Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria; Christian Doppler Laboratory for Personalized Immunotherapy, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Division of Oncology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
ESMO Open. 2023 Apr;8(2):101200. doi: 10.1016/j.esmoop.2023.101200. Epub 2023 Mar 28.
Malignant ascites is common in metastatic pancreatic cancer (mPC) and its management still remains a clinical challenge. Early identification of patients at risk for ascites development may support and guide treatment decisions.
Data of patients treated for mPC at the Medical University of Vienna between 2010 and 2019 were collected by retrospective chart review. Ascites was defined as clinically relevant accumulation of intraperitoneal fluid diagnosed by ultrasound or computer tomography scan of the abdomen. We investigated the association between general risk factors, metastatic sites, liver function, systemic inflammation as well as portal vein obstruction (PVO) and ascites development.
Among 581 patients with mPC included in this study, 122 (21.0%) developed ascites after a median of 8.7 months after diagnosis of metastatic disease. The occurrence of ascites led to an 8.9-fold increased risk of death [confidence interval (CI) 7.2-11, P < 0.001] with a median overall survival of 1 month thereafter. Clinical risk factors for ascites were male sex [hazard ratio (HR) 1.71, CI 1.00-2.90, P = 0.048], peritoneal carcinomatosis (HR 6.79, CI 4.09-11.3, P < 0.001), liver metastases (HR 2.16, CI 1.19-3.91, P = 0.011), an albumin-bilirubin (ALBI) score grade 3 (HR 6.79, CI 2.11-21.8, P = 0.001), PVO (HR 2.28, CI 1.15-4.52, P = 0.019), and an elevated C-reactive protein (CRP) (HR 4.19, CI 1.58-11.1, P = 0.004).
Survival after diagnosis of ascites is very limited in mPC patients. Male sex, liver and peritoneal metastases, impaired liver function, PVO, as well as systemic inflammation were identified as independent risk factors for ascites development in this uniquely large real-life patient cohort.
恶性腹水在转移性胰腺癌(mPC)中很常见,其管理仍然是一个临床挑战。早期识别有腹水发展风险的患者可能有助于支持和指导治疗决策。
通过回顾性病历审查,收集了 2010 年至 2019 年在维也纳医科大学接受 mPC 治疗的患者的数据。腹水定义为通过腹部超声或计算机断层扫描诊断的临床相关腹腔内液体积聚。我们研究了一般危险因素、转移部位、肝功能、全身炎症以及门静脉阻塞(PVO)与腹水发展之间的关系。
在这项研究中,纳入了 581 名 mPC 患者,其中 122 名(21.0%)在转移性疾病诊断后中位数 8.7 个月后出现腹水。腹水的发生使死亡风险增加了 8.9 倍[置信区间(CI)7.2-11,P < 0.001],此后的总生存中位数为 1 个月。腹水的临床危险因素包括男性[风险比(HR)1.71,CI 1.00-2.90,P = 0.048]、腹膜癌病(HR 6.79,CI 4.09-11.3,P < 0.001)、肝转移(HR 2.16,CI 1.19-3.91,P = 0.011)、白蛋白-胆红素(ALBI)评分 3 级(HR 6.79,CI 2.11-21.8,P = 0.001)、PVO(HR 2.28,CI 1.15-4.52,P = 0.019)和 C 反应蛋白(CRP)升高(HR 4.19,CI 1.58-11.1,P = 0.004)。
在 mPC 患者中,腹水诊断后的生存非常有限。在这个独特的大型真实患者队列中,男性、肝和腹膜转移、肝功能受损、PVO 以及全身炎症被确定为腹水发展的独立危险因素。