Pothuri Vikram, Herndon John, Ballentine Samuel J, Lim Kian-Huat, Fields Ryan C
Washington University School of Medicine, Barnes-Jewish Hospital, St. Louis, Missouri, USA.
Oncologist. 2021 Sep;26(9):722-726. doi: 10.1002/onco.13821. Epub 2021 May 26.
Herein, we report on a patient with known Lynch syndrome and periampullary adenocarcinoma that exhibited a pathological complete response to neoadjuvant nivolumab plus ipilimumab. Two MSH2 mutations, high microsatellite instability, high tumor mutational burden, and elevated PD-L1 expression were identified by next-generation sequencing and immunohistochemistry. Following FOLFIRINOX (Fluorouracil/Leucovorin/Irinotecan/Oxaliplatin) administration and disease progression, nivolumab (1 mg/kg) and ipilimumab (3 mg/kg) were administered every 3 weeks for four total cycles. The patient responded well with minimal adverse effects and significant improvement in epigastric pain, appetite, and body weight. She then underwent resection consisting of pancreaticoduodenectomy, which demonstrated pathological complete response. Complete genomic profiling of periampullary carcinomas is crucial for optimal treatment selection as true ampullary masses and pancreatic ductal adenocarcinoma have different genetic profiles. This case provides an example of a patient who may have further benefited from first-line nivolumab plus ipilimumab to avoid the reduced efficacy and significant side effects associated with chemotherapy. KEY POINTS: A patient with known Lynch syndrome and ampullary adenocarcinoma harboring two MSH2 mutations, high microsatellite instability (MSI-high), high tumor mutational burden (TMB), and elevated PD-L1 expression achieved pathological complete response with neoadjuvant nivolumab plus ipilimumab. The combination of nivolumab plus ipilimumab may be a better first-line option for patients with ampullary adenocarcinomas harboring deficient mismatch repair, MSI-high, and high TMB. Complete genomic profiling of periampullary adenocarcinomas is crucial for optimal treatment selection as true ampullary masses and pancreatic ductal adenocarcinoma have different genetic profiles. The presence of either MSI-high or high TMB could be an appropriate predictive biomarker for response to nivolumab plus ipilimumab in the context of Lynch syndrome.
在此,我们报告一例已知患有林奇综合征和壶腹周围腺癌的患者,该患者对新辅助纳武单抗加伊匹单抗表现出病理完全缓解。通过二代测序和免疫组化鉴定出两个MSH2突变、高微卫星不稳定性、高肿瘤突变负荷以及升高的PD-L1表达。在给予FOLFIRINOX(氟尿嘧啶/亚叶酸钙/伊立替康/奥沙利铂)治疗且疾病进展后,每3周给予纳武单抗(1mg/kg)和伊匹单抗(3mg/kg),共四个周期。患者反应良好,不良反应轻微,上腹部疼痛、食欲和体重有显著改善。随后她接受了包括胰十二指肠切除术在内的手术切除,显示出病理完全缓解。壶腹周围癌的完整基因组分析对于最佳治疗选择至关重要,因为真正的壶腹肿块和胰腺导管腺癌具有不同的基因谱。该病例提供了一个例子,说明患者可能从一线纳武单抗加伊匹单抗中进一步获益,以避免与化疗相关的疗效降低和显著副作用。要点:一名已知患有林奇综合征和壶腹腺癌的患者,携带两个MSH2突变、高微卫星不稳定性(MSI-High)、高肿瘤突变负荷(TMB)以及升高PD-L1表达,新辅助纳武单抗加伊匹单抗治疗后达到病理完全缓解。纳武单抗加伊匹单抗联合方案可能是具有错配修复缺陷(dMMR)、MSI-High和高TMB的壶腹腺癌患者更好的一线选择。壶腹周围腺癌的完整基因组分析对于最佳治疗选择至关重要,因为真正的壶腹肿块和胰腺导管腺癌具有不同的基因谱。在林奇综合征背景下,MSI-High或高TMB的存在可能是对纳武单抗加伊匹单抗反应的合适预测生物标志物。