Department of Surgery, McGill University Health Center, 687 Pine Avenue West, Montreal, QC, Canada.
HPB (Oxford). 2010 Feb;12(1):37-42. doi: 10.1111/j.1477-2574.2009.00119.x.
Surgery remains the only curative option for patients with colorectal cancer liver metastases (CRLM). Perioperative chemotherapeutic strategies have become increasingly popular in the treatment of CRLM. Although the role of bevacizumab (Bev) in this setting remains unclear, its widespread use has raised concerns about the use of Bev as part of perioperative chemotherapy.
We retrospectively reviewed all patients who received Bev and underwent liver resection between July 2004 and July 2008 at the McGill University Health Center. Chemotherapy-related toxicity, response to chemotherapy, surgical morbidity and mortality, liver function and survival data were assessed.
A total of 35 patients were identified. Of these, 26 (74.3%) patients received oxaliplatin-based cytotoxic chemotherapy, six (17.1%) received irinotecan-based therapy and the remainder received both agents. A total of 17 patients (48.6%) underwent portal vein embolization prior to resection and 12 (34.3%) underwent staged resection for extensive bilobar disease. A median of six cycles of preoperative Bev were administered. Nine patients (25.7%) experienced grade 3 or higher chemotherapy-related toxicities. Four events were deemed to be related to Bev. The overall response rate was 65.7% (complete and partial response). One patient progressed on therapy, but this did not prevent R0 resection. The incidence of postoperative morbidity was 42.3%. A total of 21.7% of complications were Clavien grade 3 or higher. There were no perioperative mortalities. There were no cases of severe sinusoidal injury or steatohepatitis. The Kaplan-Meier estimate of 4-year survival was 52.5%.
These data confirm the safety of chemotherapy regimens which include Bev in the perioperative setting and demonstrate that such perioperative chemotherapy in patients with CRLM does not adversely affect patient outcome. There was no increase in perioperative morbidity compared with published rates. The addition of Bev to standard chemotherapy may improve response rates, which may, in turn, impact favourably on patient survival.
手术仍然是结直肠癌肝转移(CRLM)患者的唯一治愈选择。围手术期化疗策略在 CRLM 的治疗中变得越来越流行。尽管贝伐单抗(Bev)在这种情况下的作用仍不清楚,但它的广泛应用引起了人们对将 Bev 用作围手术期化疗一部分的担忧。
我们回顾性分析了 2004 年 7 月至 2008 年 7 月在麦吉尔大学健康中心接受 Bev 治疗并接受肝切除术的所有患者。评估了化疗相关毒性、对化疗的反应、手术发病率和死亡率、肝功能和生存数据。
共确定了 35 例患者。其中,26 例(74.3%)患者接受了基于奥沙利铂的细胞毒性化疗,6 例(17.1%)患者接受了基于伊立替康的治疗,其余患者接受了这两种药物。共有 17 例(48.6%)患者在切除前进行了门静脉栓塞术,12 例(34.3%)患者因广泛的双侧疾病进行了分期切除术。中位数为 6 个周期的术前 Bev。9 例(25.7%)患者出现 3 级或更高的化疗相关毒性。有 4 例事件被认为与 Bev 有关。总的缓解率为 65.7%(完全和部分缓解)。1 例患者在治疗过程中进展,但这并未阻止 R0 切除。术后发病率为 42.3%。总共 21.7%的并发症为 Clavien 3 级或更高。围手术期无死亡。没有严重的窦状损伤或脂肪性肝炎病例。4 年生存率的 Kaplan-Meier 估计值为 52.5%。
这些数据证实了包括 Bev 在内的围手术期化疗方案的安全性,并表明 CRLM 患者的这种围手术期化疗不会对患者的预后产生不利影响。与已发表的比率相比,围手术期发病率没有增加。在标准化疗中加入 Bev 可能会提高缓解率,这反过来可能对患者的生存产生有利影响。