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Authordc.contributor.authorVillanueva Olivares, Luis Marcelo
Authordc.contributor.authorAnabalón Tohá, Jaime Andrés
Authordc.contributor.authorButte Barrios, Jean M.
Authordc.contributor.authorSalman Boghikian, Pamela Victoria
Authordc.contributor.authorPanay, Sergio
Authordc.contributor.authorMilla, Elizabeth
Authordc.contributor.authorGallardo, Carlos
Authordc.contributor.authorHoefler Steffen, Sebastián Ernesto
Authordc.contributor.authorCharles, Roberto
Authordc.contributor.authorReyes, Felipe
Authordc.contributor.authorBarajas Barajas, Olga Beatriz
Authordc.contributor.authorMatamala, Luis
Authordc.contributor.authorMolina, Angálica
Authordc.contributor.authorPortiño Roa, Sergio Fabián
Authordc.contributor.authorBerríos, Marcela
Authordc.contributor.authorCaglevic Medina, Christian Lorenzo
Authordc.contributor.authorMahave Cáceres, Mauricio Rodrigo
Admission datedc.date.accessioned2021-12-01T12:10:29Z
Available datedc.date.available2021-12-01T12:10:29Z
Publication datedc.date.issued2020
Cita de ítemdc.identifier.citationEcancer 2021, 15:1168es_ES
Identifierdc.identifier.other10.3332/ECANCER.2021.1168
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/182965
Abstractdc.description.abstractBackground: Gastric cancer is the fifth cause of cancer incidence worldwide. Multidisciplinary approaches that improve the survival are needed. Perioperative chemotherapies show improvement in pathological complete remission (pCR) and overall survival (OS), but less than 50% of the patients completed the chemotherapeutic regimen. The recent 5-fluorouracil, leucovorin, oxaliplatin, docetaxel-4 (FLOT4) study shows OS 50 months and pCR 16.6%, but only 46% of the patients completed pre- and postoperative treatment. This case series report evaluated pCR and safety in patients that received complete preoperative chemotherapeutic with FLOT. Methods: Patients received eight cycles FLOT regimen before surgery. Each cycle comprised 50 mg/m2 docetaxel intravenous (iv) on day 1, 85 mg/m2 oxaliplatin iv on day 1, 200 mg/m2 leucovorin iv on day 1 and 2,600 mg/m2 5-fluorouracil iv in a 24-hour infusion on day 1, every 2 weeks. Results: Fifty-nine patients were evaluated, 58 patients received preoperative cycles. Thirty-one patients received all eight cycles of preoperative therapy. 65.5% patients presented any major adverse event. Thirty-nine patients underwent surgery. Thirty-three biopsy reports were obtained. Six patients (18.2%) presented pCR, 13 patients (39.4%) had no lymph node involvement. OS was 21.32 months. Patients with histology of signet ring carcinoma cells had a shorter survival than other histologies. Conclusion: Total neoadjuvant with FLOT chemotherapy presents an adequate safety profile, a similar pathologic regression rate, and a slightly higher rate of completing treatment to report in perioperative FLOT regimen studies. A prospective clinical study with suitable diagnostic, staging tools and an adequate follow-up may prove total neoadjuvant chemotherapy’s efficacy.es_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherCancer Intelligencees_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
Sourcedc.sourceEcancer Medical Sciencees_ES
Keywordsdc.subjectTotal neoadjuvant chemotherapyes_ES
Keywordsdc.subjectPreoperative chemotherapyes_ES
Keywordsdc.subjectFLOTes_ES
Keywordsdc.subjectGastric Canceres_ES
Keywordsdc.subjectAdenocarcinoma of the gastro-oesophageal junctiones_ES
Keywordsdc.subjectPathological responsees_ES
Títulodc.titleTotal neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safetyes_ES
Document typedc.typeArtículo de revistaes_ES
dc.description.versiondc.description.versionVersión publicada - versión final del editores_ES
dcterms.accessRightsdcterms.accessRightsAcceso abiertoes_ES
Catalogueruchile.catalogadorcfres_ES
Indexationuchile.indexArtículo de publicación SCOPUS


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Attribution-NonCommercial-NoDerivs 3.0 United States
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 United States