Medical Oncology Department, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
Oncology and Hemato-oncology Department, University of Milan, Milan, Italy.
Oncologist. 2021 Apr;26(4):302-309. doi: 10.1002/onco.13642. Epub 2021 Jan 2.
Doublets plus anti-epidermal growth factor receptors (EGFRs) are the preferred upfront option for patients with left-sided RAS/BRAF wild-type metastatic colorectal cancer (mCRC). Initial therapy with FOLFOXIRI-bevacizumab is superior to doublets plus bevacizumab independently from primary tumor sidedness and RAS/BRAF status. No randomized comparison between FOLFOXIRI-bevacizumab versus doublets plus anti-EGFRs is available in left-sided RAS/BRAF wild-type mCRC.
We selected patients with left-sided RAS and BRAF wild-type mCRC treated with first-line FOLFOX-panitumumab or FOLFOXIRI-bevacizumab in five randomized trials: Valentino, TRIBE, TRIBE2, STEAM, and CHARTA. A propensity score-based analysis was performed to compare FOLFOXIRI-bevacizumab with FOLFOX-panitumumab.
A total of 185 patients received FOLFOX-panitumumab and 132 received FOLFOXIRI-bevacizumab. Median progression-free survival (PFS) and median overall survival (OS) were 13.3 and 33.1 months in the FOLFOXIRI-bevacizumab group compared with 11.4 and 30.3 months in the FOLFOX-panitumumab group (propensity score-adjusted hazard ratio (HR) for PFS, 0.82; 95% confidence interval (CI), 0.64-1.04; p = .11; propensity score-adjusted HR for OS, 0.80; 95% CI, 0.59-1.08; p = .14). No significant differences in overall response rate and disease control rate were observed. A statistically nonsignificant difference in favor of FOLFOXIRI-bevacizumab was observed for OS after secondary resection of metastases. Chemotherapy-related adverse events were more frequent in the FOLFOXIRI-bevacizumab group, with specific regard to grade 3 and 4 neutropenia (48% vs. 26%, adjusted p = .001).
Although randomized comparison is lacking, both FOLFOXIRI-bevacizumab and FOLFOX-panitumumab are valuable treatment options in left-sided RAS/BRAF wild-type mCRC.
A propensity score-based analysis of five trials was performed to compare FOLFOX-panitumumab versus FOLFOXIRI-bevacizumab in left-sided RAS/BRAF wild-type metastatic colorectal cancer (mCRC). No significant differences were observed, but FOLFOXIRI-bevacizumab achieved numerically superior survival outcomes versus FOLFOX-panitumumab. Chemotherapy-related adverse events were more frequent in the FOLFOXIRI-bevacizumab group. These observations suggest that although doublet chemotherapy plus anti-EGFRs remains the preferred treatment in patients with left-sided RAS/BRAF wild-type mCRC, FOLFOXIRI-bevacizumab is a valuable option able to provide similar, if not better, outcomes at the price of a moderate increase in toxicity and may be adopted based on patients' preference and potential impact on quality of life.
对于左侧 RAS/BRAF 野生型转移性结直肠癌(mCRC)患者,双药联合加抗表皮生长因子受体(EGFR)治疗是首选的初始治疗方案。与双药联合加贝伐珠单抗相比,FOLFOXIRI-贝伐珠单抗初始治疗在肿瘤原发部位和 RAS/BRAF 状态方面均具有优势。在左侧 RAS/BRAF 野生型 mCRC 中,尚无 FOLFOXIRI-贝伐珠单抗与双药联合加抗 EGFR 治疗的随机比较。
我们选择了在五项随机试验中接受一线 FOLFOX-帕尼单抗或 FOLFOXIRI-贝伐珠单抗治疗的左侧 RAS 和 BRAF 野生型 mCRC 患者:Valentino、TRIBE、TRIBE2、STEAM 和 CHARTA。进行了基于倾向评分的分析,以比较 FOLFOXIRI-贝伐珠单抗与 FOLFOX-帕尼单抗。
共有 185 例患者接受了 FOLFOX-帕尼单抗治疗,132 例患者接受了 FOLFOXIRI-贝伐珠单抗治疗。FOLFOXIRI-贝伐珠单抗组的中位无进展生存期(PFS)和中位总生存期(OS)分别为 13.3 个月和 33.1 个月,而 FOLFOX-帕尼单抗组分别为 11.4 个月和 30.3 个月(倾向评分调整后的 PFS 风险比(HR)为 0.82;95%置信区间(CI)为 0.64-1.04;p=0.11;倾向评分调整后的 OS HR 为 0.80;95%CI 为 0.59-1.08;p=0.14)。两组的总缓解率和疾病控制率无显著差异。在转移性疾病二次切除后,FOLFOXIRI-贝伐珠单抗组在 OS 方面具有统计学上的优势。FOLFOXIRI-贝伐珠单抗组的化疗相关不良反应更为频繁,特别是 3 级和 4 级中性粒细胞减少症(48% vs. 26%,调整后 p=0.001)。
尽管缺乏随机比较,但 FOLFOXIRI-贝伐珠单抗和 FOLFOX-帕尼单抗都是左侧 RAS/BRAF 野生型 mCRC 的有价值的治疗选择。
对五项试验进行了基于倾向评分的分析,以比较 FOLFOX-帕尼单抗与 FOLFOXIRI-贝伐珠单抗在左侧 RAS/BRAF 野生型转移性结直肠癌(mCRC)中的应用。虽然没有观察到显著差异,但与 FOLFOX-帕尼单抗相比,FOLFOXIRI-贝伐珠单抗在生存结果方面取得了数值上的优势。FOLFOXIRI-贝伐珠单抗组的化疗相关不良反应更为频繁。这些观察结果表明,尽管在左侧 RAS/BRAF 野生型 mCRC 患者中,双药联合加抗 EGFR 治疗仍然是首选治疗方案,但 FOLFOXIRI-贝伐珠单抗是一种有价值的选择,能够提供相似(如果不是更好)的结果,同时增加适度的毒性,并可根据患者的偏好和对生活质量的潜在影响来采用。