Herrera M A, Chu T M, Holyoke E D, Mittelman A
Ann Surg. 1977 Jan;185(1):23-30. doi: 10.1097/00000658-197701000-00004.
Palliative treatment was applied to 131 cases of unresectable or palliatively resected colorectal carcinoma being monitored with serial CEA determinations. There were 84 instances of disease progression with 67 (80%) of them showing an increase in CEA above pretreatment levels or maintaining high levels, and 17 (20%) showing a fall when compared to pretreatment values or maintaining low initial values. There was a clear-cut regression of the disease in only 9 instances. In all 9, the CEA clearly dropped or maintained low valles throughout the period of regression. No patient in regression had a rise or maintained an elevated CEA level. These changes in CEA followed closely the clinical response of our patient to the use of a particular agent, although for the Nitrosourea compounds there may be a tendency to lower the CEA regardless of the patient's tumor response to the drug. This could be due to the fact that the Nitrosoureas produce a diffuse block of cellular activity, both at the nucleous and cytoplasm; while other compounds act as alkylating agents or by inhibition of enzymes involved in the metabolism of nucleic acids (i.e., 5-FU inhibiting thymidylate synthetase). In general, longer survival was found in those patients who had initially lower levels of CEA as compared to those with high initial levels. The patients with a favorable CEA response to the treatment (falling CEA or maintained low value), even in many who did not show a clinical response had a longer survival than the group with rising or stable high levels. The main value in CEA monitoring of patients resides in its correlation with the amount of disease present and then its ability to detect progression of tumor mass which is not clinically measurable.
对131例无法切除或姑息性切除的结肠直肠癌患者进行姑息治疗,并通过连续测定癌胚抗原(CEA)进行监测。疾病进展有84例,其中67例(80%)CEA高于治疗前水平或维持在高水平,17例(20%)与治疗前值相比下降或维持在低初始值。仅9例出现明确的疾病消退。在所有9例中,疾病消退期间CEA明显下降或维持在低水平。病情消退的患者中没有CEA升高或维持在高水平的情况。CEA的这些变化与患者对特定药物使用的临床反应密切相关,尽管对于亚硝基脲类化合物,无论患者的肿瘤对药物的反应如何,都可能有降低CEA的趋势。这可能是因为亚硝基脲类在细胞核和细胞质中都会产生弥漫性的细胞活性阻滞;而其他化合物则作为烷基化剂或通过抑制参与核酸代谢的酶(如5-氟尿嘧啶抑制胸苷酸合成酶)起作用。一般来说,与初始CEA水平高的患者相比,初始CEA水平低的患者生存期更长。对治疗有良好CEA反应(CEA下降或维持在低值)的患者,即使许多患者没有临床反应,其生存期也比CEA升高或稳定在高水平的组更长。对患者进行CEA监测的主要价值在于其与现存疾病量的相关性,以及其检测临床上无法测量的肿瘤肿块进展的能力。