Loria Rossella, Vici Patrizia, Di Lisa Francesca Sofia, Soddu Silvia, Maugeri-Saccà Marcello, Bon Giulia
Cellular Network and Molecular Therapeutic Target Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Unit of Phase IV Trials, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Front Oncol. 2022 Jun 23;12:877380. doi: 10.3389/fonc.2022.877380. eCollection 2022.
Over the past two decades, cancer treatment has benefited from having a significant increase in the number of targeted drugs approved by the United States Food and Drug Administration. With the introduction of targeted therapy, a great shift towards a new era has taken place that is characterized by reduced cytotoxicity and improved clinical outcomes compared to traditional chemotherapeutic drugs. At present, targeted therapies and other systemic anti-cancer therapies available (immunotherapy, cytotoxic, endocrine therapies and others) are used alone or in combination in different settings (neoadjuvant, adjuvant, and metastatic). As a result, it is not uncommon for patients affected by an advanced malignancy to receive subsequent anti-cancer therapies. In this challenging complexity of cancer treatment, the clinical pathways of real-life patients are often not as direct as predicted by standard guidelines and clinical trials, and cross-resistance among sequential anti-cancer therapies represents an emerging issue. In this review, we summarize the main cross-resistance events described in the diverse tumor types and provide insight into the molecular mechanisms involved in this process. We also discuss the current challenges and provide perspectives for the research and development of strategies to overcome cross-resistance and proceed towards a personalized approach.
在过去二十年中,癌症治疗受益于美国食品药品监督管理局批准的靶向药物数量大幅增加。随着靶向治疗的引入,与传统化疗药物相比,一个以细胞毒性降低和临床结果改善为特征的新时代已经发生了巨大转变。目前,靶向治疗和其他可用的全身抗癌治疗方法(免疫治疗、细胞毒性治疗、内分泌治疗等)在不同情况下(新辅助、辅助和转移性)单独或联合使用。因此,患有晚期恶性肿瘤的患者接受后续抗癌治疗并不罕见。在这种具有挑战性的癌症治疗复杂性中,现实生活中患者的临床路径往往不像标准指南和临床试验所预测的那样直接,并且序贯抗癌治疗之间的交叉耐药是一个新出现的问题。在这篇综述中,我们总结了不同肿瘤类型中描述的主要交叉耐药事件,并深入探讨了这一过程中涉及的分子机制。我们还讨论了当前的挑战,并为克服交叉耐药和迈向个性化治疗方法的策略研发提供了展望。