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dc.contributor.authorBaildam, Andrew D
dc.contributor.authorZaloudik, J
dc.contributor.authorHowell, Anthony
dc.contributor.authorBarnes, Diana M
dc.contributor.authorTurnbull, Lesley
dc.contributor.authorSwindell, Ric
dc.contributor.authorMoore, Michael
dc.contributor.authorSellwood, R A
dc.date.accessioned2010-10-20T11:10:46Z
dc.date.available2010-10-20T11:10:46Z
dc.date.issued1987-05
dc.identifier.citationDNA analysis by flow cytometry, response to endocrine treatment and prognosis in advanced carcinoma of the breast. 1987, 55 (5):553-9 Br. J. Canceren
dc.identifier.issn0007-0920
dc.identifier.pmid3038158
dc.identifier.urihttp://hdl.handle.net/10541/113547
dc.description.abstractThe relationship between DNA content of mammary cancer and subsequent response to endocrine therapy was studied in 136 patients with advanced disease. All were treated with tamoxifen or ovarian ablation as first-line systemic therapy after relapse and were evaluable for response according to UICC criteria. DNA characterisation by flow cytometry was used on formalin fixed paraffin-embedded samples of tumour. Tumours were grouped according to DNA index into diploid (n = 52, 38%), 'tetraploid' (n = 46, 34%) and 'other DNA-aneuploid' (n = 38, 28%). The highest proportion of oestrogen receptor positive tumours (ER + ve) was found in the 'tetraploid' tumours (38/46, 85%, Chi-square = 8.53, P less than 0.02), and response rates, (SD + PR + CR), were 26/52 (50%), 34/46 (74%), and 15/38 (39%) respectively (Chi-square = 10.88, P less than 0.005). Patients with diploid or 'tetraploid' tumours survived longer and stayed in remission longer than those with 'other DNA-aneuploid' tumours. We suggest that 'tetraploid' or 'near tetraploid' human mammary tumours may comprise a distinct group of endocrine responsive tumours within the overall group of aneuploid tumours. The conventional interpretation of DNA histograms, grouping into diploid and aneuploid, may be masking important features of some tumour groups.
dc.language.isoenen
dc.subjectBreast Canceren
dc.subjectCancer DNAen
dc.subjectOestrogen Receptorsen
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshAged, 80 and over
dc.subject.meshBreast Neoplasms
dc.subject.meshCarcinoma, Intraductal, Noninfiltrating
dc.subject.meshDNA, Neoplasm
dc.subject.meshFemale
dc.subject.meshFlow Cytometry
dc.subject.meshHumans
dc.subject.meshMiddle Aged
dc.subject.meshPloidies
dc.subject.meshPrognosis
dc.subject.meshReceptors, Estrogen
dc.subject.meshTamoxifen
dc.subject.meshTime Factors
dc.titleDNA analysis by flow cytometry, response to endocrine treatment and prognosis in advanced carcinoma of the breast.en
dc.typeArticleen
dc.identifier.journalBritish Journal of Canceren
html.description.abstractThe relationship between DNA content of mammary cancer and subsequent response to endocrine therapy was studied in 136 patients with advanced disease. All were treated with tamoxifen or ovarian ablation as first-line systemic therapy after relapse and were evaluable for response according to UICC criteria. DNA characterisation by flow cytometry was used on formalin fixed paraffin-embedded samples of tumour. Tumours were grouped according to DNA index into diploid (n = 52, 38%), 'tetraploid' (n = 46, 34%) and 'other DNA-aneuploid' (n = 38, 28%). The highest proportion of oestrogen receptor positive tumours (ER + ve) was found in the 'tetraploid' tumours (38/46, 85%, Chi-square = 8.53, P less than 0.02), and response rates, (SD + PR + CR), were 26/52 (50%), 34/46 (74%), and 15/38 (39%) respectively (Chi-square = 10.88, P less than 0.005). Patients with diploid or 'tetraploid' tumours survived longer and stayed in remission longer than those with 'other DNA-aneuploid' tumours. We suggest that 'tetraploid' or 'near tetraploid' human mammary tumours may comprise a distinct group of endocrine responsive tumours within the overall group of aneuploid tumours. The conventional interpretation of DNA histograms, grouping into diploid and aneuploid, may be masking important features of some tumour groups.


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