Tumor heterogeneity in the clinic: is it a real problem?

Tumor heterogeneity is one of the major problems limiting the efficacy of targeted therapies and compromising treatment outcomes. A better understanding of tumor biology has advanced our knowledge of the molecular landscape of cancer to an unprecedented level. However, most patients with advanced ca...

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Main Author: Filip Janku
Format: Article
Language:English
Published: SAGE Publishing 2014-03-01
Series:Therapeutic Advances in Medical Oncology
Online Access:https://doi.org/10.1177/1758834013517414
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spelling doaj-cb8a9719eefd4387b07dc699dcd577822020-11-25T03:40:13ZengSAGE PublishingTherapeutic Advances in Medical Oncology1758-83401758-83592014-03-01610.1177/1758834013517414Tumor heterogeneity in the clinic: is it a real problem?Filip JankuTumor heterogeneity is one of the major problems limiting the efficacy of targeted therapies and compromising treatment outcomes. A better understanding of tumor biology has advanced our knowledge of the molecular landscape of cancer to an unprecedented level. However, most patients with advanced cancers treated with appropriately selected targeted therapies become resistant to the therapy, ultimately developing disease progression and succumbing to metastatic disease. Multiple factors account for therapeutic failures, which include cancer cells accumulating new molecular aberrations as a consequence of tumor progression and selection pressure of cancer therapies. Therefore, single agent targeted therapies, often administered in advanced stages, are unlikely to have a sufficiently lethal effect in most cancers. Finally, the molecular profile of cancer can change over time, which we are not able to monitor with existing strategies using tumor tissue biopsies as the gold standard for molecular diagnostics. Novel technologies focusing on testing low-risk, easily obtainable material, such as molecular cell-free DNA from plasma, can fill that gap and allow personalized therapy to be delivered in real time.https://doi.org/10.1177/1758834013517414
collection DOAJ
language English
format Article
sources DOAJ
author Filip Janku
spellingShingle Filip Janku
Tumor heterogeneity in the clinic: is it a real problem?
Therapeutic Advances in Medical Oncology
author_facet Filip Janku
author_sort Filip Janku
title Tumor heterogeneity in the clinic: is it a real problem?
title_short Tumor heterogeneity in the clinic: is it a real problem?
title_full Tumor heterogeneity in the clinic: is it a real problem?
title_fullStr Tumor heterogeneity in the clinic: is it a real problem?
title_full_unstemmed Tumor heterogeneity in the clinic: is it a real problem?
title_sort tumor heterogeneity in the clinic: is it a real problem?
publisher SAGE Publishing
series Therapeutic Advances in Medical Oncology
issn 1758-8340
1758-8359
publishDate 2014-03-01
description Tumor heterogeneity is one of the major problems limiting the efficacy of targeted therapies and compromising treatment outcomes. A better understanding of tumor biology has advanced our knowledge of the molecular landscape of cancer to an unprecedented level. However, most patients with advanced cancers treated with appropriately selected targeted therapies become resistant to the therapy, ultimately developing disease progression and succumbing to metastatic disease. Multiple factors account for therapeutic failures, which include cancer cells accumulating new molecular aberrations as a consequence of tumor progression and selection pressure of cancer therapies. Therefore, single agent targeted therapies, often administered in advanced stages, are unlikely to have a sufficiently lethal effect in most cancers. Finally, the molecular profile of cancer can change over time, which we are not able to monitor with existing strategies using tumor tissue biopsies as the gold standard for molecular diagnostics. Novel technologies focusing on testing low-risk, easily obtainable material, such as molecular cell-free DNA from plasma, can fill that gap and allow personalized therapy to be delivered in real time.
url https://doi.org/10.1177/1758834013517414
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