Long-term real-world experience with ipilimumab and non-ipilimumab therapies in advanced melanoma: the IMAGE study

被引:13
作者
Dalle, Stephane [1 ]
Mortier, Laurent [2 ]
Corrie, Pippa [3 ]
Lotem, Michal [4 ]
Board, Ruth [5 ]
Arance, Ana Maria [6 ]
Meiss, Frank [7 ]
Terheyden, Patrick [8 ]
Gutzmer, Ralf [9 ]
Buysse, Brian [10 ]
Oh, Kelly [10 ]
Brokaw, Jane [11 ]
Le, T. Kim [11 ]
Mathias, Susan D. [12 ]
Scotto, Julie [11 ]
Lord-Bessen, Jennifer [11 ]
Moshyk, Andriy [11 ]
Kotapati, Srividya [11 ]
Middleton, Mark R. [13 ]
机构
[1] Hosp Civils Lyon, Ctr Hosp Lyon Sud, F-69495 Pierre Benite, France
[2] Univ Lille, INSERM U1189, CHRU Lille, F-59037 Lille, France
[3] Cambridge Univ Hosp NHS Fdn Trust, Cambridge CB0 2QQ, England
[4] Hadassah Hebrew Univ Hosp, IL-91120 Jerusalem, Israel
[5] Royal Preston Hosp, Preston PR2 9HT, England
[6] Hosp Clin Barcelona, Barcelona 08036, Spain
[7] Med Ctr Univ Freiburg, Dept Dermatol, Fac Med, D-79104 Freiburg, Germany
[8] Univ Lubeck, D-23538 Lubeck, Germany
[9] Hannover Med Sch, D-30625 Hannover, Germany
[10] Syneos Hlth, Morrisville, NC 27560 USA
[11] Bristol Myers Squibb, Princeton, NJ 08543 USA
[12] Hlth Outcomes Solut, Winter Pk, Winter Pk, FL 32790 USA
[13] Churchill Hosp, Oxford OX3 7DQ, England
关键词
Advanced melanoma; Ipilimumab; Overall survival; Quality of life; Real-world; Subsequent therapy; METASTATIC MELANOMA; RECEIVED IPILIMUMAB; PLUS DACARBAZINE; SURVIVAL RATES; PHASE-II; MG/KG; MULTICENTER; EFFICACY; TRIALS;
D O I
10.1186/s12885-021-08032-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundIpilimumab has shown long-term overall survival (OS) in patients with advanced melanoma in clinical trials, but robust real-world evidence is lacking. We present long-term outcomes from the IMAGE study (NCT01511913) in patients receiving ipilimumab and/or non-ipilimumab (any approved treatment other than ipilimumab) systemic therapies.MethodsIMAGE was a multinational, prospective, observational study assessing adult patients with advanced melanoma treated with ipilimumab or non-ipilimumab systemic therapies between June 2012 and March 2015 with >= 3years of follow-up. Adjusted OS curves based on multivariate Cox regression models included covariate effects. Safety and patient-reported outcomes were assessed.ResultsAmong 1356 patients, 1094 (81%) received ipilimumab and 262 (19%) received non-ipilimumab index therapy (systemic therapy [chemotherapy, anti-programmed death 1 antibodies, or BRAF MEK inhibitors], radiotherapy, and radiosurgery). In the overall population, median age was 64years, 60% were male, 78% were from Europe, and 78% had received previous treatment for advanced melanoma. In the ipilimumab-treated cohort, 780 (71%) patients did not receive subsequent therapy (IPI-noOther) and 314 (29%) received subsequent non-ipilimumab therapy (IPI-Other) on study. In the non-ipilimumab-treated cohort, 205 (78%) patients remained on or received other subsequent non-ipilimumab therapy (Other-Other) and 57 (22%) received subsequent ipilimumab therapy (Other-IPI) on study. Among 1151 patients who received ipilimumab at any time during the study (IPI-noOther, IPI-Other, and Other-IPI), 296 (26%) reported CTCAE grade >= 3 treatment-related adverse events, most occurring in year 1. Ipilimumab-treated and non-ipilimumab-treated patients who switched therapy (IPI-Other and Other-IPI) had longer OS than those who did not switch (IPI-noOther and Other-Other). Patients with prior therapy who did not switch therapy (IPI-noOther and Other-Other) showed similar OS. In treatment-naive patients, those in the IPI-noOther group tended to have longer OS than those in the Other-Other group. Patient-reported outcomes were similar between treatment cohorts.ConclusionsWith long-term follow-up (>= 3years), safety and OS in this real-world population of patients treated with ipilimumab 3mg/kg were consistent with those reported in clinical trials. Patient-reported quality of life was maintained over the study period. OS analysis across both pretreated and treatment-naive patients suggested a beneficial role of ipilimumab early in treatment.Trial registration ClinicalTrials.gov, NCT01511913. Registered January 19, 2012 - Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT01511913
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