Navigation überspringen
Universitätsbibliothek Heidelberg
Status: Bibliographieeintrag

Verfügbarkeit
Standort: ---
Exemplare: ---
heiBIB
 Online-Ressource
Verfasst von:Haag, Georg Martin [VerfasserIn]   i
 Zörnig, Inka [VerfasserIn]   i
 Hassel, Jessica C. [VerfasserIn]   i
 Halama, Niels [VerfasserIn]   i
 Dick, Julika [VerfasserIn]   i
 Lang, Nina [VerfasserIn]   i
 Podola, Lilli [VerfasserIn]   i
 Ziegelmeier, Claudia [VerfasserIn]   i
 Freitag, Angelika [VerfasserIn]   i
 Beckhove, Philipp [VerfasserIn]   i
 Enk, Alexander [VerfasserIn]   i
 Jäger, Dirk [VerfasserIn]   i
Titel:Phase II trial of ipilimumab in melanoma patients with preexisting humoural immune response to NY-ESO-1
Verf.angabe:G. M. Haag, I. Zoernig, J. C. Hassel, N. Halama, J. Dick, N. Lang, L. Podola, J. Funk, C. Ziegelmeier, S. Juenger, M. Bucur, L. Umansky, C. S. Falk, A. Freitag, I. Karapanagiotou-Schenkel, P. Beckhove, A. Enk, D. Jaeger
E-Jahr:2018
Jahr:5 January 2018
Umfang:8 S.
Fussnoten:Gesehen am 15.08.2019
Titel Quelle:Enthalten in: European journal of cancer
Ort Quelle:Amsterdam [u.a.] : Elsevier, 1992
Jahr Quelle:2018
Band/Heft Quelle:90(2018), Seite 122-129
ISSN Quelle:1879-0852
Abstract:Background - Immune checkpoint therapy has dramatically changed treatment options in patients with metastatic melanoma. However, a relevant part of patients still does not respond to treatment. Data regarding the prognostic or predictive significance of preexisting immune responses against tumour antigens are conflicting. Retrospective data suggested a higher clinical benefit of ipilimumab in melanoma patients with preexisting NY-ESO-1-specific immunity. - Patients and methods - Twenty-five patients with previously untreated or treated metastatic melanoma and preexisting humoural immune response against NY-ESO-1 received ipilimumab at a dose of 10 mg/kg in week 1, 4, 7, 10 followed by 3-month maintenance treatment for a maximum of 48 weeks. Primary endpoint was the disease control rate (irCR, irPR or irSD) according to immune-related response criteria (irRC). Secondary endpoints included the disease control rate according to RECIST criteria, progression-free survival and overall survival (OS). Humoural and cellular immune responses against NY-ESO-1 were analysed from blood samples. - Results - Disease control rate according to irRC was 52%, irPR was observed in 36% of patients. Progression-free survival according to irRC was 7.8 months, according to RECIST criteria it was 2.9 months. Median OS was 22.7 months; the corresponding 1-year survival rate was 66.8%. Treatment-related grade 3 AEs occurred in 36% with no grade 4-5 AEs. No clear association was found between the presence of NY-ESO-1-specific cellular or humoural immune responses and clinical activity. - Conclusion - Ipilimumab demonstrated clinically relevant activity within this biomarker-defined population. NY-ESO-1 positivity, as a surrogate for a preexisting immune response against tumour antigens, might help identifying patients with a superior outcome from immune checkpoint blockade. Clinical trial information: NCT01216696
DOI:doi:10.1016/j.ejca.2017.12.001
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1016/j.ejca.2017.12.001
 Volltext: http://www.sciencedirect.com/science/article/pii/S0959804917314570
 DOI: https://doi.org/10.1016/j.ejca.2017.12.001
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Cancer/testis antigen
 Immunotherapy
 Ipilimumab
 Melanoma
 NY-ESO-1
K10plus-PPN:167144812X
Verknüpfungen:→ Zeitschrift

Permanenter Link auf diesen Titel (bookmarkfähig):  https://katalog.ub.uni-heidelberg.de/titel/68421099   QR-Code
zum Seitenanfang