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Preoperative Transhepatic Arterial Chemotherapy (TAC) in the Treatment of Liver Metastasis of Resectable Colorectal Cancer

Preoperative Transhepatic Arterial Chemotherapy in the Treatment of Liver Metastasis of Resectable Colorectal Cancer

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00874406
Enrollment
100
Registered
2009-04-02
Start date
2008-01-31
Completion date
2009-12-31
Last updated
2009-04-02

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

Conditions

Colorectal Cancer

Keywords

colorectal cancer, liver metastasis, neoadjuvant chemotherapy

Brief summary

The purpose of this study is to investigate whether preoperative TAC is able to improve progression free survival and overall survival in patients receiving liver metastasis resection of colorectal cancer.

Detailed description

We administered TAC(oxaliplatin,FUDR and MMC) 7 days before liver metastasis resection of colorectal cancer. The study endpoints were progression free survival and overall survival as evaluated by intent-to-treat analysis.

Interventions

tac: oxaliplatin 100mg + fudr 1g + mmc 10mg 7 days later: operation within 28 days after operation: folfox4

folfox4 will be done within 28 days after liver resection

Sponsors

Fudan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* age \<= 75 years * resectable liver metastasis * remnant liver volume \>= 70% * without other organ metastasis or peritoneum metastasis * without contradiction of cardiac and pulmonary diseases

Exclusion criteria

* age \> 75 years * unresectable liver metastasis * remnant liver volume \< 50% * with other organ metastasis or peritoneum metastasis * with contradiction of cardiac and pulmonary diseases

Design outcomes

Primary

MeasureTime frame
progression free survival5 years after operation

Secondary

MeasureTime frame
overall survival5 years after operation

Countries

China

Contacts

Primary Contactjianmin xu, MD, PHD
xujmin@yahoo.com.cn008613501984869

Outcome results

None listed

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