Fu Hai-Yan, Zhang Yi-Yang, Huang Jin-Shan, Hu Jin-Xin, Bai Kun-Hao, Wang Zhi-Qiang
State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-sen University Cancer Center, Guangzhou, P. R. China.
Department of Medical Oncology, Sun Yat-sen University Cancer Center, Guangzhou, P. R. China.
Ther Adv Med Oncol. 2025 Aug 1;17:17588359251356581. doi: 10.1177/17588359251356581. eCollection 2025.
Serum C-reactive protein (CRP) level is frequently considered a prognostic predictor of immunotherapy. However, the prognostic role of the interim serum CRP levels before the third course of immunotherapy (CRP-C3) in patients with metastatic colorectal cancer (mCRC) receiving immunotherapy remains unclear.
This study aimed to determine the predictive value of CRP-C3 for immunotherapy response and progression-free survival (PFS) and to compare its performance with other biomarkers, such as tumor mutational burden (TMB).
We conducted a retrospective cohort study of 205 patients with mCRC who received immunotherapy.
Baseline CRP (CRP-B) and CRP-C3 levels were measured in this retrospective cohort study. Clinicopathological data were retrospectively analyzed using Cox regression analyses to identify independent predictive variables for immunotherapy response and PFS, then summarized in nomograms to predict prognosis.
The median PFS periods were 8.47 months in the CRP-C3-low subgroup and 2.47 months in the CRP-C3-high subgroup ( < 0.001). The objective response rate (ORR) was 40.6% and 8.9%, respectively ( < 0.001). Although CRP-B failed in the multivariate Cox analysis, CRP-C3 performed exceptionally well, surpassing TMB levels (both < 0.001). Moreover, a prognostic model combining CRP-C3 and TMB levels could significantly stratify patients with mCRC receiving immunotherapy into low-, intermediate-, and high-risk subgroups ( < 0.001). Patients from different risk subgroups exhibited significantly different ORR (low- vs intermediate- vs high-risk groups: 59.2% vs 32.5% vs 0%, respectively, < 0.001) and Kaplan-Meier survival curves ( < 0.001).
This retrospective study indicates a potential association between decreased CRP-C3 levels and improved PFS in patients with mCRC receiving immunotherapy. The combination of CRP-C3 and TMB appeared to enhance predictive performance, suggesting their possible utility as prognostic indicators.
血清C反应蛋白(CRP)水平常被视为免疫治疗的预后预测指标。然而,接受免疫治疗的转移性结直肠癌(mCRC)患者在第三个疗程免疫治疗前的血清CRP水平(CRP-C3)的预后作用仍不清楚。
本研究旨在确定CRP-C3对免疫治疗反应和无进展生存期(PFS)的预测价值,并将其性能与其他生物标志物,如肿瘤突变负荷(TMB)进行比较。
我们对205例接受免疫治疗的mCRC患者进行了一项回顾性队列研究。
在这项回顾性队列研究中测量了基线CRP(CRP-B)和CRP-C3水平。使用Cox回归分析对临床病理数据进行回顾性分析,以确定免疫治疗反应和PFS的独立预测变量,然后汇总到列线图中以预测预后。
CRP-C3低亚组的中位PFS期为8.47个月,CRP-C3高亚组为2.47个月(<0.001)。客观缓解率(ORR)分别为40.6%和8.9%(<0.001)。虽然CRP-B在多变量Cox分析中未显示出预测价值,但CRP-C3表现出色,超过了TMB水平(均<0.001)。此外,结合CRP-C3和TMB水平的预后模型可将接受免疫治疗的mCRC患者显著分层为低、中、高风险亚组(<0.001)。来自不同风险亚组的患者表现出显著不同ORR(低风险组与中风险组与高风险组:分别为59.2% vs 32.5% vs 0%,<0.001)和Kaplan-Meier生存曲线(<0.001)。
这项回顾性研究表明,接受免疫治疗的mCRC患者CRP-C3水平降低与PFS改善之间存在潜在关联。CRP-C3和TMB的组合似乎增强了预测性能,表明它们可能作为预后指标。