Phase 3Terminated

Preoperative FOLFOX Versus Postoperative Risk-adapted Chemotherapy in Patients With Locally Advanced Rectal Cancer

Preoperative FOLFOX Versus Postoperative Risk-adapted Chemotherapy in Patients With Locally Advanced Rectal Cancer and Low Risk for Local Failure: A Randomized Phase III Trial of the German Rectal Cancer Study Group

Sponsor
Ralf Hofheinz (Academic or other)
Enrolment
215 enrolled
Conditions
Rectal Cancer
Interventions
mFOLFOX (neoadjuvant); XELOX (neoadjuvant); mFOLFOX (adjuvant); XELOX (adjuvant); Capecitabine (adjuvant); infusional 5-FU/FA "AIO" regimen (adjuvant); infusional 5-FU/FA "de Gramont" (adjuvant)
Ages
adults, older adults
Registry
NCT04495088, EUCTR2018-001356-35

Full record on ClinicalTrials.gov

From the registry

This is a multicenter, prospective, randomized, stratified, controlled, open-label study comparing preoperative FOLFOX versus postoperative risk-adapted chemotherapy in patients with locally advanced rectal cancer and low risk for local failure

Primary outcomes

  • disease-free survival

History

  1. Last registry update

  2. Primary completion

  3. Started

  4. Registered