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基于顺铂疗法与基于多西他赛疗法对一组人非小细胞肺癌异种移植瘤的临床前评估。

Preclinical assessment of cisplatin-based therapy versus docetaxel-based therapy on a panel of human non-small-cell lung cancer xenografts.

作者信息

Némati Fariba, Bras-Gonçalves Rui, Fontaine Jean-Jacques, de Pinieux Gonzague, De Cremoux Patricia, Chapelier Alain, Daniel Catherine, Laurent-Puig Pierre, Livartowski Alain, Judde Jean-Gabriel, Bordier Vincent, Poupon Marie-France, Decaudin Didier

机构信息

Preclinical Investigation Laboratory, Department of Translational Research, Hôpital Européen Georges Pompidou, Paris, France.

出版信息

Anticancer Drugs. 2009 Nov;20(10):932-40. doi: 10.1097/CAD.0b013e32833009cc.

Abstract

The success of treatment of advanced non-small-cell lung cancer (NSCLC) remains very poor. The aim of this study was, on a series of NSCLC xenografts, to compare the efficacy of standard cisplatin-based or docetaxel-based chemotherapy. Seven human xenografts were obtained from six patients (two xenografts were derived from primary or metastatic tumors of the same patient). Three xenografts were adenocarcinomas and four were squamous cell carcinomas. All xenografts reproduced the same histology as that of the patient's original tumor. Docetaxel, administered as single-agent chemotherapy, induced a significant response in five of the seven NSCLC xenografts (71%), without significant increase after combination with cisplatin, vinorelbine, or gemcitabine. Relative expression of genes putatively involved in drug response was also studied in all xenografts and did not explain the variability of drug sensitivity. In conclusion, this panel of human NSCLC xenografts reliably reproduces the data obtained in patient tumors and the relative sensitivity to docetaxel reported in NSCLC patients.

摘要

晚期非小细胞肺癌(NSCLC)的治疗效果仍然很差。本研究的目的是在一系列NSCLC异种移植模型上,比较基于顺铂或多西他赛的标准化疗方案的疗效。从6名患者中获得了7个人源异种移植模型(其中两个异种移植模型来自同一名患者的原发性或转移性肿瘤)。3个异种移植模型为腺癌,4个为鳞状细胞癌。所有异种移植模型均与患者原发肿瘤具有相同的组织学特征。多西他赛作为单药化疗,在7个NSCLC异种移植模型中有5个(71%)产生了显著反应,与顺铂、长春瑞滨或吉西他滨联合使用后无显著增加。还在所有异种移植模型中研究了可能参与药物反应的基因的相对表达,但这并不能解释药物敏感性的差异。总之,这组人源NSCLC异种移植模型可靠地再现了在患者肿瘤中获得的数据以及NSCLC患者中报道的对多西他赛的相对敏感性。

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