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DOI 10.1186/s12885-026-15682-3

Медицинская библиотека · BMC cancer · 2026

PROTECTOR / FIRE‑10: study protocol for a prospective, randomized, open-label, multicenter phase III trial to investigate the efficacy of preoperative systemic therapy in advanced colon cancer.

Siegel Robert, Dittrich Luca, Plewe Julius, Denecke Timm, Leonhardi Jakob, Tannapfel Andrea, Reinacher-Schick Anke, Raschzok Nathanael, Sauer Igor Maximilian, Lauscher Johannes, Lorenzen Sylvie, Götze Thorsten, Jelas Ivan, Stahler Arndt, Kurreck Annika, Ballhausen Alexej, Ostendorf Benjamin Nils, Haase Oliver, Pratschke Johann, Stintzing Sebastian, Modest Dominik Paul

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Аннотация

BACKGROUND

Standard of care for non-metastatic colon cancer is surgery followed by stage-guided adjuvant therapy and/or structured follow-up. Upfront surgery in resectable colon cancer is irrespective of local T/N stage, whereas adjuvant systemic therapy is recommended according to pathological staging. The role of neoadjuvant chemotherapy remains unclear. Whereas perioperative systemic therapy in colon cancer seems to be safe and may lead to pathologic downstaging, evidence on improved survival and quality of life remains scarce. The PROTECTOR / FIRE‑10 trial aims to generate evidence that perioperative systemic therapy improves survival without compromising quality of life in locally advanced, mismatch-repair proficient colon cancer patients. METHODS AND

DESIGN

Open-label, randomized, controlled, multicenter, phase III study with two parallel arms. Patients with locally advanced colon or upper rectal cancer staged cT3-4 and/or cN+ are randomized in a 2:1 fashion (favoring preoperative therapy) to investigate the efficacy, patient reported quality of life, and safety of preoperative therapy followed by surgery (Arm A) versus direct surgery followed by non-study specific stage-guided adjuvant therapy (Arm B). Stratification during randomization will be performed according to the following parameters: Fit for mFOLFOXIRI vs. mFOLFOX/CAPOX vs. 80%-mFOLFOX/CAPOX, ECOG 0 vs. ECOG 1-2, and left-sided primary vs. right-sided primary tumor. Only patients with confirmed mismatch-repair proficient and/or microsatellite stable tumor can be included. Preoperative treatment in Arm A is performed for a maximum of 6 biweekly cycles of FOLFOX/FOLFOXIRI or for a maximum of 4 triweekly cycles CAPOX (i.e., appr. 12 weeks). Patients in both arms should undergo quality-controlled surgery of the primary tumor, performed as complete mesocolic excision. Patients will be followed up with regard to relapse, survival and if applicable subsequent anti-cancer treatments until death or for at least 5 years after randomization, whichever date is earlier. DISCUSSION: The PROTECTOR / FIRE‑10 trial compares preoperative systemic therapy to upfront surgery (with stage-guided adjuvant therapy) in patients with locally advanced colon cancer. TRIAL REGISTRATION: This study is registered with clinicaltrials.gov (NCT06899477) and EudraCT (2023-508076-11-00).

Для цитирования: Siegel Robert, Dittrich Luca, Plewe Julius, Denecke Timm, Leonhardi Jakob, Tannapfel Andrea, Reinacher-Schick Anke, Raschzok Nathanael, Sauer Igor Maximilian, Lauscher Johannes, Lorenzen Sylvie, Götze Thorsten, Jelas Ivan, Stahler Arndt, Kurreck Annika, Ballhausen Alexej, Ostendorf Benjamin Nils, Haase Oliver, Pratschke Johann, Stintzing Sebastian, Modest Dominik Paul. PROTECTOR / FIRE‑10: study protocol for a prospective, randomized, open-label, multicenter phase III trial to investigate the efficacy of preoperative systemic therapy in advanced colon cancer.. BMC cancer. 2026. DOI: 10.1186/s12885-026-15682-3.

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