Uveal Melanoma: A European Network to Face the Many Challenges of a Rare Cancer.
Sophie Piperno-NeumannJose Maria PiulatsMatthias GoebelerIain GallowayIwona LugowskaJürgen Christian BeckerPia P VihinenJoachim Van CalsterTheodora HadjistilianouRui Daniel Mateus Barreiros ProençaJose Maria CaminalMuriel RogasikJean Yves BlayEllen KapiteijnPublished in: Cancers (2019)
Uveal melanoma (UM) is the most frequent primary ocular cancer in adults, accounting for 5% of all melanomas. Despite effective treatments for the primary tumour, up to 50% of UM patients will develop metastasis, leading to a very poor prognosis and a median overall survival of 6 to 12 months, with no major improvements in the last 30 years. There is no standard oncological treatment available for metastatic UM patients, and BRAF/MEK and immune checkpoint inhibitors show disappointing results when compared to cutaneous melanoma (CM). Recent advances in biology, however, identified specific gene and chromosome alterations, potentially permitting an actively tailored surveillance strategy, and dedicated clinical studies. Being a rare cancer, UM patients have to overcome issues such as identifying referral centres, having access to information, and partnering with oncologists for specific management strategies and research priorities. Here, we describe how the EUropean Rare Adult solid CAacer Network (EURACAN) will help in addressing these challenges and accelerating international collaborations to enhance the development of innovative treatments in UM.
Keyphrases
- end stage renal disease
- poor prognosis
- ejection fraction
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- prognostic factors
- public health
- papillary thyroid
- small cell lung cancer
- long non coding rna
- primary care
- palliative care
- young adults
- cell proliferation
- genome wide
- health information
- advanced cancer
- robot assisted
- rectal cancer