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Fruquintinib in Refractory Metastatic Colorectal Cancer: A Real-world Study

Fruquintinib in Refractory Metastatic Colorectal Cancer: A Real-world Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06202417
Enrollment
520
Registered
2024-01-11
Start date
2021-01-01
Completion date
2023-12-25
Last updated
2024-01-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer, Metastatic Colorectal Cancer, Refractory Colorectal Cancer

Keywords

Fruquintinib

Brief summary

Fruquintinib is an oral tyrosine kinase inhibitor (TKI), which improves progression-free survival (PFS) and overall survival (OS) in patients with refractory metastatic colorectal cancer (mCRC). Here, we explore the real-world treatment patterns of fruquintinib in the third- or late-line setting for mCRC in six centers in China.

Interventions

DRUGFruquintinib

an oral tyrosine kinase inhibitor (TKI)

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

(1) histology-confirmed metastatic CRC (mCRC); (2) disease progression on standard therapy with at least two lines of chemotherapy, including fluorouracil, oxaliplatin, and irinotecan with or without biologics such as bevacizumab and cetuximab; (3) fruquintinib administered as salvage treatment; (4) available clinical data.

Exclusion criteria

(1) lack of follow-up data; (2) fruquintinib administration as second-line treatment; (3) fruquintinib administration stopped after less than two cycles.

Design outcomes

Primary

MeasureTime frameDescription
PFSThree yearsPFS was calculated from the date of fruquintinib administration to the first observation of disease progression or death
OSThree yearsOS was defined as the time from fruquintinib administration to death
DCRDuring the medication periodDCR was determined as the proportion of patients who achieved complete response, partial response or stable disease assessed at least 6 weeks after drug administration

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026