Bullen B R, Cooper E H, Turner R, Neville A M, Giles G R, Hall R
Med Pediatr Oncol. 1977;3(3):289-300. doi: 10.1002/mpo.2950030311.
The combination of CEA, hepatic function marker enzymes, and four acute phase reactant proteins (haptoglobin, alpha 1 antitrypsin, alpha 1 acid glycoprotein, and prealbumin) has been used to monitor patients with colorectal cancer receiving chemotherapy. In 18 patients with advanced lesions who survived at least 3 months treatment the markers predicted progression in 92% of 25 incidents of progression; the mean lead time was 2.8 months. A rising CEA was only present in 28%, but in these patients it gave a mean lead time of 4 months. In the group of 14 patients with minimal residual disease progression to clinically detectable disease has occurred in 9 of them. In these cases the markers predicted progression with a mean lead time of 6 months; in a further six patients the markers have indicated progression, but as yet their disease is not detectable, the mean lead time being at least 8.6 months. CEA and the liver enzyme markers are the most sensitive indicators of progression of the minimal residual disease group.
癌胚抗原(CEA)、肝功能标记酶以及四种急性期反应蛋白(触珠蛋白、α1抗胰蛋白酶、α1酸性糖蛋白和前白蛋白)联合使用,用于监测接受化疗的结直肠癌患者。在18例晚期病变患者中,这些患者至少接受了3个月的治疗,在25次病情进展事件中,这些标志物在92%的事件中预测了病情进展;平均提前期为2.8个月。CEA升高仅出现在28%的患者中,但在这些患者中,其平均提前期为4个月。在14例微小残留病患者组中,其中9例已进展为临床可检测到的疾病。在这些病例中,标志物预测病情进展的平均提前期为6个月;在另外6例患者中,标志物已提示病情进展,但目前其疾病尚不可检测,平均提前期至少为8.6个月。CEA和肝脏酶标志物是微小残留病组病情进展最敏感的指标。