Investigational targeted therapies for the treatment of testicular germ cell tumors

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Investigational targeted therapies for the treatment of testicular germ cell tumors. / Oing, Christoph; Kollmannsberger, Christian; Oechsle, Karin; Bokemeyer, Carsten.

in: EXPERT OPIN INV DRUG, Jahrgang 25, Nr. 9, 09.2016, S. 1033-43.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{d655867410da42cc95545b5b1b48d10e,
title = "Investigational targeted therapies for the treatment of testicular germ cell tumors",
abstract = "INTRODUCTION: Germ cell tumors (GCTs) are the most common malignancy among men aged between 15 to 45. Despite high cure rates of >90% over all GCTs, 3 to 5% of patients will still die of platinum-refractory disease. New systemic treatment options are needed to improve treatment success in this challenging setting.AREAS COVERED: To review targeted treatment options and preclinical developments in platinum-refractory GCTs, a comprehensive literature search of PubMed, Medline and scientific meeting abstracts on published clinical trials and reports on molecularly targeted approaches was conducted. Outcomes of platinum-refractory disease and of patients failing high-dose chemotherapy remain poor. Currently, no molecularly targeted treatment has shown clinically meaningful activity in unselected patient populations in clinical trials, but individual patients may achieve short-lived objective responses by treatment with sunitinib, brentuximab vedotin or imatinib. Targeted trials based on molecular selection of patients have not yet been performed.EXPERT OPINION: The limited activity of targeted agents in refractory GCT is disappointing. Assessment of druggable biomarkers and marker-stratified treatment may help individual patients, but is largely lacking. The low incidence and high curability of GCTs make the design of larger clinical trials difficult. The potential of novel agents, i.e. immune-checkpoint inhibitors, remains to be elucidated.",
keywords = "Journal Article",
author = "Christoph Oing and Christian Kollmannsberger and Karin Oechsle and Carsten Bokemeyer",
year = "2016",
month = sep,
doi = "10.1080/13543784.2016.1195808",
language = "English",
volume = "25",
pages = "1033--43",
journal = "EXPERT OPIN INV DRUG",
issn = "1354-3784",
publisher = "informa healthcare",
number = "9",

}

RIS

TY - JOUR

T1 - Investigational targeted therapies for the treatment of testicular germ cell tumors

AU - Oing, Christoph

AU - Kollmannsberger, Christian

AU - Oechsle, Karin

AU - Bokemeyer, Carsten

PY - 2016/9

Y1 - 2016/9

N2 - INTRODUCTION: Germ cell tumors (GCTs) are the most common malignancy among men aged between 15 to 45. Despite high cure rates of >90% over all GCTs, 3 to 5% of patients will still die of platinum-refractory disease. New systemic treatment options are needed to improve treatment success in this challenging setting.AREAS COVERED: To review targeted treatment options and preclinical developments in platinum-refractory GCTs, a comprehensive literature search of PubMed, Medline and scientific meeting abstracts on published clinical trials and reports on molecularly targeted approaches was conducted. Outcomes of platinum-refractory disease and of patients failing high-dose chemotherapy remain poor. Currently, no molecularly targeted treatment has shown clinically meaningful activity in unselected patient populations in clinical trials, but individual patients may achieve short-lived objective responses by treatment with sunitinib, brentuximab vedotin or imatinib. Targeted trials based on molecular selection of patients have not yet been performed.EXPERT OPINION: The limited activity of targeted agents in refractory GCT is disappointing. Assessment of druggable biomarkers and marker-stratified treatment may help individual patients, but is largely lacking. The low incidence and high curability of GCTs make the design of larger clinical trials difficult. The potential of novel agents, i.e. immune-checkpoint inhibitors, remains to be elucidated.

AB - INTRODUCTION: Germ cell tumors (GCTs) are the most common malignancy among men aged between 15 to 45. Despite high cure rates of >90% over all GCTs, 3 to 5% of patients will still die of platinum-refractory disease. New systemic treatment options are needed to improve treatment success in this challenging setting.AREAS COVERED: To review targeted treatment options and preclinical developments in platinum-refractory GCTs, a comprehensive literature search of PubMed, Medline and scientific meeting abstracts on published clinical trials and reports on molecularly targeted approaches was conducted. Outcomes of platinum-refractory disease and of patients failing high-dose chemotherapy remain poor. Currently, no molecularly targeted treatment has shown clinically meaningful activity in unselected patient populations in clinical trials, but individual patients may achieve short-lived objective responses by treatment with sunitinib, brentuximab vedotin or imatinib. Targeted trials based on molecular selection of patients have not yet been performed.EXPERT OPINION: The limited activity of targeted agents in refractory GCT is disappointing. Assessment of druggable biomarkers and marker-stratified treatment may help individual patients, but is largely lacking. The low incidence and high curability of GCTs make the design of larger clinical trials difficult. The potential of novel agents, i.e. immune-checkpoint inhibitors, remains to be elucidated.

KW - Journal Article

U2 - 10.1080/13543784.2016.1195808

DO - 10.1080/13543784.2016.1195808

M3 - SCORING: Journal article

C2 - 27286362

VL - 25

SP - 1033

EP - 1043

JO - EXPERT OPIN INV DRUG

JF - EXPERT OPIN INV DRUG

SN - 1354-3784

IS - 9

ER -