Authors

Yan Gu, Wanling Yang, Min Zhang, Xiaolu Yang, Xinhua Fu*


Departments

Department of Respiratory and Critical Care Medicine, the Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia 010050, China

Abstract

Objective: To evaluation the efficacy and direct costs of Bevacizumab in managing of malignant pleural effusion (MPE) caused by lung adenocarcinoma.

Methods: Between December 2014 to December 2016, 60 untreated patients with MPE in lung adenocarcinoma were randomly assigned to one of two groups; intrapleural injection of Bevacizumab (n= 30) or intrapleural injection of OK-432 (n= 30). Adverse events were recorded and assessed. ELISA was applied to detect the serum vascular endothelial growth factor (VEGF) level.

Results: In the Bevacizumab group, fifteen (50%) and eleven (37%) patients achieved complete response (CR) and partial response (PR), respectively, 1 patient remained stable (3%), and 3 patients showed disease progression (10%). In the OK-432 group, thirteen (43%) and twelve (40%) patients achieved CR and PR, respectively, 2 patients remained stable (7%), and 4 patients showed progressed (13%). There was no statistically significant difference in the effective rate between the two groups (P> 0.05). Regarding the adverse effects, only 1 case experienced fever in the Bevacizumab group. However, for the patients in OK-432 group, chest pain, fever, dyspnea, fatigue, nausea, and anorexia were occurred in 16 (53%), 21 (70%), 5 (16.67%), 5 (16.67%), 1 (3.33%), and 7 (23.3%) cases, respectively. The incidence of adverse reactions of the patients in the OK-432 group was significantly higher than that in the Bevacizumab group (P< 0.05). In the Bevacizumab group, the serum VEGF concentration was 246.79± 179.51 pg/ml before treatment and 129.85± 113.09 pg/ml after treatment, suggesting the VEGF level was decreased in Bevacizumab group (P< 0.001). Median duration in hospital was 3 days in the Bevacizumab group, and less than 5 days in the OK-432 group (P< 0.001). The care cost was CNY 136.00±75.46 in the Bevacizumab group compared with CNY 201.33±66.00 in the OK-432 group (P< 0.001).

Conclusion: Intrapleural injection of Bevacizumab was effective and safe for MPE, and shortened the length of hospital stay, and reduced the cost of hospitalization and nursing care.

Keywords

Malignant Pleural Effusion, Bevacizumab, Vascular Endothelial Growth Factor.

DOI:

10.19193/0393-6384_2021_5_406