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

IF 1.5 Q4 ONCOLOGY
Cancer reports Pub Date : 2025-06-09 DOI:10.1002/cnr2.70186
Li Wang, Jiaqi Wu, Ping Shao, Wuping Bao, Lin Mao, Zhendong Pan, Aihua Bao, Min Zhang, Zhenghua Wu, Guorong Fan
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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.

一名KRAS突变的晚期IVB肺腺癌患者受益于Camrelizumab联合抗血管生成药物治疗:一例报告
背景:尽管Kirsten小鼠肉瘤病毒(KRAS)突变的存在预示着非小细胞癌(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+抗血管生成的程序性联合治疗更为敏感。近期NSCLC中腺癌的治疗指南和相关临床研究表明,在不能手术的IV期肺腺癌患者中,免疫检查点抑制剂联合抗血管生成药物可能会发挥协同作用,显著提高近期治疗的疗效,但具体临床指标的量化和长期随访尚缺乏。camrelizumab联合抗血管生成药物治疗kras突变的非小细胞肺癌尚无长期良好结果的报道。本文报道了一例在上海总医院接受常规化疗治疗的晚期非小细胞肺癌胸膜积液和KRAS突变患者,经免疫治疗联合抗血管生成抑制剂治疗长期(超过18个月)获益。本病例通过治疗药物调整、依从性、疗效评估、安全性评价等对患者进行药学服务,为临床提高药物治疗的疗效和安全性提供参考。截至最后一次随访日期(2023年12月),总生存期为27个月,患者目前总体状况良好,无明显不适主诉。结论ICLs联合抗血管生成治疗可能是KRAS突变晚期非小细胞肺癌患者的一种治疗选择,且具有良好的持续性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cancer reports
Cancer reports Medicine-Oncology
CiteScore
2.70
自引率
5.90%
发文量
160
审稿时长
17 weeks
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