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Real‐world treatment practice in patients with advanced melanoma in the era before ipilimumab: results from the IMAGE study

The therapeutic landscape for advanced melanoma has recently been transformed by several novel agents (immune checkpoint inhibitors and molecular‐targeted agents). The prospective, multi‐site, observational study IMAGE (ipilimumab: management of advanced melanoma in real practice) included a retrosp...

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Detalles Bibliográficos
Autores principales: Middleton, Mark R., Dalle, Stéphane, Claveau, Joel, Mut, Pilar, Hallmeyer, Sigrun, Plantin, Patrice, Highley, Martin, Kotapati, Srividya, Le, Trong Kim, Brokaw, Jane, Abernethy, Amy P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4944869/
https://www.ncbi.nlm.nih.gov/pubmed/27118102
http://dx.doi.org/10.1002/cam4.717
Descripción
Sumario:The therapeutic landscape for advanced melanoma has recently been transformed by several novel agents (immune checkpoint inhibitors and molecular‐targeted agents). The prospective, multi‐site, observational study IMAGE (ipilimumab: management of advanced melanoma in real practice) included a retrospective cohort to describe real‐world treatment prior to approval of the immune checkpoint inhibitor ipilimumab. This retrospective cohort of patients, who started second‐line/subsequent treatment (index therapy) for advanced melanoma within 3 years before ipilimumab approval, was selected randomly by chart review. Collected data included treatment history, patient outcomes, and healthcare resource utilization. All patients had ≥1 year of follow‐up data. This analysis included 177 patients from Europe (69%) and North America (31%). The most common index therapies (used alone or in combination) were fotemustine (23%), dacarbazine (21%), temozolomide (14%), and platinum‐based chemotherapy (14%). Most patients (89%) discontinued index treatment during the study period; the most common reason was disease progression (59%). Among patients with tumor assessment (153/177; 86%), 2% had complete response, 5% had partial response, and 12% had stable disease on last tumor assessment. At 1‐year study follow‐up, median progression‐free survival was 2.6 months (95% confidence interval [CI], 2.1–2.9) and median overall survival was 8.8 months (95% CI, 6.5–9.7). During follow‐up, 95% of the patients had healthcare visits for advanced melanoma, 74% of whom were hospitalized or admitted to a hospice facility. These results provide insights into patient care with advanced melanoma in the era before ipilimumab and may serve as a benchmark for new agents in future real‐world studies.