Changes over time of extracellular domain of HER2 (ECD/HER2) serum levels have prognostic value in metastatic breast cancer

被引:52
作者
Bramwell, Vivien H. C. [1 ,2 ]
Doig, Gordon S. [2 ,3 ]
Tuck, Alan B. [2 ,4 ,5 ]
Wilson, Sylvia M. [2 ,6 ]
Tonkin, Katia S. [2 ,7 ]
Tomiak, Anna [2 ,8 ]
Perera, Francisco [2 ,5 ]
Vandenberg, Theodore A. [2 ,5 ]
Chambers, Ann F. [2 ,4 ,5 ]
机构
[1] Tom Baker Canc Clin, Calgary, AB T2N 4N2, Canada
[2] London Reg Canc Program, London, ON, Canada
[3] Univ Sydney, Dept Med, Sydney, NSW 2006, Australia
[4] Univ Western Ontario, Dept Pathol, London, ON, Canada
[5] Univ Western Ontario, Dept Oncol, London, ON, Canada
[6] Univ Calgary, Dept Pharmacol & Therapeut, Calgary, AB, Canada
[7] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[8] Queens Univ, Dept Med, Kingston, ON K7L 3N6, Canada
关键词
Breast cancer; Extracellular domain of HER2; Serial samples; Survival; Tumor markers; PROGRESSION-FREE SURVIVAL; IN-SITU HYBRIDIZATION; CLINICAL UTILITY; ADJUVANT CHEMOTHERAPY; AMERICAN-SOCIETY; TUMOR-MARKERS; PHASE-II; HER-2/NEU; TRASTUZUMAB; RECOMMENDATIONS;
D O I
10.1007/s10549-008-0033-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Blood levels of the extracellular domain of HER-2/neu (ECD/HER2) have been suggested to have potential as a tumor marker in breast cancer. Our aim was to assess the prognostic value of baseline levels of ECD/HER2, but more importantly changes in levels over time, in women with metastatic breast cancer. Methods Baseline and serial levels of ECD/HER2 were measured in 158 women with newly-diagnosed metastatic breast cancer, in whom we previously performed serial measurement of plasma osteopontin. ECD/HER2 was measured in 1,282 serum samples using a validated ELISA at baseline and every 3-12 weeks during and after therapy until death (median, n = 8 samples per patient). Multivariate time-dependent survival analyses were conducted using models that right-censored patient outcomes 3, 6 and 12 months after last known ECD/HER2 measurement. Results Thirty-four patients (22%) had elevated baseline ECD/HER2 (median 10.2 ng/ml: range 4.1-40.4 ng/ml). In univariate analysis, elevated baseline ECD/HER2 was associated with short survival (P = 0.001). In a multivariate model incorporating standard clinical prognostic factors, baseline ECD/HER2 was significantly associated with survival duration (RR 1.029; P = 0.020). Presence of visceral metastases and ECOG status 2-4 also retained significance. In a multivariate model incorporating standard prognostic factors and changes in sequential ECD/HER2 levels, an ECD/HER2 increase of > 12 ng/ml at any time was the variable with most prognostic value for poor survival (RR 6.10; P = 0.0003); poor ECOG status also retained significance. Conclusion Increases over time of ECD/HER2 levels were strongly associated with poor survival in this cohort of women with metastatic breast cancer.
引用
收藏
页码:503 / 511
页数:9
相关论文
共 50 条
[1]  
Abe O, 2005, LANCET, V366, P2087, DOI 10.1016/s0140-6736(05)66544-0
[2]  
Abeloff M.D., 2004, CLINCIAL ONCOLOGY, V3rd, P2369
[3]  
Ali SM, 2002, CLIN CHEM, V48, P1314
[4]   PRACTICAL PROBLEMS IN FITTING A PROPORTIONAL HAZARDS MODEL TO DATA WITH UPDATED MEASUREMENTS OF THE COVARIATES [J].
ALTMAN, DG ;
DESTAVOLA, BL .
STATISTICS IN MEDICINE, 1994, 13 (04) :301-341
[5]  
BASELGA J, 2007, CLIN CANCER RES, V7, P2605
[6]  
Bast RC, 1996, J CLIN ONCOL, V14, P2843
[7]  
Bast RC, 1998, J CLIN ONCOL, V16, P793
[8]   2000 update of recommendations for the use of tumor markers in breast and colorectal cancer: Clinical practice guidelines of the American Society of Clinical Oncology [J].
Bast, RC ;
Ravdin, P ;
Hayes, DF ;
Bates, S ;
Fritsche, H ;
Jessup, JM ;
Kemeny, N ;
Locker, GY ;
Mennel, RG ;
Somerfield, MR .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (06) :1865-1878
[9]  
Bethune-Volters A, 2004, ANTICANCER RES, V24, P1083
[10]   Serial plasma osteopontin levels have prognostic value in metastatic breast cancer [J].
Bramwell, Vivien H. C. ;
Doig, Gordon S. ;
Tuck, Alan B. ;
Wilson, Sylvia M. ;
Tonkin, Katia S. ;
Tomiak, Anna ;
Perera, Francisco ;
Vandenberg, Theodore A. ;
Chambers, Ann F. .
CLINICAL CANCER RESEARCH, 2006, 12 (11) :3337-3343