Loosen Sven H, Ulmer Tom F, Labuhn Simon, Bednarsch Jan, Lang Sven A, Alizai Patrick H, Schneider Anne T, Vucur Mihael, Neumann Ulf P, Luedde Tom, Roderburg Christoph
Clinic for Gastroenterology, Hepatology and Infectious Diseases, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Department of Visceral and Transplantation Surgery, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074 Aachen, Germany.
Cancers (Basel). 2022 Aug 23;14(17):4073. doi: 10.3390/cancers14174073.
The prognosis of biliary tract cancer (BTC) has remained very poor. Although tumor resection represents a potentially curative therapy for selected patients, tumor recurrence is common, and 5-year survival rates have remained below 50%. As stratification algorithms comprising the parameters of individual tumor biology are missing, the identification of ideal patients for extensive tumor surgery is often challenging. The CXC chemokine family exerts decisive functions in cell-cell interactions and has only recently been associated with cancer, but little is known about their function in BTC. Here, we aim to evaluate a potential role of circulating CXCL1, CXCL10 and CXCL13 in patients with resectable BTC.
Serum levels of CXCL1, CXCL10 and CXCL13 were measured by multiplex immunoassay in a cohort of 119 BTC patients undergoing tumor resection and 50 control samples.
Circulating levels of CXCL1, CXCL10 and CXCL13 were all significantly elevated in BTC patients compared to healthy controls and increased the diagnostic power of established tumor markers such as CA19-9 when used in combination. Importantly, elevated levels of CXCL13 both before and after tumor resection identified a subgroup of patients with significantly impaired outcomes following tumor resection. As such, BTC patients with initial CXCL13 levels above the ideal prognostic cut-off value (25.01 pg/mL) had a median overall survival (OS) of 290 days compared to 969 days for patients with low initial CXCL13 levels. The prognostic value of circulating CXCL13 was further confirmed by uni- and multivariate Cox regression analyses. Finally, the individual kinetics of CXCL13 before and after tumor resection were also indicative of patient outcomes.
Our data support a fundamental role of the CXC chemokine family in BTC and identified circulating levels of CXCL13 as a previously unrecognized marker for predicting outcomes following the resection of BTC.
胆管癌(BTC)的预后一直很差。尽管肿瘤切除对部分患者而言是一种潜在的治愈性疗法,但肿瘤复发很常见,5年生存率仍低于50%。由于缺乏包含个体肿瘤生物学参数的分层算法,确定适合进行广泛肿瘤手术的理想患者往往具有挑战性。CXC趋化因子家族在细胞间相互作用中发挥着决定性作用,直到最近才与癌症相关联,但对其在BTC中的功能了解甚少。在此,我们旨在评估循环CXCL1、CXCL10和CXCL13在可切除BTC患者中的潜在作用。
通过多重免疫测定法测量了119例接受肿瘤切除的BTC患者队列和50份对照样本中CXCL1、CXCL10和CXCL13的血清水平。
与健康对照相比,BTC患者中CXCL1、CXCL10和CXCL13的循环水平均显著升高,并且在联合使用时提高了如CA19-9等既定肿瘤标志物的诊断能力。重要的是,肿瘤切除前后CXCL13水平升高均表明存在肿瘤切除后预后明显受损的患者亚组。因此,初始CXCL13水平高于理想预后临界值(25.01 pg/mL)的BTC患者的中位总生存期(OS)为290天,而初始CXCL13水平低的患者为969天。单因素和多因素Cox回归分析进一步证实了循环CXCL13的预后价值。最后,肿瘤切除前后CXCL13的个体动力学也表明了患者的预后情况。
我们的数据支持CXC趋化因子家族在BTC中起重要作用,并确定循环CXCL13水平是预测BTC切除后预后的一个此前未被认识的标志物。