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联合免疫检查点抑制治疗转移性结直肠癌进展后完全代谢缓解:1 例报告。

Complete Metabolic Response to Combined Immune Checkpoint Inhibition after Progression of Metastatic Colorectal Cancer on Pembrolizumab: A Case Report.

机构信息

Department for Medicine A, Hematology, Oncology, Hemostaseology and Pneumology, University Hospital Muenster, 48149 Muenster, Germany.

West German Cancer Center, University Hospital Muenster, 48149 Muenster, Germany.

出版信息

Int J Mol Sci. 2023 Jul 27;24(15):12056. doi: 10.3390/ijms241512056.

Abstract

DNA mismatch repair deficient (dMMR) and microsatellite instable (MSI) metastatic colorectal cancer (mCRC) can be successfully treated with FDA- and EMA-approved immune checkpoint inhibitors (ICI) pembrolizumab and nivolumab (as single agents targeting the anti-programmed cell death protein-1 (PD-1)) or combinations of a PD-1 inhibitor with ipilimumab, a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4)-targeting antibody. The best treatment strategy beyond progression on single-agent ICI therapy remains unclear. Here, we present the case of a 63-year-old male with Lynch-syndrome-associated, microsatellite instability-high (MSI-H) mCRC who achieved a rapid normalization of his tumor markers and a complete metabolic remission (CMR), currently lasting for ten months, on sequential ICI treatment with the combination of nivolumab and ipilimumab followed by nivolumab maintenance therapy after progression on single-agent anti-PD-1 ICI therapy. The therapy was well-tolerated, and no immune-related adverse events occurred. To the best of our knowledge, this is the first case of a sustained metabolic complete remission in an MSI-H mCRC patient initially progressing on single-agent anti-PD-1 therapy. Thus, dMMR mCRC patients might benefit from sequential immune checkpoint regimens even with long-term responses. However, further sophistication of clinical algorithms for treatment beyond progression on single-agent ICI therapy in MSI-mCRC is urgently needed.

摘要

DNA 错配修复缺陷(dMMR)和微卫星不稳定(MSI)转移性结直肠癌(mCRC)可以成功地用美国食品药品监督管理局(FDA)和欧洲药品管理局(EMA)批准的免疫检查点抑制剂(ICI)pembrolizumab 和 nivolumab(作为针对抗程序性细胞死亡蛋白-1(PD-1)的单一药物)或 PD-1 抑制剂与 ipilimumab(一种细胞毒性 T 淋巴细胞相关蛋白 4(CTLA-4)靶向抗体)联合治疗。在单一 ICI 治疗进展后,最佳的治疗策略尚不清楚。在这里,我们报告了一例林奇综合征相关、微卫星高度不稳定(MSI-H)mCRC 的 63 岁男性患者的病例,他在序贯 ICI 治疗中联合使用 nivolumab 和 ipilimumab 后,肿瘤标志物迅速正常化,并实现完全代谢缓解(CMR),目前已持续十个月,在单一抗 PD-1 ICI 治疗进展后继续使用 nivolumab 维持治疗。该治疗耐受良好,未发生免疫相关不良事件。据我们所知,这是首例在单一抗 PD-1 治疗进展后持续代谢完全缓解的 MSI-H mCRC 患者。因此,dMMR mCRC 患者可能受益于序贯免疫检查点方案,即使有长期反应。然而,迫切需要进一步完善用于 MSI-mCRC 中单一 ICI 治疗进展后治疗的临床算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435c/10418401/0ae8ea67bd89/ijms-24-12056-g001.jpg

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