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Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety

BACKGROUND: 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 complete...

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Autores principales: Villanueva, Luis, Anabalon, Jaime, Butte, Jean M, Salman, Pamela, Panay, Sergio, Milla, Elizabeth, Gallardo, Carlos, Hoefler, Sebastian, Charles, Roberto, Reyes, Felipe, Barajas, Olga, Matamala, Luis, Molina, Angelica, Portiño, Sergio, Berrios, Marcela, Caglevic, Christian, Mahave, Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cancer Intelligence 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929772/
https://www.ncbi.nlm.nih.gov/pubmed/33680082
http://dx.doi.org/10.3332/ecancer.2021.1168
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author Villanueva, Luis
Anabalon, Jaime
Butte, Jean M
Salman, Pamela
Panay, Sergio
Milla, Elizabeth
Gallardo, Carlos
Hoefler, Sebastian
Charles, Roberto
Reyes, Felipe
Barajas, Olga
Matamala, Luis
Molina, Angelica
Portiño, Sergio
Berrios, Marcela
Caglevic, Christian
Mahave, Mauricio
author_facet Villanueva, Luis
Anabalon, Jaime
Butte, Jean M
Salman, Pamela
Panay, Sergio
Milla, Elizabeth
Gallardo, Carlos
Hoefler, Sebastian
Charles, Roberto
Reyes, Felipe
Barajas, Olga
Matamala, Luis
Molina, Angelica
Portiño, Sergio
Berrios, Marcela
Caglevic, Christian
Mahave, Mauricio
author_sort Villanueva, Luis
collection PubMed
description BACKGROUND: 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/m(2) docetaxel intravenous (iv) on day 1, 85 mg/m(2) oxaliplatin iv on day 1, 200 mg/m(2) leucovorin iv on day 1 and 2,600 mg/m(2) 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.
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spelling pubmed-79297722021-03-05 Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety Villanueva, Luis Anabalon, Jaime Butte, Jean M Salman, Pamela Panay, Sergio Milla, Elizabeth Gallardo, Carlos Hoefler, Sebastian Charles, Roberto Reyes, Felipe Barajas, Olga Matamala, Luis Molina, Angelica Portiño, Sergio Berrios, Marcela Caglevic, Christian Mahave, Mauricio Ecancermedicalscience Clinical Study BACKGROUND: 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/m(2) docetaxel intravenous (iv) on day 1, 85 mg/m(2) oxaliplatin iv on day 1, 200 mg/m(2) leucovorin iv on day 1 and 2,600 mg/m(2) 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. Cancer Intelligence 2021-01-13 /pmc/articles/PMC7929772/ /pubmed/33680082 http://dx.doi.org/10.3332/ecancer.2021.1168 Text en © the authors; licensee ecancermedicalscience. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Villanueva, Luis
Anabalon, Jaime
Butte, Jean M
Salman, Pamela
Panay, Sergio
Milla, Elizabeth
Gallardo, Carlos
Hoefler, Sebastian
Charles, Roberto
Reyes, Felipe
Barajas, Olga
Matamala, Luis
Molina, Angelica
Portiño, Sergio
Berrios, Marcela
Caglevic, Christian
Mahave, Mauricio
Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
title Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
title_full Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
title_fullStr Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
title_full_unstemmed Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
title_short Total neoadjuvant chemotherapy with FLOT scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
title_sort total neoadjuvant chemotherapy with flot scheme in resectable adenocarcinoma of the gastro-oesophageal junction or gastric adenocarcinoma: impact on pathological complete response and safety
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7929772/
https://www.ncbi.nlm.nih.gov/pubmed/33680082
http://dx.doi.org/10.3332/ecancer.2021.1168
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