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Real World Study of Regorafenib Versus Fruquintinib in Colorectal Cancer

P

Peking University

Status

Unknown

Conditions

Colorectal Cancer

Treatments

Drug: Regorafenib
Drug: Fruquintinib

Study type

Observational

Funder types

Other

Identifiers

NCT04431791
Reg vs Fru

Details and patient eligibility

About

This is an observational, ambispective cohort study. The aim is to compare the efficacy and safety of regorafenib versus fruquintinib conducted in China. About 268 eligible metastatic colorectal cancer patients after second-line therapy will be assigned to receive either regorafenib or fruquintinib, based on decision of the gastrointestinal physician according the patients' condition.

Enrollment

268 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. signed and dated informed consent.
  2. Diagnosis of histologically confirmed colorectal cancer, stage IV.
  3. after second-line therapy.
  4. gastrointestinal physician prescribed to receive regorafenib or fruquintinib according the patients' condition.

Exclusion criteria

  1. received regorafenib or fruquintinib before third-line therapy.
  2. the clinicopathological characteristics and previous therapy were unknown.
  3. regorafenib or fruquintinib treatment is less than one cycle in the historical cohort.

Trial design

268 participants in 2 patient groups

Regorafenib
Treatment:
Drug: Regorafenib
Fruquintinib
Treatment:
Drug: Fruquintinib

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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