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OncoMatch/Clinical Trials/NCT05194878

Neoadjuvant FOLFOXIRI Versus Immediate Surgery for Stage II and III Colon Cancers

Is NCT05194878 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including neoadjuvant chemotherapyI and adjuvant chemotherapy for colon cancer stage ii.

Phase 3RecruitingSun Yat-sen UniversityNCT05194878Data as of May 2026

Treatment: neoadjuvant chemotherapyI · adjuvant chemotherapyBACKGROUND: In patients with high risk stage II and stage III colon cancer (CC), curative surgery followed by adjuvant chemotherapy with FOLFOX or CAPOX regimens has become a standard treatment. However, 20 to 30 % of these patients will develop distant metastasis, which ultimately result in death. Perioperative chemotherapy is a promising strategy with potential benefits that could be more effective at eradicating micrometastases. Moreover, shrinking tumor before surgery not only facilitate removal of all the tumor by the surgeon but also reduce tumor cell spreading during the procedure. With recent advances in radiology, preoperative computed tomography allows a good prediction of tumor stage (wall penetration and nodal involvement) prior to surgery. The investigators conducted the present randomized study to explore whether perioperative chemotherapy with FOLFOXIRI regimen compared with postoperative chemotherapy could improve disease-free survival in patients with radiologically staged, High-risk, but resectable Stage II or III colon cancer. OBJECTIVE: The primary objective of this study is to evaluate the efficacy of perioperative chemotherapy with FOLFOXIRI regimen compared to postoperative chemotherapy in patients with High-risk Resectable Stage II and III colon cancer. Secondary objectives are efficacy in terms of R0 resection rate, overall survival (OS), relapse-free survival (RFS), down-staging of primary tumors, and tolerability of perioperative therapy and postoperative complications.

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Extracted eligibility criteria

Cancer type

Colorectal Cancer

Biomarker criteria

Required: MMR proficient MMR

pMMR in immunohistochemical detection

Required: MSI MSI-H

MSI-H in MSI test

Excluded: MMR deficient MMR

dMMR in immunohistochemical detection [excluded]

Excluded: MSI MSI-L/MS-S

MSI-L/MS-S in MSI test [excluded]

Disease stage

Required: Stage II, III

Performance status

ECOG 0–1(Restricted strenuous activity)

Lab requirements

Blood counts

WBC >3.0 x109/l; Plts >100 x109/l. Anaemia (Hb < 10.0 g/dl) is not an exclusion, but should be corrected by transfusion prior to surgery and chemotherapy. If Hb remains low despite transfusions, surgery and chemotherapy can be given at the decision of the surgical and oncology teams.

Kidney function

serum creatinine was less than 1.5 times the normal value

Liver function

serum total bilirubin and ALT were less than 1.5 times the normal value

Adequate full blood count: WBC >3.0 x109/l; Plts >100 x109/l. Anaemia (Hb < 10.0 g/dl) is not an exclusion, but should be corrected by transfusion prior to surgery and chemotherapy. If Hb remains low despite transfusions, surgery and chemotherapy can be given at the decision of the surgical and oncology teams. Adequate renal biochemistry: serum creatinine was less than 1.5 times the normal value. Adequate hepatobiliary function: serum total bilirubin and ALT were less than 1.5 times the normal value.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

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