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Retrospective evaluation of the efficacy and safety of DEB-TACE combined with HAIC versus HAIC alone in patients with unresectable colorectal liver metastases (CRLM)
This study is a retrospective, non-randomized, single-arm, single-center clinical study. Patients who received DEB-TACE combined with HAIC or HAIC alone were screened from the treatment records of the Department of Interventional Radiology at Peking University Cancer Hospital between March 2015 and December 2023. The study aims to observe treatment efficacy, disease progression, and postoperative adverse reactions to evaluate the effectiveness and safety of combination therapy versus HAIC alone in patients with colorectal liver metastases (CRLM). Analyses will be conducted based on various parameters, including but not limited to HAIC perfusion regimens and drug-eluting bead tumor characteristics.
The primary endpoint of the study is progression-free survival (PFS). Secondary endpoints include overall survival (OS), objective response rate (ORR), disease control rate (DCR), and safety. PFS is defined as the time from the first DEB-TACE plus HAIC or HAIC-alone treatment to disease progression. PFS will be categorized into intrahepatic PFS and overall PFS.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| observed group | the patient treated with DEB-TACE combined with HAIC | ||
| Control group | the patient treated with HAIC only |
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| Measure | Description | Time Frame |
|---|---|---|
| Treatment efficacy-PFS | PFS is defined as the time from the date of the first DEB-TACE combined with HAIC or HAIC alone treatment to disease progression or death. PFS will be categorized into intrahepatic PFS and overall PFS. | 6-8 weeks after each treatment |
| Measure | Description | Time Frame |
|---|---|---|
| Treatment efficacy-OS | OS is defined as the time from the date of the first DEB-TACE combined with HAIC or HAIC alone treatment to death | Through study completion, an average of 1 year |
| Treatment efficacy-ORR |
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Inclusion Criteria:
Exclusion Criteria:
Presence of treatment risks or contraindications to DEB-TACE combined with HAIC or HAIC alone.
Concurrent diagnosis of other malignancies.
Underwent other local treatment modalities during the observation period.
DEB-TACE combined with HAIC or HAIC alone was used as postoperative adjuvant therapy.
Missing relevant examination results before or after treatment.
Incomplete imaging data, making response evaluation impossible.
Follow-up failure due to incorrect or missing patient information, loss to follow-up, or patient refusal.
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Patients with colorectal liver metastases who received DEB-TACE combined with HAIC or HAIC alone at the Department of Interventional Radiology, Peking University Cancer Hospital, between March 2015 and December 2023.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Aiwei Feng, MD | Contact | 88196476 | ivyfeng_1026@163.com |
| Name | Affiliation | Role |
|---|---|---|
| XU zhu, MD | Peking University Cancer Hospital & Institute | Principal Investigator |
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ORR=CR+PR
| 6-8 weeks after each treatment |
| Treatment efficacy-DCR | DCR=CR+PR+SD | 6-8 weeks after each treatment |
| treatment safety | the frequency of adverse events after treatment | within 30 days after each treatment |