None listed
Conditions
Interventions
Drug : Colorectal cancer patients treated with minimally invasive surgery followed by adjuvant FOLFOX chemotherapy were randomly assigned to two groups: the FOLFOX group, FOLFOX on postoperative day (
the control group, FOLFOX on POD 21.
FOLFOX4 chemotherapy: Leucovorin 200 mg/m2 iv over 2 hrs before 5-FU, d1 and 2
5-FU 400 mg/m2 iv bolus and then 600 mg/m2 iv over 22 hrs, d 1 and d2
Oxaliplatin 85 mg/m2 iv d1
Blood sampling is performed preoperatively, and POD 3, POD 7-9, POD 9-11, POD 21.
Sponsors
Korea University Anam Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Inclusion criteria are aged 18-80, American Society of Anesthesiologists classification = 2, Clinical stage = 3, and laparoscopic or robotic surgery.
Exclusion criteria
Exclusion criteria: Exclusion criteria are preopeartive chemotherapy or radiotherapy, prior history of other cancer, major complications (Dindo classification =3), and not having postoperative FOLFOX4 chemotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| levels of plasma VEGF, Ang-1, Ang-2, TSP-1 | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety of early FOLFOX chemotherapy | — |
Countries
Korea, Republic of
Contacts
Public ContactByung Eun Yoo
Korea University Anam Hospital
Outcome results
None listed