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A randomized clinical study to compare intrapleural infusion with intravenous infusion of bevacizumab in the management of malignant pleural effusion in patients with non-small-cell lung cancer.
Nie, Keke; Zhang, Zhen; You, Yunhong; Zhuang, Xingjun; Zhang, Chunling; Ji, Youxin.
Afiliação
  • Nie K; Department of Oncology, Qingdao Cancer Hospital, Qingdao, China.
  • Zhang Z; Department of Oncology, Qingdao Cancer Hospital, Qingdao, China.
  • You Y; Department of Oncology, Qingdao Cancer Hospital, Qingdao, China.
  • Zhuang X; Department of Oncology, PLA 971 Hospital, Qingdao, China.
  • Zhang C; Department of Oncology, Qingdao Central Hospital, the Affiliated Qingdao Central Hospital of Qingdao University, Qingdao, China.
  • Ji Y; Department of Oncology, Qingdao Central Hospital, the Affiliated Qingdao Central Hospital of Qingdao University, Qingdao, China.
Thorac Cancer ; 11(1): 8-14, 2020 01.
Article em En | MEDLINE | ID: mdl-31726490
ABSTRACT

BACKGROUND:

To compare the efficiency and toxicity of bevacizumab by intrapleural or intravenous infusion in the management of malignant pleural effusion in patients with non-small-cell lung cancer (NSCLC).

METHODS:

Sensitizing mutation negative NSCLC patients with malignant pleural effusion were randomized into two groups in 11 ratio. The pleural effusion was completely drained in 24 hours; one group received intrapleural infusion and the second group received intravenous infusion of bevacizumab at a dose of 7.5 mg per kg bodyweight. The serum vascular endothelial growth factor (VEGF) was tested before and 72 hours after injection of bevacizumab. Computerized tomography (CT) scan to evaluate pleural effusions was carried out at four weeks for each patient and their survival followed-up.

RESULTS:

A total of 67 patients were screened and 43 enrolled into the study. The response rate was 80% (16 of 20) in the intrapleural group and 66.7% (14 of 21) in the intravenous group. The median duration of response (DoR) of pleural effusion was 4.50 months and 3.70 months, respectively. The median serum VEGF level at 72 hours decreased 67.25% in the intrapleural group and 57.19% in the intravenous group compared to baseline level (P = 0.276). The median serum VEGF level at 72 hours decreased 52.02% compared to baseline level in patients' DoR less than three months and 68.33% in patients' DoR longer than three months, respectively (P = 0.014). The main side effects noted were mild to moderate hypertension, proteinuria and epistaxis.

CONCLUSIONS:

Bevacizumab intrapleural infusion had higher efficiency and higher safety than intravenous infusion in the management of malignant pleural effusion caused by NSCLC. The decreased level of serum VEGF at 72 hours after bevacizumab treatment was closely related to the response rate and duration of the response of pleural effusion.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derrame Pleural Maligno / Carcinoma Pulmonar de Células não Pequenas / Bevacizumab / Antineoplásicos Imunológicos / Neoplasias Pulmonares Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Derrame Pleural Maligno / Carcinoma Pulmonar de Células não Pequenas / Bevacizumab / Antineoplásicos Imunológicos / Neoplasias Pulmonares Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies Limite: Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article