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4.
Br J Cancer ; 107(2): 221-3, 2012 Jul 10.
Article En | MEDLINE | ID: mdl-22735901

BACKGROUND: The understanding of metastatic patterns after metachronous contralateral breast cancer (CBC) may help determine the biological nature of CBC. METHODS: A cohort of 8478 women with breast cancer treated at Guy's and St Thomas' NHS Foundation Trust between 1975 and 2006 were studied. Organ-specific 5-year cumulative incidence and incidence rate ratios were assessed for women diagnosed with unilateral breast cancer (UBC), CBC within 5 years and CBC more than 5 years of the initial diagnosis. RESULTS: Women diagnosed with CBC within 5 years had a higher incidence of metastases in all organs compared with UBC. Women with a short interval time to CBC developed metastasis more rapidly and were more likely to develop visceral and distant cutaneous metastases compared with bone metastasis. CONCLUSION: These findings explain poor prognosis of women with early occurring CBC and suggest that some of these CBCs are indicators of aggressive and/or systemic disease.


Breast Neoplasms/diagnosis , Breast Neoplasms/pathology , Neoplasms, Second Primary/diagnosis , Neoplasms, Second Primary/pathology , Breast Neoplasms/epidemiology , Cohort Studies , Female , Follow-Up Studies , Humans , Incidence , Neoplasm Metastasis , Neoplasms, Second Primary/epidemiology , Prognosis , United Kingdom/epidemiology
5.
Breast Cancer Res Treat ; 134(2): 811-4, 2012 Jul.
Article En | MEDLINE | ID: mdl-22678157

Various studies have suggested that women who smoke have a worse prognosis if they develop breast cancer. Cotinine levels have been measured in sera from 511 patients with stage I and II breast cancer diagnosed between 1975 and 1980, all of whom had complete follow-up. Although the known prognostic factors, axillary nodal status, tumour size and grade were found to be significant, there was no relationship between serum cotinine and metastasis-free survival. A point estimate of serum cotinine was not found to be a determinant of survival in women with early breast cancer.


Breast Neoplasms/blood , Breast Neoplasms/pathology , Cotinine/blood , Smoking/adverse effects , Aged , Breast Neoplasms/mortality , Cohort Studies , Disease-Free Survival , Female , Humans , Lymphatic Metastasis , Middle Aged , Prognosis , Risk Factors , Smoking/blood
7.
Int J Clin Pract ; 66(1): 28-36, 2012 Jan.
Article En | MEDLINE | ID: mdl-22145580

Zearalenone (ZEN) is a non-steroidal mycoestrogen that widely contaminates agricultural products. ZEN and its derivatives share similar molecular mechanisms and activity with estrogens and interact with ERα and ERß leading to changes in the reproductive system in both animals and humans. The reduced form of ZEN, α-ZEA ralenol, has been used as an anabolic agent for animals and also proposed as hormonal replacement therapy in postmenopausal women. Furthermore, both zearelanol ZEN and derivatives have been patented as oral contraceptives. ZEN has been widely used in the United States since 1969 to improve fattening rates in cattle by increasing growth rate and feed conversion efficiency. Evidence of human harm from this practice is provided by observations of central precocious puberty. As a result, this practice has been banned by the European Union. As ZEN has been associated with breast enlargement in humans, it has been included in many bust-enhancing dietary supplements but epidemiological evidence is lacking with regard to breast cancer risk. Extensive work with human breast cancer cell lines has shown estrogenic stimulation in those possessing ER but a reduction in DMBA-induced breast cancers in rodents given ZEN. Protein disulfide isomerase provides a molecular biomarker of dietary exposure to ZEN and its derivatives allowing the detection and control of harmful food intake. The interaction of ZEN with anti-estrogens, anticancer agents and antioxidants requires further investigation.


Breast Neoplasms/chemically induced , Estrogens, Non-Steroidal/adverse effects , Zearalenone/adverse effects , Animals , Anticarcinogenic Agents/therapeutic use , Apoptosis/drug effects , Breast Neoplasms/prevention & control , Cattle , Cell Line, Tumor , Diet/adverse effects , Disease Models, Animal , Dose-Response Relationship, Drug , Estrogens, Non-Steroidal/metabolism , Female , Food Contamination/analysis , Food Contamination/prevention & control , Growth Substances/pharmacology , Hormone Replacement Therapy , Humans , Inactivation, Metabolic/physiology , Puberty, Precocious/chemically induced , Receptors, Estrogen/drug effects , Zearalenone/metabolism , Zeranol/adverse effects , Zeranol/metabolism
8.
Eur J Surg Oncol ; 37(12): 1051-8, 2011 Dec.
Article En | MEDLINE | ID: mdl-21843919

BACKGROUND: In breast cancer patients (≥70 years), tumour resection plus tamoxifen (T + T) has a higher loco-regional relapse (LR) rate than mastectomy. This study examines factors influencing local recurrence in these cases. METHODS: Clinical records of 71 patients aged ≥70 years, randomised to the T + T arm of 2 randomised trials were reviewed. Cox Proportional Hazards model was used to determine the most significant variables. RESULTS: After 15-years follow-up, LR relapse occurred in 29/71, of whom 5 had synchronous metastatic disease. Most tumours recurred in the index quadrant. Subsequently 21/24 patients with loco-regional recurrence only had salvage mastectomy. Three variables significantly predicted LR: lympho-vascular invasion (LVI) (HR [95% CI]: 11.18 [4.47, 27.95], p < 0.01), ER negative status (HR [95% CI]: 0.27 [0.10, 0.72] p = 0.01), and tumour necrosis (HR [95% CI]: 2.65 [1.10, 6.37], p = 0.03). Final margin status was not associated with LR. CONCLUSIONS: Tumour resection + Tamoxifen in older patients results in long-term local control in the majority with most loco-regional failures being salvageable. Risk factors for LR are lympho-vascular invasion, ER status and tumour necrosis. Negative tumour excision margins did not significantly change local outcome in the absence of radiotherapy. In these older patients LVI significantly reduced survival time.


Antineoplastic Agents, Hormonal/therapeutic use , Breast Neoplasms/drug therapy , Breast Neoplasms/surgery , Mastectomy, Segmental , Neoplasm Recurrence, Local/prevention & control , Tamoxifen/therapeutic use , Age Factors , Aged , Aged, 80 and over , Biomarkers, Tumor/analysis , Breast Neoplasms/mortality , Breast Neoplasms/pathology , Disease-Free Survival , Female , Follow-Up Studies , Humans , Kaplan-Meier Estimate , Lymphatic Metastasis , Mastectomy, Modified Radical , Medical Records , Multivariate Analysis , Neoplasm Grading , Neoplasm Invasiveness , Neoplasms, Multiple Primary/diagnosis , Patient Selection , Proportional Hazards Models , Randomized Controlled Trials as Topic , Retrospective Studies , Risk Factors , Salvage Therapy , Vascular Neoplasms/secondary
9.
Br J Cancer ; 105(5): 709-22, 2011 Aug 23.
Article En | MEDLINE | ID: mdl-21772329

BACKGROUND: Breast cancer risk for postmenopausal women is positively associated with circulating concentrations of oestrogens and androgens, but the determinants of these hormones are not well understood. METHODS: Cross-sectional analyses of breast cancer risk factors and circulating hormone concentrations in more than 6000 postmenopausal women controls in 13 prospective studies. RESULTS: Concentrations of all hormones were lower in older than younger women, with the largest difference for dehydroepiandrosterone sulphate (DHEAS), whereas sex hormone-binding globulin (SHBG) was higher in the older women. Androgens were lower in women with bilateral ovariectomy than in naturally postmenopausal women, with the largest difference for free testosterone. All hormones were higher in obese than lean women, with the largest difference for free oestradiol, whereas SHBG was lower in obese women. Smokers of 15+ cigarettes per day had higher levels of all hormones than non-smokers, with the largest difference for testosterone. Drinkers of 20+ g alcohol per day had higher levels of all hormones, but lower SHBG, than non-drinkers, with the largest difference for DHEAS. Hormone concentrations were not strongly related to age at menarche, parity, age at first full-term pregnancy or family history of breast cancer. CONCLUSION: Sex hormone concentrations were strongly associated with several established or suspected risk factors for breast cancer, and may mediate the effects of these factors on breast cancer risk.


Breast Neoplasms/etiology , Carcinoma/etiology , Gonadal Steroid Hormones/blood , Postmenopause/blood , Adult , Aged , Aged, 80 and over , Breast Neoplasms/blood , Carcinoma/blood , Cross-Sectional Studies , Female , Humans , Middle Aged , Pregnancy , Retrospective Studies , Risk Factors
11.
Br J Cancer ; 103(5): 747-56, 2010 Aug 24.
Article En | MEDLINE | ID: mdl-20648013

BACKGROUND: Epidemiological studies have suggested that excessive alcohol intake increases colorectal cancer (CRC) risk. However, findings regarding tumour subsites and sex differences have been inconsistent. METHODS: We investigated the prospective associations between alcohol intake on overall and site- and sex-specific CRC risk. Analyses were conducted on 579 CRC cases and 1996 matched controls nested within the UK Dietary Cohort Consortium using standardised data obtained from food diaries as a main nutritional method and repeated using data from food frequency questionnaire (FFQ). RESULTS: Compared with individuals in the lightest category of drinkers (>0-<5 g per day), the multivariable odds ratios of CRC were 1.16 (95% confidence interval (95% CI): 0.88, 1.53) for non-drinkers, 0.91 (95% CI: 0.67, 1.24) for drinkers with 5-<15 g per day, 0.90 (95% CI: 0.65, 1.25) for drinkers with 15-<30 g per day, 1.02 (95% CI: 0.66, 1.58) for drinkers with 30-<45 g per day and 1.19 (95% CI: 0.75, 1.91) for drinkers with >or=45 g per day. No clear associations were observed between site-specific CRC risk and alcohol intake in either sex. Analyses using FFQ showed similar results. CONCLUSION: We found no significantly increased risk of CRC up to 30 g per day of alcohol intake within the UK Dietary Cohort Consortium.


Alcohol Drinking/adverse effects , Colorectal Neoplasms/etiology , Case-Control Studies , Colorectal Neoplasms/epidemiology , Diet , Female , Humans , Male , Middle Aged , Risk Factors , Smoking/adverse effects , United Kingdom/epidemiology
12.
Br J Cancer ; 103(1): 90-3, 2010 Jun 29.
Article En | MEDLINE | ID: mdl-20517309

BACKGROUND: It has been reported that there is an increased risk of cancer in individuals with elevated levels of serum gamma-glutamyl transferase (GGT). METHODS: In the Guernsey Breast Cancer Cohort Study, GGT was measured in sera from 1803 normal women. Among these women, 251 subsequently developed cancer, of whom 96 developed breast cancer. RESULTS: After adjustment for age at entry, height, weight, age at menarche and first birth with nulliparity, there was a highly significant relationship between elevated GGT and breast cancer risk. In the highest quartile, the hazard ratio (HR) was 2.17 (95% confidence interval (CI): 1.19, 3.93). When subdivided by menopausal status, there was a reduced non-significant effect in postmenopausal women, whereas for premenopausal women in the highest quartile, HR was 3.81 (95% CI: 1.37, 10.59). Premenopausal women with serum GGT levels above the normal range had a significantly elevated HR of 4.90 (95% CI: 1.86, 12.94). CONCLUSIONS: These results suggest that premenopausal women with high normal (above median) serum GGT or elevated levels (< or =40 IU l(-1)) are at increased risk of breast cancer and might benefit from close surveillance, possibly with breast magnetic resonance imaging scans. Serum GGT may mark previous exposure to carcinogens and lead to the identification of DNA adducts involved in mammary carcinogenesis.


Breast Neoplasms/etiology , gamma-Glutamyltransferase/blood , Adult , Aged , Breast Neoplasms/enzymology , Cohort Studies , Female , Humans , Menopause , Middle Aged , Risk Factors
13.
Br J Cancer ; 103(1): 94-100, 2010 Jun 29.
Article En | MEDLINE | ID: mdl-20517310

BACKGROUND: There is no consensus agreement regarding optimal management of locally excised ductal carcinoma in situ (DCIS) or features of greatest assistance in predicting disease behaviour. Cases in the UKCCCR/ANZ DCIS trial have been histologically reviewed to determine the features of prognostic importance. METHOD: A total of 72% of 1694 cases entered into the UKCCCR/ANZ DCIS trial had full pathological review. A large number of histological features were assessed, blinded to outcome and compared regarding ability to predict ipsilateral recurrence, as either DCIS or progression to invasive carcinoma. RESULTS: Pathological features associated with ipsilateral recurrence in univariate analysis included high cytonuclear grade, larger lesion size, growth pattern, presence of necrosis or chronic inflammation, incompleteness (or uncertainty of completeness) of excision and smaller margin width. Receipt of post-operative radiotherapy was also a strong prognostic factor.We report a novel sub-division of the large group of high-grade lesions, which enables identification of a very poor prognosis sub-group; namely, DCIS that is of high cytonuclear grade, predominantly (>50%) solid architecture, bearing extensive comedo-type necrosis (>50% of ducts). In addition, we found little difference in ipsilateral recurrence rates between low- and intermediate-grade groups. Hazard ratios for low, intermediate, high and the new, very high, grade were 0.42, 0.33, 0.62 and 1.00, respectively, for ipsilateral in situ or invasive recurrence. CONCLUSION: We present a novel pathological classification for DCIS with substantially better prognostic discrimination for ipsilateral recurrence than the classical categorisation based on cytonuclear grade alone.


Breast Neoplasms/pathology , Carcinoma in Situ/pathology , Carcinoma, Ductal, Breast/pathology , Neoplasm Recurrence, Local/pathology , Age Factors , Female , Humans , Inflammation/complications , Multivariate Analysis , Randomized Controlled Trials as Topic
16.
Int J Gen Med ; 3: 19-21, 2010 Apr 08.
Article En | MEDLINE | ID: mdl-20463819

Synchronous bilateral male breast cancer (MBC) is rare and only a few cases have been reported in the literature. The majority of MBC patients have no definable risk factors. We describe a case with Klinefelter's syndrome, prior thymic irradiation, testicular surgery, and first degree family history in a 61-year-old male.

17.
Climacteric ; 13(1): 4-21, 2010 Feb.
Article En | MEDLINE | ID: mdl-20067430

Breast cancer survivors frequently experience severe hot flushes as a result of their treatment. This can adversely affect their quality of life, compliance with treatment and overall survival. To relieve vasomotor symptoms, a variety of drugs have been used including clonidine, gabapentin, selective serotonin reuptake inhibitors and selective norepinephrine reuptake inhibitors. Stellate ganglion block (SGB) has recently emerged as a new technique against hot flushes and preliminary studies report encouraging efficacy with minimal complications. Other approaches include various alternative treatments and, in a few cases, hormone replacement therapy (HRT). All randomized, controlled studies of drugs, hormone treatments and alternative therapies for vasomotor symptoms have been reviewed and efficacy and safety noted. Side-effects of current medical treatments frequently outweigh the benefits--leading many patients to discontinue the medications. Statistically significant differences between placebo and test agent may not translate into a meaningful subjective benefit. Desvenlafaxine looks promising as does SGB, despite its invasive nature. The favorable safety profile of SGB is confirmed through the long experience of SGB performed for other medical purposes. The majority of non-HRT treatments for hot flushes are little better than placebo but early results from randomized trials of desvenlafaxine and pilot studies of SGB suggest that it is worthwhile to test their efficacy specifically in breast cancer survivors.


Breast Neoplasms/therapy , Hot Flashes/etiology , Hot Flashes/therapy , Amines/adverse effects , Amines/therapeutic use , Anesthetics, Local , Bupivacaine/administration & dosage , Bupivacaine/adverse effects , Clonidine/adverse effects , Clonidine/therapeutic use , Complementary Therapies , Cyclohexanecarboxylic Acids/adverse effects , Cyclohexanecarboxylic Acids/therapeutic use , Drugs, Chinese Herbal/therapeutic use , Estrogen Replacement Therapy/adverse effects , Estrogens/adverse effects , Estrogens/therapeutic use , Exercise , Female , Gabapentin , Hot Flashes/drug therapy , Humans , Middle Aged , Norepinephrine/antagonists & inhibitors , Progesterone/administration & dosage , Progesterone/therapeutic use , Quality of Life , Randomized Controlled Trials as Topic , Selective Serotonin Reuptake Inhibitors/adverse effects , Selective Serotonin Reuptake Inhibitors/therapeutic use , Stellate Ganglion/drug effects , Survivors , gamma-Aminobutyric Acid/adverse effects , gamma-Aminobutyric Acid/therapeutic use
19.
Br J Surg ; 96(4): 376-80, 2009 Apr.
Article En | MEDLINE | ID: mdl-19283743

BACKGROUND: The prognosis of patients with synchronous bilateral breast cancer (SBBC) is usually based on the tumour with the worst pathological features. There is little evidence in the literature for this assumption, potentially impairing reasoned decisions on optimal adjuvant therapy. METHODS: This was a case-control study in which 68 women with SBBC were matched with 128 women with unilateral breast cancer. Both the GuysRisk prognostic model and the Nottingham Prognostic Index were used to determine the bilateral tumour with the poorer prognosis. Controls were matched for age, menopausal status, date of diagnosis, histological type and grade, and oestrogen receptor and axillary node status. RESULTS: Both prognostic models indicated the same side tumour with the worst prognosis. Kaplan-Meier survival curves for both disease-free and overall survival showed no significant difference in outcome between the two groups. CONCLUSION: Prognosis was determined by the tumour with the worst prognosis, with no additional worsening of outcome incurred from the second tumour.


Breast Neoplasms/mortality , Adult , Aged , Aged, 80 and over , Breast Neoplasms/pathology , Breast Neoplasms/surgery , Case-Control Studies , Disease-Free Survival , Female , Humans , Kaplan-Meier Estimate , Mastectomy/mortality , Middle Aged , Prognosis , Tumor Burden
20.
Int J Clin Pract ; 62(5): 816-20, 2008 May.
Article En | MEDLINE | ID: mdl-18412934

BACKGROUND/INTRODUCTION: Radiofrequency energy has emerged as a new tool for the local destruction of cancer by inducing thermal tissue necrosis in the target region. Radiofrequency ablation (RFA) has recently been used to treat breast cancer primaries, potentially offering all the advantages of minimally invasive techniques. METHODS/EVIDENCE: Nine published studies addressing the role of RFA in the treatment of breast cancer have been identified and analysed, in six, first-line RFA was followed by surgical removal and there were 12 failures in 108 ablations. Three further studies involved RFA without subsequent excision and in 1/60 there was a local relapse after 4 months (follow-up range: 15-29 months). DISCUSSION: Existing RFA techniques may not be able to destroy the whole of the malignant lesion, because of local conditions allowing cancer cells to survive within the target area or because electrodes cannot be accurately directed to the tumour site with ultrasound. Additionally, distant in-breast cancers can be missed on pre/intraoperative imaging. Histological information is unavailable after tissue destruction so that the opportunity to reassess tumour grade based on more extensive sampling is lost, but this can be improved by more extensive sampling with vacuum-assisted core biopsy. CONCLUSIONS: Before RFA can be safely used in the treatment of breast cancer primaries, several criteria need to be met. These include development of RFA devices and techniques, standardisation of the treatment protocol, including imaging and selection of patients, and establishment of a feasible post-treatment follow-up strategy.


Breast Neoplasms/surgery , Catheter Ablation/methods , Breast Neoplasms/pathology , Clinical Protocols , Evidence-Based Medicine , Female , Humans , Mastectomy/methods , Treatment Failure
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