Division of Hematology and Oncology, Department of Medicine, University of Florida, Gainesville, FL.
Department of Health Services Research, Management and Policy, College of Public Health and Health Professions, University of Florida, Gainesville, FL.
Cancer Med. 2019 Jul;8(8):3918-3927. doi: 10.1002/cam4.2278. Epub 2019 May 23.
Dipeptidyl peptidase 4 (DPP4) is a cell surface protein that can act as a tumor suppressor or activator, depending upon the level of expression and interaction with the microenvironment and chemokines. DPP4 inhibitors are used to treat diabetes.
We conducted this Surveillance Epidemiology and Endpoint Research-Medicare database study to evaluate the role of DPP4 inhibitors on the overall survival (OS) of diabetic patients diagnosed with colorectal (CRC) and lung cancers.
Diabetic patients with CRC or lung cancer who were treated with DPP4 inhibitors exhibited a statistically significant survival advantage (hazard ratio [HR] of 0.89; CI: 0.82-0.97, P = 0.007) that remained significant after controlling for all other confounders. When DPP4 inhibitors were used in combination of metformin which is known to suppress cancer, the survival advantage was even more pronounced (HR of 0.83; CI: 0.77-0.90, P < 0.0001). Data were then analyzed separately for two cancer types. In the CRC-only cohort, the use of DPP4 inhibitors alone had a positive trend but did not meet statistically significant threshold (HR of 0.87; CI: 0.75-1.00, P = 0.055), while the combined use of DPP4 inhibitors and metformin was associated with statistically significant survival advantage (HR of 0.77; CI: 0.67-0.89, P = 0.003). Similarly, for the lung cancer cohort, use of DPP4 alone was not found to be statistically significant (HR of 0.93; CI: 0.83-1.03, P = 0.153), whereas lung cancer patients treated with the combination of DPP4 inhibitors and metformin showed statistically significant survival advantage (HR of 0.88; CI: 0.80-0.97, P = 0.010).
DPP4 inhibition in CRC and lung cancer is associated with improved OS, which possibly may be due to the effect of DPP4 inhibition on immunoregulation of cancer.
二肽基肽酶 4(DPP4)是一种细胞表面蛋白,其作用取决于表达水平以及与微环境和趋化因子的相互作用,可以作为肿瘤的抑制因子或激活因子。DPP4 抑制剂被用于治疗糖尿病。
我们开展了这项监测流行病学和终点研究-医疗保险数据库研究,以评估 DPP4 抑制剂对诊断患有结直肠癌(CRC)和肺癌的糖尿病患者总生存期(OS)的影响。
接受 DPP4 抑制剂治疗的 CRC 或肺癌合并糖尿病患者的生存优势具有统计学意义(风险比 [HR]为 0.89;95%CI:0.82-0.97,P=0.007),在控制了所有其他混杂因素后,这一结果仍然具有统计学意义。当 DPP4 抑制剂与已知具有抑制癌症作用的二甲双胍联合使用时,生存优势更为显著(HR 为 0.83;95%CI:0.77-0.90,P<0.0001)。然后分别对两种癌症类型的数据进行分析。在仅 CRC 队列中,单独使用 DPP4 抑制剂呈阳性趋势,但未达到统计学显著阈值(HR 为 0.87;95%CI:0.75-1.00,P=0.055),而联合使用 DPP4 抑制剂和二甲双胍与统计学显著的生存优势相关(HR 为 0.77;95%CI:0.67-0.89,P=0.003)。同样,对于肺癌队列,单独使用 DPP4 抑制剂未发现具有统计学意义(HR 为 0.93;95%CI:0.83-1.03,P=0.153),而接受 DPP4 抑制剂和二甲双胍联合治疗的肺癌患者显示出统计学显著的生存优势(HR 为 0.88;95%CI:0.80-0.97,P=0.010)。
CRC 和肺癌中 DPP4 的抑制与 OS 改善相关,这可能是由于 DPP4 抑制对癌症免疫调节的作用。