Department of Hematology-Oncology, Henry Ford Health System, Detroit, MI, USA.
Am J Case Rep. 2020 Jul 13;21:e923803. doi: 10.12659/AJCR.923803.
BACKGROUND Pancreatic adenocarcinoma (PDA) is associated with an 8.6-fold increased risk in Lynch syndrome patients. Here, we report the case of a Lynch syndrome PDA patient with an exceptional response to a single cycle of pembrolizumab immunotherapy. CASE REPORT A 65-year-old male patient with Lynch syndrome mismatch repair (MMR) deficient PDA with metastatic liver disease, received 1 cycle of pembrolizumab (200 mg) after progressing on 2 standard lines of treatment. His initial computed tomography (CT) showed 3×2.5 cm PDA. At that time, the disease was considered borderline resectable, and the patient received 6 cycles of FOLFIRINOX followed by chemoradiotherapy with capecitabine. A follow-up CT scan showed multiple new liver lesions. The biopsy showed metastatic PDA and tumor tissue demonstrated high microsatellite instability with abnormal/lost expression of MLH1 and PMS2 proteins. The patient was started on pembrolizumab. Only 1 cycle was given due to the development of thromboembolic complications: pulmonary embolism and myocardial infarction. His thrombophilia workup was negative. Restaging CT scans at 3, 6, and 9 months after 1 cycle of pembrolizumab revealed an excellent response with shrinkage of liver lesions. Restaging at 11 months showed the eventual resolution of most liver lesions. No new metastatic disease developed. A repeat biopsy of the dominant liver lesion showed no morphological evidence of PDA. CONCLUSIONS Only 1 cycle of pembrolizumab resulted in clinical complete response and pathologic response in metastatic PDA. We emphasize the importance of testing for MMR status and treating with immunotherapy in metastatic PDA patients with MMR deficiency.
林奇综合征(Lynch syndrome)患者患胰腺导管腺癌(PDA)的风险增加 8.6 倍。在此,我们报告了一例林奇综合征伴 PDA 的患者,其对单周期派姆单抗免疫治疗有显著反应。
一名 65 岁男性林奇综合征错配修复(MMR)缺陷 PDA 伴肝转移患者,在标准治疗方案进展后,接受了 1 周期的派姆单抗(200mg)治疗。他的初始计算机断层扫描(CT)显示 3×2.5cm 的 PDA。当时,该疾病被认为是临界可切除的,患者接受了 6 周期的 FOLFIRINOX 治疗,随后进行了卡培他滨化疗和放疗。后续 CT 扫描显示有多个新的肝脏病变。活检显示转移性 PDA,肿瘤组织表现为高度微卫星不稳定,MLH1 和 PMS2 蛋白异常/缺失表达。患者开始接受派姆单抗治疗。由于发生血栓栓塞并发症:肺栓塞和心肌梗死,仅给予 1 个周期。他的血栓形成倾向检查为阴性。派姆单抗治疗 1 周期后 3、6 和 9 个月的复查 CT 扫描显示肝脏病变有显著缩小,疗效评估为完全缓解。11 个月时的复查显示大多数肝脏病变最终得到解决。未发现新的转移性疾病。对主要肝脏病变的重复活检显示无形态学证据的 PDA。
仅 1 个周期的派姆单抗治疗导致转移性 PDA 的临床完全缓解和病理缓解。我们强调了在 MMR 缺陷的转移性 PDA 患者中检测 MMR 状态并进行免疫治疗的重要性。