Adjuvant ipilimumab versus placebo after complete resection of high-risk stage III melanoma (EORTC 18071): a randomised, double-blind, phase 3 trial.
By A. Eggermont, V. Chiarion-Sileni, J. Grob, R. Dummer, J. Wolchok, H. Schmidt, O. Hamid, C. Robert, P. Ascierto, J. Richards and 12 more. The Lancet Oncology, 2015
1,127 citations recorded by the source corpus.
Subfields: Molecular Biology, Oncology
View Paper: https://www.semanticscholar.org/paper/b03c6d9e1293305db329f498f3d6b07976548a1c
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Citations in the corpus
- Prolonged Survival in Stage III Melanoma with Ipilimumab Adjuvant Therapy (2016, result): “We previously reported the primary results of the EORTC 18071 phase 3 trial in which we compared adjuvant ipilimumab with placebo in patients with resected stage III melanoma.(11) At a median follow-up of 2.”
- Management of toxicities of immune checkpoint inhibitors. (2016, background): “Although rare and occurring in no more than 3% of patients (3% with a 10 mg/kg dose of ipilimumab [4], <1% in other studies [5,8,10,14,16,19,22]), neurological irAEs require prompt recognition and treatment to avoid substantial morbidity.”
- Cutaneous melanoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up†. (2019, background): “Therefore, additional trials are mandatory and the respective patient population should be referred to centres offering trial participation [21].”
- Management of Immune-Related Adverse Events in Patients Treated With Immune Checkpoint Inhibitor Therapy: American Society of Clinical Oncology Clinical Practice Guideline (2018, background): “The EORTC 18071 trial reported neurologic irAEs at a rate of 4% in the adjuvant ipilimumab arm.(91) Most neurologic events are mild; headache and peripheral sensory neuropathy are the most commonly encountered symptoms.”