Comparison of risk prediction scores for venous thromboembolism in cancer patients: a prospective cohort study
Nick van Es,
Marcello Di Nisio,
Gabriela Cesarman,
Ankie Kleinjan,
Hans-Martin Otten,
Isabelle Mahé,
Ineke T. Wilts,
Desirée C. Twint,
Ettore Porreca,
Oscar Arrieta,
Alain Stépanian,
Kirsten Smit,
Michele De Tursi,
Suzanne M. Bleker,
Patrick M. Bossuyt,
Rienk Nieuwland,
Pieter W. Kamphuisen,
Harry R. Büller
Affiliations
Nick van Es
Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
Marcello Di Nisio
Department of Medicine and Ageing Sciences, G. D’Annunzio University, Chieti, Italy
Gabriela Cesarman
Department of Hematology, National Cancer Institute Mexico, Mexico City, Mexico
Ankie Kleinjan
Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
Hans-Martin Otten
Department of Internal Medicine, Slotervaart hospital, Amsterdam, the Netherlands
Isabelle Mahé
Department of Internal Medicine, Hôpital Louis Mourier, Paris, France
Ineke T. Wilts
Department of Internal Medicine, University Medical Center Groningen, the Netherlands
Desirée C. Twint
Department of Internal Medicine, VU Medical Center, Amsterdam, the Netherlands
Ettore Porreca
Department of Medical, Oral and Biotechnological Sciences, G. D’Annunzio University, Chieti, Italy
Oscar Arrieta
Department of Hematology, National Cancer Institute Mexico, Mexico City, Mexico
Alain Stépanian
Department of Hematology, Hôpital Lariboisière, Paris, France
Kirsten Smit
Department of Internal Medicine, VU Medical Center, Amsterdam, the Netherlands
Michele De Tursi
Department of Medical, Oral and Biotechnological Sciences, G. D’Annunzio University, Chieti, Italy
Suzanne M. Bleker
Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
Patrick M. Bossuyt
Department of Clinical Epidemiology, Biostatistics, and Bioinformatics, Academic Medical Center, Amsterdam, the Netherlands
Rienk Nieuwland
Department of Experimental Clinical Chemistry, Academic Medical Center, Amsterdam, the Netherlands
Pieter W. Kamphuisen
Department of Internal Medicine, University Medical Center Groningen, the Netherlands;Department of Internal Medicine, Tergooi Hospital, Hilversum, the Netherlands
Harry R. Büller
Department of Vascular Medicine, Academic Medical Center, Amsterdam, the Netherlands
In ambulatory patients with solid cancer, routine thromboprophylaxis to prevent venous thromboembolism is not recommended. Several risk prediction scores to identify cancer patients at high risk of venous thromboembolism have been proposed, but their clinical usefulness remains a matter of debate. We evaluated and directly compared the performance of the Khorana, Vienna, PROTECHT, and CONKO scores in a multinational, prospective cohort study. Patients with advanced cancer were eligible if they were due to undergo chemotherapy or had started chemotherapy in the previous three months. The primary outcome was objectively confirmed symptomatic or incidental deep vein thrombosis or pulmonary embolism during a 6-month follow-up period. A total of 876 patients were enrolled, of whom 260 (30%) had not yet received chemotherapy. Fifty-three patients (6.1%) developed venous thromboembolism. The c-statistics of the scores ranged from 0.50 to 0.57. At the conventional positivity threshold of 3 points, the scores classified 13–34% of patients as high-risk; the 6-month incidence of venous thromboembolism in these patients ranged from 6.5% (95%CI: 2.8–12) for the Khorana score to 9.6% (95%CI: 6.6–13) for the PROTECHT score. High-risk patients had a significantly increased risk of venous thromboembolism when using the Vienna (subhazard ratio 1.7; 95%CI: 1.0–3.1) or PROTECHT (subhazard ratio 2.1; 95%CI: 1.2–3.6) scores. In conclusion, the prediction scores performed poorly in predicting venous thromboembolism in cancer patients. The Vienna CATS and PROTECHT scores appear to discriminate better between low- and high-risk patients, but further improvements are needed before they can be considered for introduction into clinical practice.