Total neoadjuvant chemotherapy with FLOT for resectable gastric and gastroesophageal junction adenocarcinoma: Real-world outcomes from a Chilean oncology institution.

L Luis Villanueva (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) S Sebastian Hoefler (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) M Maureen Callahan (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) A Alberto Caro (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) A Alex Contreras (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) J Jesus Rojas (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) M Macarena Vera M Maria Andrea Canals (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) P Paulina Leiva (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) C Claudia Sierra (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) N Nicole Caire (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) C Carlos Rojas (Bradford Hill Investigación Clínica, Santiago, Chile) R Rodrigo Uribe Maturana (Fundación Arturo López Pérez (FALP), Santiago, Chile) J Jean MIchel Butte (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago., Chile) R Roberto Charles (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile) M Mauricio Mahave (Instituto Oncologico Fundacion Arturo Lopez Perez, Providencia, Chile) M Manuel Meneses (Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago., Chile) C Christian Caglevic (Centro de Investigacion e Innovación en Cáncer Fundación Arturo López Pérez, Santiago, Chile)

Abstract

e15720 Background: Perioperative FLOT improves survival and pathological complete response (pCR) in resectable gastric cancer; however, postoperative chemotherapy completion remains suboptimal due to toxicity. Delivering all 8 cycles of FLOT chemotherapy preoperatively as total neoadjuvant therapy (TNT) may improve adherence and oncologic outcomes. We report safety, pathological response, and survival outcomes from a large Chilean real-world cohort treated with total neoadjuvant chemotherapy FLOT. Methods: We performed a retrospective cohort study of patients with resectable, locally advanced gastric or gastroesophageal junction adenocarcinoma (cT1–4 N+ or cT3–4 N0, M0) treated at Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile, between May 2019 and December 2024. All patients were planned to receive eight cycles of neoadjuvant FLOT chemotherapy prior to surgery. Clinical, pathological, and treatment-related variables were collected from institutional databases and medical records. Survival outcomes were estimated using the Kaplan–Meier method. Results: Ninety-one patients were included. Mean age was 58 years; 67% were male and 88% had ECOG performance status 0–1. 40.7% were diffusive pattern (signet ring cell). 74.8% patients were cT3-4 and 78% were cN+. The median number of administered FLOT cycles was 8. Grade ≥3 treatment-related adverse events occurred in 21.7%, most commonly gastrointestinal toxicity and neutropenia. Dose reductions were required in 41.8%, and permanent treatment discontinuation occurred in 17.6%. Most patients underwent total gastrectomy (76.9%) with D2 lymphadenectomy (94.5%). R0 resection was achieved in 97.8%. Pathological complete response was observed in 18.7%. 22% and 50.5% achieved ypT0 and ypN0 status respectively. The median follow-up was 43.8 months. 36-month overall survival was 78.2% and disease-free survival was 73.7%. Recurrence occurred in 22%, predominantly at distant sites such as peritoneal and liver metastases. Conclusions: Total neoadjuvant FLOT demonstrated acceptable toxicity, high complete response, R0 resection, and nodal clearance rates, and encouraging long-term survival in a real-world Chilean population. These findings support total neoadjuvant FLOT as a feasible and effective strategy for resectable gastric and gastroesophageal junction adenocarcinoma.

Article Details

Volume / Issue Vol. 44, Issue 16_suppl
Published June 01, 2026
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (18)

L

Luis Villanueva

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

S

Sebastian Hoefler

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

M

Maureen Callahan

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

A

Alberto Caro

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

A

Alex Contreras

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

J

Jesus Rojas

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

M

Macarena Vera

M

Maria Andrea Canals

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

P

Paulina Leiva

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

C

Claudia Sierra

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

N

Nicole Caire

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

C

Carlos Rojas

Bradford Hill Investigación Clínica, Santiago, Chile

R

Rodrigo Uribe Maturana

Fundación Arturo López Pérez (FALP), Santiago, Chile

J

Jean MIchel Butte

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago., Chile

R

Roberto Charles

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago, Chile

M

Mauricio Mahave

Instituto Oncologico Fundacion Arturo Lopez Perez, Providencia, Chile

M

Manuel Meneses

Instituto Oncologico Fundacion Arturo Lopez Perez, Santiago., Chile

C

Christian Caglevic

Centro de Investigacion e Innovación en Cáncer Fundación Arturo López Pérez, Santiago, Chile