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赫赛汀,一种人源化抗HER2单克隆抗体:在过表达该致癌基因的乳腺癌治疗中取得的重大进展?

[Herceptin, a monoclonal humanized antibody anti-HER2: a major therapeutic progress in breast cancers overexpressing this oncogene?].

作者信息

Beuzeboc P, Scholl S, Garau X S, Vincent-Salomon A, Cremoux P D, Couturier J, Palangié T, Pouillart P

机构信息

Service d'oncologie médicale, Institut Curie, 26, rue d'Ulm, 75005 Paris.

出版信息

Bull Cancer. 1999 Jun;86(6):544-9.

Abstract

HER2 is overexpressed in about 25% to 30% of breast cancers and associated with poor prognosis, resistance to hormonotherapy and lack of sensitivity to CMF-based adjuvant chemotherapy. Herceptin (trastuzumab), a humanized monoclonal antibody, administered as a single agent, produces objective responses in phase II trials in patients with metastatic breast cancers overexpressing HER2. It has shown a substantial benefit in a phase III trial which compares a standard first line chemotherapy (doxorubicin and cyclophosphamide or taxol alone) to the same chemotherapy with Herceptin in metastatic breast cancer. The Herceptin arm had significantly higher response rate (+ 53%), an improvement in the median duration of response (+ 57%) as well as in time to progression (+ 65%) compared to chemotherapy alone.

摘要

HER2在约25%至30%的乳腺癌中过度表达,与预后不良、激素治疗耐药以及对基于CMF的辅助化疗不敏感相关。赫赛汀(曲妥珠单抗)是一种人源化单克隆抗体,作为单一药物给药时,在HER2过度表达的转移性乳腺癌患者的II期试验中产生了客观反应。在一项III期试验中,它将标准一线化疗(单独使用阿霉素和环磷酰胺或紫杉醇)与在转移性乳腺癌中联合赫赛汀的相同化疗进行比较,显示出显著益处。与单纯化疗相比,赫赛汀组的缓解率显著更高(提高了53%),中位缓解持续时间有所改善(提高了57%),疾病进展时间也有所改善(提高了65%)。

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