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


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
29 May 2021
Historique:
received: 20 11 2020
accepted: 15 03 2021
entrez: 30 5 2021
pubmed: 31 5 2021
medline: 16 10 2021
Statut: epublish

Résumé

Ipilimumab 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. IMAGE 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 ≥3 years of follow-up. Adjusted OS curves based on multivariate Cox regression models included covariate effects. Safety and patient-reported outcomes were assessed. Among 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 64 years, 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. With long-term follow-up (≥ 3 years), safety and OS in this real-world population of patients treated with ipilimumab 3 mg/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. ClinicalTrials.gov , NCT01511913. Registered January 19, 2012 - Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT01511913.

Sections du résumé

BACKGROUND BACKGROUND
Ipilimumab 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.
METHODS METHODS
IMAGE 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 ≥3 years of follow-up. Adjusted OS curves based on multivariate Cox regression models included covariate effects. Safety and patient-reported outcomes were assessed.
RESULTS RESULTS
Among 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 64 years, 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.
CONCLUSIONS CONCLUSIONS
With long-term follow-up (≥ 3 years), safety and OS in this real-world population of patients treated with ipilimumab 3 mg/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 BACKGROUND
ClinicalTrials.gov , NCT01511913. Registered January 19, 2012 - Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT01511913.

Identifiants

pubmed: 34051732
doi: 10.1186/s12885-021-08032-y
pii: 10.1186/s12885-021-08032-y
pmc: PMC8164785
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0
Ipilimumab 0

Banques de données

ClinicalTrials.gov
['NCT01511913']

Types de publication

Clinical Trial, Phase IV Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

642

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Auteurs

Stéphane Dalle (S)

Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, 69495, Pierre-Bénite, France. stephane.dalle@chu-lyon.fr.

Laurent Mortier (L)

Université de Lille, INSERM U1189, CHRU Lille, 59037, Lille, France.

Pippa Corrie (P)

Cambridge University Hospitals NHS Foundation Trust, Cambridge, CB0 2QQ, UK.

Michal Lotem (M)

Hadassah Hebrew University Hospital, 91120, Jerusalem, Israel.

Ruth Board (R)

Royal Preston Hospital, Preston, PR2 9HT, UK.

Ana María Arance (AM)

Hospital Clínic Barcelona, 08036, Barcelona, Spain.

Frank Meiss (F)

Department of Dermatology, Faculty of Medicine, Medical Center - University of Freiburg, 79104, Freiburg, Germany.

Patrick Terheyden (P)

University of Lübeck, 23538, Lübeck, Germany.

Ralf Gutzmer (R)

Medizinische Hochschule Hannover, 30625, Hanover, Germany.

Brian Buysse (B)

Syneos Health, Morrisville, NC, 27560, USA.

Kelly Oh (K)

Syneos Health, Morrisville, NC, 27560, USA.

Jane Brokaw (J)

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

T Kim Le (TK)

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

Susan D Mathias (SD)

Health Outcomes Solutions, Winter Park, FL, 32790, USA.

Julie Scotto (J)

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

Jennifer Lord-Bessen (J)

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

Andriy Moshyk (A)

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

Srividya Kotapati (S)

Bristol Myers Squibb, Princeton, NJ, 08543, USA.

Mark R Middleton (MR)

Churchill Hospital, Oxford, OX3 7DQ, UK.

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Classifications MeSH