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Long-term real-world experience with ipilimumab and non-ipilimumab therapies in advanced melanoma: the IMAGE study.
Dalle, Stéphane; Mortier, Laurent; Corrie, Pippa; Lotem, Michal; Board, Ruth; Arance, Ana María; Meiss, Frank; Terheyden, Patrick; Gutzmer, Ralf; Buysse, Brian; Oh, Kelly; Brokaw, Jane; Le, T Kim; Mathias, Susan D; Scotto, Julie; Lord-Bessen, Jennifer; Moshyk, Andriy; Kotapati, Srividya; Middleton, Mark R.
Afiliación
  • Dalle S; Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, 69495, Pierre-Bénite, France. stephane.dalle@chu-lyon.fr.
  • Mortier L; Université de Lille, INSERM U1189, CHRU Lille, 59037, Lille, France.
  • Corrie P; Cambridge University Hospitals NHS Foundation Trust, Cambridge, CB0 2QQ, UK.
  • Lotem M; Hadassah Hebrew University Hospital, 91120, Jerusalem, Israel.
  • Board R; Royal Preston Hospital, Preston, PR2 9HT, UK.
  • Arance AM; Hospital Clínic Barcelona, 08036, Barcelona, Spain.
  • Meiss F; Department of Dermatology, Faculty of Medicine, Medical Center - University of Freiburg, 79104, Freiburg, Germany.
  • Terheyden P; University of Lübeck, 23538, Lübeck, Germany.
  • Gutzmer R; Medizinische Hochschule Hannover, 30625, Hanover, Germany.
  • Buysse B; Syneos Health, Morrisville, NC, 27560, USA.
  • Oh K; Syneos Health, Morrisville, NC, 27560, USA.
  • Brokaw J; Bristol Myers Squibb, Princeton, NJ, 08543, USA.
  • Le TK; Bristol Myers Squibb, Princeton, NJ, 08543, USA.
  • Mathias SD; Health Outcomes Solutions, Winter Park, FL, 32790, USA.
  • Scotto J; Bristol Myers Squibb, Princeton, NJ, 08543, USA.
  • Lord-Bessen J; Bristol Myers Squibb, Princeton, NJ, 08543, USA.
  • Moshyk A; Bristol Myers Squibb, Princeton, NJ, 08543, USA.
  • Kotapati S; Bristol Myers Squibb, Princeton, NJ, 08543, USA.
  • Middleton MR; Churchill Hospital, Oxford, OX3 7DQ, UK.
BMC Cancer ; 21(1): 642, 2021 May 29.
Article en En | MEDLINE | ID: mdl-34051732
ABSTRACT

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:

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:

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:

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 ClinicalTrials.gov , NCT01511913. Registered January 19, 2012 - Retrospectively registered, https//clinicaltrials.gov/ct2/show/NCT01511913.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Protocolos de Quimioterapia Combinada Antineoplásica / Ipilimumab / Inhibidores de Puntos de Control Inmunológico / Melanoma Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Protocolos de Quimioterapia Combinada Antineoplásica / Ipilimumab / Inhibidores de Puntos de Control Inmunológico / Melanoma Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Año: 2021 Tipo del documento: Article