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Adjuvant Therapy(3 vs. 6 Months) With the FOLFOX 4 or XELOX for Stage II or Stage III Colon Cancer

A Multicenter Trial Investigating the Duration of Adjuvant Therapy(3 vs. 6 Months) With the FOLFOX 4 or XELOX Regimen for Patients With High Risk Stage II or Stage III Colon Cancer

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01308086
Enrollment
2000
Registered
2011-03-03
Start date
2010-10-31
Completion date
2017-12-31
Last updated
2017-08-09

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

Conditions

CRC

Keywords

Cancer, colorectal cancer, adjuvant chemotherapy, capecitabine, oxaliplatin, 5 fluorouracil

Brief summary

The purpose of this study is to compare whether a 3-month treatment is at least not inferior to a 6-month treatment (FOLFOX-4 6 vs. 12 cycles or XELOX 4 cycles vs. 8 cycles) in terms of RFS in patients with high risk stage II or stage III radically resected colon cancer.

Detailed description

Six months of adjuvant chemotherapy with 5-FU and oxaliplatin for patients with stage III colon cancer is the world-wide standard of care, based on the MOSAIC and C-07 trials. However, it leads to significant cost, toxicity, and inconvenience. In particular, the onset of oxaliplatin induced cumulative dose-dependent neuropathies is a significant issue. The ability to maintain efficacy with a reduced duration of therapy would have clear advantage to patients, to providers, and to the health care system. Multiple large trials in the 1990s demonstrated that the previous standard of 12 months of therapy could be reduced to 6 months. A single small trial with 5-FU alone demonstrated similar outcomes for 3 versus 6 months of therapy. Thus, it is proposed to definitively evaluate the non-inferiority of 3 months of oxaliplatin-based adjuvant chemotherapy versus the current standard of 6 months. The primary endpoint will be disease-free survival (DFS). It is essential to have sufficient power to eliminate the possibility of clinically meaningful inferiority of 3 months of therapy: a huge number of patients will be necessary. Previous efforts and experience have conclusively demonstrated that in colon cancer, a single, global trial is impractical. Consequently, an international, prospective pooled analysis will be performed, gathering data of independent trials run in different countries, to answer the single primary hypothesis that 3 months of adjuvant therapy with FOLFOX/XELOX is non-inferior to the current standard of 6 months. Among six planned countries, the Greek intergroup will conduct one of these trials.

Interventions

DRUG5-Fluorouracil

5-FU 400mg/m2 Bolus and then 22 hours 5-FU 600mg/m2 IV, days 1 & 2, q2w, for 12 cycles

DRUGLeucovorin

Leucovorin 200mg/m2 IV in 2 hours, days 1 & 2, q2w, for 12 cycles

DRUGOxaliplatin

Oxaliplatin 85mg/m2 in 2 hours IV, day 1, q2w, for 12 cycles

DRUGCapecitabine

Capecitabine 1000 mg/m2 X 2 ,days 1-14, q2w, for 8 cycles

Sponsors

University Hospital of Crete
CollaboratorOTHER
Hellenic Oncology Research Group
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Histologically- - confirmed adenocarcinoma of the colon or rectum stage III or stage with at least one of the follow characteristics T4 tumours, undifferentiated tumor grade \>3, bowel obstruction or perforation, vascular or lymphatic or perineural invasion, \<12 nodes examined, Stage IV. * Signed written informed consent * Randomization between 2 -8 weeks after curative surgery * Age \>18 years * ECOG performance Status 0-1 * Pretreatment CEA within UNL * Post-menopausal women or women willing to accept the use of an effective contraception. Pre-menopausal women should have a negative pregnancy test within 72 hours prior to randomization * Men should also accept to use an effective contraception * R0 resections

Exclusion criteria

* Evidence of metastatic disease (including presence of tumor cells in ascites or peritoneal carcinomatosis resected en bloc) * Evidence of other malignancies within the last 5 years (other than curatively treated basal cell carcinoma of the skin and/or in situ carcinoma of the cervix) * No pregnant or lactating women * Presence of clinically relevant cardiovascular disease * Presenc of medical history or current evidence of CNS disease * Presence of peripheral neuropathy ≤ grade 1 (CTCAE v. 3.0) * History of clinically relevant psychiatric disability, precluding informed consent

Design outcomes

Primary

MeasureTime frame
Relapse Free Survival3-years

Secondary

MeasureTime frameDescription
Overall Survival3-years
Safety Profil according to NCI-CTAE v 3.0q2wPercentage (%) of treatments delays and interaptions in each arm Percentage (%) of dose received versus planned dose in each arm

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026