Department of Internal Medicine, Mayo Clinic, Phoenix, Arizona.
Department of Hematology and Oncology, Mayo Clinic, Phoenix, Arizona.
J Natl Compr Canc Netw. 2023 Sep;21(9):894-899. doi: 10.6004/jnccn.2023.7029.
Immune checkpoint inhibitors (ICIs) induce profound benefits in cancer patients with mismatch repair gene mutations or high levels of microsatellite instability. Herein, we present a case of a patient with history of Muir-Torre/Lynch syndrome and metastatic gastric adenocarcinoma in the presence of an MSH2 gene mutation. The patient was initially treated with a PD-1 inhibitor, pembrolizumab, but developed grade 4 myocarditis requiring treatment with infliximab and a prolonged steroid taper. Following discontinuation of pembrolizumab, surveillance testing showed no radiographic or endoscopic evidence of progression for 7 months, until biopsy results from a repeat upper endoscopy indicated local disease recurrence. The patient was subsequently rechallenged with another PD-1 inhibitor, nivolumab, at a 50% dose reduction without recurrent adverse events and eventually achieved a complete response after 13 cycles. This case highlights the relative importance of considering careful rechallenge with ICI therapy in patients with microsatellite instability-high malignancies and a high risk of severe adverse events.
免疫检查点抑制剂(ICIs)在错配修复基因突变或高水平微卫星不稳定性的癌症患者中诱导显著获益。在此,我们报告了一例 Muir-Torre/Lynch 综合征病史和转移性胃腺癌患者,存在 MSH2 基因突变。该患者最初接受 PD-1 抑制剂 pembrolizumab 治疗,但发生 4 级心肌炎,需要使用英夫利昔单抗和延长的类固醇减量治疗。停用 pembrolizumab 后,监测检查在 7 个月内没有影像学或内镜进展证据,直到重复上内窥镜检查的活检结果表明局部疾病复发。随后,该患者以 50%的剂量减少重新接受另一种 PD-1 抑制剂 nivolumab 治疗,无复发不良事件,并在 13 个周期后最终实现完全缓解。该病例强调了在微卫星不稳定高恶性和严重不良事件风险高的患者中,仔细重新考虑 ICI 治疗的相对重要性。