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...

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Autores principales: 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
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Publicado: Public Library of Science (PLoS) 2012
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Acceso en línea:https://doaj.org/article/09b8615a61a7470da45dce0f0c6aad39
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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
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