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  • 1
    In: BMJ, BMJ, Vol. 1, No. 5433 ( 1965-02-20), p. 513-513
    Type of Medium: Online Resource
    ISSN: 0959-8138 , 1468-5833
    Language: English
    Publisher: BMJ
    Publication Date: 1965
    detail.hit.zdb_id: 1479799-9
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  • 2
    In: BMJ, BMJ, Vol. 337, No. nov13 1 ( 2008-11-13), p. a2079-a2079
    Type of Medium: Online Resource
    ISSN: 0959-8138 , 1468-5833
    Language: English
    Publisher: BMJ
    Publication Date: 2008
    detail.hit.zdb_id: 1479799-9
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  • 3
    In: Ultrasound in Obstetrics & Gynecology, Wiley, Vol. 40, No. 3 ( 2012-09), p. 338-344
    Abstract: To estimate the risk of primary epithelial ovarian cancer (EOC) and slow growing borderline or Type I and aggressive Type II EOC in postmenopausal women with adnexal abnormalities on ultrasound. Methods This was a prospective cohort study in the ultrasound group of the UK Collaborative Trial of Ovarian Cancer Screening of postmenopausal women with ultrasound‐detected abnormal adnexal (unilocular, multilocular, unilocular solid and multilocular solid, solid) morphology on their first scan. Women were followed up through the national cancer registries and by postal questionnaires. Absolute risks of EOC and borderline, Type I and Type II EOC within 3 years of initial scan were calculated. Results Of 48 053 women who underwent ultrasound examination and had complete scan data, 4367 (9.1% (95% CI, 8.8–9.3%)) had abnormal adnexal morphology. Median follow‐up was 7.09 (25 th –75 th centiles, 6.03–7.92) years. Forty‐seven (32 borderline or Type I, 15 Type II) were diagnosed with EOC. The overall absolute risk of EOC associated with abnormal adnexal morphology was 1.08% (95% CI, 0.79–1.43%); for borderline and Type I it was 0.73% (95% CI, 0.5–1.03%); and for Type II it was 0.34% (95% CI, 0.33–0.79%). In the subgroup ( n = 741) with solid elements (unilocular solid, multilocular solid and solid) overall absolute risk was 4.45% (95% CI, 3.08–6.20%), for borderline and Type I it was 3.1% (95% CI, 1.9–4.6%) and for Type II it was 1.3% (95% CI, 0.6–2.4%). 11 982 women had both ovaries visualized and normal annual scans throughout the 3‐year follow‐up period. In this group, no borderline or Type I and eight Type II cancers were diagnosed. Conclusion Asymptomatic postmenopausal women with ultrasound‐detected adnexal abnormalities with solid elements have a 1 in 22 risk for EOC. Despite the higher prevalence of Type II EOC, the risk of borderline or Type I cancer in women with ultrasound abnormalities seems to be higher than does the risk of Type II cancer. This has important immediate implications for patients with incidental adnexal findings as well as for any future ultrasound‐based screening. Copyright © 2012 ISUOG. Published by John Wiley & Sons, Ltd.
    Type of Medium: Online Resource
    ISSN: 0960-7692 , 1469-0705
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2012
    detail.hit.zdb_id: 2020512-0
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  • 4
    In: BMJ, BMJ, Vol. 313, No. 7069 ( 1996-11-30), p. 1355-1358
    Type of Medium: Online Resource
    ISSN: 0959-8138 , 1468-5833
    Language: English
    Publisher: BMJ
    Publication Date: 1996
    detail.hit.zdb_id: 1479799-9
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  • 5
    Online Resource
    Online Resource
    BMJ ; 1994
    In:  International Journal of Gynecologic Cancer Vol. 4, No. 1 ( 1994-01), p. 7-18
    In: International Journal of Gynecologic Cancer, BMJ, Vol. 4, No. 1 ( 1994-01), p. 7-18
    Abstract: A review of the pathology and cytopathology of 295 endometrial adenocarcinomas treated surgically at King Edward Memorial Hospital for Women, with full 5-year follow-up, revealed 16 cases of pure serous carcinoma (USC), 10 cases of mixed serous and endometrioid carcinoma with a predominant serous component (mixed USC-EAC) and six cases of mixed serous and endometrioid carcinoma with a predominant endometrioid component (mixed EAC-USC). The mixed carcinomas may be characterized microscopically by classical serous features side by side with classical endometrioid features, or additionally by features intermediate between the two. Many of these features are reproduced in preoperative cervicovaginal smears. USC and mixed USC-EAC were found to be indistinguishable clinically and prognostically, with an identical corrected 5-year survival of 40%, although numbers are small. Mixed EAC-USC (which contained 10–25% serous differentiation in this series), however, were similar in many respects to a control population of 95 EAC of Grade 2 and 3. The corrected 5-year survival in these two groups was 67% and 79%, respectively, which is not statistically significant in this small series. This study suggests that the behavior of a mixed tumor containing 50% or more serous differentiation is similar to that of pure serous carcinoma, and that the behavior of a mixed tumor containing less than 25% serous differentiation is similar to that of the other component. Given the poor correlation between pathologic findings in curettage and subsequent hysterectomy specimens, however, identification of any significant serous element in curettage material may prove vital in optimizing surgical and adjuvant therapy.
    Type of Medium: Online Resource
    ISSN: 1048-891X , 1525-1438
    Language: English
    Publisher: BMJ
    Publication Date: 1994
    detail.hit.zdb_id: 2009072-9
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  • 6
    Online Resource
    Online Resource
    Hindawi Limited ; 2014
    In:  Surgery Research and Practice Vol. 2014 ( 2014), p. 1-6
    In: Surgery Research and Practice, Hindawi Limited, Vol. 2014 ( 2014), p. 1-6
    Abstract: Objective. This study assesses the role of preoperative serum CA125 levels in the planning treatment options for women diagnosed with uterine cancer. Material and Method. Ninety five consecutive patients diagnosed with uterine cancer during a four-year period were identified. Age ranged from 35 to 89 years with a mean age of 69 years. The preoperative CA125 levels were dichotomised at 28 U/mL (using ROC analysis to identify the best discriminating threshold for 5-year survival). This level was then correlated with preoperative prognostic indicators: patient age, tumour grade, and histopathological tumour cell type. Survival data was plotted using Kaplan-Meier curves and analysed using the log-rank test. Univariate and multivariate analysis were performed to identify the predictors of overall survival. Results. The mean age of patients was 69 years (range: 35–89). On univariate analysis, the use of preoperative CA125 levels of greater or less than 28 U/mL correlated significantly with age ( P = 0.01 ) , the grade of disease ( P = 0.02 ) and unfavourable tissue type ( P = 0.03 ) . This threshold CA125 level had a sensitivity of 75%, specificity of 76%, positive predictive value of 35% and negative predicative value of 96.25%, and a likelihood ratio of 3.12 for predicting nodal disease. Using a threshold of preoperative CA125 level of 28 U/mL (area under curve: 0.60) was also a significant predictor of 5-year survival (log-rank test, P = 0.01 ). Using Cox multivariate survival analysis to identify predictive preoperative factors overall, unfavourable cell type was the strongest predictor of survival (Chi square = 36.5, df = 4, and P = 0.001 ), followed by preoperative CA125 level (CA125  〉  28 U/mL, P = 0.011 ) and unfavourable preoperative grade ( P = 0.017 ). Amongst patients with a favourable histological tissue type (endometrioid), preoperative CA125 levels predicted overall survival (Chi square = 6.039, df = 2, P = 0.02 ); however unfavourable preoperative grade did not ( P = 0.5 ). Overall, at five-year follow-up, while there were no deaths among the women with preoperative serum CA125 less than 12 U/mL, eleven of the twenty-three deaths (47.82%) in the study occurred in women with a preoperative CA125 more than 28 U/mL. Conclusions. A preoperative CA125 assay for women with uterine cancer is a relatively inexpensive, reproducible, and objective test which provides valuable information regarding the risk of metastatic disease and overall likelihood of long term survival. Patients with a low likelihood of metastatic/nodal disease (favourable tissue type and CA125 level  〈  28 U/mL) and significant comorbidities may benefit from avoiding an extended complete staging procedure. Alternatively, a high level of CA125 may prompt further imaging and multidisciplinary discussions to plan for individualised management and consideration for recruitment to clinical trials.
    Type of Medium: Online Resource
    ISSN: 2356-7759 , 2356-6124
    Language: English
    Publisher: Hindawi Limited
    Publication Date: 2014
    detail.hit.zdb_id: 2775994-5
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