal cancer. This multicenter phase 2 study investigated the efficacy of the addition of the epidermal growth factor receptor (EGFR) inhibitor panitumumab to a preoperative CRT regimen with carboplatin, paclitaxel, and radiation therapy in patients with resectable esophageal cancer. Methods and Materials Patients with resectable cT1N1M0 or cT2-3N0 to -2M0 tumors received preoperative CRT consisting of panitumumab (6 mg/kg) on days 1, 15, and 29, weekly administrations of carboplatin (area under the curve [AUC] = 2), and paclitaxel (50 mg/m2 ) for 5 weeks and concurrent radiation therapy (41.4 Gy in 23 fractions, 5 days per week), followed by surgery. Primary endpoint was pathologic complete response (pCR) rate. We aimed at a pCR rate of more than 40%. Furthermore, we explored the predictive value of biomarkers (EGFR, HER 2, and P53) for pCR. Results From January 2010 until December 2011, 90 patients were enrolled. Patients were diagnosed predominantly with adenocarcinoma (AC) (80%), T3 disease (89%), and were node positive (81%). Three patients were not resected due to progressive disease. The primary aim was unmet, with a pCR rate of 22%. Patients with AC and squamous cell carcinoma reached a pCR of 14% and 47%, respectively. R0 resection was achieved in 95% of the patients. Main grade 3 toxicities were rash (12%), fatigue (11%), and nonfebrile neutropenia (11%). None of the biomarkers was predictive for response. Conclusions The addition of panitumumab to CRT with carboplatin and paclitaxel was safe and well tolerated but could not improve pCR rate to the preset criterion of 40%.</description><subject>Adenocarcinoma - chemistry</subject><subject>Adenocarcinoma - mortality</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - therapy</subject><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Monoclonal - administration &amp; dosage</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antineoplastic Agents - administration &amp; dosage</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - adverse effects</subject><subject>Area Under Curve</subject><subject>BIOLOGICAL MARKERS</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Carboplatin - administration &amp; dosage</subject><subject>Carcinoma, Squamous Cell - chemistry</subject><subject>Carcinoma, Squamous Cell - mortality</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - therapy</subject><subject>CARCINOMAS</subject><subject>Chemoradiotherapy - methods</subject><subject>CHEMOTHERAPY</subject><subject>DIAGNOSIS</subject><subject>Dose Fractionation</subject><subject>Drug Administration Schedule</subject><subject>Esophageal Neoplasms - chemistry</subject><subject>Esophageal Neoplasms - mortality</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Esophageal Neoplasms - therapy</subject><subject>ESOPHAGUS</subject><subject>FATIGUE</subject><subject>Feasibility Studies</subject><subject>Female</subject><subject>GROWTH FACTORS</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Staging</subject><subject>Paclitaxel - administration &amp; dosage</subject><subject>PATIENTS</subject><subject>Preoperative Care - methods</subject><subject>Radiology</subject><subject>RADIOLOGY AND NUCLEAR MEDICINE</subject><subject>RADIOTHERAPY</subject><subject>Receptor, Epidermal Growth Factor - antagonists &amp; inhibitors</subject><subject>RECEPTORS</subject><subject>SURGERY</subject><subject>TOXICITY</subject><issn>0360-3016</issn><issn>1879-355X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk2L1TAUhosoznX0H4gU3Li513y2jQthKOMHDHhxruguJOm5Ntc2qUk6cLf-clM6unDjKpyc53zwvqconmO0wwhXr087ewpeTzuCMNshvkOEPCg2uKnFlnL-7WGxQbRCW5rhi-JJjCeEEMY1e1xcEI4FF4Juil_7AH6CoJK9g7LtYfRBdTaH3pWHPiemc2ld2fpRW7d-f7WpL_fK2TSP86h0efQhx8mCS3HNfoYIJik9QHkd_dSr76CGslXOQHiz9C33V-2hvE1zd35aPDqqIcKz-_ey-PLu-tB-2N58ev-xvbrZGsZ42mqiK3ZstCCAKaa6azrRUUFUjWoiDGggShMhEOOaU1FjahrSsI5zhZkmHb0sXq59fUxWRmMTmN545_KmkhBGECM8U69Wagr-5wwxydFGA8OgHPg5SswrjLK-vMooW1ETfIwBjnIKdlThLDGSi0fyJFeP5OKRRFxmj3LZi_sJsx6h-1v0x5QMvF0ByGrcWQjLspCl62xYdu28_d-EfxuYwTpr1PADzhBPfg4uKy2xjEQiebvcyXImmCFUEYLpb23HuXQ</recordid><startdate>20140901</startdate><enddate>20140901</enddate><creator>Kordes, Sil, MD</creator><creator>van Berge Henegouwen, Mark I., MD, PhD</creator><creator>Hulshof, Maarten C., MD, PhD</creator><creator>Bergman, Jacques J.G.H.M., MD, PhD</creator><creator>van der Vliet, Hans J., MD, PhD</creator><creator>Kapiteijn, Ellen, MD, PhD</creator><creator>van Laarhoven, Hanneke W.M., MD, PhD</creator><creator>Richel, Dick J., MD, PhD</creator><creator>Klinkenbijl, Jean H.G., MD, PhD</creator><creator>Meijer, Sybren L., MD, PhD</creator><creator>Wilmink, Johanna W., MD, PhD</creator><general>Elsevier Inc</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>7X8</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0002-9796-1734</orcidid></search><sort><creationdate>20140901</creationdate><title>Preoperative Chemoradiation Therapy in Combination With Panitumumab for Patients With Resectable Esophageal Cancer: The PACT Study</title><author>Kordes, Sil, MD ; van Berge Henegouwen, Mark I., MD, PhD ; Hulshof, Maarten C., MD, PhD ; Bergman, Jacques J.G.H.M., MD, PhD ; van der Vliet, Hans J., MD, PhD ; Kapiteijn, Ellen, MD, PhD ; van Laarhoven, Hanneke W.M., MD, PhD ; Richel, Dick J., MD, PhD ; Klinkenbijl, Jean H.G., MD, PhD ; Meijer, Sybren L., MD, PhD ; Wilmink, Johanna W., MD, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-b2b64f8b92e1313bd8d9d392a70729cebe2ab299045b539713c8284d55a14b2d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenocarcinoma - chemistry</topic><topic>Adenocarcinoma - mortality</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - therapy</topic><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Monoclonal - administration &amp; dosage</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antineoplastic Agents - administration &amp; dosage</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</topic><topic>Antineoplastic Combined Chemotherapy Protocols - adverse effects</topic><topic>Area Under Curve</topic><topic>BIOLOGICAL MARKERS</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Carboplatin - administration &amp; dosage</topic><topic>Carcinoma, Squamous Cell - chemistry</topic><topic>Carcinoma, Squamous Cell - mortality</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - therapy</topic><topic>CARCINOMAS</topic><topic>Chemoradiotherapy - methods</topic><topic>CHEMOTHERAPY</topic><topic>DIAGNOSIS</topic><topic>Dose Fractionation</topic><topic>Drug Administration Schedule</topic><topic>Esophageal Neoplasms - chemistry</topic><topic>Esophageal Neoplasms - mortality</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Esophageal Neoplasms - therapy</topic><topic>ESOPHAGUS</topic><topic>FATIGUE</topic><topic>Feasibility Studies</topic><topic>Female</topic><topic>GROWTH FACTORS</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasm Staging</topic><topic>Paclitaxel - administration &amp; dosage</topic><topic>PATIENTS</topic><topic>Preoperative Care - methods</topic><topic>Radiology</topic><topic>RADIOLOGY AND NUCLEAR MEDICINE</topic><topic>RADIOTHERAPY</topic><topic>Receptor, Epidermal Growth Factor - antagonists &amp; inhibitors</topic><topic>RECEPTORS</topic><topic>SURGERY</topic><topic>TOXICITY</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kordes, Sil, MD</creatorcontrib><creatorcontrib>van Berge Henegouwen, Mark I., MD, PhD</creatorcontrib><creatorcontrib>Hulshof, Maarten C., MD, PhD</creatorcontrib><creatorcontrib>Bergman, Jacques J.G.H.M., MD, PhD</creatorcontrib><creatorcontrib>van der Vliet, Hans J., MD, PhD</creatorcontrib><creatorcontrib>Kapiteijn, Ellen, MD, PhD</creatorcontrib><creatorcontrib>van Laarhoven, Hanneke W.M., MD, PhD</creatorcontrib><creatorcontrib>Richel, Dick J., MD, PhD</creatorcontrib><creatorcontrib>Klinkenbijl, Jean H.G., MD, PhD</creatorcontrib><creatorcontrib>Meijer, Sybren L., MD, PhD</creatorcontrib><creatorcontrib>Wilmink, Johanna W., MD, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><jtitle>International journal of radiation oncology, biology, physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kordes, Sil, MD</au><au>van Berge Henegouwen, Mark I., MD, PhD</au><au>Hulshof, Maarten C., MD, PhD</au><au>Bergman, Jacques J.G.H.M., MD, PhD</au><au>van der Vliet, Hans J., MD, PhD</au><au>Kapiteijn, Ellen, MD, PhD</au><au>van Laarhoven, Hanneke W.M., MD, PhD</au><au>Richel, Dick J., MD, PhD</au><au>Klinkenbijl, Jean H.G., MD, PhD</au><au>Meijer, Sybren L., MD, PhD</au><au>Wilmink, Johanna W., MD, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preoperative Chemoradiation Therapy in Combination With Panitumumab for Patients With Resectable Esophageal Cancer: The PACT Study</atitle><jtitle>International journal of radiation oncology, biology, physics</jtitle><addtitle>Int J Radiat Oncol Biol Phys</addtitle><date>2014-09-01</date><risdate>2014</risdate><volume>90</volume><issue>1</issue><spage>190</spage><epage>196</epage><pages>190-196</pages><issn>0360-3016</issn><eissn>1879-355X</eissn><abstract>Purpose Preoperative chemoradiation therapy (CRT) has become the standard treatment strategy for patients with resectable esophageal cancer. This multicenter phase 2 study investigated the efficacy of the addition of the epidermal growth factor receptor (EGFR) inhibitor panitumumab to a preoperative CRT regimen with carboplatin, paclitaxel, and radiation therapy in patients with resectable esophageal cancer. Methods and Materials Patients with resectable cT1N1M0 or cT2-3N0 to -2M0 tumors received preoperative CRT consisting of panitumumab (6 mg/kg) on days 1, 15, and 29, weekly administrations of carboplatin (area under the curve [AUC] = 2), and paclitaxel (50 mg/m2 ) for 5 weeks and concurrent radiation therapy (41.4 Gy in 23 fractions, 5 days per week), followed by surgery. Primary endpoint was pathologic complete response (pCR) rate. We aimed at a pCR rate of more than 40%. Furthermore, we explored the predictive value of biomarkers (EGFR, HER 2, and P53) for pCR. Results From January 2010 until December 2011, 90 patients were enrolled. Patients were diagnosed predominantly with adenocarcinoma (AC) (80%), T3 disease (89%), and were node positive (81%). Three patients were not resected due to progressive disease. The primary aim was unmet, with a pCR rate of 22%. Patients with AC and squamous cell carcinoma reached a pCR of 14% and 47%, respectively. R0 resection was achieved in 95% of the patients. Main grade 3 toxicities were rash (12%), fatigue (11%), and nonfebrile neutropenia (11%). None of the biomarkers was predictive for response. Conclusions The addition of panitumumab to CRT with carboplatin and paclitaxel was safe and well tolerated but could not improve pCR rate to the preset criterion of 40%.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25195993</pmid><doi>10.1016/j.ijrobp.2014.05.022</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-9796-1734</orcidid></addata></record>
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ispartof International journal of radiation oncology, biology, physics, 2014-09, Vol.90 (1), p.190-196
issn 0360-3016
1879-355X
language eng
recordid cdi_osti_scitechconnect_22420425
source MEDLINE; Elsevier ScienceDirect Journals
subjects Adenocarcinoma - chemistry
Adenocarcinoma - mortality
Adenocarcinoma - pathology
Adenocarcinoma - therapy
Adult
Aged
Antibodies, Monoclonal - administration & dosage
Antibodies, Monoclonal - adverse effects
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - adverse effects
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - adverse effects
Area Under Curve
BIOLOGICAL MARKERS
Biomarkers, Tumor - analysis
Carboplatin - administration & dosage
Carcinoma, Squamous Cell - chemistry
Carcinoma, Squamous Cell - mortality
Carcinoma, Squamous Cell - pathology
Carcinoma, Squamous Cell - therapy
CARCINOMAS
Chemoradiotherapy - methods
CHEMOTHERAPY
DIAGNOSIS
Dose Fractionation
Drug Administration Schedule
Esophageal Neoplasms - chemistry
Esophageal Neoplasms - mortality
Esophageal Neoplasms - pathology
Esophageal Neoplasms - therapy
ESOPHAGUS
FATIGUE
Feasibility Studies
Female
GROWTH FACTORS
Hematology, Oncology and Palliative Medicine
Humans
Male
Middle Aged
Neoplasm Staging
Paclitaxel - administration & dosage
PATIENTS
Preoperative Care - methods
Radiology
RADIOLOGY AND NUCLEAR MEDICINE
RADIOTHERAPY
Receptor, Epidermal Growth Factor - antagonists & inhibitors
RECEPTORS
SURGERY
TOXICITY
title Preoperative Chemoradiation Therapy in Combination With Panitumumab for Patients With Resectable Esophageal Cancer: The PACT Study
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