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 |
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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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fullrecord | <record><control><sourceid>proquest_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_22420425</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0360301614006221</els_id><sourcerecordid>1561035556</sourcerecordid><originalsourceid>FETCH-LOGICAL-c445t-b2b64f8b92e1313bd8d9d392a70729cebe2ab299045b539713c8284d55a14b2d3</originalsourceid><addsrcrecordid>eNqFkk2L1TAUhosoznX0H4gU3Li513y2jQthKOMHDHhxruguJOm5Ntc2qUk6cLf-clM6unDjKpyc53zwvqconmO0wwhXr087ewpeTzuCMNshvkOEPCg2uKnFlnL-7WGxQbRCW5rhi-JJjCeEEMY1e1xcEI4FF4Juil_7AH6CoJK9g7LtYfRBdTaH3pWHPiemc2ld2fpRW7d-f7WpL_fK2TSP86h0efQhx8mCS3HNfoYIJik9QHkd_dSr76CGslXOQHiz9C33V-2hvE1zd35aPDqqIcKz-_ey-PLu-tB-2N58ev-xvbrZGsZ42mqiK3ZstCCAKaa6azrRUUFUjWoiDGggShMhEOOaU1FjahrSsI5zhZkmHb0sXq59fUxWRmMTmN545_KmkhBGECM8U69Wagr-5wwxydFGA8OgHPg5SswrjLK-vMooW1ETfIwBjnIKdlThLDGSi0fyJFeP5OKRRFxmj3LZi_sJsx6h-1v0x5QMvF0ByGrcWQjLspCl62xYdu28_d-EfxuYwTpr1PADzhBPfg4uKy2xjEQiebvcyXImmCFUEYLpb23HuXQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1561035556</pqid></control><display><type>article</type><title>Preoperative Chemoradiation Therapy in Combination With Panitumumab for Patients With Resectable Esophageal Cancer: The PACT Study</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 & dosage</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - adverse effects</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration & 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 & 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 & 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 & 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 & dosage</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - adverse effects</topic><topic>Antineoplastic Combined Chemotherapy Protocols - administration & 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 & 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 & 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 & 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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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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