Medical Oncology, Complejo Hospitalario Universitario de Ourense, Orense, Spain.
Medical Oncology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Clin Colorectal Cancer. 2020 Sep;19(3):165-177. doi: 10.1016/j.clcc.2020.04.003. Epub 2020 Apr 20.
Colorectal cancer (CRC) is a public health problem: it is the third most common cancer in men (746,000 new cases/year) and the second in women (614,000 new cases/year), representing the second leading cause of death by cancer worldwide. The survival of patients with metastatic CRC (mCRC) has increased prominently in recent years, reaching a median of 25 to 30 months. A growing number of patients with mCRC are candidates to receive a treatment in third line or beyond, although the optimal drug regimen and sequence are still unknown. In this situation of refractoriness, there are several alternatives: (1) To administer sequentially the 2 oral drugs approved in this indication: trifluridine/tipiracil and regorafenib, which have shown a statistically significant benefit in progression-free survival and overall survival with a different toxicity profile. (2) To administer cetuximab or panitumumab in treatment-naive patients with RAS wild type, which is increasingly rare because these drugs are usually indicated in first- or second-line. (3) To reuse drugs already administered that were discontinued owing to toxicity or progression (oxaliplatin, irinotecan, fluoropyrimidine, antiangiogenics, anti-epidermal growth factor receptor [if RAS wild-type]). High-quality evidence is limited, but this strategy is often used in routine clinical practice in the absence of alternative therapies especially in patients with good performance status. (4) To use specific treatments for very selected populations, such as trastuzumab/lapatinib in mCRC human epidermal growth factor receptor 2-positive, immunotherapy in microsatellite instability, intrahepatic therapies in limited disease or primarily located in the liver, although the main recommendation is to include patients in clinical trials.
结直肠癌(CRC)是一个公共卫生问题:它是男性中第三常见的癌症(每年有 746,000 例新发病例),在女性中排名第二(每年有 614,000 例新发病例),是全球癌症死亡的第二大主要原因。近年来,转移性结直肠癌(mCRC)患者的生存率显著提高,中位生存期达到 25 至 30 个月。越来越多的 mCRC 患者有资格接受三线或以上治疗,尽管最佳药物方案和顺序仍不清楚。在这种耐药情况下,有几种选择:(1)依次给予这两种在该适应证中批准的口服药物:替氟尿苷/盐酸替匹嘧啶和瑞戈非尼,它们在无进展生存期和总生存期方面显示出统计学上的显著获益,且毒性谱不同。(2)在 RAS 野生型的初治患者中给予西妥昔单抗或帕尼单抗,由于这些药物通常在一线或二线治疗中使用,因此这种情况越来越少见。(3)重新使用因毒性或进展而停用的已用药物(奥沙利铂、伊立替康、氟嘧啶、抗血管生成药物、抗表皮生长因子受体[如果 RAS 野生型])。高质量证据有限,但在缺乏替代疗法的情况下,特别是在身体状况良好的患者中,这种策略通常在常规临床实践中使用。(4)对非常特定的人群使用特定的治疗方法,例如 mCRC 人类表皮生长因子受体 2 阳性患者的曲妥珠单抗/拉帕替尼、微卫星不稳定性患者的免疫疗法、局限于肝脏或主要位于肝脏的疾病的肝内治疗,尽管主要建议是将患者纳入临床试验。