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find Keyword "胸膜肿瘤" 3 results
  • Raltitrexed plus Cisplatin for Malignant Pleural Mesothelioma: A Systematic Review

    Objective To systematically evaluate the clinical effectiveness and safety of raltitrexed plus cisplatin in the treatment of malignant pleural mesothelioma (MPM) when compared with other chemotherapy regimens. Methods We electronically searched PubMed, Embase, The Cochrane Library and Chinese Biomedicine Database to March, 2007. Randomized controlled trials (RCTs) and quasi-RCTs were identified, and Revman 4.2.10 was applied for statistical analyses. Results One RCT involving 250 patients was included, which compared raltitrexed plus cisplatin versus cisplatin alone in the treatment of MPM. In the intention-to-treat population, the median survival time was statistically longer in the raltitrexed plus cisplatin group as compared to cisplatin alone group. (11.4 versus 8.8 months, P=0.048). The incidence of grade 3/4 toxicities was similar between the two groups. Conclusion The current evidence available showed that, the combination of raltitrexed and cisplatin may prolong the survival time for MPM patients, with a low incidence of grade 3/4 toxicities. However, more high-quality RCTs are required to further define its clinical effectiveness.

    Release date:2016-08-25 03:36 Export PDF Favorites Scan
  • Evidence-based Treatment for a Patient with Malignant Pleural Mesothelioma

    Objective To formulate an evidence-based treatment plan for a patient with malignant pleural mesothelioma.Methods Based on an adequate assessment of the patient’s condition and using the principle of PICO, we searched The Cochrane Library (Issue 1, 2007), PubMed (1996 to February 2007) and EMbase (1974 to February 2007) to identify the best available clinical evidence. Results Five randomized controlled trials, 4 systematic reviews and 1 health economic evaluation were included. According to the current evidence, as well as the patient’s clinical condition and preference, 5 cycles of raltitrexed plus cisplatin were given to the patient along with thoracic drainage and other symptomatic treatment. And the follow-up after 4 months indicated that this treatment plan was appropriate for the patient. Conclusion Evidence-based approaches helped us to prepare the most appropriate chemotherapy plan for this patient and will help improve the therapeutic results for patients with malignant pleural mesothelioma.

    Release date:2016-09-07 02:12 Export PDF Favorites Scan
  • 胸膜上皮样血管内皮细胞瘤一例并文献复习

    目的探讨胸膜上皮样血管内皮细胞瘤(PEH)的临床表现、影像、病理学特征、诊断、鉴别诊断、治疗及预后, 提高对该病的诊治水平。 方法以"胸膜上皮样血管内皮细胞瘤"为检索词检索了四川大学华西医院2007年1月至2014年12月的住院患者资料, 仅有1例呼吸内科收治的患者符合条件, 就此回顾性分析其临床特点, 并进行相关文献复习。以"胸膜上皮样血管内皮细胞瘤"为检索词检索万方数据库和中国期刊网全文数据库, 以"pleural epithelioid hemangioendothelioma"为检索词检索PubMed、Embase、Ovid及Cochrane数据库, 检索时间为1975年1月至2015年4月。 结果68岁女性患者, 临床表现胸背痛, 查体发现除左侧胸腔积液体征外, 有新近发生的脊柱侧弯畸形及杵状指。胸部增强CT示左侧胸膜弥漫增厚伴胸腔大量积液, 部分包裹, 左肺舌叶及下叶压迫性不张, 不张舌叶内见密度减低影, 右肺散在结节。经胸膜活检获得病理, 组织学上查见异型细胞巢, 进一步免疫组化染色血小板内皮细胞黏附分子(CD31)蛋白阳性, 至此明确诊断。本例患者拒绝化疗, 明确诊断11个月后死亡。文献复习显示, 在上述数据库中共检索到74篇文献, 经筛选后, 有26篇文献40例患者明确诊断为PEH且具备相应临床资料, 符合检索条件。此类患者主要的临床表现为胸痛及呼吸困难, 影像学主要表现为胸腔积液, 胸膜不规则增厚, 组织病理学呈现血管内皮源性免疫标志物阳性。 结论PEH为罕见的低度恶性血管源性肿瘤, 病因不清, 临床表现及影像学不具有特征性, 与肿瘤胸膜转移、胸膜间皮瘤等疾病易混淆, 其诊断主要依靠活检组织病理学检查。现有的治疗手段有限, 尚无有效的治疗措施。预后与性别、年龄及病变累计范围等多种因素有关。

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