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Undetectable Preoperative Levels of Serum CA 19-9 Correlate with Improved Survival for Patients with Resectable Pancreatic Adenocarcinoma

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Abstract

Background: Serum levels of CA19-9 have been shown to correlate with both recurrence and survival in patients with pancreatic cancer. However, little is known about the prognosis for patients with undetectable levels of serum CA19-9.

Methods :One hundred twenty-nine patients with pancreatic cancer who underwent preoperative assessment of serum CA19-9 followed by resection with curative intent between 1990 and 2002 were retrospectively analyzed. Data collected included preoperative serum CA19-9 level (U/mL), age, pathologic staging, and survival. Data were analyzed with the SAS system according to four distinct preoperative serum CA19-9 levels: undetectable, normal (<37), 38–200, and ⦔200 U/mL.

Results: Serum CA19-9 levels ranged from undetectable to 16,300 U/mL. Stage III/IV disease accounted for 86%, 67%, 59%, and 53% of patients in the four CA19-9 groups. The overall median and 5-year survivals were 19 months and 11%, respectively. Survival was similar between nonsecretors and those with normal CA 19-9 levels. However, both groups had statistically significant prolonged survival compared with the two groups with elevated CA 19-9 levels (P = .003). The only factors that were significant on univariate and multivariate analysis for overall survival were lymph node positivity (P = .015 and .002) and CA 19-9 grouping (P = .003 and P < .0001). Although this group of patients presented with predominately advanced-stage disease, their overall survival was superior.

Conclusions: These findings suggest that patients who present with undetectable preoperative CA19-9 levels and potentially resectable pancreatic cancer, regardless of advanced stage, should be considered candidates for aggressive therapy.

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REFERENCES

  1. Koprowski H, Steplewski Z, Mitchell K, et al. Colorectal carcinoma antigens detected by hybridoma antibodies. Somatic Cell Genetics 1979;5:957–71.

    PubMed  CAS  Google Scholar 

  2. Glenn J, Steinberg WM, Kurtzman SH, et al. Evaluation of the utility of a radioimmunoassay for serum CA 19-9 levels in patients before and after treatment of carcinoma of the pancreas. J Clin Oncol 1988;6:462–8.

    PubMed  CAS  Google Scholar 

  3. Sperti C, Pasquali C, Catalini S, et al. CA 19-9 as a prognostic index after resection for pancreatic cancer. J Surg Oncol 1993;52:137–41.

    PubMed  CAS  Google Scholar 

  4. Montgomery RC, Hoffman JP, Riley LB, et al. Prediction of recurrence and survival by post-resection CA 19-9 values in patients with adenocarcinoma of the pancreas. Ann Surg Oncol 1997;4:551–6.

    PubMed  CAS  Google Scholar 

  5. Safi F, Schlosser W, Falkenreck S, Beger HG. Prognostic values of CA 19-9 serum course in pancreatic cancer. Hepatogastroenterology 1998;45:253–9.

    PubMed  CAS  Google Scholar 

  6. Halm U, Schumann T, Schiefke I, et al. Decrease of CA 19-9 during chemotherapy with gemcitabine predicts survival time in patients with advanced pancreatic cancer. Br J Cancer 2000;82:1013–6.

    PubMed  CAS  Google Scholar 

  7. Magnani J, Nilsson B, Brockhaus M, et al. A monoclonal antibody-defined antigen associated with gastrointestinal cancer is a ganglioside containing sialylated lacto-N-fucopenteose II. J Biological Chem 1982;257:14365–9.

    CAS  Google Scholar 

  8. Ritts RE, Pitt HA. CA 19-9 in pancreatic cancer. Surg Oncol Clin North Am 1998;7:93–100.

    CAS  Google Scholar 

  9. Lamerz R. Role of tumour markers, cytogenetics. Ann Oncol1990;10(Supp. 4):145–9.

    Google Scholar 

  10. Brockhaus M, Wysocka M, Magnani JL, Steplewski Z, Koprowski H, Ginsburg V. Normal salivary mucin contains the gastrointestinal cancer associated antigen detected by monoclonal antibody CA 19-9 in the serum mucin of patients. Vox Sang 1985;48:34–8.

    Article  PubMed  CAS  Google Scholar 

  11. Kalthoff H, Kreiker C, Schmiegel WH, Greten H, Thiele HG. Characterization of CA 19-9 bearing mucins as physiological exocrine pancreatic secretion products. Cancer Res 1986;46:3605–7.

    PubMed  CAS  Google Scholar 

  12. Safi F, Beger HG, Bittner R, Buchler M, Krautzberger W. CA 19-9 and pancreatic adenocarcinoma. Cancer 1986;57:779–83.

    PubMed  CAS  Google Scholar 

  13. Tian F, Appert HE, Myles J, Howard JM. Prognostic value of serum CA 19-9 levels in pancreatic adenocarcinoma. Ann Surg 1992;215:350–5.

    PubMed  CAS  Google Scholar 

  14. Heinemann V, Schermuly MM, Stieber P, Schulz L, Jungst D, Wilkowski R, Schalhorn A. CA 19-9: A predictor of response in pancreatic cancer treated with gemcitabine and cisplatin. Anticancer Res 1999;19:2433–6.

    PubMed  CAS  Google Scholar 

  15. Magnani JL, Steplewski Z, Koprowski H, Ginsburg V. Identification of the gastrointestinal and pancreatic cancer-associated antigen detected by monoclonal antibody 19-9 in the sera of patients as a mucin. Cancer Res 1983;43:5489–92.

    CAS  PubMed  Google Scholar 

  16. Koprowski H, Brockhaus M, Blaszczyk M, Magnani J, Steplewski Z, Ginsburg V. Lewis blood type may affect the incidence of gastrointestinal cancer. Lancet 1982;1:1332–3.

    PubMed  CAS  Google Scholar 

  17. Kawa S, Oguchi H, Kobayashi T, et al. Elevated serum levels of Dupan-2 in pancreatic cancer patients negative for Lewis blood group phenotype. Br J Cancer 1991;64:899–902.

    PubMed  CAS  Google Scholar 

  18. Yazawa S, Nishihara S, Iwasaki H, et al. Genetic and enzymatic evidence for Lewis enzyme expression in Lewis-negative cancer patients. Cancer Res 1995;55:1473–8.

    PubMed  CAS  Google Scholar 

  19. Hirano K, Kawa S, Oguchi H, et al. Loss of Lewis antigen expression on erythrocytes in some cancer patients with high serum CA 19-9 levels. JNCI 1987;79:1261–8.

    PubMed  CAS  Google Scholar 

  20. Narimatsu H, Iwasaki H, Nakayama F, et al. Lewis and secretor gene dosages affect CA 19-9 and DU-PAN-2 serum levels in normal individuals and colorectal cancer patients. Cancer Res 1998;58:512–8.

    PubMed  CAS  Google Scholar 

  21. Orntoft TF, Vestergaard EM, Holmes E, et al. Influence of Lewis α1–3/4-L-fucosyltransferase (FUT3) gene mutations on enzyme activity, erythrocyte phenotyping, and circulating tumor marker sialyl-Lewis a levels. J Biol Chem 1996;271:32260–8.

    PubMed  CAS  Google Scholar 

  22. Lim JE, Chien MW, Earle CC. Prognostic factors following curative resection for pancreatic adenocarcinoma: a population-based, linked database analysis of 396 patients. Ann Surg 2003;237:74–85.

    Article  PubMed  Google Scholar 

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Correspondence to Adam C. Berger MD.

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Berger, A.C., Meszoely, I.M., Ross, E.A. et al. Undetectable Preoperative Levels of Serum CA 19-9 Correlate with Improved Survival for Patients with Resectable Pancreatic Adenocarcinoma. Ann Surg Oncol 11, 644–649 (2004). https://doi.org/10.1245/ASO.2004.11.025

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  • DOI: https://doi.org/10.1245/ASO.2004.11.025

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