Pessaux P
Pôle de pathologies digestives et hépatiques et de la transplantation, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Université de Strasbourg, 67200 Strasbourg, France.
J Chir (Paris). 2010 Jan;147 Suppl 1:S7-S11. doi: 10.1016/S0021-7697(10)70002-8.
Hepatotoxic effect of oxaliplatin and irinotecan on the non-tumourous liver parenchyma has been reported. These two main drugs have been linked to injuries such as vascular changes (sinusoidal obstruction syndrome (SOS) and chemotherapy-associated steatohepatitis (CASH)). Oxaliplatin-based regimens have been associated with an increased risk of vascular lesions and irinotecan-containing regimens have been also associated with increased risks of steatosis and steatohepatitis. SOS increased morbidity after major liver resection, mostly after administration of more than six cycles of neoadjuvant systemic chemotherapy. CASH increased morbidity and mortality rates after hepatectomy. Preliminary results demonstrated that the addition of targeted molecular therapy (bevacizumab or cetuximab) to conventional chemotherapy does not increase the postoperative morbidity and mortality rates after hepatectomy. Furthermore, there was no additional injury to the non-tumorous liver parenchyma.
已有报道奥沙利铂和伊立替康对非肿瘤性肝实质具有肝毒性作用。这两种主要药物与诸如血管变化(窦性阻塞综合征(SOS)和化疗相关脂肪性肝炎(CASH))等损伤有关。基于奥沙利铂的方案与血管病变风险增加相关,而含伊立替康的方案也与脂肪变性和脂肪性肝炎风险增加相关。SOS会增加大肝切除术后的发病率,大多发生在给予六个以上周期的新辅助全身化疗后。CASH会增加肝切除术后的发病率和死亡率。初步结果表明,在传统化疗中添加靶向分子疗法(贝伐单抗或西妥昔单抗)不会增加肝切除术后的术后发病率和死亡率。此外,对非肿瘤性肝实质没有额外损伤。