The Efficacy and Safety of TAS-102(Suyuan) Combined With Bevacizumab as First-line Therapy in Patients With Advanced Colorectal Cancer

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-85
SponsorThe Second Affiliated Hospital of Shandong First Medical University

About this trial

To evaluate the efficacy and safety of TAS-102 combined with bevacizumab as first-line therapy in patients with advanced colorectal cancer who could not tolerate or did not receive combined chemotherapy

Eligibility criteria

Qualifiers

Age ≥18 years

Life expectancy of at least 3 months

Definitive histological or cytological evidence of adenocarcinoma of the colon or rectum;

Patients who had not previously received first-line chemotherapy or targeted therapy for metastatic colorectal cancer, or who had received adjuvant chemotherapy after radical resection and had relapsed 12 months after completion of adjuvant chemotherapy;

Disqualifiers

the presence of other active malignancies at the same time, excluding those that have not been diagnosed for more than 5 years or are considered curable with adequate treatment,

the known presence of brain or pial metastases,

systemic active infection (ie, infection leading to body temperature ≥38 ° C-RRB- ,

clinically significant intestinal obstruction, pulmonary fibrosis, renal failure, liver failure, or symptomatic cerebrovascular disease,

Trial design

Treatments tested in this trial

  • Tas-102(Suyuan) combined with bevacizumab

Treatment groups

50 Participants
are divided into 1 treatment group