Cargando…

Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up

LESSONS LEARNED. Adding docetaxel to the modified FOLFOX7 backbone (DOF) is a feasible three‐drug combination therapy for advanced gastric cancer with high activity, providing evidence that leucovorin is not necessary in this setting. The DOF regimen represents an alternative to the FLOT (5‐FU 2,600...

Descripción completa

Detalles Bibliográficos
Autores principales: Rosenberg, Ari Joseph, Rademaker, Alfred, Hochster, Howard S., Ryan, Theresa, Hensing, Thomas, Shankaran, Veena, Baddi, Lisa, Mahalingam, Devalingam, Mulcahy, Mary F., Benson, Al B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693711/
https://www.ncbi.nlm.nih.gov/pubmed/31138725
http://dx.doi.org/10.1634/theoncologist.2019-0330
_version_ 1783443725365542912
author Rosenberg, Ari Joseph
Rademaker, Alfred
Hochster, Howard S.
Ryan, Theresa
Hensing, Thomas
Shankaran, Veena
Baddi, Lisa
Mahalingam, Devalingam
Mulcahy, Mary F.
Benson, Al B.
author_facet Rosenberg, Ari Joseph
Rademaker, Alfred
Hochster, Howard S.
Ryan, Theresa
Hensing, Thomas
Shankaran, Veena
Baddi, Lisa
Mahalingam, Devalingam
Mulcahy, Mary F.
Benson, Al B.
author_sort Rosenberg, Ari Joseph
collection PubMed
description LESSONS LEARNED. Adding docetaxel to the modified FOLFOX7 backbone (DOF) is a feasible three‐drug combination therapy for advanced gastric cancer with high activity, providing evidence that leucovorin is not necessary in this setting. The DOF regimen represents an alternative to the FLOT (5‐FU 2,600 mg/m(2) as 24‐hour infusion with leucovorin 200 mg/m(2), oxaliplatin 85 mg/m(2), and docetaxel 50 mg/m(2)) regimen that can be considered in select patients with advanced gastric cancer and is a potential choice in the curative setting. BACKGROUND. The combination of docetaxel, cisplatin, and 5‐fluorouracil (5‐FU) demonstrates high response rates in advanced gastric cancer, albeit with increased toxicity. Given the efficacy of platinum‐taxane‐fluoropyrimidine regimens, this phase II study evaluated the efficacy and toxicity of docetaxel, oxaliplatin, and 5‐FU (DOF) for the treatment of metastatic or unresectable gastric or gastroesophageal junction (GEJ) adenocarcinoma. METHODS. Patients with metastatic or unresectable gastric or GEJ adenocarcinoma with no prior therapy for metastatic disease received docetaxel 50 mg/m(2) on day 1, oxaliplatin 85 mg/m(2) on day 1, and 5‐FU 2,400 mg/m(2) continuous intravenous infusion over 46 hours; cycles were repeated every 2 weeks. The primary endpoint was overall response rate (ORR). RESULTS. Forty‐four patients were enrolled. Assessment of treatment response and toxicity was feasible in 41 and 43 patients, respectively. ORR was 73.2% (68.3% partial response; 4.9% complete response). Therapy was discontinued for progressive disease in 53%, toxicity in 26%, and death on treatment in 16%. Two patients underwent surgical resection. Thirty‐three patients (76.7%) received at least seven cycles (7–34). Grade 3–4 toxicities occurred in 31 patients (72.1%), including neutropenia (23.3%), neurologic (20.9%), and diarrhea (14.0%). Median overall survival was 10.3 months. CONCLUSION. DOF demonstrates a high response rate, expected safety profile, and prolonged survival and remains an option for select patients with unresectable or metastatic gastric or GEJ adenocarcinoma.
format Online
Article
Text
id pubmed-6693711
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-66937112019-08-17 Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up Rosenberg, Ari Joseph Rademaker, Alfred Hochster, Howard S. Ryan, Theresa Hensing, Thomas Shankaran, Veena Baddi, Lisa Mahalingam, Devalingam Mulcahy, Mary F. Benson, Al B. Oncologist Clinical Trial Results LESSONS LEARNED. Adding docetaxel to the modified FOLFOX7 backbone (DOF) is a feasible three‐drug combination therapy for advanced gastric cancer with high activity, providing evidence that leucovorin is not necessary in this setting. The DOF regimen represents an alternative to the FLOT (5‐FU 2,600 mg/m(2) as 24‐hour infusion with leucovorin 200 mg/m(2), oxaliplatin 85 mg/m(2), and docetaxel 50 mg/m(2)) regimen that can be considered in select patients with advanced gastric cancer and is a potential choice in the curative setting. BACKGROUND. The combination of docetaxel, cisplatin, and 5‐fluorouracil (5‐FU) demonstrates high response rates in advanced gastric cancer, albeit with increased toxicity. Given the efficacy of platinum‐taxane‐fluoropyrimidine regimens, this phase II study evaluated the efficacy and toxicity of docetaxel, oxaliplatin, and 5‐FU (DOF) for the treatment of metastatic or unresectable gastric or gastroesophageal junction (GEJ) adenocarcinoma. METHODS. Patients with metastatic or unresectable gastric or GEJ adenocarcinoma with no prior therapy for metastatic disease received docetaxel 50 mg/m(2) on day 1, oxaliplatin 85 mg/m(2) on day 1, and 5‐FU 2,400 mg/m(2) continuous intravenous infusion over 46 hours; cycles were repeated every 2 weeks. The primary endpoint was overall response rate (ORR). RESULTS. Forty‐four patients were enrolled. Assessment of treatment response and toxicity was feasible in 41 and 43 patients, respectively. ORR was 73.2% (68.3% partial response; 4.9% complete response). Therapy was discontinued for progressive disease in 53%, toxicity in 26%, and death on treatment in 16%. Two patients underwent surgical resection. Thirty‐three patients (76.7%) received at least seven cycles (7–34). Grade 3–4 toxicities occurred in 31 patients (72.1%), including neutropenia (23.3%), neurologic (20.9%), and diarrhea (14.0%). Median overall survival was 10.3 months. CONCLUSION. DOF demonstrates a high response rate, expected safety profile, and prolonged survival and remains an option for select patients with unresectable or metastatic gastric or GEJ adenocarcinoma. John Wiley & Sons, Inc. 2019-05-28 2019-08 /pmc/articles/PMC6693711/ /pubmed/31138725 http://dx.doi.org/10.1634/theoncologist.2019-0330 Text en © AlphaMed Press; the data published online to support this summary are the property of the authors
spellingShingle Clinical Trial Results
Rosenberg, Ari Joseph
Rademaker, Alfred
Hochster, Howard S.
Ryan, Theresa
Hensing, Thomas
Shankaran, Veena
Baddi, Lisa
Mahalingam, Devalingam
Mulcahy, Mary F.
Benson, Al B.
Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up
title Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up
title_full Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up
title_fullStr Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up
title_full_unstemmed Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up
title_short Docetaxel, Oxaliplatin, and 5‐Fluorouracil (DOF) in Metastatic and Unresectable Gastric/Gastroesophageal Junction Adenocarcinoma: A Phase II Study with Long‐Term Follow‐Up
title_sort docetaxel, oxaliplatin, and 5‐fluorouracil (dof) in metastatic and unresectable gastric/gastroesophageal junction adenocarcinoma: a phase ii study with long‐term follow‐up
topic Clinical Trial Results
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693711/
https://www.ncbi.nlm.nih.gov/pubmed/31138725
http://dx.doi.org/10.1634/theoncologist.2019-0330
work_keys_str_mv AT rosenbergarijoseph docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT rademakeralfred docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT hochsterhowards docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT ryantheresa docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT hensingthomas docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT shankaranveena docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT baddilisa docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT mahalingamdevalingam docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT mulcahymaryf docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup
AT bensonalb docetaxeloxaliplatinand5fluorouracildofinmetastaticandunresectablegastricgastroesophagealjunctionadenocarcinomaaphaseiistudywithlongtermfollowup