Department of Medical Oncology, Guangxi Medical University Cancer Hospital, No. 71 Hedi Road, Nanning, 530021, Guangxi, China.
Department of Gastroenterology, First Affiliated Hospital of Guangxi Medical University, No.6 Shuangyong Road, Nanning, 530021, Guangxi, China.
J Gastrointest Cancer. 2024 Dec;55(4):1620-1627. doi: 10.1007/s12029-024-01108-5. Epub 2024 Sep 24.
Fruquintinib has received approval for the management of patients with chemotherapy-resistant metastatic colorectal cancer (mCRC). However, combination of fruquintinib with immune checkpoint inhibitors (ICIs) is yet to be extensively studied. This study aims to assess the clinical efficacy, safety, and prognostic indicators of treatment regimen combining fruquintinib with ICIs in mCRC patients.
We analyzed data from mCRC patients who were administered fruquintinib either as a monotherapy or in conjunction with ICIs following conventional chemotherapy. Parameters such as the objective response rate (ORR), disease control rate (DCR), overall survival (OS), progression-free survival (PFS), and incidence of adverse events were meticulously evaluated. Furthermore, the relationship between blood markers and patient prognosis was examined.
A total of 72 mCRC patients were included in this study, with a median observation period of 48 months, 19 were treated with fruquintinib alone, while 53 received a combination therapy involving fruquintinib and ICIs. The combined therapy group exhibited superior ORR and DCR compared to the fruquintinib monotherapy group. Additionally, significant improvements in OS and PFS were observed in the combined treatment group. The occurrence of adverse events was generally manageable and well-tolerated across both groups, with no significant difference in incidence rates. Notably, albumin levels were identified as a prognostic marker for PFS and OS in the univariate Cox regression analysis.
The combination of fruquintinib with ICIs demonstrated enhanced clinical efficacy and improved survival outcomes compared to fruquintinib monotherapy in mCRC patients. The safety of the combination regimen was deemed manageable and acceptable.
呋喹替尼已获批用于治疗化疗耐药的转移性结直肠癌(mCRC)患者。然而,呋喹替尼联合免疫检查点抑制剂(ICI)的治疗方案尚未得到广泛研究。本研究旨在评估联合使用呋喹替尼和 ICI 治疗 mCRC 患者的临床疗效、安全性和预后指标。
我们分析了接受呋喹替尼单药或在常规化疗后联合 ICI 治疗的 mCRC 患者的数据。仔细评估了客观缓解率(ORR)、疾病控制率(DCR)、总生存期(OS)、无进展生存期(PFS)和不良事件发生率等参数。此外,还研究了血液标志物与患者预后的关系。
本研究共纳入 72 例 mCRC 患者,中位观察期为 48 个月,19 例患者接受呋喹替尼单药治疗,53 例患者接受呋喹替尼联合 ICI 治疗。联合治疗组的 ORR 和 DCR 均优于呋喹替尼单药组。此外,联合治疗组的 OS 和 PFS 均有显著改善。两组不良事件的发生总体上均可管理且耐受良好,发生率无显著差异。值得注意的是,单因素 Cox 回归分析显示,白蛋白水平是 PFS 和 OS 的预后标志物。
与呋喹替尼单药治疗相比,呋喹替尼联合 ICI 治疗 mCRC 患者的临床疗效增强,生存结局改善。联合治疗方案的安全性可管理且可接受。