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Characteristics and survival of patients with advanced cancer and p53 mutations

P53 mutations are associated with invasive tumors in mouse models. We assessed the p53mutations and survival in patients with advanced cancer treated in the Phase I Program. Of 691 tested patients, 273 (39.5%) had p53 mutations. Patients with p53 mutations were older (p<.0001) and had higher numb...

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Autores principales: Said, Rabih, Ye, Yang, Hong, David S., Janku, Filip, Fu, Siqing, Naing, Aung, Wheler, Jennifer J., Kurzrock, Razelle, Thomas, Christoforos, Palmer, Gary A., Hess, Kenneth R., Aldape, Kenneth, Tsimberidou, Apostolia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116527/
https://www.ncbi.nlm.nih.gov/pubmed/25003695
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author Said, Rabih
Ye, Yang
Hong, David S.
Janku, Filip
Fu, Siqing
Naing, Aung
Wheler, Jennifer J.
Kurzrock, Razelle
Thomas, Christoforos
Palmer, Gary A.
Hess, Kenneth R.
Aldape, Kenneth
Tsimberidou, Apostolia M.
author_facet Said, Rabih
Ye, Yang
Hong, David S.
Janku, Filip
Fu, Siqing
Naing, Aung
Wheler, Jennifer J.
Kurzrock, Razelle
Thomas, Christoforos
Palmer, Gary A.
Hess, Kenneth R.
Aldape, Kenneth
Tsimberidou, Apostolia M.
author_sort Said, Rabih
collection PubMed
description P53 mutations are associated with invasive tumors in mouse models. We assessed the p53mutations and survival in patients with advanced cancer treated in the Phase I Program. Of 691 tested patients, 273 (39.5%) had p53 mutations. Patients with p53 mutations were older (p<.0001) and had higher numbers of liver metastases (p=.005). P53 mutations were associated with higher numbers of other aberrations; PTEN (p=.0005) and HER2 (p=.003)aberrations were more common in the p53 mutation group. No survival difference was observed between patients with p53 mutations and those with wild-type p53. In patients with wild-type p53 and other aberrations, patients treated with matched-therapy against the additional aberrations had longer survival compared to those treated with non-matched-therapy or those who received no therapy (median survival, 26.0 vs. 11.8 vs. 9.8 months, respectively; p= .0007). Results were confirmed in a multivariate analysis (p= .0002). In the p53 mutation group with additional aberrations, those who received matched-therapy against the additional aberrations had survival similar to those treated with non-matched-therapy or those who received no therapy (p=.15). In conclusion, our results demonstrated resistance to matched-targeted therapy to the other aberrations in patients with p53 mutations and emphasize the need to overcome this resistance.
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spelling pubmed-41165272014-08-04 Characteristics and survival of patients with advanced cancer and p53 mutations Said, Rabih Ye, Yang Hong, David S. Janku, Filip Fu, Siqing Naing, Aung Wheler, Jennifer J. Kurzrock, Razelle Thomas, Christoforos Palmer, Gary A. Hess, Kenneth R. Aldape, Kenneth Tsimberidou, Apostolia M. Oncotarget Research Paper P53 mutations are associated with invasive tumors in mouse models. We assessed the p53mutations and survival in patients with advanced cancer treated in the Phase I Program. Of 691 tested patients, 273 (39.5%) had p53 mutations. Patients with p53 mutations were older (p<.0001) and had higher numbers of liver metastases (p=.005). P53 mutations were associated with higher numbers of other aberrations; PTEN (p=.0005) and HER2 (p=.003)aberrations were more common in the p53 mutation group. No survival difference was observed between patients with p53 mutations and those with wild-type p53. In patients with wild-type p53 and other aberrations, patients treated with matched-therapy against the additional aberrations had longer survival compared to those treated with non-matched-therapy or those who received no therapy (median survival, 26.0 vs. 11.8 vs. 9.8 months, respectively; p= .0007). Results were confirmed in a multivariate analysis (p= .0002). In the p53 mutation group with additional aberrations, those who received matched-therapy against the additional aberrations had survival similar to those treated with non-matched-therapy or those who received no therapy (p=.15). In conclusion, our results demonstrated resistance to matched-targeted therapy to the other aberrations in patients with p53 mutations and emphasize the need to overcome this resistance. Impact Journals LLC 2014-05-25 /pmc/articles/PMC4116527/ /pubmed/25003695 Text en Copyright: © 2014 Said et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Said, Rabih
Ye, Yang
Hong, David S.
Janku, Filip
Fu, Siqing
Naing, Aung
Wheler, Jennifer J.
Kurzrock, Razelle
Thomas, Christoforos
Palmer, Gary A.
Hess, Kenneth R.
Aldape, Kenneth
Tsimberidou, Apostolia M.
Characteristics and survival of patients with advanced cancer and p53 mutations
title Characteristics and survival of patients with advanced cancer and p53 mutations
title_full Characteristics and survival of patients with advanced cancer and p53 mutations
title_fullStr Characteristics and survival of patients with advanced cancer and p53 mutations
title_full_unstemmed Characteristics and survival of patients with advanced cancer and p53 mutations
title_short Characteristics and survival of patients with advanced cancer and p53 mutations
title_sort characteristics and survival of patients with advanced cancer and p53 mutations
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4116527/
https://www.ncbi.nlm.nih.gov/pubmed/25003695
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