Acta Oncologica · 2019 · 14 citations · 14 references
MedicineNuclear MedicineOncologyDiagnostic ImagingDiagnostic RadiologyTransplant ImmunologyPositron Emission TomographyPost-therapy ImagingRelapsed DiseaseResponse AssessmentTherapy Response AssessmentTreatment Response Monitoring18F-fluorodeoxyglucose Positron Emission TomographyDisease Relapse PredictionEnd-of-treatment ImagingFluorine-18 Fluorodeoxyglucose Positron Emission TomographyInterim Positron Emission TomographyPositron Emission Tomography Response AssessmentPost-treatment Response AssessmentTherapy Response Evaluation
Background: Fluorine-18-fluorodeoxyglucose positron emission tomography (PET) has an established and central role in diagnosis, staging and response evaluation of lymphoproliferative diseases. It has shown a high sensitivity and specificity at diagnosis in posttransplant lymphoproliferative disorders (PTLDs). However, little is known about the performance of interim and end of treatment (EOT) PET in PTLD patients with regards to response assessment, relapse prediction and outcome.Methods: We performed a single-center retrospective study in which we analyzed consecutive patients diagnosed with CD20-positive PTLD after solid organ transplantation between 2008 and 2017, who all received risk-stratified sequential treatment according to the PTLD-1 phase II trial. Interim and EOT PET studies were scored according to the Deauville criteria.Results: Forty-one patients were included with median follow-up of 41.5 months (range 1–108). Positive and negative predictive values for disease recurrence were 13% and 85% for interim and 33% and 87% for EOT PET, respectively. There was no significant difference in overall survival, progression-free survival nor time to progression between negative versus positive patients on interim and EOT scans.Conclusions: Negative interim and/or negative end of treatment PET identify PTLD patients with low risk of disease recurrence.
14
Sally F. Barrington, N. George Mikhaeel, Lale Kostakoğlu et al. · Journal of Clinical Oncology · 2014 · 1.6K citations · Full text
Malik E. Juweid, Gregory A. Wiseman, Julie M. Vose et al. · Journal of Clinical Oncology · 2005 · 387 citations · Full text
Medicine, Nuclear Medicine, Oncology +17