Trials / Recruiting
RecruitingNCT06447727
Efficacy and Safety of 90Y Microsphere Combined With FOLFIRI and Bevacizumab in Second-line Treatment of CRLM
Efficacy and Safety of 90Y Microsphere Combined With FOLFIRI and Bevacizumab in Second-line Treatment of Colorectal Cancer Liver Metastasis
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 30 (estimated)
- Sponsor
- Zhongda Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
To observe the PFS of yttrium \[90Y\] microsphere injection combined with FOLFIRI and bevacizumab in second-line treatment of CRLM.
Detailed description
This study is a prospective, multicenter, observational, cohort study to observe the efficacy and safety of selective internal radiation therapy (SIRT) with yttrium \[90Y\] microsphere injection combined with FOLFIRI and bevacizumab as second-line therapy in patients with colorectal cancer liver metastases.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | SIRT with Yttrium-90 Microspheres | Selective Internal Radiation Therapy (SIRT) with Yttrium-90 \[90Y\] Microspheres Injection |
| DRUG | FOLFIRI and Bevacizumab | FOLFIRI and Bevacizumab |
Timeline
- Start date
- 2024-05-20
- Primary completion
- 2025-11-30
- Completion
- 2025-11-30
- First posted
- 2024-06-07
- Last updated
- 2024-06-07
Locations
1 site across 1 country: China
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06447727. Inclusion in this directory is not an endorsement.