نتایج جستجو برای: ipilimumab

تعداد نتایج: 1961  

Journal: :Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2015
Vera Montes Sandra Sousa Fernando Pita Rui Guerreiro Cátia Carmona

In daily clinical practice, there is a growing number of patients receiving new biological agents used in the treatment of malignancies. Ipilimumab is a fully humanized monoclonal antibody approved for patients with melanoma. It acts as an immune checkpoint inhibitor, binding and blocking cytotoxic T-lymphocyte antigen-4 in order to increase the antitumor immune response. There are several repo...

2014
Claire Roddie Karl S Peggs

Ipilimumab is a fully human immunoglobulin subclass G1 anticytotoxic-T-lymphocyte-antigen-4 monoclonal antibody. It has been approved by the US Food and Drug Administration (FDA) and the European Medicines Agency for use in advanced melanoma following clear evidence of survival benefit in randomized Phase III studies. It is also under investigation as a treatment for other solid tumors such as ...

Journal: :Cancer immunology research 2016
Sebastian Theurich Sacha I Rothschild Michael Hoffmann Mario Fabri Andrea Sommer Maria Garcia-Marquez Martin Thelen Catherine Schill Ramona Merki Thomas Schmid Dieter Koeberle Alfred Zippelius Christian Baues Cornelia Mauch Christian Tigges Alexander Kreuter Jan Borggrefe Michael von Bergwelt-Baildon Max Schlaak

Immune checkpoint inhibition with ipilimumab has revolutionized cancer immunotherapy and significantly improved outcomes of patients with advanced malignant melanoma. Local peripheral treatments (LPT), such as radiotherapy or electrochemotherapy, have been shown to modulate systemic immune responses, and preliminary data have raised the hypothesis that the combination of LPT with systemic immun...

2013
Van Anh Trinh Brenda Hagen

Ipilimumab, a fully human anti-CTLA-4 antibody, has been approved for the treatment of unresectable or metastatic melanoma based on its survival benefit demonstrated in randomized phase III studies. The current approved dosing schedule of ipilimumab is 3 mg/kg as a 90-min intravenous infusion every 3 weeks for a total of 4 doses. The immune-mediated mechanism of action of ipilimumab can result ...

2012
Stephanie Andrews Rita Holden

When diagnosed in its early stages, melanoma is highly treatable and associated with good long-term outcomes; however, the prognosis is much poorer for patients diagnosed with advanced or metastatic melanoma. For decades, available treatments were effective in only a few patients and associated with significant safety concerns. Ipilimumab is a novel immunotherapy which has proved to be an excit...

Journal: :Cancer immunology research 2014
F Stephen Hodi Donald Lawrence Cecilia Lezcano Xinqi Wu Jun Zhou Tetsuro Sasada Wanyong Zeng Anita Giobbie-Hurder Michael B Atkins Nageatte Ibrahim Philip Friedlander Keith T Flaherty George F Murphy Scott Rodig Elsa F Velazquez Martin C Mihm Sara Russell Pamela J DiPiro Jeffrey T Yap Nikhil Ramaiya Annick D Van den Abbeele Maria Gargano David McDermott

Ipilimumab improves survival in advanced melanoma and can induce immune-mediated tumor vasculopathy. Besides promoting angiogenesis, vascular endothelial growth factor (VEGF) suppresses dendritic cell maturation and modulates lymphocyte endothelial trafficking. This study investigated the combination of CTLA4 blockade with ipilimumab and VEGF inhibition with bevacizumab. Patients with metastati...

Journal: :Clinical oncology (Royal College of Radiologists (Great Britain)) 2016
T Carter H Shaw D Cohn-Brown K Chester P Mulholland

The median survival in glioblastoma is just over a year, with no standard second-line therapy. Ipilimumab is an immune checkpoint inhibitor that activates the anti-tumour immune response by cytotoxic T-lymphocyte antigen-4 blockade. There is significant evidence supporting its role in the treatment of malignant melanoma, including in patients with brain metastases. The addition of the anti-angi...

2014
Stephanie Du Four Angela Hong Matthew Chan Michail Charakidis Johnny Duerinck Sofie Wilgenhof Wei Wang Linda Feng Alex Michotte Meena Okera Brindha Shivalingam Gerald Fogarty Richard Kefford Bart Neyns

Four cases previously treated with ipilimumab with a total of six histologically confirmed symptomatic lesions of RNB without any sign of active tumour following stereotactic irradiation of MBM are reported. These lesions were all originally thought to be disease recurrence. In two cases, ipilimumab was given prior to SRT; in the other two ipilimumab was given after SRT. The average time from f...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2016
Heather L McArthur Adi Diab David B Page Jianda Yuan Stephen B Solomon Virgilio Sacchini Christopher Comstock Jeremy C Durack Majid Maybody Janice Sung Arielle Ginsberg Phillip Wong Afsar Barlas Zhiwan Dong Chunjun Zhao Brian Blum Sujata Patil Deirdre Neville Elizabeth A Comen Elizabeth A Morris Alan Kotin Edi Brogi Y Hannah Wen Monica Morrow Mario E Lacouture Padmanee Sharma James P Allison Clifford A Hudis Jedd D Wolchok Larry Norton

PURPOSE To assess the safety and tolerability of preoperative cryoablation-mediated tumor antigen presentation and/or ipilimumab-mediated immune modulation in women with operable breast cancer. EXPERIMENTAL DESIGN In this pilot study, 19 women with breast cancer for whom mastectomy was planned were treated with preoperative tumor cryoablation (n = 7), single-dose ipilimumab at 10 mg/kg (n = 6...

2015
Matthew Hellmann Suresh Ramalingam Martin Reck Ken O'Byrne Luis Paz-Ares Christopher T Harbison Prabhu Bhagavatheeswaran Faith Nathan Julie Brahmer

Background Patients with advanced NSCLC are treated with first-line PT-DC, which is associated with a median OS of 8–10 months and 1-year and 2-year survival rates of 30–40% and 10–15%, respectively. Nivolumab (a fully human IgG4 anti-programmed death-1 immune checkpoint inhibitor antibody) alone and in combination with ipilimumab (a fully human IgG4 cytotoxic T-lymphocyte antigen-4 immune chec...

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