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