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Regorafenib Treatment Patterns and Survival Outcomes in Advanced Colorectal Cancer: A Real-world Study

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Unknown

Conditions

Advanced Colorectal Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT04835324
ChineseAcademyMedicalSciences

Details and patient eligibility

About

This is a multi-center, retrospective, real-world study. The purpose of this study is to observe the effectiveness and safety of regorafenib in Chinese advanced colorectal cancer patients.

The main observational goals include overall survival(OS), 6 month OS rate, 1 year OS rate, and treatment time failure (TTF), other study goals include objective response rate( ORR)、Disease control rate(DCR)and adverse event(AE) of regorafenib.

Enrollment

650 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Patients with colorectal cancer confirmed by pathological tissue or cytology;
  2. The pathological type of colorectal tumor was adenocarcinoma;
  3. Patients with recurrent or metastatic, unresectable advanced colorectal cancer;
  4. Patients who received regorafenib at least one period treatment.

Exclusion criteria

  1. Patients participating in other interventional clinical studies while taking regorafenib;
  2. Patients with other malignant tumors within 5 years before regorafenib treatment, except for cured cervical carcinoma in situ, skin squamous cell carcinoma or basal cell carcinoma, early papillary thyroid carcinoma, etc.;
  3. The investigator deems that there are other factors that are not suitable for patients who participate in this study.

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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