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

Published

Journal Article

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.

Full Text

Cited Authors

  • Middleton, MR; Dalle, S; Claveau, J; Mut, P; Hallmeyer, S; Plantin, P; Highley, M; Kotapati, S; Le, TK; Brokaw, J; Abernethy, AP

Published Date

  • July 2016

Published In

Volume / Issue

  • 5 / 7

Start / End Page

  • 1436 - 1443

PubMed ID

  • 27118102

Pubmed Central ID

  • 27118102

Electronic International Standard Serial Number (EISSN)

  • 2045-7634

International Standard Serial Number (ISSN)

  • 2045-7634

Digital Object Identifier (DOI)

  • 10.1002/cam4.717

Language

  • eng