SG Moscati Hospital, Division of Medical Oncology, Avellino, Italy.
Expert Opin Investig Drugs. 2010 May;19(5):631-9. doi: 10.1517/13543781003767434.
Lung cancer is the leading cause of cancer-related mortality worldwide. NSCLC accounts for > 80% of all lung cancers. The treatment of advanced fit NSCLC patients seems to have reached a plateau. Considerable efforts have been initiated to identify new biological agents.
Diagnosis of NSCLC histotype is becoming extremely important to address treatment. While non-squamous histology could start to benefit from the administration of several new drugs only recently, non-adenocarcinoma subtype seems to benefit from the administration of figitumumab (CP-751,871) a fully human anti-IGF 1 receptor (IGF-1R) mAb. In this paper, we reviewed the IGF-1R pathway and its inhibitors.
Approaches targeting IGF-1R include small-molecule IGF-1R tyrosine kinase inhibitors (TKIs), which are in preclinical and early clinical phases of development, and the mAbs, among which figitumumab is being investigated in Phase III trials of advanced NSCLC.
Figitumumab reported interesting results in the treatment of advanced non-adenocarcinoma NSCLC patients. Overall, in order to administer the optimal treatment to patients, a more definite histological diagnosis is mandatory.
肺癌是全球癌症相关死亡的主要原因。非小细胞肺癌 (NSCLC) 占所有肺癌的 80%以上。晚期适合治疗的 NSCLC 患者的治疗似乎已经达到了一个平台期。已经发起了相当多的努力来寻找新的生物制剂。
非小细胞肺癌组织类型的诊断对于解决治疗问题变得极为重要。虽然非鳞状组织学最近才开始受益于几种新药的应用,但非腺癌亚型似乎受益于 figitumumab(CP-751,871)的应用,figitumumab 是一种完全人源抗 IGF1 受体 (IGF-1R) mAb。在本文中,我们回顾了 IGF-1R 通路及其抑制剂。
针对 IGF-1R 的方法包括小分子 IGF-1R 酪氨酸激酶抑制剂 (TKI),它们处于临床前和早期临床开发阶段,以及 mAb,其中 figitumumab 正在晚期 NSCLC 的 III 期试验中进行研究。
figitumumab 在治疗晚期非腺癌 NSCLC 患者方面取得了有趣的结果。总的来说,为了给患者提供最佳治疗,更明确的组织学诊断是必要的。