The New England Journal of Medicine
e-mail icon  FREE NEJM E-TOC    HOME   |   SUBSCRIBE   |   CURRENT ISSUE   |   PAST ISSUES   |   COLLECTIONS   |    Advanced Search
Sign in | Get NEJM's E-Mail Table of Contents — Free | Subscribe
 
Original Article
PreviousPrevious
Volume 331:81-84 July 14, 1994 Number 2
NextNext

Diabetes and the Risk of Pancreatic Cancer
Lucio Gullo, Raffaele Pezzilli, Antonio Maria Morselli-Labate, for Italian Pancreatic Cancer Study Group

 

This Article
-Abstract

Commentary
-Letters

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited

More Information
-PubMed Citation
ABSTRACT

Background Diabetes and pancreatic cancer are known to be associated, but the cause of the association and whether diabetes is a risk factor for pancreatic cancer remain controversial.

Methods A total of 720 patients with pancreatic cancer and 720 control patients from 14 Italian centers were enrolled in the study. All subjects were interviewed personally and in detail about their clinical history. The diagnosis of diabetes was based on criteria recommended by the American Diabetes Association.

Results One hundred sixty-four patients with pancreatic cancer (22.8 percent) and 60 controls (8.3 percent) had diabetes. In the majority of the patients with pancreatic cancer (56.1 percent), diabetes was diagnosed either concomitantly with the cancer (in 40.2 percent), or within two years before the diagnosis of cancer (in 15.9 percent). The association between the two conditions was significant (odds ratio, 3.04; 95 percent confidence interval, 2.21 to 4.17). However, when only patients with diabetes of three or more years' duration were considered, the association was no longer significant (odds ratio, 1.43; 95 percent confidence interval, 0.98 to 2.07). All the patients with pancreatic cancer whose diabetes had been diagnosed before the cancer had non-insulin-dependent diabetes; all but one of the control patients with diabetes had the non-insulin-dependent form of the disease.

Conclusions Diabetes in patients with pancreatic cancer is frequently of recent onset and is presumably caused by the tumor. Diabetes is not a risk factor for pancreatic cancer.


Diabetes mellitus is known to occur more frequently in patients with pancreatic cancer than in the general population,1,2,3,4,5,6 and it has repeatedly been claimed that diabetes is a risk factor for the tumor6,7,8,9,10,11,12,13,14,15,16,17,18. The increased frequency of diabetes in patients with pancreatic cancer is well established,19,20 but the nature of this association is unknown21. A relevant question is whether diabetes in patients with pancreatic cancer represents a preexisting condition or whether it is secondary to the tumor. A corollary of this question is whether diabetes is a risk factor for pancreatic cancer. Several studies have found that this is the case,6,7,8,9,10,11,12,13,14,15,16,17,18 but others have not22,23,24,25,26,27,28. None of the previous studies addressed the question of which type of diabetes might be a risk factor for pancreatic cancer: insulin-dependent diabetes, non-insulin-dependent diabetes, or both. In an attempt to answer these questions, we carried out a multicenter study of a large series of patients with pancreatic cancer.

Methods

This work, part of a multicenter study of the risk factors for pancreatic cancer in Italy, involved 14 Italian university and community hospitals with experience in the management of pancreatic disease29. All study subjects were patients who were hospitalized in 13 of the study centers between January 1987 and December 1989 and in the 14th center, in Bologna, between January 1987 and December 1992. Of the 76,144 patients hospitalized at the 14 centers during the study, 738 had pancreatic cancer. We studied 720 of them (415 men [57.6 percent] and 305 women [42.4 percent]); the mean age was 62.6 years (range, 22 to 79). The diagnosis of pancreatic cancer was based on the clinical history. It was confirmed by histologic findings in 512 of the patients (71.1 percent) and by surgery in 48 (6.7 percent); in the other 160 patients (22.2 percent), the diagnosis was confirmed by typical findings on at least three imaging procedures (ultrasonography, computed tomography, endoscopic retrograde cholangiopancreatography, or angiography), as well as by the clinical course.

For each patient, a control subject matched for sex, age (±5 years), social class, and geographic region was selected at random from the patients hospitalized at the same time in the same facility for acute nonmalignant disorders. The most frequent diagnoses in the control group were fractures, minor trauma, abdominal hernias, and disorders of the skin, throat, nose, or ear.

All the study subjects were interviewed personally about their medical history; special attention was paid to the presence of diabetes, the patient's age at the time of diagnosis, the type of diabetes, and the treatment received for it. Members of the immediate family were also interviewed in most cases. When possible, the results of previous blood tests, including the glucose concentration, were noted. Patients who were not able to provide detailed information, either because of the severity of their illness or for other reasons, were not included in the study; of the 738 patients with pancreatic cancer who were initially eligible for the study, 18 (2.4 percent) were excluded on this account. Of the 728 eligible controls, 8 (1.1 percent) were excluded because of insufficient cooperation.

The diagnosis of diabetes was based on the criteria recommended by the American Diabetes Association30: an unequivocal elevation of the plasma glucose concentration ( >= 200 mg per deciliter [11.1 mmol per liter]) along with the classic symptoms of diabetes such as polydipsia, polyuria, polyphagia, and weight loss; and a fasting plasma glucose concentration greater than or equal to 140 mg per deciliter (7.8 mmol per liter) on more than one occasion.

Statistical Analysis

The chi-square test and the Mann-Whitney U test were used to compare the clinical characteristics of the case patients and control patients; Yates' correction was applied to two-by-two tables. The clinical duration of diabetes in the two groups of patients was compared by means of a log-linear model. A conditional logistic model for matched case-control studies was used in the analysis of the association between diabetes and pancreatic cancer. All statistical evaluations were performed with BMDP statistical software31 on a personal computer.

Results

One hundred sixty-four patients (96 men and 68 women) with pancreatic cancer had diabetes (22.8 percent), as did 60 patients (30 men and 30 women) without pancreatic cancer (8.3 percent). In the group of 164 case patients, the mean age was 64.4 years (range, 36 to 79) when pancreatic cancer was diagnosed and 59.4 years (range, 35 to 79) when diabetes was diagnosed. In the 60 controls, the mean age at the time of the diagnosis of diabetes was 56.1 years (range, 25 to 78). There was a family history of diabetes in 67 of the 164 case patients with diabetes (40.9 percent) and in 24 of the 60 control patients with diabetes (40.0 percent). None of these differences were significant. Among the case patients with diabetes, 127 (77.4 percent) had cancer in the head of the pancreas, and 31 (18.9 percent) in the body or tail of the pancreas (or both); the cancer was diffuse in the other 6 case patients (3.7 percent). The tumor was resectable in 31 case patients (18.9 percent).

Table 1 shows the distribution of case and control patients according to the clinical duration of diabetes. In 92 of the 164 case patients (56.1 percent), diabetes was diagnosed either at the same time as the pancreatic cancer (40.2 percent) or within two years before the diagnosis of cancer (15.9 percent). The diagnosis of diabetes preceded the diagnosis of pancreatic cancer by 3 to 4 years in 11 case patients (6.7 percent), by 5 to 9 years in 27 (16.5 percent), and by 10 or more years in 34 (20.7 percent). The frequency of recent-onset diabetes (zero to two years' duration) was significantly higher in the case patients than in the control patients (56.0 percent vs. 13.3 percent, P<0.001), whereas the frequency of long-standing diabetes (10 or more years' duration) was significantly higher in the control patients (53.3 percent vs. 20.7 percent, P<0.001).

View this table:
[in this window]
[in a new window]
 
Table 1. Clinical Duration of Diabetes in Case and Control Patients.

 
Table 2 shows some of the clinical characteristics of the patients with pancreatic cancer who had diabetes of recent onset and those without diabetes. There were no significant differences between the two groups in sex, age at the time of the diagnosis of pancreatic cancer, or location of the tumor. In the group of patients with a recent diagnosis of diabetes, a family history of diabetes was significantly more frequent (P = 0.003), and resectability of the tumor significantly less frequent (P = 0.04).

View this table:
[in this window]
[in a new window]
 
Table 2. Clinical Characteristics of Patients with Pancreatic Cancer Who Had Diabetes of Recent Onset (Zero to Two Years' Duration) and Patients with Pancreatic Cancer Who Did Not Have Diabetes.

 
Table 3 shows the frequency and clinical duration of diabetes in the case and control patients, as well as the estimated odds ratios. When all case patients with diabetes were considered, a significant association between diabetes and pancreatic cancer was found (odds ratio, 3.04; 95 percent confidence interval, 2.21 to 4.17). However, the association was not significant in patients with diabetes of three or more years' duration (odds ratio, 1.43; 95 percent confidence interval, 0.98 to 2.07). This decline in the risk of diabetes was more rapid among the women than among the men: for women, the estimated risk fell below the level of significance with diabetes of one or more years' duration (odds ratio, 1.38; 95 percent confidence interval, 0.83 to 2.30); for men, it was of borderline significance with diabetes of three or more years' duration (odds ratio, 1.75; 95 percent confidence interval, 1.06 to 2.89) and fell below the level of significance only with diabetes of seven or more years' duration (odds ratio, 1.71; 95 percent confidence interval, 0.94 to 3.11). Among women, men, and both sexes combined, the odds ratio was less than 1 for diabetes of 15 or more years' duration.

View this table:
[in this window]
[in a new window]
 
Table 3. Frequency of Diabetes and Odds Ratio, According to the Duration of Diabetes in Patients with Pancreatic Cancer and in Control Patients.

 
All the patients with pancreatic cancer in whom diabetes had been recognized before the tumor were considered to have non-insulin-dependent diabetes. Among the control patients with diabetes, all had the non-insulin-dependent form of the disease except one, who had insulin-dependent diabetes. In 90.0 percent of the case patients and 91.7 percent of the controls, treatment consisted of oral antidiabetic agents or dietary modifications.

Discussion

We found a significant association between diabetes and pancreatic cancer. However, we found no association between diabetes and pancreatic cancer among patients with long-standing diabetes. The increased prevalence of diabetes in patients with pancreatic cancer is apparently due largely to diabetes of recent onset, presumably caused by the tumor.

Many studies6,7,8,9,10,11,12,13,14,15,16,17,18 have concluded that diabetes is a risk factor for pancreatic cancer. However, the duration of the diabetes before the diagnosis of pancreatic cancer was not ascertained in these investigations. Other methodologic differences between our study and earlier work include the small numbers of patients, the use of mailed questionnaires and death certificates, and possibly unrepresentative control groups in previous studies.

In our patients with pancreatic cancer who had diabetes that was diagnosed at the same time as or shortly before the tumor, it is likely that the diabetes was a consequence of the tumor. Pancreatic cancer can cause diabetes by destroying islet cells2,3,32 or by causing peripheral resistance to insulin33. Such insulin resistance frequently occurs early in the course of the disease,19,20,34 which may explain why diabetes can appear before the symptoms of the pancreatic tumor.

As compared with the case patients who did not have diabetes, those with diabetes that was presumably secondary to pancreatic cancer were significantly more likely to have a family history of diabetes and an unresectable tumor, suggesting that a hereditary predisposition to diabetes and a larger tumor size contribute to the development of diabetes. The absence of a relation between the location of the cancer and the frequency of diabetes would be compatible with a dependence of tumor-related diabetes on humoral factors. Green et al.3 found no relation between the location of the pancreatic tumor and the frequency of recent-onset diabetes, but they also reported no relation between a family history of diabetes or the size of the tumor and the incidence of diabetes.

In our study, all the patients with pancreatic cancer in whom the diagnosis of diabetes preceded the diagnosis of cancer were considered to have non-insulin-dependent diabetes. All the control patients with diabetes also had the non-insulin-dependent form of the disease except one, who had insulin-dependent diabetes. Most of the case patients (90 percent) and control patients (92 percent) were treated with oral antidiabetic agents or dietary modifications.

The prevalence of diabetes in our control subjects (8.3 percent) was similar to that reported in the Italian population of a corresponding age (7 percent)35. We did not use the glucose-tolerance test to diagnose diabetes; for this reason, we may have underestimated the percentages of patients with diabetes. However, in patients with cancer, the glucose-tolerance test frequently yields false positive results36.

Supported by grants (880716 and 892616) from the Centro Nazionale delle Ricerche.

We are indebted to Miss Janice Capan for assistance in translating the manuscript.


Source Information

From the Institute of Medicine and Gastroenterology, University of Bologna, St. Orsola Hospital, Bologna, Italy. The members of the Italian Pancreatic Cancer Study Group include Patrizia Priori, M.D., Orazio Campione, M.D., Riccardo Casadei, M.D., Maria Brambati, M.D., Carlo Lesi, M.D., and Antonio Frena, M.D. (Bologna); Alberto Malesci, M.D., and Alessandro Zerbi, M.D. (Milan); Angelo Andriulli, M.D., and Patrizio Acquadro, M.D. (Turin); Alessandro D'Ambrosi, M.D., and Vittorio Alvisi, M.D. (Ferrara); Giuseppe Montalto, M.D., and Antonio Carroccio, M.D. (Palermo); Valerio De Conca, M.D., Alberto Mornese, M.D., and Carlo Mansi, M.D. (Genoa); Carlo Battistini, M.D. (Parma); Cosimo Sperti, M.D., and Claudio Pasquali, M.D. (Padua); Luigi Gaeta, M.D., and Mario Mazzeo, M.D. (Naples); and Martina Felder, M.D. (Bolzano).

Address reprint requests to Professor Gullo at the Istituto di Clinica Medica e Gastroenterologia, Ospedale S. Orsola, Via Massarenti, 9, 40138 Bologna, Italy.

References

  1. Marble A. Diabetes and cancer. N Engl J Med 1934;211:339-349. 
  2. Bell ET. Carcinoma of the pancreas. I. A clinical and pathologic study of 609 necropsied cases. II. The relation of carcinoma of the pancreas to diabetes mellitus. Am J Pathol 1957;33:499-523.
  3. Green RC Jr, Baggenstoss AH, Sprague RG. Diabetes mellitus in association with primary carcinoma of the pancreas. Diabetes 1958;7:308-311. [Medline]
  4. Clark CG, Mitchell PEG. Diabetes mellitus and primary carcinoma of the pancreas. BMJ 1961;2:1259-1262. [Medline]
  5. Karmody AJ, Kyle J. The association between carcinoma of the pancreas and diabetes mellitus. Br J Surg 1969;56:362-364. [Medline]
  6. Kessler II. Cancer mortality among diabetics. J Natl Cancer Inst 1970;44:673-686.
  7. Wynder EL, Mabuchi K, Maruchi N, Fortner JG. Epidemiology of cancer of the pancreas. J Natl Cancer Inst 1973;50:645-667.
  8. Blot WJ, Fraumeni JF Jr, Stone BJ. Geographic correlates of pancreas cancer in the United States. Cancer 1978;42:373-380. [Medline]
  9. Whittemore AS, Paffenbarger RS Jr, Anderson K, Halpern J. Early precursors of pancreatic cancer in college men. J Chronic Dis 1983;36:251-256. [CrossRef][Medline]
  10. Norell S, Ahlbom A, Erwald R, et al. Diabetes, gall stone disease, and pancreatic cancer. Br J Cancer 1986;54:377-378. [Medline]
  11. Hiatt RA, Klatsky AL, Armstrong MA. Pancreatic cancer, blood glucose and beverage consumption. Int J Cancer 1988;41:794-797. [Medline]
  12. Mills PK, Beeson WL, Abbey DE, Fraser GE, Phillips RL. Dietary habits and past medical history as related to fatal pancreas cancer risk among Adventists. Cancer 1988;61:2578-2585. [CrossRef][Medline]
  13. Cuzick J, Babiker AG. Pancreatic cancer, alcohol, diabetes mellitus and gall-bladder disease. Int J Cancer 1989;43:415-421. [Medline]
  14. Farrow DC, Davis S. Risk of pancreatic cancer in relation to medical history and the use of tobacco, alcohol and coffee. Int J Cancer 1990;45:816-820. [Medline]
  15. Jain M, Howe GR, St Louis P, Miller AB. Coffee and alcohol as determinants of risk of pancreas cancer: a case-control study from Toronto. Int J Cancer 1991;47:384-389. [Medline]
  16. Bueno de Mesquita HB, Maisonneuve P, Moerman CJ, Walker AM. Aspects of medical history and exocrine carcinoma of the pancreas: a population-based case-control study in the Netherlands. Int J Cancer 1992;52:17-23. [Medline]
  17. Friedman GD, van den Eeden SK. Risk factors for pancreatic cancer: an exploratory study. Int J Epidemiol 1993;22:30-37. [Free Full Text]
  18. Kalapothaki V, Tzonou A, Hsieh C-C, Toupadaki N, Karakatsani A, Trichopoulos D. Tobacco, ethanol, coffee, pancreatitis, diabetes mellitus, and cholelithiasis as risk factors for pancreatic carcinoma. Cancer Causes Control 1993;4:375-382. [CrossRef][Medline]
  19. Schwartz SS, Zeidler A, Moossa AR, Kuku SF, Rubenstein AH. A prospective study of glucose tolerance, insulin, C-peptide, and glucagon responses in patients with pancreatic carcinoma. Am J Dig Dis 1978;23:1107-1114. [CrossRef][Medline]
  20. Permert J, Ihse I, Jorfeldt L, von Schenck H, Arnqvist HJ, Larsson J. Pancreatic cancer is associated with impaired glucose metabolism. Eur J Surg 1993;159:101-107. [Medline]
  21. Warshaw AL, Fernandez-del Castillo C. Pancreatic carcinoma. N Engl J Med 1992;326:455-465. [Medline]
  22. Lin RS, Kessler II. A multifactorial model for pancreatic cancer in man: epidemiologic evidence. JAMA 1981;245:147-152. [Abstract]
  23. Ragozzino M, Melton LJ III, Chu CP, Palumbo PJ. Subsequent cancer risk in the incidence cohort of Rochester, Minnesota, residents with diabetes mellitus. J Chronic Dis 1982;35:13-19. [CrossRef][Medline]
  24. Gold EB, Gordis L, Diener MD, et al. Diet and other risk factors for cancer of the pancreas. Cancer 1985;55:460-467. [CrossRef][Medline]
  25. Green A, Jensen OM. Frequency of cancer among insulin-treated diabetic patients in Denmark. Diabetologia 1985;28:128-130. [Medline]
  26. O'Mara BA, Byers T, Schoenfeld E. Diabetes mellitus and cancer risk: a multisite case-control study. J Chronic Dis 1985;38:435-441. [CrossRef][Medline]
  27. Mack TM, Yu MC, Hanisch R, Henderson BE. Pancreas cancer and smoking, beverage consumption, and past medical history. J Natl Cancer Inst 1986;76:49-60.
  28. La Vecchia C, Negri E, D'Avanzo B, et al. Medical history, diet and pancreatic cancer. Oncology 1990;47:463-466. [Medline]
  29. Gullo L, Pezzilli R, Morselli Labate AM, Italian Pancreatic Cancer Study Group. Coffee and cancer of the pancreas: an Italian multicenter study. Digestion 1993;54:279-279.abstract 
  30. National Diabetes Data Group. Classification and diagnosis of diabetes mellitus and other categories of glucose intolerance. Diabetes 1979;28:1039-1057. [Medline]
  31. Dixon WJ, Brown MB, Engelman L, Jennrich RI. BMDP statistical software manual. Berkeley: University of California Press, 1990.
  32. Grauer FW. Pancreatic carcinoma: a review of thirty-four autopsies. Arch Intern Med 1939;63:884-898. [CrossRef]
  33. Permert J, Larsson J, Westermark GT, et al. Islet amyloid polypeptide in patients with pancreatic cancer and diabetes. N Engl J Med 1994;330:313-318. [Free Full Text]
  34. Gullo L, Ancona D, Pezzilli R, Casadei R, Campione O. Glucose tolerance and insulin secretion in pancreatic cancer. Ital J Gastroenterol 1993;25:487-489. [Medline]
  35. Morsiani M. Epidemiologia del diabete in Italia. Metabolismo Oggi 1987;4:3-10.
  36. Glicksman AS, Rawson RW. Diabetes and altered carbohydrate metabolism in patients with cancer. Cancer 1956;9:1127-1134. [Medline]

 

This Article
-Abstract

Commentary
-Letters

Tools and Services
-Add to Personal Archive
-Add to Citation Manager
-Notify a Friend
-E-mail When Cited

More Information
-PubMed Citation

Related Letters:

Pancreatic Cancer and Diabetes
Balkau B., Barrett-Connor E., Eschwege E., Jones S.C., Alberti K.G.M.M., O'Shea R. S., Strom B. L., Berlin J. A., Gullo L., Pezzilli R., Morselli-Labate A. M.
Extract | Full Text  
N Engl J Med 1994; 331:1526-1528, Dec 1, 1994. Correspondence

This article has been cited by other articles:



HOME  |  SUBSCRIBE  |  SEARCH  |  CURRENT ISSUE  |  PAST ISSUES  |  COLLECTIONS  |  PRIVACY  |  HELP  |  beta.nejm.org

Comments and questions? Please contact us.

The New England Journal of Medicine is owned, published, and copyrighted © 2008 Massachusetts Medical Society. All rights reserved.