Thromb Haemost 2014; 112(06): 1129-1136
DOI: 10.1160/th14-04-0351
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Impact of anatomical location of lower limb venous thrombus on the risk of subsequent cancer

Jean-Philippe Galanaud
1   Clinical Investigation Center and Department of Internal Medicine, Montpellier University Hospital, Montpellier, France
,
Anne Cécile Arnoult
2   Department of Vascular Medicine, Grenoble University Hospital, Grenoble, France
3   Clinical Investigation Center, Grenoble University Hospital, Grenoble, France
,
Marie-Antoinette Sevestre
4   Department of Vascular Medicine, Amiens University Hospital, Amiens, France
,
Céline Genty
3   Clinical Investigation Center, Grenoble University Hospital, Grenoble, France
,
Michael Bonaldi
5   Department of Cardiology, Chalon sur Saône Hospital, Chalon sur Saône, France
,
Audrey Guyard
3   Clinical Investigation Center, Grenoble University Hospital, Grenoble, France
,
Pascal Giordana
6   Vascular Medicine Physician, Nice, France
,
Olivier Pichot
7   Vascular Medicine Physician, Grenoble, France
,
Marc Colonna
8   Registry of cancer of Isère, Grenoble University Hospital, Grenoble, France
,
Isabelle Quéré
1   Clinical Investigation Center and Department of Internal Medicine, Montpellier University Hospital, Montpellier, France
,
Jean-Luc Bosson
3   Clinical Investigation Center, Grenoble University Hospital, Grenoble, France
,
for the OPTIMEV-SFMV Investigators› Institutsangaben

Financial support: This study was supported by grants from the French Ministry of Health, the French Society of Vascular Medicine and Sanofi-Aventis.
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Publikationsverlauf

Received: 16. April 2014

Accepted after minor revision: 20. Juni 2014

Publikationsdatum:
29. November 2017 (online)

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Summary

After a proximal deep-vein thrombosis (P-DVT), the risk of diagnosis of a previously unsuspected cancer is high. Isolated distal DVT (iDDVT; i.e. infra-popliteal DVT without pulmonary embolism [PE]) and isolated superficial-vein thrombosis (iSVT; i.e. without concomitant DVT and PE) are at least as frequent as P-DVT but their association with subsequent cancer is uncertain. We exploited data from the OPTIMEV prospective, observational, multicentre study to i) compare the risk of subsequent cancer three years after a first objectively confirmed iSVT, iD-DVT and iP-DVT in patients without a prior history of cancer or of venous thromboembolism, ii) assess predictors of subsequent cancer in cases of iD-DVT. The overall cumulative rates of cancer among the 304 patients with iSVT, 536 patients with iD-DVT, and 327 patients with iP-DVT were similar (3.4% 95% confidence interval [1.8–6.2], 3.9% [2.5–5.9] and 3.9% [2.3–6.8], respectively), regardless of whether the index venous thromboembolic event was unprovoked or associated with a major transient risk factor. Neither anatomical (muscular vs deep-calf DVT) nor ultrasound scan characteristics (number of thrombosed veins, clot diameter under compression) seemed strongly associated with the risk of cancer in cases of iD-DVT. In patients managed in routine practice, all the different clinical expressions of lower limb venous thromboembolism are associated with a similar risk of subsequent cancer. From a clinical practice point of view, this suggests that cancer screening, without discussing the necessity, or not, of such screening, should not differ between a deepproximal, deep-distal or superficial location of thrombosis.

Note: Part of this study was presented as an oral presentation at the 54th American Society of Hematology Annual Meeting, 8 to 11 December 2012, Atlanta, GA, USA.