Abstract 345P
Background
Venous thromboembolism (VTE) is a common event in brain tumour patients. The risk is further believed to increase with the addition of bevacizumab. In view of limited literature addressing this issue, we found the need to conduct this study.
Methods
The database of the adult patients with primary brain tumour on bevacizumab therapy, was utilised to see the occurrence of VTE. The demographics were noted and Khorana score was calculated. Pearson correlation analysis was done and the Pearson correlation coefficient was estimated between Khorana score and VTE. P-value <0.05 was considered statistically significant.
Results
Out of 80 patients, 7 (8.8%) had VTE events after starting bevacizumab. It was diagnosed as deep vein thrombosis (DVT) in 4 (5%) patients and pulmonary thromboembolism (PTE) in 3 (3.8%) patients. Also, out of all, 43 (53.8%) patients belonged to the low risk category of Khorana score, while 37 (46.2%) patients were in the intermediate category. There was no significant association between Khorana scores obtained and VTE (fisher exact test, p-value = 0.171). Table: 345P
Khorana score and VTE
Khorana sore | Venous thromboembolism (VTE) | |
Yes | No | |
0 | 2 (4.7%) | 41 (95.3%) |
1 | 4 (12.1%) | 29 (87.9%) |
2 | 1 (25%) | 3 (75%) |
3 | 0 | 0 |
Conclusions
The incidence of VTE in primary primary brain tumour patients receiving bevacizumab therapy is low. Low and intermediate risk Khorana scores are unable to predict the risk of VTE in our population.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
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