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What is the future potential of the PI3K pathway in colorectal cancer treatment?

机译:PI3K途径在结直肠癌治疗中的未来潜力是什么?

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Therapeutic options for treating patients with metastatic colorectal cancer (CRC) have increased markedly over the past decade. Recent improvements in overall survival rates from 10 to 24 months have been achieved through the introduction of molecularly targeted agents to complement traditional cytotoxics, including agents directed against the EGF receptor (EGFR) pathway (cetuximab and panitumumab) and angiogenesis (bevacizumab, aflibercept and regorafenib). This progress has spurred intense efforts to develop further compounds that target key molecular pathways driving carcinogenesis. One major focus has been on the inhibition of oncogenic PI3K signaling, with diverse inhibitors currently in Phase I/II clinical trials. While achieving clear responses in some cancers, activity in CRC has been modest, with disease stabilization observed in approximately 10% of patients. Here, we discuss the potential opportunities of targeting the PI3K pathway in treating patients with metastatic CRC.
机译:在过去的十年中,治疗转移性结直肠癌(CRC)患者的治疗选择显着增加。通过引入分子靶向药物来补充传统的细胞毒剂,包括针对EGF受体(EGFR)途径的药物(西妥昔单抗和帕尼单抗)和血管生成(贝伐单抗,阿柏西普和雷戈非尼),最近实现了10至24个月的总体生存率的改善。 )。这项进展促使人们大力努力开发进一步的化合物,这些化合物靶向驱动致癌作用的关键分子途径。一个主要的焦点是抑制致癌的PI3K信号传导,目前在I / II期临床试验中使用了多种抑制剂。虽然在某些癌症中获得了明确的反应,但CRC的活性仍然很低,大约10%的患者观察到疾病稳定。在这里,我们讨论了靶向PI3K途径治疗转移性CRC患者的潜在机会。

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