Prediction of response to immune checkpoint inhibitor therapy using 18F-FDG PET/CT in patients with melanoma.


Journal

Medicine
ISSN: 1536-5964
Titre abrégé: Medicine (Baltimore)
Pays: United States
ID NLM: 2985248R

Informations de publication

Date de publication:
Jul 2019
Historique:
entrez: 24 7 2019
pubmed: 25 7 2019
medline: 3 8 2019
Statut: ppublish

Résumé

We aimed to assess serial F-FDG PET/CT imaging according to morphological (RECIST1.1, iRECIST) and functional (PERCIST, PECRIT) criteria to predict clinical response to therapy in patients with advanced melanoma receiving immune checkpoint blocking agents.Retrospective data collection and analysis was done for 37 patients with unresectable metastatic cutaneous melanoma eligible for immunotherapy (cycles: 4 for ipilimumab and pembrolizumab/ 6 for nivolumab).F-FDG PET/CT imaging was performed prior to (F-FDG PET/CT 0) and 14 weeks after ICI onset (F-FDG PET/CT 1). Some cases during the follow-up required imaging (F-FDG PET/CT 2). Assessment of patient response to treatment was done according to RECIST1.1, iRECIST, PERCIST and PECRIT criteria.Among 37 assessed patients, 27 had 1 line of ICI, 8 had 2 lines of ICI and 2 patients had 3 lines of ICI: total of 49 PET/CTs. Mean time between initiation of ICI and F-FDG PET/CT (1 or 2) were respectively 13.82 ± 4.32 and 24.73 ± 9.53 weeks. Time between F-FDG PET/CT 1 and F-FDG PET/CT 2 was at mean +/- SD: 11.19w ± 5.59. Median PFS was 29.62 months (range 22.52-36.71) (P = .001: RECIST 1.1), (P < .0001: iRECIST), (P = .000: PERCIST), (P = .072: PECRIT). Median OS was 36.62 months (30.46-42.78) (P = .005: RECIST 1.1), (P < .0001: iRECIST), (P = .001: PERCIST), (P = .082 PECRIT).F-FDG PET/CT could detect eventual ICI-response in patients with metastatic melanoma undergoing ICI using iRECIST and PERCIST criteria.

Identifiants

pubmed: 31335691
doi: 10.1097/MD.0000000000016417
pii: 00005792-201907190-00026
pmc: PMC6708819
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Antineoplastic Agents, Immunological 0
Ipilimumab 0
Radiopharmaceuticals 0
Fluorodeoxyglucose F18 0Z5B2CJX4D
Nivolumab 31YO63LBSN
pembrolizumab DPT0O3T46P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e16417

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Auteurs

Karim Amrane (K)

Oncology Department.

Delphine Le Goupil (D)

Oncology Department.

Gilles Quere (G)

Oncology Department.

Olivier Delcroix (O)

Nuclear Medicine Department.

Sylvie Gouva (S)

Oncology Department.

Ulrike Schick (U)

Radiotherapy department, University Hospital Morvan, 29609 Brest Cedex.

Pierre-Yves Salaun (PY)

Nuclear Medicine Department.
EA 3878 GETBO IFR 148, Brest.
Université of Bretagne Occidentale.

Ronan Abgral (R)

Nuclear Medicine Department.
EA 3878 GETBO IFR 148, Brest.
Université of Bretagne Occidentale.

Zarrin Alavi (Z)

Brest Medical University Hospital- Inserm CIC 1412, France.

Nathalie Keromnes (N)

Nuclear Medicine Department.

Solène Querellou (S)

Nuclear Medicine Department.
EA 3878 GETBO IFR 148, Brest.
Université of Bretagne Occidentale.

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Classifications MeSH