Department of Biotherapy, Cancer Center, West China Hospital of Sichuan University, Chengdu, China.
Department of Abdominal Oncology, Cancer Center, West China Hospital of Sichuan University, Chengdu, China.
Cancer Med. 2021 May;10(10):3388-3402. doi: 10.1002/cam4.3876. Epub 2021 May 3.
To compare the efficacy of first-line bevacizumab plus chemotherapy with cetuximab plus chemotherapy based on the stratification of metastatic colorectal cancer (mCRC) patients with mucinous adenocarcinoma (MA) or mucinous component (MC).
A retrospective study involving all mCRC patients receiving first-line bevacizumab-based or cetuximab-based chemotherapy at our hospital from September 2013 to January 2020 was conducted. Overall survival (OS), progression-free survival (PFS), and objective response rate (ORR) were compared between the cetuximab-chemotherapy group and the bevacizumab-chemotherapy group on the basis of the conventional pathological classification of MA or MC.
A total of 620 patients with mCRC were included in our study, consisting of 141 (22.7%) patients with MA/MC and 479 (77.3%) patients with non-mucinous adenocarcinoma (NMA). In the MA/MC cohort, patients who were treated with bevacizumab-based chemotherapy were associated with significantly better OS than those treated with cetuximab-base chemotherapy (30.0 vs. 26.3 months, p = 0.002), irrespective of tumor sites. The efficacy of bevacizumab-based chemotherapy was higher in nearly all subgroups as shown in the subgroup analysis. In the NMA cohort, median OS was better in the cetuximab plus chemotherapy group than that in the bevacizumab plus chemotherapy group (32.2 vs. 27.0 months, p = 0.005) for left-side mCRC patients, whereas OS was significantly longer in the bevacizumab plus chemotherapy group for right-side mCRC patients (26.0 vs. 20.9 months, p = 0.013).
Conventional pathological classification (e.g. MA/MC) should be considered when tailoring the individualized optimal treatment for mCRC. Bevacizumab plus chemotherapy as first-line therapy may be the optimal option for patients with MA/MC.
比较转移性结直肠癌(mCRC)患者中黏液腺癌(MA)或黏液成分(MC)分层一线贝伐珠单抗联合化疗与西妥昔单抗联合化疗的疗效。
回顾性分析 2013 年 9 月至 2020 年 1 月我院收治的所有接受一线贝伐珠单抗或西妥昔单抗化疗的 mCRC 患者。根据 MA 或 MC 的常规病理分类,比较西妥昔单抗化疗组与贝伐珠单抗化疗组的总生存期(OS)、无进展生存期(PFS)和客观缓解率(ORR)。
本研究共纳入 620 例 mCRC 患者,其中 MA/MC 患者 141 例(22.7%),非黏液性腺癌(NMA)患者 479 例(77.3%)。在 MA/MC 队列中,接受贝伐珠单抗化疗的患者的 OS 明显长于接受西妥昔单抗化疗的患者(30.0 与 26.3 个月,p=0.002),且与肿瘤部位无关。在亚组分析中,贝伐珠单抗化疗的疗效在几乎所有亚组中均较高。在 NMA 队列中,左半结肠癌患者中,西妥昔单抗联合化疗组的中位 OS 长于贝伐珠单抗联合化疗组(32.2 与 27.0 个月,p=0.005),而右半结肠癌患者中,贝伐珠单抗联合化疗组的 OS 明显长于西妥昔单抗联合化疗组(26.0 与 20.9 个月,p=0.013)。
在为 mCRC 患者制定个体化最佳治疗方案时,应考虑常规病理分类(如 MA/MC)。贝伐珠单抗联合化疗作为一线治疗可能是 MA/MC 患者的最佳选择。