Kalavska Katarina, Chovanec Michal, Zatovicova Miriam, Takacova Martina, Gronesova Paulina, Svetlovska Daniela, Baratova Magdalena, Miskovska Vera, Obertova Jana, Palacka Patrik, Rajec Jan, Sycova-Mila Zuzana, Cierna Zuzana, Kajo Karol, Spanik Stanislav, Babal Pavel, Mardiak Jozef, Pastorekova Silvia, Mego Michal
Translational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Department of Oncology, National Cancer Institute, 833 10 Bratislava, Slovakia; Cancer Research Institute, Biomedical Research Center, Slovak Academy of Sciences, 811 04 Bratislava, Slovakia.
Translational Research Unit, Faculty of Medicine, Comenius University, 811 02 Bratislava, Slovakia; Department of Oncology, National Cancer Institute, 833 10 Bratislava, Slovakia; Second Department of Oncology, Faculty of Medicine, Comenius University and National Cancer Institute, 833 10 Bratislava, Slovakia.
Oncol Lett. 2016 Oct;12(4):2590-2598. doi: 10.3892/ol.2016.5010. Epub 2016 Aug 16.
Despite the fact that testicular germ cell tumors (TGCTs) are one of the most chemosensitive solid tumors, a small proportion of patients fail to be cured following cisplatin-based first line chemotherapy. Upregulation of carbonic anhydrase IX (CA IX) in various solid tumors is associated with poor outcome. The current prospective study investigated the prognostic value of serum CA IX level in TGCTs. In total, 83 patients (16 non-metastatic following orchiectomy with no evidence of disease, 57 metastatic chemotherapy-naïve and 10 metastatic relapsed chemotherapy-pretreated) starting adjuvant and/or new line of chemotherapy and 35 healthy controls were enrolled in the study. Serum CA IX values were determined using an enzyme-linked immunosorbent assay, and intratumoral CA IX was analyzed by immunohistochemistry. Metastatic chemotherapy-naïve patients had significantly higher mean CA IX serum levels than healthy controls (490.6 vs. 249.6 pg/ml, P=0.005), while there was no difference in serum CA IX levels in non-metastatic or relapsed TGCT patients compared with healthy controls. There was no significant difference in the mean serum CA IX levels between different groups of patients and between the first and second cycle of chemotherapy, nor association with patients/tumor characteristics. Serum CA IX was not prognostic for progression-free survival [hazard ratio (HR)=0.81, P=0.730] or overall survival (HR=0.64, P=0.480). However, there was a significant association between intratumoral CA IX expression and serum CA IX concentration (rho=0.51, P=0.040). These results suggest that serum CA IX level correlates with tumor CA IX expression in TGCT patients, but fails to exhibit either a prognostic value or an association with patients/tumor characteristics.
尽管睾丸生殖细胞肿瘤(TGCTs)是化疗敏感性最高的实体瘤之一,但仍有一小部分患者在接受以顺铂为基础的一线化疗后未能治愈。多种实体瘤中碳酸酐酶IX(CA IX)的上调与不良预后相关。本前瞻性研究探讨了血清CA IX水平在TGCTs中的预后价值。该研究共纳入了83例开始辅助化疗和/或新的化疗方案的患者(16例睾丸切除术后无疾病证据的非转移性患者、57例未经化疗的转移性患者和10例经化疗预处理的转移性复发患者)以及35名健康对照者。采用酶联免疫吸附测定法测定血清CA IX值,通过免疫组织化学分析肿瘤内CA IX。未经化疗的转移性患者的平均血清CA IX水平显著高于健康对照者(490.6 vs. 249.6 pg/ml,P = 0.005),而非转移性或复发TGCT患者的血清CA IX水平与健康对照者相比无差异。不同组患者之间以及化疗第一周期和第二周期之间的平均血清CA IX水平无显著差异,也与患者/肿瘤特征无关。血清CA IX对无进展生存期[风险比(HR)= 0.81,P = 0.730]或总生存期(HR = 0.64,P = 0.480)无预后价值。然而,肿瘤内CA IX表达与血清CA IX浓度之间存在显著相关性(rho = 0.51,P = 0.040)。这些结果表明,TGCT患者血清CA IX水平与肿瘤CA IX表达相关,但既不具有预后价值,也与患者/肿瘤特征无关。