Di Nicolantonio Federica, Martini Miriam, Molinari Francesca, Sartore-Bianchi Andrea, Arena Sabrina, Saletti Piercarlo, De Dosso Sara, Mazzucchelli Luca, Frattini Milo, Siena Salvatore, Bardelli Alberto
Laboratory of Molecular Genetics, The Oncogenomics Center, Institute for Cancer Research and Treatment, University of Torino, Medical School, Candiolo, Torino, Italy.
J Clin Oncol. 2008 Dec 10;26(35):5705-12. doi: 10.1200/JCO.2008.18.0786. Epub 2008 Nov 10.
PURPOSE Cetuximab or panitumumab are effective in 10% to 20% unselected metastatic colorectal cancer (CRC) patients. KRAS mutations account for approximately 30% to 40% patients who are not responsive. The serine-threonine kinase BRAF is the principal effector of KRAS. We hypothesized that, in KRAS wild-type patients, BRAF mutations could have a predictive/prognostic value. PATIENTS AND METHODS We retrospectively analyzed objective tumor responses, time to progression, overall survival (OS), and the mutational status of KRAS and BRAF in 113 tumors from cetuximab- or panitumumab-treated metastatic CRC patients. The effect of the BRAF V600E mutation on cetuximab or panitumumab response was also assessed using cellular models of CRC. Results KRAS mutations were present in 30% of the patients and were associated with resistance to cetuximab or panitumumab (P = .011). The BRAF V600E mutation was detected in 11 of 79 patients who had wild-type KRAS. None of the BRAF-mutated patients responded to treatment, whereas none of the responders carried BRAF mutations (P = .029). BRAF-mutated patients had significantly shorter progression-free survival (P = .011) and OS (P < .0001) than wild-type patients. In CRC cells, the introduction of BRAF V600E allele impaired the therapeutic effect of cetuximab or panitumumab. Treatment with the BRAF inhibitor sorafenib restored sensitivity to panitumumab or cetuximab of CRC cells carrying the V600E allele. CONCLUSION BRAF wild-type is required for response to panitumumab or cetuximab and could be used to select patients who are eligible for the treatment. Double-hit therapies aimed at simultaneous inhibition of epidermal growth factor receptor and BRAF warrant exploration in CRC patients carrying the V600E oncogenic mutation.
目的 西妥昔单抗或帕尼单抗对10%至20%未经选择的转移性结直肠癌(CRC)患者有效。KRAS突变约占30%至40%无反应患者的原因。丝氨酸 - 苏氨酸激酶BRAF是KRAS的主要效应器。我们假设,在KRAS野生型患者中,BRAF突变可能具有预测/预后价值。患者与方法 我们回顾性分析了113例接受西妥昔单抗或帕尼单抗治疗的转移性CRC患者肿瘤的客观反应、进展时间、总生存期(OS)以及KRAS和BRAF的突变状态。还使用CRC细胞模型评估了BRAF V600E突变对西妥昔单抗或帕尼单抗反应的影响。结果 30%的患者存在KRAS突变,且与对西妥昔单抗或帕尼单抗耐药相关(P = 0.011)。在79例KRAS野生型患者中,有11例检测到BRAF V600E突变。BRAF突变的患者均未对治疗产生反应,而所有有反应的患者均未携带BRAF突变(P = 0.029)。BRAF突变患者的无进展生存期(P = 0.011)和总生存期(P < 0.0001)明显短于野生型患者。在CRC细胞中,引入BRAF V600E等位基因会损害西妥昔单抗或帕尼单抗的治疗效果。用BRAF抑制剂索拉非尼治疗可恢复携带V600E等位基因的CRC细胞对帕尼单抗或西妥昔单抗的敏感性。结论 对帕尼单抗或西妥昔单抗产生反应需要BRAF野生型,其可用于选择适合该治疗的患者。针对同时抑制表皮生长因子受体和BRAF的双重打击疗法值得在携带V600E致癌突变的CRC患者中探索。