author_facet Aust, Stefanie
Schwameis, Richard
Gagic, Tamara
Müllauer, Leonhard
Langthaler, Eva
Prager, Gerald
Grech, Christina
Reinthaller, Alexander
Krainer, Michael
Pils, Dietmar
Grimm, Christoph
Polterauer, Stephan
Aust, Stefanie
Schwameis, Richard
Gagic, Tamara
Müllauer, Leonhard
Langthaler, Eva
Prager, Gerald
Grech, Christina
Reinthaller, Alexander
Krainer, Michael
Pils, Dietmar
Grimm, Christoph
Polterauer, Stephan
author Aust, Stefanie
Schwameis, Richard
Gagic, Tamara
Müllauer, Leonhard
Langthaler, Eva
Prager, Gerald
Grech, Christina
Reinthaller, Alexander
Krainer, Michael
Pils, Dietmar
Grimm, Christoph
Polterauer, Stephan
spellingShingle Aust, Stefanie
Schwameis, Richard
Gagic, Tamara
Müllauer, Leonhard
Langthaler, Eva
Prager, Gerald
Grech, Christina
Reinthaller, Alexander
Krainer, Michael
Pils, Dietmar
Grimm, Christoph
Polterauer, Stephan
Cancers
Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
Cancer Research
Oncology
author_sort aust, stefanie
spelling Aust, Stefanie Schwameis, Richard Gagic, Tamara Müllauer, Leonhard Langthaler, Eva Prager, Gerald Grech, Christina Reinthaller, Alexander Krainer, Michael Pils, Dietmar Grimm, Christoph Polterauer, Stephan 2072-6694 MDPI AG Cancer Research Oncology http://dx.doi.org/10.3390/cancers12030548 <jats:p>Background: Treating cancer according to its molecular alterations (i.e., targeted treatment, TT) is the goal of precision medicine tumor boards (PTBs). Their clinical applicability has been evaluated for ovarian cancer patients in this analysis. Methods: All consecutive ovarian cancer patients discussed in a PTB at the Medical University of Vienna, Austria, from April 2015 to April 2019 were included (n = 44). Results: In 38/44 (86%) cases, at least one mutation, deletion or amplification was detected. The most frequently altered genes were p53 (64%), PI3K pathway (18%), KRAS (14%), BRCA1 (11%) and BRCA2 (2%). In 31 patients (70%) a TT was recommended. A total of 12/31 patients (39%) received the recommended therapy. Median time from indication for PTB to TT start was 65 days (15–216). Median time to treatment failure was 2.7 months (0.2–13.2). Clinical benefit rate (CBR) was 42%. Reasons for treatment discontinuation were disease progression (42%), poor performance status (PS &gt; 2; 25%), death (17%) or treatment related side effects (8%). In 61% the TT was not administered—mainly due to PS &gt; 2. Conclusion: Even though a TT recommendation can be derived frequently, clinical applicability remains limited due to poor patients’ general condition after exploitation of standard treatment. However, we observed antitumor activity in a substantial number of heavily pretreated patients.</jats:p> Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer Cancers
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title Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_unstemmed Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_full Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_fullStr Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_full_unstemmed Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_short Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_sort precision medicine tumor boards: clinical applicability of personalized treatment concepts in ovarian cancer
topic Cancer Research
Oncology
url http://dx.doi.org/10.3390/cancers12030548
publishDate 2020
physical 548
description <jats:p>Background: Treating cancer according to its molecular alterations (i.e., targeted treatment, TT) is the goal of precision medicine tumor boards (PTBs). Their clinical applicability has been evaluated for ovarian cancer patients in this analysis. Methods: All consecutive ovarian cancer patients discussed in a PTB at the Medical University of Vienna, Austria, from April 2015 to April 2019 were included (n = 44). Results: In 38/44 (86%) cases, at least one mutation, deletion or amplification was detected. The most frequently altered genes were p53 (64%), PI3K pathway (18%), KRAS (14%), BRCA1 (11%) and BRCA2 (2%). In 31 patients (70%) a TT was recommended. A total of 12/31 patients (39%) received the recommended therapy. Median time from indication for PTB to TT start was 65 days (15–216). Median time to treatment failure was 2.7 months (0.2–13.2). Clinical benefit rate (CBR) was 42%. Reasons for treatment discontinuation were disease progression (42%), poor performance status (PS &gt; 2; 25%), death (17%) or treatment related side effects (8%). In 61% the TT was not administered—mainly due to PS &gt; 2. Conclusion: Even though a TT recommendation can be derived frequently, clinical applicability remains limited due to poor patients’ general condition after exploitation of standard treatment. However, we observed antitumor activity in a substantial number of heavily pretreated patients.</jats:p>
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author Aust, Stefanie, Schwameis, Richard, Gagic, Tamara, Müllauer, Leonhard, Langthaler, Eva, Prager, Gerald, Grech, Christina, Reinthaller, Alexander, Krainer, Michael, Pils, Dietmar, Grimm, Christoph, Polterauer, Stephan
author_facet Aust, Stefanie, Schwameis, Richard, Gagic, Tamara, Müllauer, Leonhard, Langthaler, Eva, Prager, Gerald, Grech, Christina, Reinthaller, Alexander, Krainer, Michael, Pils, Dietmar, Grimm, Christoph, Polterauer, Stephan, Aust, Stefanie, Schwameis, Richard, Gagic, Tamara, Müllauer, Leonhard, Langthaler, Eva, Prager, Gerald, Grech, Christina, Reinthaller, Alexander, Krainer, Michael, Pils, Dietmar, Grimm, Christoph, Polterauer, Stephan
author_sort aust, stefanie
container_issue 3
container_start_page 0
container_title Cancers
container_volume 12
description <jats:p>Background: Treating cancer according to its molecular alterations (i.e., targeted treatment, TT) is the goal of precision medicine tumor boards (PTBs). Their clinical applicability has been evaluated for ovarian cancer patients in this analysis. Methods: All consecutive ovarian cancer patients discussed in a PTB at the Medical University of Vienna, Austria, from April 2015 to April 2019 were included (n = 44). Results: In 38/44 (86%) cases, at least one mutation, deletion or amplification was detected. The most frequently altered genes were p53 (64%), PI3K pathway (18%), KRAS (14%), BRCA1 (11%) and BRCA2 (2%). In 31 patients (70%) a TT was recommended. A total of 12/31 patients (39%) received the recommended therapy. Median time from indication for PTB to TT start was 65 days (15–216). Median time to treatment failure was 2.7 months (0.2–13.2). Clinical benefit rate (CBR) was 42%. Reasons for treatment discontinuation were disease progression (42%), poor performance status (PS &gt; 2; 25%), death (17%) or treatment related side effects (8%). In 61% the TT was not administered—mainly due to PS &gt; 2. Conclusion: Even though a TT recommendation can be derived frequently, clinical applicability remains limited due to poor patients’ general condition after exploitation of standard treatment. However, we observed antitumor activity in a substantial number of heavily pretreated patients.</jats:p>
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spelling Aust, Stefanie Schwameis, Richard Gagic, Tamara Müllauer, Leonhard Langthaler, Eva Prager, Gerald Grech, Christina Reinthaller, Alexander Krainer, Michael Pils, Dietmar Grimm, Christoph Polterauer, Stephan 2072-6694 MDPI AG Cancer Research Oncology http://dx.doi.org/10.3390/cancers12030548 <jats:p>Background: Treating cancer according to its molecular alterations (i.e., targeted treatment, TT) is the goal of precision medicine tumor boards (PTBs). Their clinical applicability has been evaluated for ovarian cancer patients in this analysis. Methods: All consecutive ovarian cancer patients discussed in a PTB at the Medical University of Vienna, Austria, from April 2015 to April 2019 were included (n = 44). Results: In 38/44 (86%) cases, at least one mutation, deletion or amplification was detected. The most frequently altered genes were p53 (64%), PI3K pathway (18%), KRAS (14%), BRCA1 (11%) and BRCA2 (2%). In 31 patients (70%) a TT was recommended. A total of 12/31 patients (39%) received the recommended therapy. Median time from indication for PTB to TT start was 65 days (15–216). Median time to treatment failure was 2.7 months (0.2–13.2). Clinical benefit rate (CBR) was 42%. Reasons for treatment discontinuation were disease progression (42%), poor performance status (PS &gt; 2; 25%), death (17%) or treatment related side effects (8%). In 61% the TT was not administered—mainly due to PS &gt; 2. Conclusion: Even though a TT recommendation can be derived frequently, clinical applicability remains limited due to poor patients’ general condition after exploitation of standard treatment. However, we observed antitumor activity in a substantial number of heavily pretreated patients.</jats:p> Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer Cancers
spellingShingle Aust, Stefanie, Schwameis, Richard, Gagic, Tamara, Müllauer, Leonhard, Langthaler, Eva, Prager, Gerald, Grech, Christina, Reinthaller, Alexander, Krainer, Michael, Pils, Dietmar, Grimm, Christoph, Polterauer, Stephan, Cancers, Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer, Cancer Research, Oncology
title Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_full Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_fullStr Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_full_unstemmed Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_short Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
title_sort precision medicine tumor boards: clinical applicability of personalized treatment concepts in ovarian cancer
title_unstemmed Precision Medicine Tumor Boards: Clinical Applicability of Personalized Treatment Concepts in Ovarian Cancer
topic Cancer Research, Oncology
url http://dx.doi.org/10.3390/cancers12030548