Benoist Stéphane, Nordlinger Bernard
Department of Digestive and Oncologic Surgery, AP-HP, Hôpital Ambroise Paré Boulogne, Université Versailles Saint Quentin en Yvelines, Versailles, Cedex, France.
Ann Surg Oncol. 2009 Sep;16(9):2385-90. doi: 10.1245/s10434-009-0492-7. Epub 2009 Jun 25.
Liver metastases develop in 40-50% of patients with colorectal cancer and represent the major cause of death in this disease. Surgical resection remains the only treatment procedure that can ensure long-term survival and provide cure when liver metastases can be totally resected with clear margins, when the primary cancer is controlled, and when there is no nonresectable extrahepatic disease. Five-year survival rate after surgical resection of colorectal metastases varies from 25% to 55%, but cancer relapse is observed in most patients.
To review the potential benefits and disadvantages of neoadjuvant chemotherapy administered before surgery to patients with initially resectable metastases.
European Organization for Research and Treatment of Cancer (EORTC) study 40983 has shown that neoadjuvant chemotherapy could reduce the risk of relapse by one-quarter, and allows to test the chemosensitivity of the cancer, to help to determine the appropriateness of further treatments, and to observe progressive disease, which contraindicates immediate surgery. Neoadjuvant chemotherapy can induce damage to the remnant liver. Oxaliplatin-based combination regimen is associated with increased risk of vascular lesions, whereas irinotecan-containing regimens have been associated with increased risks of steatosis and steatohepatitis. Analysis of EORTC study 40983 showed that administration of six cycles of neoadjuvant systemic chemotherapy with 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) was associated with moderate increase of the risk of reversible complications after surgery, but mortality rate was below 1% and not increased. If patients are not overtreated, chemotherapy before surgery is well tolerated. The integration of novel targeted agents in combination with cytotoxic drugs is a promising way to improve outcome in patients with advanced colorectal cancer. Preliminary trials have shown that targeted agents combined with cytotoxic regimens can increase tumor response rates. Another impact of preoperative chemotherapy is that metastases that respond to treatment may no longer be visible on computed tomography (CT) scan or at surgery. Patients should be carefully monitored and receive surgery before metastases disappear.
Treatment of most patients with liver metastases-those with resectable metastases as well as those with initially unresectable metastases-should start with chemotherapy. If drugs are well chosen and the duration of treatment is monitored with care during multidisciplinary meetings, benefits largely outweigh potential disadvantages.
40%-50%的结直肠癌患者会发生肝转移,这是该疾病的主要死亡原因。手术切除仍然是唯一能够确保长期生存并实现治愈的治疗方法,前提是肝转移灶能够在切缘阴性的情况下完全切除,原发癌得到控制,且不存在不可切除的肝外疾病。结直肠癌肝转移灶手术切除后的五年生存率在25%至55%之间,但大多数患者会出现癌症复发。
回顾术前对初始可切除转移灶患者进行新辅助化疗的潜在益处和弊端。
欧洲癌症研究与治疗组织(EORTC)的40983研究表明,新辅助化疗可将复发风险降低四分之一,并能够检测癌症的化疗敏感性,有助于确定后续治疗的适宜性,以及观察疾病进展情况,而疾病进展则提示不宜立即手术。新辅助化疗可对残余肝脏造成损害。基于奥沙利铂的联合方案与血管病变风险增加相关,而含伊立替康的方案则与脂肪变性和脂肪性肝炎风险增加相关。对EORTC 40983研究的分析表明,采用5-氟尿嘧啶、亚叶酸钙和奥沙利铂(FOLFOX)进行六个周期的新辅助全身化疗与术后可逆性并发症风险的适度增加相关,但死亡率低于1%且未升高。如果不对患者进行过度治疗,术前化疗的耐受性良好。将新型靶向药物与细胞毒性药物联合使用是改善晚期结直肠癌患者预后的一种有前景的方法。初步试验表明,靶向药物与细胞毒性方案联合使用可提高肿瘤反应率。术前化疗的另一个影响是,对治疗有反应的转移灶在计算机断层扫描(CT)或手术中可能不再可见。应仔细监测患者,并在转移灶消失前进行手术。
大多数肝转移患者(包括可切除转移灶患者以及初始不可切除转移灶患者)的治疗应从化疗开始。如果药物选择得当,且在多学科会诊期间仔细监测治疗时长,益处将大大超过潜在弊端。