Unit of Medical Oncology 2, Azienda Ospedaliero-Universitaria Pisana, via Roma 57, 56126 Pisa, Italy.
Br J Cancer. 2013 Jun 25;108(12):2549-56. doi: 10.1038/bjc.2013.245. Epub 2013 May 23.
The FOLFOXIRI regimen produces a high rate of radiological and histopathological responses. Bevacizumab added to chemotherapy showed an improvement in pathological response and necrosis of colorectal liver metastases (CLMs). FOLFOXIRI plus bevacizumab produced promising early clinical results and is under investigation in several randomised trials, although no data are currently available on its effects on response of CLMs and on liver toxicities.
Starting from 499 patients enrolled in first-line phase II/III trials, we selected on the basis of tissue sample availability 18 patients treated with FOLFOXIRI/XELOXIRI and 24 patients treated with FOLFOXIRI plus bevacizumab who underwent secondary resection of CLMs. The 28 untreated patients who underwent primary resection of CLMs were included as control group. Responses of CLMs and chemotherapy-induced toxicities were assessed.
Among the patients, 63% of those treated with FOLFOXIRI plus bevacizumab, as compared with 28% of those treated with only FOLFOXIRI/XELOXIRI, showed a histopathological response (P=0.033). In the two groups, 52% and 12.5%, respectively, showed necrosis ≥50% (P=0.017). The incidence of liver toxicities was not significantly increased in patients treated with FOLFOXIRI plus bevacizumab.
The addition of bevacizumab to FOLFOXIRI produces high rates of pathologic responses and necrosis of CLM without increasing liver toxicity.
FOLFOXIRI 方案产生了高比例的影像学和组织病理学反应。贝伐单抗联合化疗显示出改善结直肠肝转移瘤(CLM)的病理反应和坏死的作用。FOLFOXIRI 联合贝伐单抗产生了有前景的早期临床结果,正在几项随机试验中进行研究,尽管目前尚无关于其对 CLM 反应和肝脏毒性的影响的数据。
我们从接受一线二线/三期试验的 499 名患者中选择了基于组织样本可用性的 18 名接受 FOLFOXIRI/XELOXIRI 和 24 名接受 FOLFOXIRI 联合贝伐单抗治疗的患者,他们接受了 CLM 的二次切除术。28 名未经治疗的接受 CLM 初次切除术的患者作为对照组。评估了 CLM 的反应和化疗诱导的毒性。
在接受 FOLFOXIRI 联合贝伐单抗治疗的患者中,有 63%的患者表现出组织病理学反应,而仅接受 FOLFOXIRI/XELOXIRI 治疗的患者中,这一比例为 28%(P=0.033)。在这两组患者中,分别有 52%和 12.5%的患者出现了≥50%的坏死(P=0.017)。接受 FOLFOXIRI 联合贝伐单抗治疗的患者中,肝脏毒性的发生率没有显著增加。
贝伐单抗联合 FOLFOXIRI 可提高 CLM 的病理反应和坏死率,而不增加肝脏毒性。