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 |
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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. |
doi_str_mv | 10.1002/ijc.10208 |
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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 < 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.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.10208</identifier><identifier>PMID: 11920599</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>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</subject><ispartof>International journal of cancer, 2002-03, Vol.98 (3), p.450-455</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4528-7bef6418291cf7458396af3f0fb07cd5443e315c5b2dde3d6071d8d822da75313</citedby><cites>FETCH-LOGICAL-c4528-7bef6418291cf7458396af3f0fb07cd5443e315c5b2dde3d6071d8d822da75313</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fijc.10208$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.10208$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13567376$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11920599$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takamura, Yuuki</creatorcontrib><creatorcontrib>Kobayashi, Hisayuki</creatorcontrib><creatorcontrib>Taguchi, Tetsuya</creatorcontrib><creatorcontrib>Motomura, Kazuyoshi</creatorcontrib><creatorcontrib>Inaji, Hideo</creatorcontrib><creatorcontrib>Noguchi, Shinzaburo</creatorcontrib><title>Prediction of chemotherapeutic response by collagen gel droplet embedded culture‐drug sensitivity test in human breast cancers</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><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.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>Biopsy</subject><subject>breast cancer</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Chemotherapy</subject><subject>Collagen</subject><subject>collagen gel droplet</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Docetaxel</subject><subject>Drug Screening Assays, Antitumor</subject><subject>drug sensitivity test</subject><subject>Epirubicin - administration & dosage</subject><subject>Female</subject><subject>Gels</subject><subject>Gynecology. 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 & 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 & dosage</topic><topic>Docetaxel</topic><topic>Drug Screening Assays, Antitumor</topic><topic>drug sensitivity test</topic><topic>Epirubicin - administration & 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 & 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 < 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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