Skip to content

Radiomics Assess of Bevacizumab Plus Chemo in Colorectal Cancer Liver Metastases

A Radiomics Approach to Predict the Effect of Bevacizumab Plus Chemotherapy in Patients With Liver Metastases of Colorectal Cancer: A Prospective Multi-Centers Trial

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04213222
Acronym
ROBOT
Enrollment
300
Registered
2019-12-30
Start date
2020-10-31
Completion date
2023-12-31
Last updated
2020-08-11

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

Conditions

Colon Cancer, Liver Metastases, Rectal Cancer

Keywords

colorectal cancer, liver metastasis, bevacizumab

Brief summary

Colorectal carcinoma with liver metastasis is one of the major problems bothering physicians worldwide. Bevacizumab combined with chemotherapy is the standard treatment recommended by several guidelines. Despite the high cost, a certain portion of patients couldn't benefit from this therapy. This study is aiming to find out the specific type of patients who would respond to bevacizumab by Radiomics approach, and evaluate the prediction value of this imaging model with clinical and genetic factors.

Interventions

DRUGBevacizumab

bevacizumab combined with chemotherapy

Sponsors

Peking University People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Colorectal carcinoma confirmed by pathological result. 2. Liver metastasis confirmed by imaging studies. 3. Treatment of bevacizumab combined with chemotherapy chosen by MDT team. 4. ECOG: 0-2. 5. Normal laboratory studies including liver\\renal\\bone marrow functions. 6. Expected lifespan more than 3 months.

Exclusion criteria

1. Previous treatment of colorectal cancer with liver metastasis. 2. Diagnosed with other malignancies. 3. Couldn't finish the trial due to several reasons such as allergy to chemotherapy drugs\\pregnancy or lactation\\chronic heart disease\\unable to sustain further treatment.

Design outcomes

Primary

MeasureTime frame
estimated ORR6-8 weeks

Secondary

MeasureTime frame
estimated PFS3 years
estimated OS3 years

Countries

China

Contacts

Primary ContactYudi Bao, MD
ggpptang@gmail.com8613810355879

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026