Moisuc Diana Cornelia, Constantinescu Daniela, Marinca Mihai Vasile, Gafton Bogdan, Pavel-Tanasa Mariana, Cianga Petru
Immunology Department, "Grigore T. Popa" University of Medicine and Pharmacy, 700115 Iasi, Romania.
Immunology Department, "St. Spiridon" Hospital, 700111 Iasi, Romania.
Cancers (Basel). 2024 Jan 16;16(2):385. doi: 10.3390/cancers16020385.
Colorectal cancer (CRC) ranks as second most common cause of cancer-related deaths. The CRC management considerably improved in recent years, especially due to biological therapies such as bevacizumab. The lack of predictive or prognostic biomarkers remains one of the major disadvantages of using bevacizumab in the CRC management. We performed a prospective study to analyze the prognostic and predictive roles of three potential serum biomarkers (Cyclophilin A (CypA), copeptin and Tie2) investigated by ELISA in 56 patients with metastatic CRC undergoing bevacizumab and chemotherapy between May 2019 and September 2021 at baseline and after one and six months of therapy. We showed that low levels of CypA at baseline and after one month of treatment were associated with better overall survival (OS) (42 versus 24 months, = 0.029 at baseline; 42 versus 25 months, = 0.039 after one month). For copeptin and Tie2, Kaplan-Meier curves showed no correlation between these biomarkers and OS or progression-free survival. When adjusting for baseline and post-treatment factors, a multivariate Cox analysis showed that low values of CypA at baseline and after one month of treatment were independent prognostic factors for OS and correlated with a better prognosis in metastatic CRC patients.
结直肠癌(CRC)是癌症相关死亡的第二大常见原因。近年来,CRC的治疗有了显著改善,尤其是由于贝伐单抗等生物疗法。缺乏预测或预后生物标志物仍然是在CRC治疗中使用贝伐单抗的主要缺点之一。我们进行了一项前瞻性研究,以分析通过酶联免疫吸附测定(ELISA)检测的三种潜在血清生物标志物(亲环素A(CypA)、 copeptin和Tie2)在2019年5月至2021年9月期间接受贝伐单抗和化疗的56例转移性CRC患者基线时以及治疗1个月和6个月后的预后和预测作用。我们发现,基线时和治疗1个月后CypA水平较低与更好的总生存期(OS)相关(分别为42个月对24个月,基线时P = 0.029;42个月对25个月,1个月后P = 0.039)。对于copeptin和Tie2,Kaplan-Meier曲线显示这些生物标志物与OS或无进展生存期之间无相关性。在对基线和治疗后因素进行调整后,多变量Cox分析显示,基线时和治疗1个月后CypA值较低是OS的独立预后因素,并且与转移性CRC患者的更好预后相关。