Zielgerichtete Therapie des Mammakarzinoms

Standard

Zielgerichtete Therapie des Mammakarzinoms. / Seiffert, Katharina; Schmalfeldt, Barbara; Müller, Volkmar.

In: DEUT MED WOCHENSCHR, Vol. 142, No. 22, 11.2017, p. 1669-1675.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

APA

Vancouver

Bibtex

@article{e44f34f40f504ed489747220a947fe4d,
title = "Zielgerichtete Therapie des Mammakarzinoms",
abstract = "Within the last years, significant improvements have been achieved in breast cancer treatment, particularly with the development of targeted therapies. Major progress has been made in identifying the drivers malignant growth in oestrogen-receptor-positive breast cancer and the mechanisms of resistance to endocrine therapy. This progress has translated into several targeted therapies that enhance the efficacy of endocrine therapy; inhibitors of the cyclin-dependent kinases CDK4 and CDK6 like palbociclib and inhibitors of mTOR substantially improve progression-free survival. For patients with HER2-positive disease the addition of Pertuzumab to Trastuzumab in combination with chemotherapy has been a significant improvement in anti-HER2 therapy in early as well as metastatic breast cancer. Evidence-based further line therapy options in the metastatic setting include T-DM1 and in later lines Lapatinib. For triple negative disease the angiogenesis inhibitor Bevacizumab is approved, which increases progression free survival. Immune checkpoint inhibitors, PARP-inhibitors or anti-androgens represent promising strategies, all of which are currently being evaluated in clinical trials. The development of predictive biomarkers to guide targeted therapies is still the subject of research.",
keywords = "Antineoplastic Agents, Breast Neoplasms, Disease-Free Survival, Female, Humans, Molecular Targeted Therapy, Journal Article",
author = "Katharina Seiffert and Barbara Schmalfeldt and Volkmar M{\"u}ller",
note = "{\textcopyright} Georg Thieme Verlag KG Stuttgart · New York.",
year = "2017",
month = nov,
doi = "10.1055/s-0043-108468",
language = "Deutsch",
volume = "142",
pages = "1669--1675",
journal = "DEUT MED WOCHENSCHR",
issn = "0012-0472",
publisher = "Georg Thieme Verlag KG",
number = "22",

}

RIS

TY - JOUR

T1 - Zielgerichtete Therapie des Mammakarzinoms

AU - Seiffert, Katharina

AU - Schmalfeldt, Barbara

AU - Müller, Volkmar

N1 - © Georg Thieme Verlag KG Stuttgart · New York.

PY - 2017/11

Y1 - 2017/11

N2 - Within the last years, significant improvements have been achieved in breast cancer treatment, particularly with the development of targeted therapies. Major progress has been made in identifying the drivers malignant growth in oestrogen-receptor-positive breast cancer and the mechanisms of resistance to endocrine therapy. This progress has translated into several targeted therapies that enhance the efficacy of endocrine therapy; inhibitors of the cyclin-dependent kinases CDK4 and CDK6 like palbociclib and inhibitors of mTOR substantially improve progression-free survival. For patients with HER2-positive disease the addition of Pertuzumab to Trastuzumab in combination with chemotherapy has been a significant improvement in anti-HER2 therapy in early as well as metastatic breast cancer. Evidence-based further line therapy options in the metastatic setting include T-DM1 and in later lines Lapatinib. For triple negative disease the angiogenesis inhibitor Bevacizumab is approved, which increases progression free survival. Immune checkpoint inhibitors, PARP-inhibitors or anti-androgens represent promising strategies, all of which are currently being evaluated in clinical trials. The development of predictive biomarkers to guide targeted therapies is still the subject of research.

AB - Within the last years, significant improvements have been achieved in breast cancer treatment, particularly with the development of targeted therapies. Major progress has been made in identifying the drivers malignant growth in oestrogen-receptor-positive breast cancer and the mechanisms of resistance to endocrine therapy. This progress has translated into several targeted therapies that enhance the efficacy of endocrine therapy; inhibitors of the cyclin-dependent kinases CDK4 and CDK6 like palbociclib and inhibitors of mTOR substantially improve progression-free survival. For patients with HER2-positive disease the addition of Pertuzumab to Trastuzumab in combination with chemotherapy has been a significant improvement in anti-HER2 therapy in early as well as metastatic breast cancer. Evidence-based further line therapy options in the metastatic setting include T-DM1 and in later lines Lapatinib. For triple negative disease the angiogenesis inhibitor Bevacizumab is approved, which increases progression free survival. Immune checkpoint inhibitors, PARP-inhibitors or anti-androgens represent promising strategies, all of which are currently being evaluated in clinical trials. The development of predictive biomarkers to guide targeted therapies is still the subject of research.

KW - Antineoplastic Agents

KW - Breast Neoplasms

KW - Disease-Free Survival

KW - Female

KW - Humans

KW - Molecular Targeted Therapy

KW - Journal Article

U2 - 10.1055/s-0043-108468

DO - 10.1055/s-0043-108468

M3 - SCORING: Zeitschriftenaufsatz

C2 - 29078212

VL - 142

SP - 1669

EP - 1675

JO - DEUT MED WOCHENSCHR

JF - DEUT MED WOCHENSCHR

SN - 0012-0472

IS - 22

ER -