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一例KRAS突变的晚期IVB期肺腺癌患者,从卡瑞利珠单抗联合抗血管生成药物治疗中获益:病例报告

An Advanced IVB Lung Adenocarcinoma Patient With KRAS Mutations, Benefited From Camrelizumab Combined With Anti-Angiogenic Agents for Therapy: A Case Report.

作者信息

Wang Li, Wu Jiaqi, Shao Ping, Bao Wuping, Mao Lin, Pan Zhendong, Bao Aihua, Zhang Min, Wu Zhenghua, Fan Guorong

机构信息

School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.

Department of Clinical Pharmacy, Shanghai General Hospital, Shanghai Jiao Tong University, School of Medicine, Shanghai, China.

出版信息

Cancer Rep (Hoboken). 2025 Jun;8(6):e70186. doi: 10.1002/cnr2.70186.

Abstract

BACKGROUND

Although the presence of Kirsten murine sarcoma virus (KRAS) mutations predicts a failure of non-small cell carcinoma (NSCLC) patients to benefit from epidermal growth factor receptor (EGFR)-tyrosine kinase inhibitor (TKI) therapy it may be more sensitive to programmed combination therapy of programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors + anti-angiogenesis. Recent treatment guidelines and clinical studies related to adenocarcinoma in NSCLC have indicated that in patients with inoperable stage IV lung adenocarcinoma, immune checkpoint inhibitors in combination with anti-angiogenic drugs may exert a synergistic effect and significantly improve the efficacy of near-term treatment, but quantification and long-term follow-up of specific clinical indicators are still lacking. No previous cases of long-term good results with camrelizumab combined with anti-angiogenic agents for KRAS-mutated NSCLC have been described.

CASE

This manuscript reports a case of a patient with advanced NSCLC with pleural effusion and KRAS mutations treated poorly with conventional chemotherapy who had long-term (more than 18 months) benefit with immunotherapy combined with an anti-angiogenic inhibitor in Shanghai General Hospital. In this case, pharmaceutical care of the patient was carried out through therapeutic drug adjustment, compliance, efficacy assessment, and safety evaluation to provide a reference for improving the efficacy and safety of drug therapy in clinical practice. As of the last follow-up date (December 2023), overall survival was 27 months, and the patient is currently in good general condition with no significant complaints of discomfort.

CONCLUSION

ICLs in combination with antiangiogenic therapy may be a therapeutic option for patients with KRAS mutations in advanced non-small cell lung cancer with good persistence.

摘要

背景

尽管 Kirsten 鼠肉瘤病毒(KRAS)突变的存在预示着非小细胞肺癌(NSCLC)患者无法从表皮生长因子受体(EGFR)-酪氨酸激酶抑制剂(TKI)治疗中获益,但它可能对程序性死亡 1(PD-1)/程序性死亡配体 1(PD-L1)抑制剂联合抗血管生成的程序性联合治疗更敏感。近期与 NSCLC 腺癌相关的治疗指南和临床研究表明,在无法手术的 IV 期肺腺癌患者中,免疫检查点抑制剂与抗血管生成药物联合使用可能发挥协同作用,并显著提高近期治疗效果,但仍缺乏特定临床指标的量化和长期随访。此前尚无关于卡瑞利珠单抗联合抗血管生成药物治疗 KRAS 突变型 NSCLC 取得长期良好疗效的病例报道。

病例

本手稿报告了 1 例晚期 NSCLC 伴胸腔积液且 KRAS 突变的患者,该患者接受传统化疗效果不佳,在上海交通大学医学院附属瑞金医院接受免疫治疗联合抗血管生成抑制剂后获得了长期(超过 18 个月)获益。在该病例中,通过治疗药物调整、依从性、疗效评估和安全性评价对患者进行药学监护,为提高临床实践中药物治疗的疗效和安全性提供参考。截至最后随访日期(2023 年 12 月),总生存期为 27 个月,患者目前一般状况良好,无明显不适主诉。

结论

免疫检查点抑制剂联合抗血管生成治疗可能是晚期非小细胞肺癌 KRAS 突变患者具有良好持久性的一种治疗选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24b8/12147042/b14b0404732c/CNR2-8-e70186-g001.jpg

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