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Journal article

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

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/cam4.717

Authors


More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Oncology
Role:
Author
ORCID:
0000-0003-0167-1685


Publisher:
Wiley
Journal:
Cancer Medicine More from this journal
Volume:
5
Issue:
7
Pages:
1436-1443
Publication date:
2016-04-26
Acceptance date:
2016-03-07
DOI:
EISSN:
2045-7634
Pmid:
27118102


Language:
English
Keywords:
Pubs id:
pubs:719949
UUID:
uuid:2f5f77c9-eec8-45ac-b8ec-c49f7825c70b
Local pid:
pubs:719949
Source identifiers:
719949
Deposit date:
2017-10-03

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