Prediction of chemotherapeutic response by collagen gel droplet embedded culture‐drug sensitivity test in human breast cancers

Collagen gel droplet embedded culture‐drug sensitivity test (CD‐DST) is the newly developed in vitro chemosensitivity test that has several advantages over the conventional ones. The aim of the present study is to examine the clinical usefulness of this test in the prediction of response to chemothe...

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Veröffentlicht in:International journal of cancer 2002-03, Vol.98 (3), p.450-455
Hauptverfasser: Takamura, Yuuki, Kobayashi, Hisayuki, Taguchi, Tetsuya, Motomura, Kazuyoshi, Inaji, Hideo, Noguchi, Shinzaburo
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container_end_page 455
container_issue 3
container_start_page 450
container_title International journal of cancer
container_volume 98
creator Takamura, Yuuki
Kobayashi, Hisayuki
Taguchi, Tetsuya
Motomura, Kazuyoshi
Inaji, Hideo
Noguchi, Shinzaburo
description Collagen gel droplet embedded culture‐drug sensitivity test (CD‐DST) is the newly developed in vitro chemosensitivity test that has several advantages over the conventional ones. The aim of the present study is to examine the clinical usefulness of this test in the prediction of response to chemotherapy in breast cancer patients. Seventy patients with primary (n = 45) or locally recurrent (n = 25) breast cancers were recruited, and each patient underwent tumor biopsy before chemotherapy. The biopsy specimens were used for CD‐DST and immunohistological examination of 6 biological markers (P‐gp, erbB2, p53, BCL2, MIB1 and ER‐α). As chemotherapy, cyclophosphamide 600 mg/m2 plus epirubicin 60 mg/m2 q3w (CE, n = 28) or docetaxel 60 mg/m2 q3w (DOC, n = 42) was given. Interpretable results using the CD‐DST assay were obtained from 84.3% (59/70) of tumor specimens studied. Of the 18 tumors diagnosed as CE sensitive by CD‐DST, 15 (83.3%) exhibited a response to CE therapy and none of the 5 tumors diagnosed as CE resistant by CD‐DST exhibited a response to CE therapy. Of the 14 tumors diagnosed as DOC sensitive by CD‐DST, 13 (92.9%) exhibited a response to DOC therapy and only one of the 22 tumors diagnosed as DOC resistant by CD‐DST exhibited a response to DOC therapy. P‐gp expression was found to exhibit a significant (p < 0.05) association with the resistance to CE therapy but not to DOC therapy. Diagnostic accuracy (72.7%) achieved by P‐gp was lower than that (87.0%) achieved by CD‐DST in CE therapy. Expressions of other biological markers (erbB2, p53, BCL2, MIB1 and ER‐α) were not significantly associated with response to CE or DOC therapy. These results demonstrate that CD‐DST can predict the response to CE and DOC therapy with a high accuracy in breast cancer patients and seems to be superior to the conventional predictors. © 2002 Wiley‐Liss, Inc.
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The aim of the present study is to examine the clinical usefulness of this test in the prediction of response to chemotherapy in breast cancer patients. Seventy patients with primary (n = 45) or locally recurrent (n = 25) breast cancers were recruited, and each patient underwent tumor biopsy before chemotherapy. The biopsy specimens were used for CD‐DST and immunohistological examination of 6 biological markers (P‐gp, erbB2, p53, BCL2, MIB1 and ER‐α). As chemotherapy, cyclophosphamide 600 mg/m2 plus epirubicin 60 mg/m2 q3w (CE, n = 28) or docetaxel 60 mg/m2 q3w (DOC, n = 42) was given. Interpretable results using the CD‐DST assay were obtained from 84.3% (59/70) of tumor specimens studied. Of the 18 tumors diagnosed as CE sensitive by CD‐DST, 15 (83.3%) exhibited a response to CE therapy and none of the 5 tumors diagnosed as CE resistant by CD‐DST exhibited a response to CE therapy. Of the 14 tumors diagnosed as DOC sensitive by CD‐DST, 13 (92.9%) exhibited a response to DOC therapy and only one of the 22 tumors diagnosed as DOC resistant by CD‐DST exhibited a response to DOC therapy. P‐gp expression was found to exhibit a significant (p &lt; 0.05) association with the resistance to CE therapy but not to DOC therapy. Diagnostic accuracy (72.7%) achieved by P‐gp was lower than that (87.0%) achieved by CD‐DST in CE therapy. Expressions of other biological markers (erbB2, p53, BCL2, MIB1 and ER‐α) were not significantly associated with response to CE or DOC therapy. 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The aim of the present study is to examine the clinical usefulness of this test in the prediction of response to chemotherapy in breast cancer patients. Seventy patients with primary (n = 45) or locally recurrent (n = 25) breast cancers were recruited, and each patient underwent tumor biopsy before chemotherapy. The biopsy specimens were used for CD‐DST and immunohistological examination of 6 biological markers (P‐gp, erbB2, p53, BCL2, MIB1 and ER‐α). As chemotherapy, cyclophosphamide 600 mg/m2 plus epirubicin 60 mg/m2 q3w (CE, n = 28) or docetaxel 60 mg/m2 q3w (DOC, n = 42) was given. Interpretable results using the CD‐DST assay were obtained from 84.3% (59/70) of tumor specimens studied. Of the 18 tumors diagnosed as CE sensitive by CD‐DST, 15 (83.3%) exhibited a response to CE therapy and none of the 5 tumors diagnosed as CE resistant by CD‐DST exhibited a response to CE therapy. Of the 14 tumors diagnosed as DOC sensitive by CD‐DST, 13 (92.9%) exhibited a response to DOC therapy and only one of the 22 tumors diagnosed as DOC resistant by CD‐DST exhibited a response to DOC therapy. P‐gp expression was found to exhibit a significant (p &lt; 0.05) association with the resistance to CE therapy but not to DOC therapy. Diagnostic accuracy (72.7%) achieved by P‐gp was lower than that (87.0%) achieved by CD‐DST in CE therapy. Expressions of other biological markers (erbB2, p53, BCL2, MIB1 and ER‐α) were not significantly associated with response to CE or DOC therapy. 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Andrology. Obstetrics</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - drug therapy</subject><subject>Neoplasm Recurrence, Local - metabolism</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Neoplasm Staging</subject><subject>Paclitaxel - analogs &amp; derivatives</subject><subject>Paclitaxel - therapeutic use</subject><subject>Pharmacology. Drug treatments</subject><subject>Predictive Value of Tests</subject><subject>Taxoids</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kLlOxDAQQC0EguUo-AHkhoIi4COOkxKtOIUEBdSRY493jXLJdkDb8Ql8I1-CYVeiopoZzdMcD6FjSs4pIezCveqUMFJuoRkllcwIo2IbzVKPZJLyYg_th_BKCKWC5Ltoj9KKEVFVM_Tx5ME4Hd3Q48FivYRuiEvwaoQpOo09hHHoA-BmhfXQtmoBPV5Ai40fxhYihq4BY8BgPbVx8vD18Wn8tMAB-uCie3NxhSOEiF2Pl1Onetx4UKnWqtfgwyHasaoNcLSJB-jl-up5fps9PN7czS8fMp0LVmayAVvktGQV1VbmouRVoSy3xDZEaiPynAOnQouGpWu4KYikpjQlY0ZJwSk_QGfrudoPIXiw9ehdp_yqpqT-sVgni_WvxcSerNlxajowf-RGWwJON4AKWrXWp19c-OO4KCSXReIu1ty7a2H1_8b67n6-Xv0NvkSMaw</recordid><startdate>20020320</startdate><enddate>20020320</enddate><creator>Takamura, Yuuki</creator><creator>Kobayashi, Hisayuki</creator><creator>Taguchi, Tetsuya</creator><creator>Motomura, Kazuyoshi</creator><creator>Inaji, Hideo</creator><creator>Noguchi, Shinzaburo</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20020320</creationdate><title>Prediction of chemotherapeutic response by collagen gel droplet embedded culture‐drug sensitivity test in human breast cancers</title><author>Takamura, Yuuki ; Kobayashi, Hisayuki ; Taguchi, Tetsuya ; Motomura, Kazuyoshi ; Inaji, Hideo ; Noguchi, Shinzaburo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4528-7bef6418291cf7458396af3f0fb07cd5443e315c5b2dde3d6071d8d822da75313</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>Biopsy</topic><topic>breast cancer</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Chemotherapy</topic><topic>Collagen</topic><topic>collagen gel droplet</topic><topic>Cyclophosphamide - administration &amp; dosage</topic><topic>Docetaxel</topic><topic>Drug Screening Assays, Antitumor</topic><topic>drug sensitivity test</topic><topic>Epirubicin - administration &amp; dosage</topic><topic>Female</topic><topic>Gels</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - drug therapy</topic><topic>Neoplasm Recurrence, Local - metabolism</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Neoplasm Staging</topic><topic>Paclitaxel - analogs &amp; derivatives</topic><topic>Paclitaxel - therapeutic use</topic><topic>Pharmacology. Drug treatments</topic><topic>Predictive Value of Tests</topic><topic>Taxoids</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takamura, Yuuki</creatorcontrib><creatorcontrib>Kobayashi, Hisayuki</creatorcontrib><creatorcontrib>Taguchi, Tetsuya</creatorcontrib><creatorcontrib>Motomura, Kazuyoshi</creatorcontrib><creatorcontrib>Inaji, Hideo</creatorcontrib><creatorcontrib>Noguchi, Shinzaburo</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takamura, Yuuki</au><au>Kobayashi, Hisayuki</au><au>Taguchi, Tetsuya</au><au>Motomura, Kazuyoshi</au><au>Inaji, Hideo</au><au>Noguchi, Shinzaburo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prediction of chemotherapeutic response by collagen gel droplet embedded culture‐drug sensitivity test in human breast cancers</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2002-03-20</date><risdate>2002</risdate><volume>98</volume><issue>3</issue><spage>450</spage><epage>455</epage><pages>450-455</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>Collagen gel droplet embedded culture‐drug sensitivity test (CD‐DST) is the newly developed in vitro chemosensitivity test that has several advantages over the conventional ones. The aim of the present study is to examine the clinical usefulness of this test in the prediction of response to chemotherapy in breast cancer patients. Seventy patients with primary (n = 45) or locally recurrent (n = 25) breast cancers were recruited, and each patient underwent tumor biopsy before chemotherapy. The biopsy specimens were used for CD‐DST and immunohistological examination of 6 biological markers (P‐gp, erbB2, p53, BCL2, MIB1 and ER‐α). As chemotherapy, cyclophosphamide 600 mg/m2 plus epirubicin 60 mg/m2 q3w (CE, n = 28) or docetaxel 60 mg/m2 q3w (DOC, n = 42) was given. Interpretable results using the CD‐DST assay were obtained from 84.3% (59/70) of tumor specimens studied. Of the 18 tumors diagnosed as CE sensitive by CD‐DST, 15 (83.3%) exhibited a response to CE therapy and none of the 5 tumors diagnosed as CE resistant by CD‐DST exhibited a response to CE therapy. Of the 14 tumors diagnosed as DOC sensitive by CD‐DST, 13 (92.9%) exhibited a response to DOC therapy and only one of the 22 tumors diagnosed as DOC resistant by CD‐DST exhibited a response to DOC therapy. P‐gp expression was found to exhibit a significant (p &lt; 0.05) association with the resistance to CE therapy but not to DOC therapy. Diagnostic accuracy (72.7%) achieved by P‐gp was lower than that (87.0%) achieved by CD‐DST in CE therapy. Expressions of other biological markers (erbB2, p53, BCL2, MIB1 and ER‐α) were not significantly associated with response to CE or DOC therapy. These results demonstrate that CD‐DST can predict the response to CE and DOC therapy with a high accuracy in breast cancer patients and seems to be superior to the conventional predictors. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>11920599</pmid><doi>10.1002/ijc.10208</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Biomarkers, Tumor - metabolism
Biopsy
breast cancer
Breast Neoplasms - drug therapy
Breast Neoplasms - metabolism
Breast Neoplasms - pathology
Chemotherapy
Collagen
collagen gel droplet
Cyclophosphamide - administration & dosage
Docetaxel
Drug Screening Assays, Antitumor
drug sensitivity test
Epirubicin - administration & dosage
Female
Gels
Gynecology. Andrology. Obstetrics
Humans
Immunoenzyme Techniques
Mammary gland diseases
Medical sciences
Middle Aged
Neoplasm Recurrence, Local - drug therapy
Neoplasm Recurrence, Local - metabolism
Neoplasm Recurrence, Local - pathology
Neoplasm Staging
Paclitaxel - analogs & derivatives
Paclitaxel - therapeutic use
Pharmacology. Drug treatments
Predictive Value of Tests
Taxoids
Tumors
title Prediction of chemotherapeutic response by collagen gel droplet embedded culture‐drug sensitivity test in human breast cancers
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