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Upper GI: Perioperative chemotherapy gastric (FLOT4 vs MAGIC)

Free question published 17 August 2026

Upper GIPerioperative chemotherapy gastric (FLOT4 vs MAGIC)

A 58-year-old man has a cT3N1M0 adenocarcinoma of the gastric body. He is fit (WHO performance status 0) with no significant comorbidity and is planned for radical gastrectomy with perioperative chemotherapy. Which perioperative chemotherapy regimen should be preferred?

  1. AGemcitabine and capecitabine (GEMCAP)
  2. BEpirubicin, cisplatin and capecitabine (ECX)
  3. CEpirubicin, cisplatin and 5-fluorouracil (ECF)
  4. DFluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT)
  5. ECisplatin and capecitabine plus trastuzumab

Why D is correct

The FLOT4 trial showed that perioperative FLOT improved median overall survival to 50 months versus 35 months with ECF/ECX (HR 0.77; p=0.012) and achieved a higher pathological complete response rate (16% versus 6%) in resectable gastric or gastro-oesophageal junction adenocarcinoma. FLOT is therefore the preferred perioperative regimen for fit patients, superseding the MAGIC (ECF) regimen.

And why the others are not

  • AGEMCAP is an induction regimen in locally advanced pancreatic cancer (SCALOP), not a perioperative gastric cancer regimen.
  • BECX was part of the ECF/ECX comparator arm shown to be inferior to FLOT in FLOT4.
  • CECF was the comparator (MAGIC-type) arm in FLOT4 and was inferior to FLOT for both survival and pathological response.
  • ECisplatin-capecitabine plus trastuzumab is the regimen for HER2-positive metastatic disease, not the standard perioperative regimen for localised gastric cancer.

Source FLOT4 - Perioperative FLOT versus ECF/ECX in resectable gastric or GOJ adenocarcinomaAl-Batran SE, Homann N, Pauligk C, et al. Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): a randomised, phase 2/3 trial. Lancet. 2019;393(10184):1948-1957.

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