Keshaviah A, Dellapasqua S, Rotmensz N, Lindtner J, Crivellari D, Collins J, Colleoni M, Thürlimann B, Mendiola C, Aebi S, Price K N, Pagani O, Simoncini E, Castiglione Gertsch M, Gelber R D, Coates A S, Goldhirsch A
International Breast Cancer Study Group Statistical Center, Dana-Farber Cancer Institute, Boston, MA, USA.
Ann Oncol. 2007 Apr;18(4):701-8. doi: 10.1093/annonc/mdl492. Epub 2007 Jan 20.
We evaluated the ability of CA15-3 and alkaline phosphatase (ALP) to predict breast cancer recurrence.
Data from seven International Breast Cancer Study Group trials were combined. The primary end point was relapse-free survival (RFS) (time from randomization to first breast cancer recurrence), and analyses included 3953 patients with one or more CA15-3 and ALP measurement during their RFS period. CA15-3 was considered abnormal if >30 U/ml or >50% higher than the first value recorded; ALP was recorded as normal, abnormal, or equivocal. Cox proportional hazards models with a time-varying indicator for abnormal CA15-3 and/or ALP were utilized.
Overall, 784 patients (20%) had a recurrence, before which 274 (35%) had one or more abnormal CA15-3 and 35 (4%) had one or more abnormal ALP. Risk of recurrence increased by 30% for patients with abnormal CA15-3 [hazard ratio (HR) = 1.30; P = 0.0005], and by 4% for those with abnormal ALP (HR = 1.04; P = 0.82). Recurrence risk was greatest for patients with either (HR = 2.40; P < 0.0001) and with both (HR = 4.69; P < 0.0001) biomarkers abnormal. ALP better predicted liver recurrence.
CA15-3 was better able to predict breast cancer recurrence than ALP, but use of both biomarkers together provided a better early indicator of recurrence. Whether routine use of these biomarkers improves overall survival remains an open question.
我们评估了CA15 - 3和碱性磷酸酶(ALP)预测乳腺癌复发的能力。
合并了来自七项国际乳腺癌研究组试验的数据。主要终点是无复发生存期(RFS)(从随机分组到首次乳腺癌复发的时间),分析纳入了3953例在其RFS期间进行过一次或多次CA15 - 3和ALP测量的患者。如果CA15 - 3>30 U/ml或比首次记录值高>50%,则认为其异常;ALP记录为正常、异常或不确定。使用具有随时间变化的CA15 - 3和/或ALP异常指标的Cox比例风险模型。
总体而言,784例患者(20%)出现复发,在此之前,274例(35%)有一次或多次CA15 - 3异常,35例(4%)有一次或多次ALP异常。CA15 - 3异常的患者复发风险增加30%[风险比(HR)= 1.30;P = 0.0005],ALP异常的患者复发风险增加4%(HR = 1.04;P = 0.82)。两种生物标志物均异常的患者复发风险最高(HR = 2.40;P < 0.0001),两种生物标志物都异常的患者复发风险最高(HR = 4.69;P < 0.0001)。ALP能更好地预测肝转移复发。
CA15 - 3比ALP更能预测乳腺癌复发,但同时使用这两种生物标志物能更好地早期提示复发。这些生物标志物的常规使用是否能改善总体生存率仍是一个悬而未决的问题。