窦性心动过缓在信迪利单抗联合化疗治疗晚期胃腺癌疗效中的预测价值
Predictive Value of Sinus Bradycardia in the Efficacy of Sintilimab Combined with Chemotherapy for Advanced Gastric Adenocarcinoma
DOI: 10.12677/acm.2026.161162, PDF,    科研立项经费支持
作者: 朱忠平, 董娟娟*:安徽医科大学第四附属医院肿瘤内科,安徽 合肥
关键词: 胃腺癌信迪利单抗窦性心动过缓化疗预后Gastric Adenocarcinoma Sintilimab Sinus Bradycardia Chemotherapy Prognosis
摘要: 目的:探讨窦性心动过缓在接受信迪利单抗联合化疗治疗晚期胃腺癌中的预后预测价值。方法:回顾性分析2022年1月1日至2025年1月1日在安徽医科大学第四附属医院(附属巢湖医院)接受信迪利单抗联合化疗一线治疗的晚期胃腺癌患者68例临床资料。评估窦性心动过缓(Sinus Bradycardia, SBc)与无进展生存期(PFS)的关系。结果:在68例患者中,16例(23.5%)患者发生SBc。发生SBc组患者的中位PFS显著优于未发生SBc组(11.1个月vs 5.9个月;P < 0.001);未发生腹腔转移患者的PFS优于发生腹腔转移患者(6.7个月vs 5.1个月;P = 0.028)。COX回归分析表明SBc的发生是PFS的独立预测因子(HR6.176, 95% CI 2.349~16.240, P < 0.001)。结论:SBc与信迪利单抗联合化疗治疗胃腺癌患者的疗效相关,可能是一种抗肿瘤免疫反应的临床指标。
Abstract: Objective: To investigate the prognostic value of sinus bradycardia in patients with advanced gastric adenocarcinoma treated with sintilimab combined with chemotherapy. Methods: A retrospective analysis was conducted on the clinical data of 68 patients with advanced gastric adenocarcinoma who received first-line treatment with sintilimab combined with chemotherapy at the Fourth Affiliated Hospital of Anhui Medical University (Affiliated Chaohu Hospital) between January 1, 2022, and January 1, 2025. The relationship between sinus bradycardia (SBc) and progression-free survival (PFS) was evaluated. Results: Among the 68 patients, 16 (23.5%) developed SBc. The median PFS in the SBc group was significantly longer than that in the non-SBc group (11.1 months vs. 5.9 months; P < 0.001). COX regression analysis indicated that the occurrence of SBc was an independent predictor of PFS (HR 6.176, 95% CI 2.349~16.240, P < 0.001). Conclusion: SBc is associated with the efficacy of sintilimab combined with chemotherapy in patients with gastric adenocarcinoma and may serve as a clinical indicator of anti-tumor immune response.
文章引用:朱忠平, 董娟娟. 窦性心动过缓在信迪利单抗联合化疗治疗晚期胃腺癌疗效中的预测价值[J]. 临床医学进展, 2026, 16(1): 1247-1256. https://doi.org/10.12677/acm.2026.161162

参考文献

[1] Zhang, L., Wang, W., Ge, S., Li, H., Bai, M., Duan, J., et al. (2023) Sintilimab Plus Apatinib and Chemotherapy as Second-/Third-Line Treatment for Advanced Gastric or Gastroesophageal Junction Adenocarcinoma: A Prospective, Single-Arm, Phase II Trial. BMC Cancer, 23, Article No. 211. [Google Scholar] [CrossRef] [PubMed]
[2] Wang, G., Huang, Y., Zhou, L., Yang, H., Lin, H., Zhou, S., et al. (2024) Immunotherapy and Targeted Therapy as First-Line Treatment for Advanced Gastric Cancer. Critical Reviews in Oncology/Hematology, 198, Article ID: 104197. [Google Scholar] [CrossRef] [PubMed]
[3] Jiang, H., Yu, X., Li, N., Kong, M., Ma, Z., Zhou, D., et al. (2022) Efficacy and Safety of Neoadjuvant Sintilimab, Oxaliplatin and Capecitabine in Patients with Locally Advanced, Resectable Gastric or Gastroesophageal Junction Adenocarcinoma: Early Results of a Phase 2 Study. Journal for ImmunoTherapy of Cancer, 10, e003635. [Google Scholar] [CrossRef] [PubMed]
[4] Wang, Y., Zhao, J., Yu, H., Wang, J., Zhang, N. and Cao, B. (2021) Efficacy and Safety of Sintilimab-Based Regimens against Advanced Gastric and Gastroesophageal Junction Adenocarcinoma. Journal of Cancer Research and Therapeutics, 17, 1234-1240. [Google Scholar] [CrossRef] [PubMed]
[5] Lu, G., Tu, J., Tu, J. and Jiang, R. (2025) Case Report: Chemotherapy Plus Sintilimab for the Treatment of Gastroesophageal Junction Hepatoid Adenocarcinoma with Liver Metastasis: A Case Study with Literature Review. Frontiers in Immunology, 16, Article 1513604. [Google Scholar] [CrossRef] [PubMed]
[6] Tan, S., Zheng, Q., Zhang, W., Zhou, M., Xia, C. and Feng, W. (2024) Prognostic Value of Inflammatory Markers NLR, PLR, and LMR in Gastric Cancer Patients Treated with Immune Checkpoint Inhibitors: A Meta-Analysis and Systematic Review. Frontiers in Immunology, 15, Article 1408700. [Google Scholar] [CrossRef] [PubMed]
[7] He, X., Du, B., Wu, T. and Shen, H. (2024) Prognostic Analysis of Related Factors of Adverse Reactions to Immunotherapy in Advanced Gastric Cancer and Establishment of a Nomogram Model. World Journal of Gastrointestinal Oncology, 16, 1268-1280. [Google Scholar] [CrossRef] [PubMed]
[8] Tocchetti, C.G., Farmakis, D., Koop, Y., Andres, M.S., Couch, L.S., Formisano, L., et al. (2024) Cardiovascular Toxicities of Immune Therapies for Cancer—A Scientific Statement of the Heart Failure Association (HFA) of the esc and the esc Council of Cardio‐Oncology. European Journal of Heart Failure, 26, 2055-2076. [Google Scholar] [CrossRef] [PubMed]
[9] Palaskas, N.L., Ali, H., Koutroumpakis, E., Ganatra, S. and Deswal, A. (2024) Cardiovascular Toxicity of Immune Therapies for Cancer. BMJ, 385, e075859. [Google Scholar] [CrossRef] [PubMed]
[10] Zhao, C. (2024) Correlation between Thyroid Dysfunction and Efficacy of Immune Checkpoint Inhibitors in Patients with Advanced Solid Tumors. Discover Oncology, 15, Article No. 663. [Google Scholar] [CrossRef] [PubMed]
[11] 阴明妹. 信迪利单抗联合SOX方案在HER-2阴性晚期胃癌一线治疗的疗效及疗效预测因子分析[D]: [硕士学位论文]. 开封: 河南大学, 2023.
[12] 顾晓凌, 吴冠楠, 王栋, 等. 免疫检查点抑制剂相关甲状腺不良事件对PD-1单抗治疗非小细胞肺癌的预测价值[J]. 东南国防医药, 2023, 25(1): 7-12.
[13] Ou, W., Zhou, C., Zhu, X., Lin, L. and Xu, Q. (2021) Prognostic Significance of Preoperative Lymphocyte-To-C-Reactive Protein Ratio in Patients with Non-Metastatic Colorectal Cancer. OncoTargets and Therapy, 14, 337-346. [Google Scholar] [CrossRef] [PubMed]
[14] LV, B., Wang, Y., Ma, D., Cheng, W., Liu, J., Yong, T., et al. (2022) Immunotherapy: Reshape the Tumor Immune Microenvironment. Frontiers in Immunology, 13, Article 744142. [Google Scholar] [CrossRef] [PubMed]
[15] Ogata, T., Satake, H., Ogata, M., Hatachi, Y., Inoue, K., Hamada, M., et al. (2018) Neutrophil-To-Lymphocyte Ratio as a Predictive or Prognostic Factor for Gastric Cancer Treated with Nivolumab: A Multicenter Retrospective Study. Oncotarget, 9, 34520-34527.
[16] Zhang, T., Lv, H., Li, J., Zhang, S., Zhang, J., Wang, S., et al. (2024) The Impact of Immune-Related Adverse Events on the Outcome of Advanced Gastric Cancer Patients with Immune Checkpoint Inhibitor Treatment. Frontiers in Immunology, 15, Article 1503316. [Google Scholar] [CrossRef] [PubMed]
[17] Niu, C., Zhu, K., Zhang, J., Joshi, U., Liu, H., Zahid, S., et al. (2023) Analysis of Immune‐Related Adverse Events in Gastrointestinal Malignancy Patients Treated with Immune Checkpoint Inhibitors. International Journal of Cancer, 154, 1261-1271. [Google Scholar] [CrossRef] [PubMed]
[18] Wang, H., Chen, J., Gao, W., Wu, Y., Wang, X., Lin, F., et al. (2024) Construction of a Nomogram with Irae and Clinic Character to Predict the Survival of Advanced G/GEJ Adenocarcinoma Patients Undergoing Anti-PD-1 Treatment. Frontiers in Immunology, 15, Article 1432281. [Google Scholar] [CrossRef] [PubMed]
[19] Hao, W., Liu, W., Chang, R., Yang, M., Xin, K., Liu, J., et al. (2024) Safety and Clinical Efficacy of Immune Checkpoint Inhibitors in Advanced Gastric Cancer in the Real World. Journal of Cancer Research and Clinical Oncology, 150, Article No. 180. [Google Scholar] [CrossRef] [PubMed]
[20] Lu, L., Xing, K., Wei, W., Ling, Y., Li, P., Li, S., et al. (2021) Immune‐related Adverse Events Predict Responses to PD‐1 Blockade Immunotherapy in Hepatocellular Carcinoma. International Journal of Cancer, 149, 959-966. [Google Scholar] [CrossRef] [PubMed]
[21] Fukushima, T., Kobayashi, S. and Ueno, M. (2024) The Correlation between Immune-Related Adverse Events and Efficacy of Immune Checkpoint Inhibitors. Japanese Journal of Clinical Oncology, 54, 949-958. [Google Scholar] [CrossRef] [PubMed]
[22] Joseph, L., Nickel, A.C., Patel, A., et al. (2021) Incidence of Cancer Treatment Induced Arrhythmia Associated with Immune Checkpoint Inhibitors. Journal of Atrial Fibrillation, 13, Article 2461. [Google Scholar] [CrossRef] [PubMed]