Serum Diagnosis of Pancreatic Adenocarcinoma Using Surface-Enhanced Laser Desorption and Ionization Mass Spectrometry
Purpose: Each year in the United States, ∼ 30,000 people die from pancreatic cancer. Fewer than 5% of patients survive >5 years after diagnosis, because most patients present with advanced disease. Early diagnosis may improve the prognosis of patients with pancreatic cancer. Experimental Design:...
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Veröffentlicht in: | Clinical cancer research 2004-02, Vol.10 (3), p.860-868 |
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Zusammenfassung: | Purpose: Each year in the United States, ∼ 30,000 people die from pancreatic cancer. Fewer than 5% of patients survive >5 years after
diagnosis, because most patients present with advanced disease. Early diagnosis may improve the prognosis of patients with
pancreatic cancer.
Experimental Design: In an attempt to improve on current approaches to the serological diagnosis of pancreatic cancer, we analyzed serum samples
from patients with and without pancreatic cancer using surface-enhanced laser desorption and ionization (SELDI) protein chip
mass spectrometry. Using a case-control study design, serum samples from 60 patients with resectable pancreatic adenocarcinoma
were compared with samples from 60 age- and sex-matched patients with nonmalignant pancreatic diseases, as well as 60 age-
and sex-matched healthy controls. To increase the number of proteins potentially identifiable, serum was fractionated using
anion exchange and profiled on two ProteinChip surfaces (metal affinity capture and weak cation exchange).
Results: We determined a minimum set of protein peaks able to discriminate between patient groups and used the unified maximum separability
algorithm to compare the performance of the individual marker panels alone or in conjunction with CA19–9. Among the peaks
identified by SELDI profiling that had the ability to distinguish between patient groups, the 2 most discriminating protein
peaks could differentiate patients with pancreatic cancer from healthy controls with a sensitivity of 78% and specificity
of 97%. These 2 markers performed significantly better than the current standard serum marker, CA19–9 ( P < 0.05). The diagnostic accuracy of the 2 markers was improved by using them in combination with CA 19-9. Similarly, a combination
of 3 SELDI markers and CA19–9 was superior to CA19–9 alone in distinguishing individuals with pancreatic cancer from the combined
pancreatic disease controls and healthy subject groups ( P = 0.078). SELDI markers were also better than CA19–9 in distinguishing patients with pancreatic cancer from those with pancreatitis.
Conclusion: SELDI profiling of serum can be used to accurately differentiate patients with pancreatic cancer from those with other pancreatic
diseases and from healthy controls. |
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ISSN: | 1078-0432 1557-3265 |
DOI: | 10.1158/1078-0432.CCR-1167-3 |