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Combination of docetaxel-carboplatin for adjuvant chemotherapy of epithelial ovarian,primary peritoneal and fallopian tube cancers:a meta-analysis 被引量:1
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作者 Hongxiao Chen Yang Rao Pengpeng Qu 《The Chinese-German Journal of Clinical Oncology》 CAS 2010年第8期475-481,共7页
Objective: The aim of this study was to compare the efficacies and safeties of the combination of docetaxel- carboplatin with the combination of non docetaxel-carboplatin as first-line chemotherapy for advanced epith... Objective: The aim of this study was to compare the efficacies and safeties of the combination of docetaxel- carboplatin with the combination of non docetaxel-carboplatin as first-line chemotherapy for advanced epithelial ovarian, pri- mary peritoneal or fallopian tube cancers. Methods: Relevant articles were identified from MEDLINE (1993-2010), EMBASE (1980-2010), MEDION, the Cochrane library, Science Citation Index Expanded databases, hand searching of reference lists from primary articles and reviews, conference abstracts and contact with experts in the field. The review included 5 relevant primary studies (1430 women). Data was extracted for study characteristics and quality. Bivariate random-effect model meta- analysis was used to estimate diagnostic accuracy of the various index tests. A quantitative meta-analysis was carried out by two reviewers based on the inclusion criteria from all available studies. Results: The frequency of the subgroup analysis of toxicity showed that toxicity action of combination of docetaxel-carboplatin was more severe than that of non docetaxel- carboplatin group (OR = 1.33, 95% CI = 1.13-1.56, P = 0.0005), whereas that of clinical responses was equivalent in com- parison combination of docetaxel-carboplatin with combination of paclitaxel-carboplatin or docetaxel-cisplatin (OR = 1.0, 95% CI = 0.87-1.16, P = 0.95). There were heterogeneity (X2 = 79.36, P 〈 0.00001) and inconsistency (83.6%) in toxicity analysis among the trials, while neither heterogeneity (x2 = 3.21, P = 0.99) nor inconsistency (F = 0%) in clinical responses among the trials. Conclusion: The safety of combination of docetaxel-carboplatin is less than that of combination of paclitaxel- carboplatin or docetaxel-cisplatin. However, the clinical responses of combination of docetaxel-carboplatin are comparable with combination of paclitaxel-carboplatin or docetaxel-cisplatin. 展开更多
关键词 docetaxel-carboplatin META-ANALYSIS adjuvant chemotherapy epithelial ovarian cancer primary peritoneal cancer fallopian tube cancer
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Primary peritoneal carcinoma metastasizing to breast: a single case report and literature review from clinic to biology 被引量:2
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作者 Ji-Yuan Sun Wondwossen Gebre +3 位作者 Yi-Min Dong Xiao Shaun Rachel Robbins Alida Podrumar 《Cancer Biology & Medicine》 SCIE CAS CSCD 2016年第3期389-395,共7页
Primary peritoneal carcinoma(PPC) is a type of rare malignant epithelial tumor. Metastasis from PPC to breast has been rarely reported. PPC originates de novo from the peritoneal tissues rather than invasion or metast... Primary peritoneal carcinoma(PPC) is a type of rare malignant epithelial tumor. Metastasis from PPC to breast has been rarely reported. PPC originates de novo from the peritoneal tissues rather than invasion or metastasis from adjacent or remote organs.PPCs have been implicated in many cases of carcinomas of unknown primary origin. It is similar to ovarian cancer(Ov Ca),because it shares the same common embryonic origin, the coelomic epithelium(mesodermal origin). The mechanism of oncogenesis remains elusive. In this article, we report a rare case of PPC in a patient 10 years after total abdominal hysterectomy and bilateral salpingooophorectomy for uterine leiomyoma, which was widely spread in the abdomen and metastasized to the colon, liver and distant organs including breast. The treatment is similar to that of primary ovarian cancer. We also reviewed the primary peritoneal cancer metastatic to breast and discuss the possible mechanisms and biology of primary peritoneal cancer,using experimental and animal model. 展开更多
关键词 primary peritoneal cancer breast cancer metastasis WT1 differential diagnosis
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