New MUC1 serum immunoassay differentiates pancreatic cancer from pancreatitis

被引:105
作者
Gold, DV
Modrak, DE
Ying, ZL
Cardillo, TM
Sharkey, RM
Goldenberg, DM
机构
[1] Garden State Canc Ctr, Ctr Mol Med & Immunol, Belleville, NJ 07109 USA
[2] Immunomed Inc, Morris Plains, NJ USA
[3] Columbia Univ, Dept Stat, New York, NY USA
关键词
D O I
10.1200/JCO.2005.02.8282
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To evaluate a new immunoassay for identification and quantitation of MUC1 in the sera of patients with pancreatic cancer or pancreatitis. The sensitivity and specificity of the assay are examined and compared to results from a CA19-9 immunoassay. Methods An in vitro enzyme immunoassay was established with monoclonal antibody PAM4 as the capture reagent, and a polyclonal anti-MUC1 antibody as the probe. Patient sera were obtained from healthy, adult patients with acute and chronic pancreatitis, and those with pancreatic and other forms of cancer, and were measured for PAM4-reactive MUC1. Results At a cutoff of 10.2 units/mL, 41 (77%) of 53 pancreatic cancer patients, none of the healthy individuals (n = 43), and only four (5%) of 87 patients with pancreatitis were positive above this value. Among nonpancreatic cancers investigated, colorectal cancers gave the highest percentage of positives (14%; five of 36). Overall, the sensitivity and specificity of the immunioassay for pancreatic cancer were 77% and 95%, respectively. Receiver operator characteristic analyses for discrimination of pancreatic cancer from pancreatitis provided an area under the curve of 0.89 (95% CI, 0.82 to 0.93), with a specificity of 95.4% and a positive likelihood ratio of 16.8. A direct pair-wise comparison of PAM4 and CA19-9 immunoassays for discrimination of pancreatic cancer and pancreatitis resulted in a significant difference (P < .003), with the PAM4 immunoassay demonstrating superior sensitivity and specificity. Conclusion The high sensitivity and specificity observed suggest that the PAM4-based immunoassay of circulating MUC1 may be useful in the diagnosis of pancreatic cancer.
引用
收藏
页码:252 / 258
页数:7
相关论文
共 45 条
[1]  
Andrianifahanana M, 2001, CLIN CANCER RES, V7, P4033
[2]  
BAECKSTROM D, 1991, J BIOL CHEM, V266, P21537
[3]  
BAECKSTROM D, 1993, CANCER RES, V53, P755
[4]   THE PROGNOSTIC VALUE OF THE MONOCLONAL-ANTIBODIES HMFG1 AND HMFG2 IN BREAST-CANCER [J].
BERRY, N ;
JONES, DB ;
SMALLWOOD, J ;
TAYLOR, I ;
KIRKHAM, N ;
TAYLORPAPADIMITRIOU, J .
BRITISH JOURNAL OF CANCER, 1985, 51 (02) :179-186
[5]   Expression of core 2 β-1,6-N-acetylglucosaminyltransferase in a human pancreatic cancer cell line results in altered expression of MUC1 tumor-associated epitopes [J].
Beum, PV ;
Singh, J ;
Burdick, M ;
Hollingsworth, MA ;
Cheng, PW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (35) :24641-24648
[6]   O-linked glycosylation in the mammary gland: Changes that occur during malignancy [J].
Burchell, JM ;
Mungul, A ;
Taylor-Papadimitriou, J .
JOURNAL OF MAMMARY GLAND BIOLOGY AND NEOPLASIA, 2001, 6 (03) :355-364
[7]   Oligosaccharides expressed an MUC1 produced by pancreatic and colon tumor cell lines [J].
Burdick, MD ;
Harris, A ;
Reid, CJ ;
Iwamura, T ;
Hollingsworth, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (39) :24198-24202
[8]   Assessing clinical benefit in the treatment of pancreas cancer: Gemcitabine compared to 5-fluorouracil [J].
Burris, H ;
Storniolo, AM .
EUROPEAN JOURNAL OF CANCER, 1997, 33 :S18-S22
[9]   Improvements in survival and clinical benefit with gemcitabine as first-line therapy for patients with advanced pancreas cancer: A randomized trial [J].
Burris, HA ;
Moore, MJ ;
Andersen, J ;
Green, MR ;
Rothenberg, ML ;
Madiano, MR ;
Cripps, MC ;
Portenoy, RK ;
Storniolo, AM ;
Tarassoff, P ;
Nelson, R ;
Dorr, FA ;
Stephens, CD ;
VanHoff, DD .
JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (06) :2403-2413
[10]  
Cardillo TM, 2001, CLIN CANCER RES, V7, P3186