Apixaban reduced venous thromboembolism incidence from 10.2% to 4.2%, HR 0.41, in high-risk ambulatory cancer patients with Khorana score ≥2 over 6 months.
This review outlines current challenges in predicting and managing cancer-associated VTE, emphasizing the need for personalized risk assessment and safer therapeutic strategies in complex oncology populations.
Effect estimate: HR 0.41 (95% CI 0.26–0.65)
Absolute Event Rate: 4.2% vs 10.2%
Cancer-associated venous thromboembolism (CA-VTE) is a significant complication in oncology, contributing to morbidity, mortality, and increased healthcare utilization. Due to multiple patient- and disease-related factors, patients with cancer are at a markedly elevated risk for VTE, particularly within the first 6 months of diagnosis. The aim of this review is to provide an overview of current challenges and unmet needs in CA-VTE prediction, prevention and management. While the Khorana score remains the most widely used risk stratification tool, its limited sensitivity has prompted the development of more refined models such as PROTECHT, CONKO, ONKOTEV, Vienna-CATS, and COMPASS-CAT. These models incorporate additional clinical variables including cancer subtype, systemic therapies, comorbidities, and emerging biomarkers. However important gaps remain, particularly in addressing bleeding risk, underrepresented racial/ethnic groups, and adapting to novel cancer therapeutics. Recent clinical trials (AVERT, CASSINI) have supported the use of direct oral anticoagulants (DOACs) for primary and secondary prophylaxis in select high-risk populations. However, anticoagulation strategies in complex populations, including those with thrombocytopenia, brain tumors, or concurrent antiplatelet therapy, remain areas of active investigation. Future directions include the integration of genomics, proteomics, and machine learning into risk modeling to enable precision medicine approaches. Ongoing clinical trials are testing the promise of safer prophylactic and therapeutic strategies. Personalized risk assessment and treatment of CA-VTE remain essential to improving patient outcomes in oncology. By consolidating existing evidence and identifying key unmet needs, this review seeks to guide more personalized and effective management of CA-VTE.
Nusrat et al. (Thu,) conducted a review in Ambulatory adult patients with various cancers initiating chemotherapy, Khorana score used for risk stratification (n=4,066). Apixaban vs. Placebo was evaluated on Incidence of venous thromboembolism (VTE) (HR 0.41, 95% CI 0.26–0.65). Apixaban reduced venous thromboembolism incidence from 10.2% to 4.2%, HR 0.41, in high-risk ambulatory cancer patients with Khorana score ≥2 over 6 months.