Safety and efficacy of a docetaxel-5FU-oxaliplatin regimen with or without trastuzumab in neoadjuvant treatment of localized gastric or gastroesophageal junction cancer: A retrospective study.

Gastric cancer Neoadjuvant chemotherapy Retrospective study TeFOX

Journal

World journal of gastrointestinal oncology
ISSN: 1948-5204
Titre abrégé: World J Gastrointest Oncol
Pays: China
ID NLM: 101532470

Informations de publication

Date de publication:
15 Aug 2019
Historique:
received: 18 03 2019
revised: 07 06 2019
accepted: 20 06 2019
entrez: 23 8 2019
pubmed: 23 8 2019
medline: 23 8 2019
Statut: ppublish

Résumé

Triplet chemotherapy, with docetaxel-5FU-oxaliplatin FLOT regimen recently became the standard perioperative treatment for localized gastric cancer (GC). An adapted regimen called TeFOX was recently tested in metastatic setting and gave promising results. To determine safety and efficacy of TeFOX perioperative regimen. This monocentric retrospective study aims to test efficacy and safety of the perioperative TeFOX regimen given alone or in combination with trastuzumab in patients with localized GC. TeFOX consist in docetaxel (50 mg/m²) with oxaliplatin 85 mg/m² and and leucovorin (400 mg/m Thirty-three consecutive patients were included in this retrospective study. Eighteen patients have a gastroesophageal junction cancer and 11 have a GC. Median follow-up of surviving patients was 32 mo. R0 resection was obtained in 30 (91) patients. Twelve patients (36) had a pathological complete response and 8 (24) patients a nearly complete pathological response. Median OS and PFS were not reached at data base lock. We have observed 6 metastatic relapses and 1 localized relapse. No relapse was observed in patients with pathological complete responses. The most common grade 3-4 adverse events were peripheral neuropathy (21) and asthenia (20). TeFOX regimen could be safely administrated in perioperative treatment of localized GC. TeFOX and the FLOT regimen have comparable efficacy and safety profiles.

Sections du résumé

BACKGROUND BACKGROUND
Triplet chemotherapy, with docetaxel-5FU-oxaliplatin FLOT regimen recently became the standard perioperative treatment for localized gastric cancer (GC). An adapted regimen called TeFOX was recently tested in metastatic setting and gave promising results.
AIM OBJECTIVE
To determine safety and efficacy of TeFOX perioperative regimen.
METHODS METHODS
This monocentric retrospective study aims to test efficacy and safety of the perioperative TeFOX regimen given alone or in combination with trastuzumab in patients with localized GC. TeFOX consist in docetaxel (50 mg/m²) with oxaliplatin 85 mg/m² and and leucovorin (400 mg/m
RESULTS RESULTS
Thirty-three consecutive patients were included in this retrospective study. Eighteen patients have a gastroesophageal junction cancer and 11 have a GC. Median follow-up of surviving patients was 32 mo. R0 resection was obtained in 30 (91) patients. Twelve patients (36) had a pathological complete response and 8 (24) patients a nearly complete pathological response. Median OS and PFS were not reached at data base lock. We have observed 6 metastatic relapses and 1 localized relapse. No relapse was observed in patients with pathological complete responses. The most common grade 3-4 adverse events were peripheral neuropathy (21) and asthenia (20).
CONCLUSION CONCLUSIONS
TeFOX regimen could be safely administrated in perioperative treatment of localized GC. TeFOX and the FLOT regimen have comparable efficacy and safety profiles.

Identifiants

pubmed: 31435464
doi: 10.4251/wjgo.v11.i8.634
pmc: PMC6700033
doi:

Types de publication

Journal Article

Langues

eng

Pagination

634-641

Déclaration de conflit d'intérêts

Conflict-of-interest statement: All authors have no conflict of interests.

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Auteurs

Valeria Basso (V)

Department of Surgery, Centre Georges Francois Leclerc, Dijon 21000, France.

David Orry (D)

Department of Surgery, Centre Georges Francois Leclerc, Dijon 21000, France.

Jean Fraisse (J)

Department of Surgery, Centre Georges Francois Leclerc, Dijon 21000, France.

Julie Vincent (J)

Department of Medical Oncology, Centre Georges Francois Leclerc, Dijon 21000, France.

Audrey Hennequin (A)

Department of Medical Oncology, Centre Georges Francois Leclerc, Dijon 21000, France.

Leila Bengrine (L)

Department of Medical Oncology, Centre Georges Francois Leclerc, Dijon 21000, France.

Francois Ghiringhelli (F)

Department of Medical Oncology, Centre Georges Francois Leclerc, Dijon 21000, France. fghiringhelli@cgfl.fr.

Classifications MeSH