Devine P.L., McGuckin M.A., Quin R.J., Ward B.G.
Department of Obstetrics and Gynaecology, University of Queensland, Australia.
Int J Gynecol Cancer. 1995 May;5(3):170-178. doi: 10.1046/j.1525-1438.1995.05030170.x.
The serum markers CA125, CASA and TPS were compared, with particular reference to the clinical applications of these tumor markers in the management of patients with ovarian cancer (discrimination of benign and malignant disease; indicating prognosis; predicting preclinical recurrence), (i) Using recommended cut-off points, CASA (>/=4 U ml-1 and TPS (>/=80 U l-1 showed similar sensitivities in ovarian carcinoma (56% and 57% respectively), though these were lower than with CA125 (85% >/= 35 U ml-1). The combined use of CA125 with either CASA or TPS at higher cut-off points excluding benign disease (CA125> 345 U ml-1; CASA> 6 U ml-1; TPS> 359 U l-1) improved the discrimination of ovarian cancer from benign adnexal masses (100% positive predictive value with 65% of ovarian cancers detected with CA125-CASA, 61% with CA125-TPS vs 46% with CA125 alone). The combined preoperative use of these markers may therefore assist the general gynecologist in avoiding potentially difficult oncologic surgery. (ii) TPS was the best preoperative indicator of prognosis, possibly due to its association with cell proliferation, while CASA was superior as a postoperative prechemotherapeutic prognostic indicator, possibly due to it being a more accurate indicator of residual disease than the other markers, or the surgeons' assessment. Similarly, CASA gave the best differentiation of patients with minimal residual disease (<1 cm) into those with a good or poor prognosis, (iii) CA125 and CASA each detected preclinical recurrence after surgery and adjuvant therapy in seven of 11 patients (mean lead times 4.6 and 3.1 months respectively) while TPS detected four of these patients (mean lead time 2.4 months). The combined use of CA125 with either assay led to the preclinical detection of eight of 11 patients, with the mean lead time increased to 5.3 months with the CA125-CASA combination.
对血清标志物CA125、CASA和TPS进行了比较,特别提及这些肿瘤标志物在卵巢癌患者管理中的临床应用(鉴别良性和恶性疾病;指示预后;预测临床前复发)。(i) 使用推荐的临界值,CASA(≥4 U/ml)和TPS(≥80 U/l)在卵巢癌中的敏感性相似(分别为56%和57%),尽管低于CA125(≥35 U/ml时为85%)。在排除良性疾病的较高临界值下(CA125>345 U/ml;CASA>6 U/ml;TPS>359 U/l),将CA125与CASA或TPS联合使用可提高卵巢癌与良性附件肿块的鉴别能力(CA125-CASA检测到65%的卵巢癌,CA125-TPS检测到61%的卵巢癌,单独使用CA125检测到46%的卵巢癌,阳性预测值均为100%)。因此,术前联合使用这些标志物可能有助于普通妇科医生避免潜在的困难肿瘤手术。(ii) TPS是最佳的术前预后指标,可能因其与细胞增殖有关,而CASA作为术后化疗前的预后指标更优,可能是因为它比其他标志物或外科医生的评估更准确地指示残留疾病。同样,CASA对微小残留疾病(<1 cm)患者的预后区分最佳,分为预后良好或不良两类。(iii) CA125和CASA在11例患者中有7例检测到术后和辅助治疗后的临床前复发(平均提前时间分别为4.6个月和3.1个月),而TPS检测到其中4例(平均提前时间2.4个月)。将CA125与任何一种检测方法联合使用可在11例患者中临床前检测到8例,CA125-CASA联合使用时平均提前时间增加到5.3个月。