Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer.
<h4>Background</h4>Preclinical data support further investigation of ascorbic acid in pancreatic cancer. There are currently insufficient safety data in human subjects, particularly when ascorbic acid is combined with chemotherapy.<h4>Methods and findings</h4>14 subjects with...
Guardado en:
Autores principales: | , , , , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Public Library of Science (PLoS)
2012
|
Materias: | |
Acceso en línea: | https://doaj.org/article/09b8615a61a7470da45dce0f0c6aad39 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:09b8615a61a7470da45dce0f0c6aad39 |
---|---|
record_format |
dspace |
spelling |
oai:doaj.org-article:09b8615a61a7470da45dce0f0c6aad392021-11-18T07:30:13ZPhase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer.1932-620310.1371/journal.pone.0029794https://doaj.org/article/09b8615a61a7470da45dce0f0c6aad392012-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/22272248/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Background</h4>Preclinical data support further investigation of ascorbic acid in pancreatic cancer. There are currently insufficient safety data in human subjects, particularly when ascorbic acid is combined with chemotherapy.<h4>Methods and findings</h4>14 subjects with metastatic stage IV pancreatic cancer were recruited to receive an eight week cycle of intravenous ascorbic acid (three infusions per week), using a dose escalation design, along with standard treatment of gemcitabine and erlotinib. Of 14 recruited subjects enrolled, nine completed the study (three in each dosage tier). There were fifteen non-serious adverse events and eight serious adverse events, all likely related to progression of disease or treatment with gemcitabine or erlotinib. Applying RECIST 1.0 criteria, seven of the nine subjects had stable disease while the other two had progressive disease.<h4>Conclusions</h4>These initial safety data do not reveal increased toxicity with the addition of ascorbic acid to gemcitabine and erlotinib in pancreatic cancer patients. This, combined with the observed response to treatment, suggests the need for a phase II study of longer duration.<h4>Trial registration</h4>Clinicaltrials.gov NCT00954525.Daniel A MontiEdith MitchellAnthony J BazzanSusan LittmanGeorge ZabreckyCharles J YeoMadhaven V PillaiAndrew B NewbergSandeep DeshmukhMark LevinePublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 7, Iss 1, p e29794 (2012) |
institution |
DOAJ |
collection |
DOAJ |
language |
EN |
topic |
Medicine R Science Q |
spellingShingle |
Medicine R Science Q Daniel A Monti Edith Mitchell Anthony J Bazzan Susan Littman George Zabrecky Charles J Yeo Madhaven V Pillai Andrew B Newberg Sandeep Deshmukh Mark Levine Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
description |
<h4>Background</h4>Preclinical data support further investigation of ascorbic acid in pancreatic cancer. There are currently insufficient safety data in human subjects, particularly when ascorbic acid is combined with chemotherapy.<h4>Methods and findings</h4>14 subjects with metastatic stage IV pancreatic cancer were recruited to receive an eight week cycle of intravenous ascorbic acid (three infusions per week), using a dose escalation design, along with standard treatment of gemcitabine and erlotinib. Of 14 recruited subjects enrolled, nine completed the study (three in each dosage tier). There were fifteen non-serious adverse events and eight serious adverse events, all likely related to progression of disease or treatment with gemcitabine or erlotinib. Applying RECIST 1.0 criteria, seven of the nine subjects had stable disease while the other two had progressive disease.<h4>Conclusions</h4>These initial safety data do not reveal increased toxicity with the addition of ascorbic acid to gemcitabine and erlotinib in pancreatic cancer patients. This, combined with the observed response to treatment, suggests the need for a phase II study of longer duration.<h4>Trial registration</h4>Clinicaltrials.gov NCT00954525. |
format |
article |
author |
Daniel A Monti Edith Mitchell Anthony J Bazzan Susan Littman George Zabrecky Charles J Yeo Madhaven V Pillai Andrew B Newberg Sandeep Deshmukh Mark Levine |
author_facet |
Daniel A Monti Edith Mitchell Anthony J Bazzan Susan Littman George Zabrecky Charles J Yeo Madhaven V Pillai Andrew B Newberg Sandeep Deshmukh Mark Levine |
author_sort |
Daniel A Monti |
title |
Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
title_short |
Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
title_full |
Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
title_fullStr |
Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
title_full_unstemmed |
Phase I evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
title_sort |
phase i evaluation of intravenous ascorbic acid in combination with gemcitabine and erlotinib in patients with metastatic pancreatic cancer. |
publisher |
Public Library of Science (PLoS) |
publishDate |
2012 |
url |
https://doaj.org/article/09b8615a61a7470da45dce0f0c6aad39 |
work_keys_str_mv |
AT danielamonti phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT edithmitchell phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT anthonyjbazzan phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT susanlittman phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT georgezabrecky phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT charlesjyeo phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT madhavenvpillai phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT andrewbnewberg phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT sandeepdeshmukh phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer AT marklevine phaseievaluationofintravenousascorbicacidincombinationwithgemcitabineanderlotinibinpatientswithmetastaticpancreaticcancer |
_version_ |
1718423330105589760 |