J Exp Clin Cancer Res 2013, 32:9 PubMedCentralPubMedCrossRef
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J Exp Clin Cancer Res 2013, 32:9.PubMedCentralPubMedCrossRef

Competing interests The authors declare that they have no competing interests. Authors’ contributions ZH, CS, MH, QC and XY conceived and designed the study, performed the experiments and wrote the paper. ZH, CS, WA, YB, and XY contributed to the writing and to the critical reading of the paper. ZH, MH, LR, WA, and QS performed patient collection and clinical data interpretation. ZH, CS, MH, YB, and QC participated performed the statistical analysis. All authors read and approved the final manuscript.”
“Background Historically, patients with unresectable Stage III or Stage IV (advanced) melanoma had limited treatment options and INCB024360 poor survival outcomes, with older patients having a particularly dismal prognosis [1, 2]. In 2010, there were

an estimated 13.6 melanoma-related deaths per 100 000 US inhabitants aged > 65 years compared with 1.2 per 100 000 US inhabitants aged ≤ 65 years [3]. Current epidemiological data suggest the incidence of melanoma continues Acalabrutinib to rise in the elderly population despite indications that it has plateaued in younger people [3, 4]. Combined with a rapid increase in the proportion of elderly people, this has resulted in melanoma becoming an increasingly important health concern in the developed world [5]. A number of explanations for the poor prognosis Carnitine palmitoyltransferase II of elderly patients with melanoma have been proposed. Older melanoma patients may be more predisposed to distant metastasis arising from the haematological distribution of tumour cells than younger patients due to changes in lymphatic drainage with ageing [6]. In addition, elderly patients present with thicker melanomas, a higher mitotic

rate and increased incidence of ulceration [7], all of which are associated with a worse prognosis [1]. It is likely, however, that the high mortality rates among elderly patients result from a number of age-related variables preventing optimal management of this disease [8]. One confounding factor that may contribute to the poor prognosis of elderly patients with metastatic melanoma is a weakening of the immune system with age, a process referred to as immunosenescence. Therefore, the possibility of using immune-based therapies to promote immune function is an attractive therapeutic option [8, 9]. In 2011, the novel immunotherapy agent ipilimumab was the first agent approved for the treatment of patients with advanced melanoma in over three decades [10]. Ipilimumab is a fully human monoclonal antibody directed against cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4), a negative regulator of T-cell-mediated immune responses. By blocking CTLA-4, ipilimumab enables prolonged T-cell activation, proliferation and tumour infiltration, thereby potentiating endogenous antitumour responses [11].

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