Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Establishment and validation of the deep learning model of Cetuximab efficacy in simultaneous RAS wild unresectable CRLM patients
Ras wild unresectable CRLM patients with primary tumor resection followed by Cetuximab in combination with chemotherapy were included in this study. The tumor response was assessed by local MDT group. Based on tumor response, almost 100 CRLM patients were classified into two groups (Clinician drived regimen vs Multi-omics model drived regimen). They will be the prospective cohort to validate our deep learning model for predicting Cetuximab efficacy.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| ARM A | Active Comparator | Chemotherapy regimens are determined based on the clinical experience of specialists |
|
| ARM B | Experimental | Chemotherapy regimens are determined based on the multimodal deep learning signature |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Cetuximab | Drug | AEM A:The specialist's decision to add cetuximab to chemotherapy will be based on their own judgment ARM B:The patient's CT imaging,genetic mutation information were input into the signature, and the FOLFOX+cetuximab regimen was selected when the output label was 1. FOLFOX+bevacizumab chemotherapy regimen was selected when the output label was 0 |
| Measure | Description | Time Frame |
|---|---|---|
| response rate | response rate will be assessed by local MDT | 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| progression free survival | progression free survival will be assessed by local MDT every two months during treatment, and telephone follow-up every three month after treatment | 3 years |
| overall survival |
Not provided
Inclusion Criteria:
Exclusion Criteria:
Not provided
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jianmin Xu, MD | Contact | +86-021-64041990 | xujmin@aliyun.com | |
| Wenju Chang, MD | Contact | +86-021-64041990 | chang.wenju@zs-hospital.sh.cn |
| Name | Affiliation | Role |
|---|---|---|
| Jianmin Xu, MD | Fudan University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Zhongshan Hospital, Fudan University | Shanghai | Shanghai Municipality | 200032 | China | ||
| Zhongshan hosptial, Fudan University |
Not provided
| ID | Term |
|---|---|
| D000068818 | Cetuximab |
| ID | Term |
|---|---|
| D061067 | Antibodies, Monoclonal, Humanized |
| D000911 | Antibodies, Monoclonal |
| D000906 | Antibodies |
| D007136 | Immunoglobulins |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
overall survival will be assessed by researchers every two months during treatment, and telephone follow-up every three month after treatment
| 3 years |
| Shanghai |
| 200032 |
| China |
| D007162 |
| Immunoproteins |
| D001798 | Blood Proteins |
| D011506 | Proteins |
| D000602 | Amino Acids, Peptides, and Proteins |
| D012712 | Serum Globulins |
| D005916 | Globulins |