| Online-Ressource |
Verfasst von: | Haag, Georg Martin [VerfasserIn]  |
| Zörnig, Inka [VerfasserIn]  |
| Hassel, Jessica C. [VerfasserIn]  |
| Halama, Niels [VerfasserIn]  |
| Dick, Julika [VerfasserIn]  |
| Lang, Nina [VerfasserIn]  |
| Podola, Lilli [VerfasserIn]  |
| Ziegelmeier, Claudia [VerfasserIn]  |
| Freitag, Angelika [VerfasserIn]  |
| Beckhove, Philipp [VerfasserIn]  |
| Enk, Alexander [VerfasserIn]  |
| Jäger, Dirk [VerfasserIn]  |
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 |
Phase II trial of ipilimumab in melanoma patients with preexisting humoural immune response to NY-ESO-1 / Haag, Georg Martin [VerfasserIn]; 5 January 2018 (Online-Ressource)