ArticleBritish journal of cancer2004
A prognostic index for operable, node-negative breast cancer.
Article in British journal of cancer, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
7 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- p27(Kip1) as a prognostic factor in breast cancer: a systematic review and meta-analysis.Journal of cellular and molecular medicine · 2010Pooled it
- Pooled it
- Bcl-2 expression and prognostic significance in feline invasive mammary carcinomas: a retrospective observational study.BMC veterinary research · 2019Article
- Loss of nuclear localized and tyrosine phosphorylated Stat5 in breast cancer predicts poor clinical outcome and increased risk of antiestrogen therapy failure.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2011Article
- A mechanism misregulating p27 in tumors discovered in a functional genomic screen.PLoS genetics · 2007Article
- Re: p27(Kip1) and cyclin E expression and breast cancer survival after treatment with adjuvant chemotherapy.Journal of the National Cancer Institute · 2007Article
- p27(Kip1) and cyclin E expression and breast cancer survival after treatment with adjuvant chemotherapy.Journal of the National Cancer Institute · 2006Article
Corrections and comments
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Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Clinical data and samples from patients diagnosed, more than 10 years previously, with operable node-negative breast cancer (participants in the Scottish Adjuvant Tamoxifen trial), were revisited. Cases with two distinct categories of outcome were selected; more than 10 years disease-free survival ('good outcome') or distant relapse within 6 years of diagnosis ('poor outcome'). An initial set of cases was analysed for a range of putative prognostic markers and a prognostic index, distinguishing the two outcome categories, was calculated. This index was then validated by testing its predictive power on a second, independent set of cases. A combination of histological grade plus immunochemical staining for BCL-2, p27 and Cyclin D1, generated a useful prognostic index for tamoxifen-treated patients but not for those treated by surgery alone. The value of the index was confirmed in a second set of tamoxifen-treated, early stage breast cancers. Overall, it correctly predicted good and poor outcome in 79 and 74% of cases, respectively (odds ratio 11.0). Other markers assessed added little to prediction of outcome. In the case of molecular assays, sensitivity and reliability were compromised by the age of the tissue specimens and the variability of fixation protocols. In selecting patients for adjuvant systemic chemotherapy, the proposed index improves considerably on current international guidelines and matches the performance reported for 'gene-expression signature' analysis.
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