A Clinical-Genetic Risk Score for Predicting Cancer-Associated Venous Thromboembolism: A Development and Validation Study Involving Two Independent Prospective Cohorts

Author:

Muñoz Andrés12ORCID,Ay Cihan34,Grilz Ella3,López Sonia5,Font Carme26ORCID,Pachón Vanesa27,Castellón Victoria28,Martínez-Marín Virginia29,Salgado Mercedes210,Martínez Eva211,Calzas Julia212ORCID,Ortega Laura12ORCID,Rupérez Ana213ORCID,Salas Eduardo14ORCID,Pabinger Ingrid3,Soria Jose Manuel5ORCID

Affiliation:

1. Medical Oncology, Hospital General Universitario Gregorio Marañón, Madrid, Spain

2. Cancer and Thrombosis Working Section, Spanish Society of Medical Oncology (SEOM), Madrid, Spain

3. Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria

4. I.M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia

5. Genomics of Complex Diseases Unit, Biomedical Research Institute Sant Pau (IIB-Sant Pau), Barcelona, Spain

6. Medical Oncology, Hospital Clínic, Barcelona, Spain

7. Medical Oncology, Hospital Universitario Ramón y Cajal Madrid, Madrid, Spain

8. Medical Oncology, Complejo Hospitalario de Torrecárdenas, Almería, Spain

9. Medical Oncology, Hospital Universitario La Paz, Madrid, Spain

10. Medical Oncology, Complejo Hospitalario Universitario de Ourense, Ourense, Spain

11. Medical Oncology, Hospital Universitario Marqués de Valdecilla, Santander, Spain

12. Medical Oncology, Hospital Universitario de Fuenlabrada, Madrid, Spain

13. Medical Oncology, Fundación Jiménez Díaz, Madrid, Spain

14. Scientific Department, Gendiag.exe, Barcelona, Spain

Abstract

PURPOSE Venous thromboembolism (VTE) is a leading cause of death among patients with cancer. The Khorana score was developed for assessing the risk of VTE in outpatients with cancer receiving chemotherapy, but its accuracy in identifying patients at high risk has been questioned. The aim of this study was to develop and validate a clinical-genetic score that improves the assessment of VTE risk in oncology outpatients within 6 months of diagnosis. METHODS The new score was developed using the data of 364 outpatients belonging to the Spanish ONCOTHROMB 12-01 population. In this cohort, clinical data associated with the risk of VTE were collected at the time of diagnosis, including the Khorana score. These patients were also genotyped for the 51 genetic variants known to be associated with VTE. Multivariate logistic regression was performed to determine the weight of each genetic and clinical variable in relation to VTE risk, allowing a clinical-genetic risk score (the ONCOTHROMB score) to be developed. The Khorana and the ONCOTHROMB scores were then compared via the area under the receiver operating characteristic curve (AUC), calibration, and the number of patients needed to treat. The new score was then validated in a study of 263 patients in the Vienna Cancer and Thrombosis Study population. RESULTS Nine genetic variants, tumor site, TNM stage, and a body mass index of > 25 kg/m2 were found to be associated with VTE and were used to build the ONCOTHROMB score, which better predicted the overall risk of VTE than did the Khorana score (AUC, 0.781 v 0.580; P < .001). Similar AUC results were recorded in the validation study the Vienna Cancer and Thrombosis Study cohort involving patients with the same type of tumor (AUC for the ONCOTHROMB score v the Khorana score: 0.686 v 0.577; P < .001) and with all type of tumors (AUC for the ONCOTHROMB score v the Khorana score: 0.720 v 0.561; P < .0001). CONCLUSION The ONCOTHROMB score for VTE risk in outpatients with cancer, which takes into account both clinical and genetic variables, better identifies patients who might benefit from primary thromboprophylaxis than does the Khorana score.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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