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卵巢癌的诊断
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作者 sudha sundar Richard D Neal +1 位作者 刘晨 王淑珍 《英国医学杂志中文版》 2016年第12期697-703,共7页
卵巢癌是全球女性第七位最常见的癌症,2012年,有23.9万新发病例。和许多其他类型的癌症一样,不同地区卵巢癌的发病率和病死率差异很大,经济发达地区的发病率更高。卵巢癌发病率最高的年龄组是50-70岁,75%的病例发生在55岁以后308... 卵巢癌是全球女性第七位最常见的癌症,2012年,有23.9万新发病例。和许多其他类型的癌症一样,不同地区卵巢癌的发病率和病死率差异很大,经济发达地区的发病率更高。卵巢癌发病率最高的年龄组是50-70岁,75%的病例发生在55岁以后3080%的病例在出现症状时已处于疾病晚期,5年生存率很低。在英国,各分期卵巢癌总的5年生存率为46%。 展开更多
关键词 卵巢癌 常见癌症 新发病例 发病率
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Heterogeneity of germline variants in high risk breast and ovarian cancer susceptibility genes in India
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作者 Archana Sharma-Oates Abeer M.Shaaban +3 位作者 Ian Tomlinson Luke Wynne Jean-Baptiste Cazier sudha sundar 《Precision Clinical Medicine》 2018年第2期75-87,共13页
Breast and ovarian cancers now account for one in three cancers in Indian women and their incidence is rising.Major differences in the clinical presentation of breast and ovarian cancers exist between India and the Un... Breast and ovarian cancers now account for one in three cancers in Indian women and their incidence is rising.Major differences in the clinical presentation of breast and ovarian cancers exist between India and the United Kingdom.For example,Indian patients with breast cancer typically present a decade earlier than in the UK.Reasons for this could be multifactorial,including differences in underlying biology,environmental risks,and other systematic factors including access to screening.One possible explanation lies in variable incidence or penetrance of germline mutations in genes such as BRCA1 and BRCA2.We performed a methodical database and literature review to investigate the prevalence and spectrum of high-risk cancer susceptibility genes in Indian patients with breast and ovarian cancers.We identified 148 articles,but most studies were small,with inconsistent inclusion criteria and based on heterogeneous technologies,so that mutation frequency could not be reliably ascertained.Data were also often lacking on penetrance,histopathology,and survival outcomes.After filtering out unsuitable studies,only 13 remained,comprising 1028 patients.Large-scale research studies are urgently needed to determine mutation prevalence,spectra,and clinico-pathological features,and hence derive guidelines for screening,treatment,and prevention specific to the Indian population. 展开更多
关键词 BRCA1 BRCA2 hereditary cancer sporadic cancer INDIA breast cancer ovarian cancer
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Corrigendum to:Heterogeneity of germline variants in high risk breast and ovarian cancer susceptibility genes in India
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作者 Archana Sharma-Oates Abeer M.Shaaban +3 位作者 Ian Tomlinson Luke Wynne Jean-Baptiste Cazier sudha sundar 《Precision Clinical Medicine》 2018年第3期134-134,共1页
This is a correction notice for article pby010(Heterogeneity of germline variants in high risk breast and ovarian cancer susceptibility genes in India;DOI:https://doi.org/10.1093/pcmedi/pby010),published on 22 Septemb... This is a correction notice for article pby010(Heterogeneity of germline variants in high risk breast and ovarian cancer susceptibility genes in India;DOI:https://doi.org/10.1093/pcmedi/pby010),published on 22 September 2018.All authors were mistakenly listed as being affiliated with the following:‘Centre for Computational Biology,Institute of Cancer and Genomic Sciences,College of Medical and Dental Sciences,Haworth Building,University of Birmingham,Edgbaston,Birmingham,B152TT,UK.’Their affiliations should instead have been given as follows. 展开更多
关键词 BREAST cancer SUSCEPTIBILITY
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