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Radiotherapy for oesophagus carcinoma: the impact of p53 on treatment outcome
Background and purpose: Wildtype p53 protein plays an important role in the cellular response to ionizing radiation and other DNA damaging agents and is mutated in many human tumours. We evaluated the relationship of the immunohistochemically determined p53 protein status and the disease control wit...
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Published in: | Radiotherapy and oncology 1998-02, Vol.46 (2), p.179-184 |
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creator | Pomp, Jacqueline Davelaar, Jacob Blom, Jan van Krimpen, Cees Zwinderman, Aeilko Quint, Wilhelmus Immerzeel, Jos |
description | Background and purpose: Wildtype p53 protein plays an important role in the cellular response to ionizing radiation and other DNA damaging agents and is mutated in many human tumours. We evaluated the relationship of the immunohistochemically determined p53 protein status and the disease control with radiotherapy alone for carcinoma of the oesophagus.
Materials and methods: Immunostaining for p53 protein was performed on paraffin-embedded specimens from 69 patients with adeno- and squamous cell carcinoma of the oesophagus. All patients were treated by radiotherapy exclusively, consisting of a combination of external irradiation and intraluminal brachytherapy, using two different dose levels.
Results: Fifty-four percent (37/69) of the tumours showed overexpression of the p53 protein. No difference in pre-treatment parameters for p53-positive and p53-negative cases was detected. In multivariate analysis p53 was significantly associated with overall survival (OS) next to weight loss, tumour stage and N-stage. For metastatic-free survival (MFS) p53 status proved to be the sole independent prognostic factor. The influence of p53 on local recurrence-free survival (LRFS), however, was not as strong as on OS and MFS.
Conclusions: Immunohistochemically detected overexpression of mutated p53 protein in oesophagus carcinoma was an independent prognostic factor in a group of patients treated with radiotherapy alone. |
doi_str_mv | 10.1016/S0167-8140(97)00163-1 |
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Materials and methods: Immunostaining for p53 protein was performed on paraffin-embedded specimens from 69 patients with adeno- and squamous cell carcinoma of the oesophagus. All patients were treated by radiotherapy exclusively, consisting of a combination of external irradiation and intraluminal brachytherapy, using two different dose levels.
Results: Fifty-four percent (37/69) of the tumours showed overexpression of the p53 protein. No difference in pre-treatment parameters for p53-positive and p53-negative cases was detected. In multivariate analysis p53 was significantly associated with overall survival (OS) next to weight loss, tumour stage and N-stage. For metastatic-free survival (MFS) p53 status proved to be the sole independent prognostic factor. The influence of p53 on local recurrence-free survival (LRFS), however, was not as strong as on OS and MFS.
Conclusions: Immunohistochemically detected overexpression of mutated p53 protein in oesophagus carcinoma was an independent prognostic factor in a group of patients treated with radiotherapy alone.</description><identifier>ISSN: 0167-8140</identifier><identifier>EISSN: 1879-0887</identifier><identifier>DOI: 10.1016/S0167-8140(97)00163-1</identifier><identifier>PMID: 9510045</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Adenocarcinoma - metabolism ; Adenocarcinoma - pathology ; Adenocarcinoma - radiotherapy ; Aged ; Carcinoma, Squamous Cell - metabolism ; Carcinoma, Squamous Cell - pathology ; Carcinoma, Squamous Cell - radiotherapy ; Esophageal Neoplasms - diagnostic imaging ; Esophageal Neoplasms - metabolism ; Esophageal Neoplasms - pathology ; Female ; Follow-Up Studies ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Oesophageal carcinoma ; p53 expression ; Prognosis ; Prospective Studies ; Radiation Tolerance - physiology ; Radionuclide Imaging ; Radiotherapy ; Treatment Outcome ; Tumor Suppressor Protein p53 - biosynthesis ; Tumor Suppressor Protein p53 - physiology</subject><ispartof>Radiotherapy and oncology, 1998-02, Vol.46 (2), p.179-184</ispartof><rights>1998 Elsevier Science Ireland Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c360t-faac64aedda73b65069206bcdc545e3d08334de925426a5429440b1c3c01a7a53</citedby><cites>FETCH-LOGICAL-c360t-faac64aedda73b65069206bcdc545e3d08334de925426a5429440b1c3c01a7a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9510045$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pomp, Jacqueline</creatorcontrib><creatorcontrib>Davelaar, Jacob</creatorcontrib><creatorcontrib>Blom, Jan</creatorcontrib><creatorcontrib>van Krimpen, Cees</creatorcontrib><creatorcontrib>Zwinderman, Aeilko</creatorcontrib><creatorcontrib>Quint, Wilhelmus</creatorcontrib><creatorcontrib>Immerzeel, Jos</creatorcontrib><title>Radiotherapy for oesophagus carcinoma: the impact of p53 on treatment outcome</title><title>Radiotherapy and oncology</title><addtitle>Radiother Oncol</addtitle><description>Background and purpose: Wildtype p53 protein plays an important role in the cellular response to ionizing radiation and other DNA damaging agents and is mutated in many human tumours. We evaluated the relationship of the immunohistochemically determined p53 protein status and the disease control with radiotherapy alone for carcinoma of the oesophagus.
Materials and methods: Immunostaining for p53 protein was performed on paraffin-embedded specimens from 69 patients with adeno- and squamous cell carcinoma of the oesophagus. All patients were treated by radiotherapy exclusively, consisting of a combination of external irradiation and intraluminal brachytherapy, using two different dose levels.
Results: Fifty-four percent (37/69) of the tumours showed overexpression of the p53 protein. No difference in pre-treatment parameters for p53-positive and p53-negative cases was detected. In multivariate analysis p53 was significantly associated with overall survival (OS) next to weight loss, tumour stage and N-stage. For metastatic-free survival (MFS) p53 status proved to be the sole independent prognostic factor. The influence of p53 on local recurrence-free survival (LRFS), however, was not as strong as on OS and MFS.
Conclusions: Immunohistochemically detected overexpression of mutated p53 protein in oesophagus carcinoma was an independent prognostic factor in a group of patients treated with radiotherapy alone.</description><subject>Adenocarcinoma - metabolism</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenocarcinoma - radiotherapy</subject><subject>Aged</subject><subject>Carcinoma, Squamous Cell - metabolism</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Carcinoma, Squamous Cell - radiotherapy</subject><subject>Esophageal Neoplasms - diagnostic imaging</subject><subject>Esophageal Neoplasms - metabolism</subject><subject>Esophageal Neoplasms - pathology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oesophageal carcinoma</subject><subject>p53 expression</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Radiation Tolerance - physiology</subject><subject>Radionuclide Imaging</subject><subject>Radiotherapy</subject><subject>Treatment Outcome</subject><subject>Tumor Suppressor Protein p53 - biosynthesis</subject><subject>Tumor Suppressor Protein p53 - physiology</subject><issn>0167-8140</issn><issn>1879-0887</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkE1PHDEMhqMKBFvan4CUU0UPA85kMpn0ghDqBxIIibbnyJt4StDOZEhmkPj3DeyKKxdbtl_7lR_GjgWcChDt2e8SdNWJBk6M_gqlkpX4wFai06aCrtN7bPUmOWQfc34AgBqkPmAHRgmARq3YzR36EOd7Sjg98z4mHinH6R7_LZk7TC6MccBvvCh4GCZ0M489n5TkceRzIpwHGktvmV0c6BPb73GT6fMuH7G_P77_ufxVXd_-vLq8uK6cbGGuekTXNkjeo5brVkFramjXzjvVKJIeOikbT6ZWTd1iCaZpYC2cdCBQo5JH7Mv27pTi40J5tkPIjjYbHCku2WqjJRioi1BthS7FnBP1dkphwPRsBdgXjPYVo31hZI22rxitKHvHO4NlPZB_29pxK_Pz7ZzKl0-Bks0u0OjIh0Rutj6Gdxz-A6r9gXk</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>Pomp, Jacqueline</creator><creator>Davelaar, Jacob</creator><creator>Blom, Jan</creator><creator>van Krimpen, Cees</creator><creator>Zwinderman, Aeilko</creator><creator>Quint, Wilhelmus</creator><creator>Immerzeel, Jos</creator><general>Elsevier Ireland Ltd</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></search><sort><creationdate>19980201</creationdate><title>Radiotherapy for oesophagus carcinoma: the impact of p53 on treatment outcome</title><author>Pomp, Jacqueline ; Davelaar, Jacob ; Blom, Jan ; van Krimpen, Cees ; Zwinderman, Aeilko ; Quint, Wilhelmus ; Immerzeel, Jos</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c360t-faac64aedda73b65069206bcdc545e3d08334de925426a5429440b1c3c01a7a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Adenocarcinoma - metabolism</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenocarcinoma - radiotherapy</topic><topic>Aged</topic><topic>Carcinoma, Squamous Cell - metabolism</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Carcinoma, Squamous Cell - radiotherapy</topic><topic>Esophageal Neoplasms - diagnostic imaging</topic><topic>Esophageal Neoplasms - metabolism</topic><topic>Esophageal Neoplasms - pathology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oesophageal carcinoma</topic><topic>p53 expression</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Radiation Tolerance - physiology</topic><topic>Radionuclide Imaging</topic><topic>Radiotherapy</topic><topic>Treatment Outcome</topic><topic>Tumor Suppressor Protein p53 - biosynthesis</topic><topic>Tumor Suppressor Protein p53 - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pomp, Jacqueline</creatorcontrib><creatorcontrib>Davelaar, Jacob</creatorcontrib><creatorcontrib>Blom, Jan</creatorcontrib><creatorcontrib>van Krimpen, Cees</creatorcontrib><creatorcontrib>Zwinderman, Aeilko</creatorcontrib><creatorcontrib>Quint, Wilhelmus</creatorcontrib><creatorcontrib>Immerzeel, Jos</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><jtitle>Radiotherapy and oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pomp, Jacqueline</au><au>Davelaar, Jacob</au><au>Blom, Jan</au><au>van Krimpen, Cees</au><au>Zwinderman, Aeilko</au><au>Quint, Wilhelmus</au><au>Immerzeel, Jos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Radiotherapy for oesophagus carcinoma: the impact of p53 on treatment outcome</atitle><jtitle>Radiotherapy and oncology</jtitle><addtitle>Radiother Oncol</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>46</volume><issue>2</issue><spage>179</spage><epage>184</epage><pages>179-184</pages><issn>0167-8140</issn><eissn>1879-0887</eissn><abstract>Background and purpose: Wildtype p53 protein plays an important role in the cellular response to ionizing radiation and other DNA damaging agents and is mutated in many human tumours. We evaluated the relationship of the immunohistochemically determined p53 protein status and the disease control with radiotherapy alone for carcinoma of the oesophagus.
Materials and methods: Immunostaining for p53 protein was performed on paraffin-embedded specimens from 69 patients with adeno- and squamous cell carcinoma of the oesophagus. All patients were treated by radiotherapy exclusively, consisting of a combination of external irradiation and intraluminal brachytherapy, using two different dose levels.
Results: Fifty-four percent (37/69) of the tumours showed overexpression of the p53 protein. No difference in pre-treatment parameters for p53-positive and p53-negative cases was detected. In multivariate analysis p53 was significantly associated with overall survival (OS) next to weight loss, tumour stage and N-stage. For metastatic-free survival (MFS) p53 status proved to be the sole independent prognostic factor. The influence of p53 on local recurrence-free survival (LRFS), however, was not as strong as on OS and MFS.
Conclusions: Immunohistochemically detected overexpression of mutated p53 protein in oesophagus carcinoma was an independent prognostic factor in a group of patients treated with radiotherapy alone.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>9510045</pmid><doi>10.1016/S0167-8140(97)00163-1</doi><tpages>6</tpages></addata></record> |
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subjects | Adenocarcinoma - metabolism Adenocarcinoma - pathology Adenocarcinoma - radiotherapy Aged Carcinoma, Squamous Cell - metabolism Carcinoma, Squamous Cell - pathology Carcinoma, Squamous Cell - radiotherapy Esophageal Neoplasms - diagnostic imaging Esophageal Neoplasms - metabolism Esophageal Neoplasms - pathology Female Follow-Up Studies Humans Immunohistochemistry Male Middle Aged Oesophageal carcinoma p53 expression Prognosis Prospective Studies Radiation Tolerance - physiology Radionuclide Imaging Radiotherapy Treatment Outcome Tumor Suppressor Protein p53 - biosynthesis Tumor Suppressor Protein p53 - physiology |
title | Radiotherapy for oesophagus carcinoma: the impact of p53 on treatment outcome |
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