ConditionOverall Response Rate
Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorQingdao Central Hospital
About this trial
The purpose of this study is to explore the efficacy and safety ofof bevacizumab plus cisplatin compare with cisplatin in the treatment of malignant serous effusion in patients with advanced adenocarcinoma
Eligibility criteria
Qualifiers
Voluntarily sign informed consent;
Treatment naive serous effusion of patients with adenocarcinoma without activating gene mutation.
Eastern Cooperative Oncology Group (ECOG) score ≤ 2;
Survival is expected to exceed 3 months
Disqualifiers
The subject had received anti-vascular endothelial growth factor (VEGF) small molecule tyrosine kinase inhibitors or monoclonal antibodies in the past 4 weeks; The subject had participated any clinical trials in the past 4 weeks; The subject had previously received bevacizumab of pleural perfusion therapy;
Trial design
Treatments tested in this trial
- Intracavity injection of bevacizumab 7.5mg/kg plus cisplatin 40mg/m2
- cisplatin 40mg/m2 intracavity injection
Treatment groups
60 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov