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Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer

The purpose of this study was to evaluate the effect of obesity and obesity-associated factors on the outcomes of patients with cervical cancer. Outcomes were evaluated in 591 patients with FIGO Ib to IV cervical cancer treated uniformly with definitive radiation. Patients were stratified into 3 gro...

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Autores principales: Grigsby, Perry, Elhammali, Adnan, Ruiz, Fiona, Markovina, Stephanie, McLellan, Michael D., Miller, Christopher A., Chundury, Anupama, Ta, Ngoc-Anh L., Rashmi, Ramachandran, Pfeifer, John D., Fulton, Robert S., DeWees, Todd, Schwarz, Julie K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790521/
https://www.ncbi.nlm.nih.gov/pubmed/29423104
http://dx.doi.org/10.18632/oncotarget.23664
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author Grigsby, Perry
Elhammali, Adnan
Ruiz, Fiona
Markovina, Stephanie
McLellan, Michael D.
Miller, Christopher A.
Chundury, Anupama
Ta, Ngoc-Anh L.
Rashmi, Ramachandran
Pfeifer, John D.
Fulton, Robert S.
DeWees, Todd
Schwarz, Julie K.
author_facet Grigsby, Perry
Elhammali, Adnan
Ruiz, Fiona
Markovina, Stephanie
McLellan, Michael D.
Miller, Christopher A.
Chundury, Anupama
Ta, Ngoc-Anh L.
Rashmi, Ramachandran
Pfeifer, John D.
Fulton, Robert S.
DeWees, Todd
Schwarz, Julie K.
author_sort Grigsby, Perry
collection PubMed
description The purpose of this study was to evaluate the effect of obesity and obesity-associated factors on the outcomes of patients with cervical cancer. Outcomes were evaluated in 591 patients with FIGO Ib to IV cervical cancer treated uniformly with definitive radiation. Patients were stratified into 3 groups based upon pretreatment Body Mass Index (BMI): A ≤ 18.5; B 18.6 – 34.9; and C ≥ 35. The 5-year freedom from failure rates were 58, 59, and 73% for BMI groups A, B, and C (p = 0.01). Overall survival rates were 50, 59, and 68%, respectively (p = 0.02). High expression of phosphorylated AKT (pAKT) was associated with poor outcomes only in non-obese patients. Obese patients with PI3K pathway mutant tumors had a trend toward favorable outcomes, while a similar effect was not observed in non-obese patients. Compared to similar tumors from non-obese hosts, PIK3CA and PTEN mutant tumors from obese patients failed to express high levels of phosphorylated AKT and its downstream targets. These results show that patients with obesity at the time of diagnosis of cervical cancer exhibit improved outcomes after radiation. PI3K/AKT pathway mutations are common in obese patients, but are not associated with activation of AKT signaling.
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spelling pubmed-57905212018-02-08 Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer Grigsby, Perry Elhammali, Adnan Ruiz, Fiona Markovina, Stephanie McLellan, Michael D. Miller, Christopher A. Chundury, Anupama Ta, Ngoc-Anh L. Rashmi, Ramachandran Pfeifer, John D. Fulton, Robert S. DeWees, Todd Schwarz, Julie K. Oncotarget Research Paper The purpose of this study was to evaluate the effect of obesity and obesity-associated factors on the outcomes of patients with cervical cancer. Outcomes were evaluated in 591 patients with FIGO Ib to IV cervical cancer treated uniformly with definitive radiation. Patients were stratified into 3 groups based upon pretreatment Body Mass Index (BMI): A ≤ 18.5; B 18.6 – 34.9; and C ≥ 35. The 5-year freedom from failure rates were 58, 59, and 73% for BMI groups A, B, and C (p = 0.01). Overall survival rates were 50, 59, and 68%, respectively (p = 0.02). High expression of phosphorylated AKT (pAKT) was associated with poor outcomes only in non-obese patients. Obese patients with PI3K pathway mutant tumors had a trend toward favorable outcomes, while a similar effect was not observed in non-obese patients. Compared to similar tumors from non-obese hosts, PIK3CA and PTEN mutant tumors from obese patients failed to express high levels of phosphorylated AKT and its downstream targets. These results show that patients with obesity at the time of diagnosis of cervical cancer exhibit improved outcomes after radiation. PI3K/AKT pathway mutations are common in obese patients, but are not associated with activation of AKT signaling. Impact Journals LLC 2017-12-23 /pmc/articles/PMC5790521/ /pubmed/29423104 http://dx.doi.org/10.18632/oncotarget.23664 Text en Copyright: © 2018 Grigsby et al. 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/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Grigsby, Perry
Elhammali, Adnan
Ruiz, Fiona
Markovina, Stephanie
McLellan, Michael D.
Miller, Christopher A.
Chundury, Anupama
Ta, Ngoc-Anh L.
Rashmi, Ramachandran
Pfeifer, John D.
Fulton, Robert S.
DeWees, Todd
Schwarz, Julie K.
Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer
title Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer
title_full Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer
title_fullStr Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer
title_full_unstemmed Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer
title_short Clinical outcomes and differential effects of PI3K pathway mutation in obese versus non-obese patients with cervical cancer
title_sort clinical outcomes and differential effects of pi3k pathway mutation in obese versus non-obese patients with cervical cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5790521/
https://www.ncbi.nlm.nih.gov/pubmed/29423104
http://dx.doi.org/10.18632/oncotarget.23664
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