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author_facet Lux, Michael
Nabieva, Naiba
Hartkopf, Andreas
Huober, Jens
Volz, Bernhard
Taran, Florin-Andrei
Overkamp, Friedrich
Kolberg, Hans-Christian
Hadji, Peyman
Tesch, Hans
Häberle, Lothar
Ettl, Johannes
Lüftner, Diana
Wallwiener, Markus
Müller, Volkmar
Beckmann, Matthias
Belleville, Erik
Wimberger, Pauline
Hielscher, Carsten
Geberth, Matthias
Abenhardt, Wolfgang
Kurbacher, Christian
Wuerstlein, Rachel
Thomssen, Christoph
Untch, Michael
Fasching, Peter
Janni, Wolfgang
Fehm, Tanja
Wallwiener, Diethelm
Schneeweiss, Andreas
Brucker, Sara
Lux, Michael
Nabieva, Naiba
Hartkopf, Andreas
Huober, Jens
Volz, Bernhard
Taran, Florin-Andrei
Overkamp, Friedrich
Kolberg, Hans-Christian
Hadji, Peyman
Tesch, Hans
Häberle, Lothar
Ettl, Johannes
Lüftner, Diana
Wallwiener, Markus
Müller, Volkmar
Beckmann, Matthias
Belleville, Erik
Wimberger, Pauline
Hielscher, Carsten
Geberth, Matthias
Abenhardt, Wolfgang
Kurbacher, Christian
Wuerstlein, Rachel
Thomssen, Christoph
Untch, Michael
Fasching, Peter
Janni, Wolfgang
Fehm, Tanja
Wallwiener, Diethelm
Schneeweiss, Andreas
Brucker, Sara
author Lux, Michael
Nabieva, Naiba
Hartkopf, Andreas
Huober, Jens
Volz, Bernhard
Taran, Florin-Andrei
Overkamp, Friedrich
Kolberg, Hans-Christian
Hadji, Peyman
Tesch, Hans
Häberle, Lothar
Ettl, Johannes
Lüftner, Diana
Wallwiener, Markus
Müller, Volkmar
Beckmann, Matthias
Belleville, Erik
Wimberger, Pauline
Hielscher, Carsten
Geberth, Matthias
Abenhardt, Wolfgang
Kurbacher, Christian
Wuerstlein, Rachel
Thomssen, Christoph
Untch, Michael
Fasching, Peter
Janni, Wolfgang
Fehm, Tanja
Wallwiener, Diethelm
Schneeweiss, Andreas
Brucker, Sara
spellingShingle Lux, Michael
Nabieva, Naiba
Hartkopf, Andreas
Huober, Jens
Volz, Bernhard
Taran, Florin-Andrei
Overkamp, Friedrich
Kolberg, Hans-Christian
Hadji, Peyman
Tesch, Hans
Häberle, Lothar
Ettl, Johannes
Lüftner, Diana
Wallwiener, Markus
Müller, Volkmar
Beckmann, Matthias
Belleville, Erik
Wimberger, Pauline
Hielscher, Carsten
Geberth, Matthias
Abenhardt, Wolfgang
Kurbacher, Christian
Wuerstlein, Rachel
Thomssen, Christoph
Untch, Michael
Fasching, Peter
Janni, Wolfgang
Fehm, Tanja
Wallwiener, Diethelm
Schneeweiss, Andreas
Brucker, Sara
Cancers
Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
Cancer Research
Oncology
author_sort lux, michael
spelling Lux, Michael Nabieva, Naiba Hartkopf, Andreas Huober, Jens Volz, Bernhard Taran, Florin-Andrei Overkamp, Friedrich Kolberg, Hans-Christian Hadji, Peyman Tesch, Hans Häberle, Lothar Ettl, Johannes Lüftner, Diana Wallwiener, Markus Müller, Volkmar Beckmann, Matthias Belleville, Erik Wimberger, Pauline Hielscher, Carsten Geberth, Matthias Abenhardt, Wolfgang Kurbacher, Christian Wuerstlein, Rachel Thomssen, Christoph Untch, Michael Fasching, Peter Janni, Wolfgang Fehm, Tanja Wallwiener, Diethelm Schneeweiss, Andreas Brucker, Sara 2072-6694 MDPI AG Cancer Research Oncology http://dx.doi.org/10.3390/cancers11010010 <jats:p>This study presents comprehensive real-world data on the use of anti-human epidermal growth factor receptor 2 (HER2) therapies in patients with HER2-positive metastatic breast cancer (MBC). Specifically, it describes therapy patterns with trastuzumab (H), pertuzumab + trastuzumab (PH), lapatinib (L), and trastuzumab emtansine (T-DM1). The PRAEGNANT study is a real-time, real-world registry for MBC patients. All therapy lines are documented. This analysis describes the utilization of anti-HER2 therapies as well as therapy sequences. Among 1936 patients in PRAEGNANT, 451 were HER2-positive (23.3%). In the analysis set (417 patients), 53% of whom were included in PRAEGNANT in the first-line setting, 241 were treated with H, 237 with PH, 85 with L, and 125 with T-DM1 during the course of their therapies. The sequence PH → T-DM1 was administered in 51 patients. Higher Eastern Cooperative Oncology Group (ECOG) scores, negative hormone receptor status, and visceral or brain metastases were associated with more frequent use of this therapy sequence. Most patients received T-DM1 after treatment with pertuzumab. Both novel therapies (PH and T-DM1) are utilized in a high proportion of HER2-positive breast cancer patients. As most patients receive T-DM1 after PH, real-world data may help to clarify whether the efficacy of this sequence is similar to that in the approval study.</jats:p> Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry Cancers
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title Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_unstemmed Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_full Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_fullStr Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_full_unstemmed Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_short Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_sort therapy landscape in patients with metastatic her2-positive breast cancer: data from the praegnant real-world breast cancer registry
topic Cancer Research
Oncology
url http://dx.doi.org/10.3390/cancers11010010
publishDate 2018
physical 10
description <jats:p>This study presents comprehensive real-world data on the use of anti-human epidermal growth factor receptor 2 (HER2) therapies in patients with HER2-positive metastatic breast cancer (MBC). Specifically, it describes therapy patterns with trastuzumab (H), pertuzumab + trastuzumab (PH), lapatinib (L), and trastuzumab emtansine (T-DM1). The PRAEGNANT study is a real-time, real-world registry for MBC patients. All therapy lines are documented. This analysis describes the utilization of anti-HER2 therapies as well as therapy sequences. Among 1936 patients in PRAEGNANT, 451 were HER2-positive (23.3%). In the analysis set (417 patients), 53% of whom were included in PRAEGNANT in the first-line setting, 241 were treated with H, 237 with PH, 85 with L, and 125 with T-DM1 during the course of their therapies. The sequence PH → T-DM1 was administered in 51 patients. Higher Eastern Cooperative Oncology Group (ECOG) scores, negative hormone receptor status, and visceral or brain metastases were associated with more frequent use of this therapy sequence. Most patients received T-DM1 after treatment with pertuzumab. Both novel therapies (PH and T-DM1) are utilized in a high proportion of HER2-positive breast cancer patients. As most patients receive T-DM1 after PH, real-world data may help to clarify whether the efficacy of this sequence is similar to that in the approval study.</jats:p>
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author Lux, Michael, Nabieva, Naiba, Hartkopf, Andreas, Huober, Jens, Volz, Bernhard, Taran, Florin-Andrei, Overkamp, Friedrich, Kolberg, Hans-Christian, Hadji, Peyman, Tesch, Hans, Häberle, Lothar, Ettl, Johannes, Lüftner, Diana, Wallwiener, Markus, Müller, Volkmar, Beckmann, Matthias, Belleville, Erik, Wimberger, Pauline, Hielscher, Carsten, Geberth, Matthias, Abenhardt, Wolfgang, Kurbacher, Christian, Wuerstlein, Rachel, Thomssen, Christoph, Untch, Michael, Fasching, Peter, Janni, Wolfgang, Fehm, Tanja, Wallwiener, Diethelm, Schneeweiss, Andreas, Brucker, Sara
author_facet Lux, Michael, Nabieva, Naiba, Hartkopf, Andreas, Huober, Jens, Volz, Bernhard, Taran, Florin-Andrei, Overkamp, Friedrich, Kolberg, Hans-Christian, Hadji, Peyman, Tesch, Hans, Häberle, Lothar, Ettl, Johannes, Lüftner, Diana, Wallwiener, Markus, Müller, Volkmar, Beckmann, Matthias, Belleville, Erik, Wimberger, Pauline, Hielscher, Carsten, Geberth, Matthias, Abenhardt, Wolfgang, Kurbacher, Christian, Wuerstlein, Rachel, Thomssen, Christoph, Untch, Michael, Fasching, Peter, Janni, Wolfgang, Fehm, Tanja, Wallwiener, Diethelm, Schneeweiss, Andreas, Brucker, Sara, Lux, Michael, Nabieva, Naiba, Hartkopf, Andreas, Huober, Jens, Volz, Bernhard, Taran, Florin-Andrei, Overkamp, Friedrich, Kolberg, Hans-Christian, Hadji, Peyman, Tesch, Hans, Häberle, Lothar, Ettl, Johannes, Lüftner, Diana, Wallwiener, Markus, Müller, Volkmar, Beckmann, Matthias, Belleville, Erik, Wimberger, Pauline, Hielscher, Carsten, Geberth, Matthias, Abenhardt, Wolfgang, Kurbacher, Christian, Wuerstlein, Rachel, Thomssen, Christoph, Untch, Michael, Fasching, Peter, Janni, Wolfgang, Fehm, Tanja, Wallwiener, Diethelm, Schneeweiss, Andreas, Brucker, Sara
author_sort lux, michael
container_issue 1
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container_title Cancers
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description <jats:p>This study presents comprehensive real-world data on the use of anti-human epidermal growth factor receptor 2 (HER2) therapies in patients with HER2-positive metastatic breast cancer (MBC). Specifically, it describes therapy patterns with trastuzumab (H), pertuzumab + trastuzumab (PH), lapatinib (L), and trastuzumab emtansine (T-DM1). The PRAEGNANT study is a real-time, real-world registry for MBC patients. All therapy lines are documented. This analysis describes the utilization of anti-HER2 therapies as well as therapy sequences. Among 1936 patients in PRAEGNANT, 451 were HER2-positive (23.3%). In the analysis set (417 patients), 53% of whom were included in PRAEGNANT in the first-line setting, 241 were treated with H, 237 with PH, 85 with L, and 125 with T-DM1 during the course of their therapies. The sequence PH → T-DM1 was administered in 51 patients. Higher Eastern Cooperative Oncology Group (ECOG) scores, negative hormone receptor status, and visceral or brain metastases were associated with more frequent use of this therapy sequence. Most patients received T-DM1 after treatment with pertuzumab. Both novel therapies (PH and T-DM1) are utilized in a high proportion of HER2-positive breast cancer patients. As most patients receive T-DM1 after PH, real-world data may help to clarify whether the efficacy of this sequence is similar to that in the approval study.</jats:p>
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spelling Lux, Michael Nabieva, Naiba Hartkopf, Andreas Huober, Jens Volz, Bernhard Taran, Florin-Andrei Overkamp, Friedrich Kolberg, Hans-Christian Hadji, Peyman Tesch, Hans Häberle, Lothar Ettl, Johannes Lüftner, Diana Wallwiener, Markus Müller, Volkmar Beckmann, Matthias Belleville, Erik Wimberger, Pauline Hielscher, Carsten Geberth, Matthias Abenhardt, Wolfgang Kurbacher, Christian Wuerstlein, Rachel Thomssen, Christoph Untch, Michael Fasching, Peter Janni, Wolfgang Fehm, Tanja Wallwiener, Diethelm Schneeweiss, Andreas Brucker, Sara 2072-6694 MDPI AG Cancer Research Oncology http://dx.doi.org/10.3390/cancers11010010 <jats:p>This study presents comprehensive real-world data on the use of anti-human epidermal growth factor receptor 2 (HER2) therapies in patients with HER2-positive metastatic breast cancer (MBC). Specifically, it describes therapy patterns with trastuzumab (H), pertuzumab + trastuzumab (PH), lapatinib (L), and trastuzumab emtansine (T-DM1). The PRAEGNANT study is a real-time, real-world registry for MBC patients. All therapy lines are documented. This analysis describes the utilization of anti-HER2 therapies as well as therapy sequences. Among 1936 patients in PRAEGNANT, 451 were HER2-positive (23.3%). In the analysis set (417 patients), 53% of whom were included in PRAEGNANT in the first-line setting, 241 were treated with H, 237 with PH, 85 with L, and 125 with T-DM1 during the course of their therapies. The sequence PH → T-DM1 was administered in 51 patients. Higher Eastern Cooperative Oncology Group (ECOG) scores, negative hormone receptor status, and visceral or brain metastases were associated with more frequent use of this therapy sequence. Most patients received T-DM1 after treatment with pertuzumab. Both novel therapies (PH and T-DM1) are utilized in a high proportion of HER2-positive breast cancer patients. As most patients receive T-DM1 after PH, real-world data may help to clarify whether the efficacy of this sequence is similar to that in the approval study.</jats:p> Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry Cancers
spellingShingle Lux, Michael, Nabieva, Naiba, Hartkopf, Andreas, Huober, Jens, Volz, Bernhard, Taran, Florin-Andrei, Overkamp, Friedrich, Kolberg, Hans-Christian, Hadji, Peyman, Tesch, Hans, Häberle, Lothar, Ettl, Johannes, Lüftner, Diana, Wallwiener, Markus, Müller, Volkmar, Beckmann, Matthias, Belleville, Erik, Wimberger, Pauline, Hielscher, Carsten, Geberth, Matthias, Abenhardt, Wolfgang, Kurbacher, Christian, Wuerstlein, Rachel, Thomssen, Christoph, Untch, Michael, Fasching, Peter, Janni, Wolfgang, Fehm, Tanja, Wallwiener, Diethelm, Schneeweiss, Andreas, Brucker, Sara, Cancers, Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry, Cancer Research, Oncology
title Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_full Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_fullStr Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_full_unstemmed Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_short Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
title_sort therapy landscape in patients with metastatic her2-positive breast cancer: data from the praegnant real-world breast cancer registry
title_unstemmed Therapy Landscape in Patients with Metastatic HER2-Positive Breast Cancer: Data from the PRAEGNANT Real-World Breast Cancer Registry
topic Cancer Research, Oncology
url http://dx.doi.org/10.3390/cancers11010010