Hematology/Oncology Division, Penn State Hershey Cancer Institute, Penn State Hershey Medical Center, Hershey, PA USA.
Cancer Biol Ther. 2013 Aug;14(8):711-9. doi: 10.4161/cbt.25310. Epub 2013 Jun 13.
Colorectal cancer patients with BRAF-mutant tumors have a more aggressive, rapidly progressing disease that is in critical need of novel therapeutic approaches. Indeed, whereas the median overall survival (OS) of colorectal cancer (CRC) patients receiving standard-of-care therapy is approximately two years or more if their tumors express wild-type BRAF and wild-type KRAS, median OS is less than twelve months with tumors expressing V600E-mutant BRAF and wild-type KRAS. Pro-apoptotic receptor agonists are a class of biologic agents under development to induce tumor-specific apoptosis and are being combined with classical chemotherapy or targeted agents in clinical trials. Herein, we present the case of a patient with bulky V600E-mutant BRAF hepatic flexure colon carcinoma, treated initially with FOLFOX plus bevacizumab neoadjuvant therapy and surgery. The patient had a rapid tumor relapse with metastatic disease to the liver and lung, and was enrolled in a phase 1b open-label clinical study, where he received the FOLFIRI regimen in combination with the pro-apoptotic receptor agonist dulanermin (rhApo2L/TRAIL). The patient maintained stable disease through 25 doses administered every two weeks before his disease progressed. After coming off study, the patient underwent surgical debulking and received intraperitoneal hyperthermic chemotherapy. He subsequently relapsed and was treated with FOLFIRI plus cetuximab. At the time of this report, the patient remains on active treatment. It is unclear what effect dulanermin may have had on the course of his disease, but it is noteworthy that the patient remained on FOLFIRI plus dulanermin therapy for a period that exceeded the median OS for patients with advanced, aggressive BRAF-mutant CRC. It is also noteworthy that at the time of this report the patient's overall survival since diagnosis has exceeded 30 months, which is beyond what is generally observed even for patients with CRC harboring wild-type BRAF and wild-type KRAS.
结直肠癌患者的 BRAF 突变肿瘤具有侵袭性更强、进展迅速的特点,迫切需要新的治疗方法。事实上,如果结直肠癌患者的肿瘤表达野生型 BRAF 和野生型 KRAS,接受标准治疗的中位总生存期(OS)约为两年或更长时间;而如果肿瘤表达 V600E 突变 BRAF 和野生型 KRAS,则中位 OS 不到 12 个月。促凋亡受体激动剂是一类正在开发中的生物制剂,用于诱导肿瘤特异性凋亡,并在临床试验中与经典化疗或靶向药物联合使用。在此,我们报告了一名 V600E 突变 BRAF 肝曲结肠癌大块患者的病例,该患者最初接受 FOLFOX 联合贝伐单抗新辅助治疗和手术治疗。患者肿瘤快速复发,出现肝和肺转移,随后入组了一项 1b 期开放标签临床试验,接受 FOLFIRI 方案联合促凋亡受体激动剂杜拉鲁单抗(rhApo2L/TRAIL)治疗。患者在每两周接受 25 剂治疗期间疾病保持稳定,随后疾病进展。停药后,患者接受了手术去瘤和腹腔内高温化疗。随后疾病复发,接受 FOLFIRI 联合西妥昔单抗治疗。在报告时,患者仍在接受积极治疗。目前尚不清楚杜拉鲁单抗对其疾病进程的影响,但值得注意的是,该患者接受 FOLFIRI 联合杜拉鲁单抗治疗的时间超过了晚期侵袭性 BRAF 突变结直肠癌患者的中位 OS。同样值得注意的是,在报告时,患者自诊断以来的总生存期已超过 30 个月,这超过了即使是携带野生型 BRAF 和野生型 KRAS 的结直肠癌患者通常观察到的生存期。