Cargando…

Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients

A proof-of-concept study was conducted to assess whether patients with advanced stage IV cancer for whom predominantly no standard therapy was available could benefit from comprehensive molecular profiling of their tumor tissue to provide targeted therapy. Tumor samples of 83 patients were collected...

Descripción completa

Detalles Bibliográficos
Autores principales: Samsen, Alexandra, von der Heyde, Silvia, Bokemeyer, Carsten, David, Kerstin A., Flath, Bernd, Graap, Max, Grebenstein, Bianca, Heflik, Ludger, Hollburg, Wiebke, Layer, Peter, von Leitner, Eike, Overkamp, Friedrich, Saeger, Wolfgang, Schneider, Sandra, von Seydewitz, Cay-Uwe, Stang, Axel, Stein, Alexander, Zornig, Carsten, Juhl, Hartmut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205171/
https://www.ncbi.nlm.nih.gov/pubmed/30410678
http://dx.doi.org/10.18632/oncotarget.26198
_version_ 1783366158302314496
author Samsen, Alexandra
von der Heyde, Silvia
Bokemeyer, Carsten
David, Kerstin A.
Flath, Bernd
Graap, Max
Grebenstein, Bianca
Heflik, Ludger
Hollburg, Wiebke
Layer, Peter
von Leitner, Eike
Overkamp, Friedrich
Saeger, Wolfgang
Schneider, Sandra
von Seydewitz, Cay-Uwe
Stang, Axel
Stein, Alexander
Zornig, Carsten
Juhl, Hartmut
author_facet Samsen, Alexandra
von der Heyde, Silvia
Bokemeyer, Carsten
David, Kerstin A.
Flath, Bernd
Graap, Max
Grebenstein, Bianca
Heflik, Ludger
Hollburg, Wiebke
Layer, Peter
von Leitner, Eike
Overkamp, Friedrich
Saeger, Wolfgang
Schneider, Sandra
von Seydewitz, Cay-Uwe
Stang, Axel
Stein, Alexander
Zornig, Carsten
Juhl, Hartmut
author_sort Samsen, Alexandra
collection PubMed
description A proof-of-concept study was conducted to assess whether patients with advanced stage IV cancer for whom predominantly no standard therapy was available could benefit from comprehensive molecular profiling of their tumor tissue to provide targeted therapy. Tumor samples of 83 patients were collected under highly standardized conditions and analyzed using immunohistochemistry, next-generation sequencing and phosphoprotein profiling. Expression and phosphorylation of key oncogenic pathways were measured to identify targets at the (phospho-) proteomic level. At genomic level, 50 oncogenes and tumor suppressor genes were analyzed. Based on molecular profiling, targeted therapies were decided by the attending oncologist. Accordingly, 28 patients who met the defined criteria fell in two equal-sized groups. One group received targeted therapies while the other did not. Following six months of treatment, disease control was achieved by 49% of patients receiving targeted therapy (complete remission, 14%; partial remission, 21%; stable disease, 14%; disease progression, 36%; death, 14%) and 21% of patients receiving non-targeted therapy (stable disease, 21%; disease progression, 64%; death, 14%). Individual patients experienced dramatic responses to a therapy which otherwise would not have been applied. This approach clarifies the value of multi-omic molecular profiling for cancer diagnostics.
format Online
Article
Text
id pubmed-6205171
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Impact Journals LLC
record_format MEDLINE/PubMed
spelling pubmed-62051712018-11-08 Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients Samsen, Alexandra von der Heyde, Silvia Bokemeyer, Carsten David, Kerstin A. Flath, Bernd Graap, Max Grebenstein, Bianca Heflik, Ludger Hollburg, Wiebke Layer, Peter von Leitner, Eike Overkamp, Friedrich Saeger, Wolfgang Schneider, Sandra von Seydewitz, Cay-Uwe Stang, Axel Stein, Alexander Zornig, Carsten Juhl, Hartmut Oncotarget Research Paper A proof-of-concept study was conducted to assess whether patients with advanced stage IV cancer for whom predominantly no standard therapy was available could benefit from comprehensive molecular profiling of their tumor tissue to provide targeted therapy. Tumor samples of 83 patients were collected under highly standardized conditions and analyzed using immunohistochemistry, next-generation sequencing and phosphoprotein profiling. Expression and phosphorylation of key oncogenic pathways were measured to identify targets at the (phospho-) proteomic level. At genomic level, 50 oncogenes and tumor suppressor genes were analyzed. Based on molecular profiling, targeted therapies were decided by the attending oncologist. Accordingly, 28 patients who met the defined criteria fell in two equal-sized groups. One group received targeted therapies while the other did not. Following six months of treatment, disease control was achieved by 49% of patients receiving targeted therapy (complete remission, 14%; partial remission, 21%; stable disease, 14%; disease progression, 36%; death, 14%) and 21% of patients receiving non-targeted therapy (stable disease, 21%; disease progression, 64%; death, 14%). Individual patients experienced dramatic responses to a therapy which otherwise would not have been applied. This approach clarifies the value of multi-omic molecular profiling for cancer diagnostics. Impact Journals LLC 2018-10-05 /pmc/articles/PMC6205171/ /pubmed/30410678 http://dx.doi.org/10.18632/oncotarget.26198 Text en Copyright: © 2018 Samsen et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Samsen, Alexandra
von der Heyde, Silvia
Bokemeyer, Carsten
David, Kerstin A.
Flath, Bernd
Graap, Max
Grebenstein, Bianca
Heflik, Ludger
Hollburg, Wiebke
Layer, Peter
von Leitner, Eike
Overkamp, Friedrich
Saeger, Wolfgang
Schneider, Sandra
von Seydewitz, Cay-Uwe
Stang, Axel
Stein, Alexander
Zornig, Carsten
Juhl, Hartmut
Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
title Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
title_full Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
title_fullStr Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
title_full_unstemmed Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
title_short Multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
title_sort multi-omic based molecular profiling of advanced cancer identifies treatable targets and improves survival in individual patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205171/
https://www.ncbi.nlm.nih.gov/pubmed/30410678
http://dx.doi.org/10.18632/oncotarget.26198
work_keys_str_mv AT samsenalexandra multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT vonderheydesilvia multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT bokemeyercarsten multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT davidkerstina multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT flathbernd multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT graapmax multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT grebensteinbianca multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT heflikludger multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT hollburgwiebke multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT layerpeter multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT vonleitnereike multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT overkampfriedrich multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT saegerwolfgang multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT schneidersandra multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT vonseydewitzcayuwe multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT stangaxel multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT steinalexander multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT zornigcarsten multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients
AT juhlhartmut multiomicbasedmolecularprofilingofadvancedcanceridentifiestreatabletargetsandimprovessurvivalinindividualpatients