Riechelmann Rachel, Grothey Axel
Instituto do Cancer do Estado de São Paulo, Av. Doutor Arnaldo 251, 5° Andar, CEP 01246-000, São Paulo, SP, Brazil.
Mayo Clinic, Rochester, MN, USA.
Ther Adv Med Oncol. 2017 Feb;9(2):106-126. doi: 10.1177/1758834016676703. Epub 2016 Nov 10.
Even though significant improvements in the treatment of colorectal cancer (CRC) have been made in recent years, survival rates for metastatic colorectal cancer (mCRC) are poor. Effective treatment options for metastatic colorectal cancer remain limited, and new therapeutic strategies are desperately needed. Several tyrosine kinase inhibitors (TKIs) and monoclonal antibodies (mAbs) that target angiogenesis, a critical process for facilitating tumor cell growth, invasion, and metastasis, are either approved or in clinical development for the treatment of mCRC. Many of these agents have shown efficacy in mCRC, both as single agents and in combination with standard chemotherapy regimens. However, there is a need for predictive markers of response to identify those patients most likely to benefit from antiangiogenic therapy, and, to date, no markers of this type have been validated in patients. Additionally, because antiangiogenic agents typically cause cytostatic as opposed to cytotoxic antitumor effects, it is important to determine the best strategies for evaluating therapeutic response in mCRC to ensure maximum clinical benefit. In this review, we summarize the efficacy and tolerability of approved and investigational antiangiogenic agents for the treatment of mCRC. We also discuss potential markers of response to antiangiogenic agents and how these markers, along with appropriate endpoint selection, can improve clinical trial design.
尽管近年来结直肠癌(CRC)的治疗取得了显著进展,但转移性结直肠癌(mCRC)的生存率仍然很低。转移性结直肠癌的有效治疗选择仍然有限,迫切需要新的治疗策略。几种靶向血管生成(促进肿瘤细胞生长、侵袭和转移的关键过程)的酪氨酸激酶抑制剂(TKIs)和单克隆抗体(mAbs)已被批准用于治疗mCRC或正处于临床开发阶段。这些药物中的许多已在mCRC中显示出疗效,无论是作为单一药物还是与标准化疗方案联合使用。然而,需要预测反应的标志物来识别那些最有可能从抗血管生成治疗中获益的患者,而迄今为止,这类标志物尚未在患者中得到验证。此外,由于抗血管生成药物通常产生细胞抑制作用而非细胞毒性抗肿瘤作用,因此确定评估mCRC治疗反应的最佳策略以确保最大临床获益非常重要。在本综述中,我们总结了已批准和正在研究的抗血管生成药物治疗mCRC的疗效和耐受性。我们还讨论了对抗血管生成药物反应的潜在标志物,以及这些标志物如何与适当的终点选择一起改善临床试验设计。