Fremal Maroš, Chedia Mária
Department of Oncology, Milosrdní Bratia University Hospital, Bratislava, Slovakia.
Department of Radiology, Milosrdní Bratia University Hospital, Bratislava, Slovakia.
Case Rep Oncol. 2025 Jun 12;18(1):920-928. doi: 10.1159/000546328. eCollection 2025 Jan-Dec.
Pegylated liposomal irinotecan (nal-IRI) in combination with fluorouracil (5-FU) and leucovorin (LV) has achieved a median overall survival of 6.1 months in patients with metastatic pancreatic ductal adenocarcinoma who progressed on gemcitabine-based chemotherapy. The case of a patient with considerable long-term survival on second-line nal-IRI-based therapy is presented.
A 70-year-old male presented with weight loss and abdominal pain in July 2018, was diagnosed with stage IB PDAC (pT2, pN0, M0), and underwent successful R0 resection. Adjuvant chemotherapy with FOLFIRINOX (5-FU, LV, irinotecan, and oxaliplatin) was given for 9 cycles between September 2018 and January 2019, and the patient remained recurrence-free until a computed tomography scan revealed soft tissue mesenteric infiltrations in July 2020. First-line palliative chemotherapy with nab-paclitaxel + gemcitabine was initiated and continued until January 2022 when disease progression in the form of two metastatic hepatic lesions was observed. Second-line palliative chemotherapy with nal-IRI 129 mg on day 1 + capecitabine (CAP) 4,000 mg daily for the first 7 days of each 14-day cycle was initiated (due to previous 5-FU intolerance). Response (reduced oncomarkers) was observed, and treatment with nal-IRI + CAP continued, with liver-directed treatment in September 2023, until February 2024. During second-line therapy, side effects (mild diarrhoea) were infrequent and manageable.
This patient achieved an extraordinary survival of 25 months with second-line treatment with nal-IRI + CAP. Nal-IRI-based therapy has the potential to provide long-term survival in the presence of favourable prognostic factors such as moderately elevated carbohydrate antigen 19-9 levels.
聚乙二醇化脂质体伊立替康(nal-IRI)联合氟尿嘧啶(5-FU)和亚叶酸钙(LV),在接受过吉西他滨为基础化疗后病情进展的转移性胰腺导管腺癌患者中,实现了6.1个月的中位总生存期。本文介绍了一名接受二线nal-IRI为基础治疗后长期存活的患者病例。
一名70岁男性于2018年7月出现体重减轻和腹痛,被诊断为IB期胰腺导管腺癌(pT2,pN0,M0),并成功接受了R0切除。2018年9月至2019年1月期间给予FOLFIRINOX(5-FU、LV、伊立替康和奥沙利铂)辅助化疗9个周期,患者一直无复发,直到2020年7月计算机断层扫描显示肠系膜软组织浸润。开始一线姑息化疗,使用白蛋白结合型紫杉醇+吉西他滨,并持续至2022年1月,此时观察到出现两个转移性肝病灶的疾病进展。开始二线姑息化疗,每14天为一个周期,第1天使用nal-IRI 129 mg+卡培他滨(CAP)4000 mg,连用7天(因之前不耐受5-FU)。观察到有反应(肿瘤标志物降低),继续使用nal-IRI+CAP治疗,并于2023年9月进行肝脏定向治疗,直至2024年2月。在二线治疗期间,副作用(轻度腹泻)很少见且可控。
该患者接受nal-IRI+CAP二线治疗后获得了25个月的超长生存期。基于nal-IRI的治疗在存在如糖类抗原19-9水平适度升高这类有利预后因素的情况下,有提供长期生存的潜力。