False positive FDG uptake in melanoma patients treated with talimogene laherparepvec (T-VEC).
Aged
Antineoplastic Agents, Immunological
/ therapeutic use
Biological Products
/ therapeutic use
Cohort Studies
False Positive Reactions
Female
Fluorodeoxyglucose F18
Herpesvirus 1, Human
Humans
Lymph Nodes
/ diagnostic imaging
Male
Melanoma
/ drug therapy
Oncolytic Virotherapy
Positron Emission Tomography Computed Tomography
Radiopharmaceuticals
Retrospective Studies
Skin Neoplasms
/ drug therapy
Melanoma, Cutaneous Malignant
FDG-PET/CT
cutaneous melanoma
false positive FDG uptake
talimogene laherparevec (T-VEC)
Journal
Journal of surgical oncology
ISSN: 1096-9098
Titre abrégé: J Surg Oncol
Pays: United States
ID NLM: 0222643
Informations de publication
Date de publication:
Dec 2021
Dec 2021
Historique:
revised:
18
06
2021
received:
10
02
2021
accepted:
01
07
2021
pubmed:
9
7
2021
medline:
10
11
2021
entrez:
8
7
2021
Statut:
ppublish
Résumé
Talimogene laherparepvec (T-VEC) is a genetically modified herpes simplex virus-1-based oncolytic immunotherapy and has been approved for the local treatment of unresectable (stage IIIB/C and IVM1a) cutaneous melanoma. During T-VEC treatment, tumor response is often evaluated using [18F]2-fluoro-2-deoxy- d-glucose(FDG) positron emission tomography/computed tomography (PET/CT). In a Dutch cohort (n = 173), almost one-third of patients developed new-onset FDG uptake in uninjected locoregional lymph nodes during T-VEC. In 36 out of 53 (68%) patients with new nodal FDG uptake, nuclear medicine physicians classified this FDG uptake as "suspected metastases" without clinical or pathological confirmation in the majority of patients. These false positive results indicate that new-onset FDG uptake in locoregional lymph nodes during T-VEC treatment does not necessarily reflect progressive disease, but may be associated with immune infiltration. In current clinical practice, physicians should be aware of the high false positive rate of FDG uptake during treatment with T-VEC in patients with melanoma. Therefore, pathological examination of lymph node lesions with new FDG uptake is recommended to differentiate between progressive disease and immune infiltration after treatment with T-VEC.
Identifiants
pubmed: 34235758
doi: 10.1002/jso.26607
pmc: PMC8596632
doi:
Substances chimiques
Antineoplastic Agents, Immunological
0
Biological Products
0
Radiopharmaceuticals
0
talimogene laherparepvec
0
Fluorodeoxyglucose F18
0Z5B2CJX4D
Types de publication
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
1161-1165Informations de copyright
© 2021 The Authors. Journal of Surgical Oncology published by Wiley Periodicals LLC.
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