Thromb Haemost 2011; 106(02): 371-378
DOI: 10.1160/TH10-12-0789
Cellular Proteolysis and Oncology
Schattauer GmbH

Symptomatic and incidental thromboembolism are both associated with mortality in pancreatic cancer

Laurel A. Menapace
1   James P. Wilmot Cancer Center, and the Department of Medicine, University of Rochester, Rochester, New York, USA
,
Derick R. Peterson
1   James P. Wilmot Cancer Center, and the Department of Medicine, University of Rochester, Rochester, New York, USA
2   Department of Biostatistics, University of Rochester, Rochester, New York, USA
,
Andrea Berry
1   James P. Wilmot Cancer Center, and the Department of Medicine, University of Rochester, Rochester, New York, USA
2   Department of Biostatistics, University of Rochester, Rochester, New York, USA
,
Tarek Sousou
1   James P. Wilmot Cancer Center, and the Department of Medicine, University of Rochester, Rochester, New York, USA
,
Alok A. Khorana
1   James P. Wilmot Cancer Center, and the Department of Medicine, University of Rochester, Rochester, New York, USA
› Author Affiliations
Further Information

Publication History

Received: 15 December 2010

Accepted after major revision: 03 May 2011

Publication Date:
25 November 2017 (online)

Summary

Pancreatic cancer is known to be associated with VTE, but contemporary rates of incidental and symptomatic VTE events and their association with mortality are incompletely understood. We conducted a retrospective cohort study of consecutive pancreatic adenocarcinoma patients at the University of Rochester from 2006–2009. Data were analysed using a Cox model with time-dependent covariates. A total of 1,151 radiologic exams of 135 patients were included. Forty-seven patients (34.8%) experienced VTE including 12 pulmonary emboli (PE), 28 deep-vein thromboses (DVTs) and 47 visceral vein events. Incidental events comprised 33.3% of PEs, 21.4% of DVTs and 100% of visceral VTE. Median (95% CI) conditional survival beyond three months was 233 (162–322) more days for those without VTE, which was significantly greater than 12 (3–60) days for those with DVT as first event (p<0.0001) and 87 (14–322) days with visceral first events (p=0.022). In multivariate analysis, DVT (HR 25, 95% CI 10–63, p <0.0001), PE (HR 8.9, 95% CI 2.5–31.7, p = 0.007) and incidental visceral events (HR 2.6, 95% CI 1.6–4.2, p =0.0001) were all associated with mortality, though anticoagulants reduced these risks by 70% (26–88%, p = 0.009). In conclusion, VTE occurs in over one-third of contemporary pancreatic cancer patients and, whether symptomatic or incidental, is strongly associated with worsened mortality. The role of anticoagulation in treating incidental or visceral VTE warrants further study.

Note: The abstract of this manuscript was presented at the Annual Meeting of the American Society of Hematology, Orlando, FL, USA on December 5, 2010.

 
  • References

  • 1 Lyman GH, Khorana AA. Cancer, clots and consensus: new understanding of an old problem. J Clin Oncol 2009; 27: 4821-4826.
  • 2 Gladish GW, Choe DH, Marom EM. et al. Incidental pulmonary emboli in oncology patients: prevalence, CT evaluation, and natural history. Radiology 2006; 240: 246-255.
  • 3 O’Connell CL, Boswell WD, Duddalwar V. et al. Unsuspected pulmonary emboli in cancer patients: clinical correlates and relevance. J Clin Oncol 2006; 24: 4928-4932.
  • 4 Singh R, Sousou T, Mohile S. et al. High rates of symptomatic and incidental thromboembolic events in gastrointestinal cancer patients. J Thromb Haemost 2010; 8: 1879-1881.
  • 5 Sebastian AJ, Paddon AJ. Clinically unsuspected pulmonary embolism–an important secondary finding in oncology CT. Clin Radiol 2006; 61: 81-85.
  • 6 Cronin CG, Lohan DG, Keane M. et al. Prevalence and significance of asymptomatic venous thromboembolic disease found on oncologic staging CT. AJR Am J Roentgenol 2007; 189: 162-170.
  • 7 Browne AM, Cronin CG, English C. et al. Unsuspected pulmonary emboli in oncology patients undergoing routine computed tomography imaging. J Thorac Oncol 2010; 5: 798-803.
  • 8 Sorensen HT, Mellemkjaer L, Olsen JH. et al. Prognosis of cancers associated with venous thromboembolism. N Engl J Med 2000; 343: 1846-1850.
  • 9 Khorana AA. Venous thromboembolism and prognosis in cancer. Thromb Res 2010; 125: 490-493.
  • 10 O’Connell C, Razavi P, Ghalichi M. et al. Unsuspected pulmonary emboli adversely impact survival in patients with cancer undergoing routine staging MDCT scanning. J Thromb Haemost 2011; 9: 305-311.
  • 11 Khorana AA, Fine RL. Pancreatic cancer and thromboembolic disease. Lancet Oncol 2004; 5: 655-663.
  • 12 Mandala M, Reni M, Cascinu S. et al. Venous thromboembolism predicts poor prognosis in irresectable pancreatic cancer patients. Ann Oncol 2007; 18: 1660-1665.
  • 13 Khorana AA, Connolly GC. Assessing risk of venous thromboembolism in the patient with cancer. J Clin Oncol 2009; 27: 4839-4847.
  • 14 Khorana AA, Francis CW, Culakova E. et al. Frequency, risk factors, and trends for venous thromboembolism among hospitalized cancer patients. Cancer 2007; 110: 2339-2346.
  • 15 Khorana AA, Francis CW, Culakova E. et al. Risk factors for chemotherapy-associated venous thromboembolism in a prospective observational study. Cancer 2005; 104: 2822-2829.
  • 16 Douma RA, Kok MG, Verberne LM. et al. Incidental venous thromboembolism in cancer patients: prevalence and consequence. Thromb Res 2010; 125: e306-309.