Department of Medical Oncology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100032, China.
Department of Medical Oncology, The General Hospital of People's Liberation Army, Beijing, 100853, China.
Cancer Immunol Immunother. 2022 Jun;71(6):1443-1451. doi: 10.1007/s00262-021-03083-3. Epub 2021 Oct 24.
Treatment strategies are limited for patients with chemotherapy refractory microsatellite stable (MSS) colorectal cancer. We aim to evaluate the efficacy and safety of immune checkpoint inhibitors (ICIs) combined with regorafenib in this population in routine clinical practice.
We retrospectively analyzed patients with advanced or metastatic colorectal cancer who received at least one dose of ICIs combined with regorafenib in 14 Chinese medical centers. The primary outcome was objective response rate (ORR). This study was registered at ClinicalTrials.gov on February 2020 (NCT04771715).
Eighty-four patients received ICIs combined with regorafenib from January 2019 to January 2021. Most patients (91%) received two or more systemic treatment lines before the study treatment. Seventy-six patients (90%) had confirmed MSS status. At a median follow-up of 5.5 months, four patients achieved partial response (5%) and 37 patients achieved stable disease (45%) as the best response. The median progression-free survival (PFS) was 3.1 months, and the median overall survival was 17.3 months. Eleven patients (13%) remained progression-free for more than 6 months. Baseline liver metastasis (HR 1.98, 95%CI 1.07-3.69, P = 0.03) and neutrophil-lymphocyte ratio (NLR) of ≥ 1.5 (HR 2.83, 95%CI 1.00-7.98, P = 0.05) were associated with shorter PFS in multivariate analysis. Grade 3 or higher treatment-related adverse events (TRAEs) occurred in 16 patients (19%).
The combination of ICIs with regorafenib can be a valuable treatment option for a proportion of patients with chemotherapy refractory MSS colorectal cancer. Patients with no liver metastasis and a low NLR at baseline may derive most benefit from this strategy.
对于化疗耐药的微卫星稳定(MSS)结直肠癌患者,治疗策略有限。我们旨在评估免疫检查点抑制剂(ICIs)联合regorafenib 在常规临床实践中对此类人群的疗效和安全性。
我们回顾性分析了 14 家中国医疗中心的至少接受一剂 ICIs 联合regorafenib 治疗的晚期或转移性结直肠癌患者。主要结局是客观缓解率(ORR)。这项研究于 2020 年 2 月在 ClinicalTrials.gov 注册(NCT04771715)。
84 例患者于 2019 年 1 月至 2021 年 1 月接受了 ICIs 联合regorafenib 治疗。大多数患者(91%)在研究治疗前接受了两种或更多种系统治疗。76 例患者(90%)有确证的 MSS 状态。在中位随访 5.5 个月时,4 例患者达到部分缓解(5%),37 例患者达到最佳疾病稳定(45%)。中位无进展生存期(PFS)为 3.1 个月,中位总生存期为 17.3 个月。11 例(13%)患者无进展时间超过 6 个月。多变量分析显示,基线时肝转移(HR 1.98,95%CI 1.07-3.69,P=0.03)和中性粒细胞-淋巴细胞比值(NLR)≥1.5(HR 2.83,95%CI 1.00-7.98,P=0.05)与 PFS 较短相关。16 例患者(19%)发生 3 级或更高级别的治疗相关不良事件(TRAEs)。
ICIs 联合 regorafenib 可为一部分化疗耐药的 MSS 结直肠癌患者提供有价值的治疗选择。基线时无肝转移和 NLR 较低的患者可能从该策略中获益最大。