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间皮素-CA-125 相互作用抑制在间皮瘤患者中的抗间皮素单克隆抗体 MORAb-009:对癌症治疗的影响。

Inhibition of mesothelin-CA-125 interaction in patients with mesothelioma by the anti-mesothelin monoclonal antibody MORAb-009: Implications for cancer therapy.

机构信息

Laboratory of Molecular Biology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-4264, USA.

出版信息

Lung Cancer. 2010 Jun;68(3):455-9. doi: 10.1016/j.lungcan.2009.07.016. Epub 2009 Sep 9.

Abstract

BACKGROUND

Mesothelin, a tumor differentiation antigen highly expressed in mesothelioma and ovarian cancer, is the receptor for CA-125 (MUC 16) and this interaction may play a role in tumor metastasis. MORAb-009 is a chimeric anti-mesothelin monoclonal antibody.

METHODS

Twenty-four patients with mesothelin expressing cancers were treated on a phase I study of MORAb-009 administered as an intravenous infusion (12.5-400mg/m(2)) weeklyx4 doses with 2 weeks off before the next cycle. This report summarizes the effect of MORAb-009 on serum CA-125 kinetics in the eight patients with mesothelioma who had CA-125 levels measured before and at different time-points following therapy.

RESULTS

MORAb-009 treatment led to a marked increase in serum CA-125 levels in all patients including those without elevated CA-125 levels before therapy. The increase in CA-125 levels was not due to disease progression since CA-125 levels decreased rapidly after stopping MORAb-009 therapy. No patients had signs of peritoneal or pleural inflammation as the possible cause of CA-125 rise. In addition, the elevated CA-125 levels were not due to MORAb-009 interfering with the laboratory assay used to measure CA-125.

CONCLUSION

The increase in serum CA-125 produced by treatment with MORAb-009 is most likely due to MORAb-009 inhibiting the binding of tumor shed CA-125 to mesothelin present on mesothelial cells lining the pleural and peritoneal cavities. Inhibiting the mesothelin-CA-125 interaction could be a useful strategy to prevent tumor metastasis in mesotheliomas and ovarian cancer.

摘要

背景

间皮素是一种在间皮瘤和卵巢癌中高度表达的肿瘤分化抗原,是 CA-125(MUC16)的受体,这种相互作用可能在肿瘤转移中发挥作用。MORAb-009 是一种嵌合型抗间皮素单克隆抗体。

方法

24 例表达间皮素的癌症患者参加了一项 MORAb-009 的 I 期研究,该研究采用静脉输注(12.5-400mg/m²),每周 4 次剂量,每个周期之间休息 2 周。本报告总结了 MORAb-009 对 8 例间皮瘤患者血清 CA-125 动力学的影响,这些患者在治疗前和治疗后不同时间点测量了 CA-125 水平。

结果

MORAb-009 治疗导致所有患者的血清 CA-125 水平显著升高,包括治疗前 CA-125 水平不升高的患者。CA-125 水平的升高不是由于疾病进展,因为在停止 MORAb-009 治疗后 CA-125 水平迅速下降。没有患者出现腹膜或胸膜炎症等可能导致 CA-125 升高的迹象。此外,升高的 CA-125 水平不是由于 MORAb-009 干扰用于测量 CA-125 的实验室检测。

结论

用 MORAb-009 治疗引起的血清 CA-125 升高很可能是由于 MORAb-009 抑制肿瘤脱落的 CA-125 与存在于胸膜和腹膜腔衬里间皮细胞上的间皮素结合。抑制间皮素-CA-125 相互作用可能是预防间皮瘤和卵巢癌肿瘤转移的一种有用策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2744/2864325/8d62fc584ab1/nihms137646f1.jpg

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