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Follicular Lymphoma Treated with First-Line Immunochemotherapy: A Review of PET/CT in Patients Who Did Not Achieve a Complete Metabolic Response in the GALLIUM Study.
Barrington, Sally F; Mir, Farheen; El-Galaly, Tarec Christoffer; Knapp, Andrea; Nielsen, Tina G; Sahin, Denis; Wenger, Michael; Kostakoglu, Lale; Trotman, Judith; Meignan, Michel.
Afiliação
  • Barrington SF; School of Biomedical Engineering and Imaging Sciences, King's College London and Guy's and St. Thomas' PET Centre, King's College London, King's Health Partners, London, United Kingdom; sally.barrington@kcl.ac.uk.
  • Mir F; Department of Haematology, Royal Marsden NHS Foundation Trust, London, United Kingdom.
  • El-Galaly TC; Department of Hematology, Aalborg University Hospital, Aalborg, Denmark.
  • Knapp A; Product Development Oncology, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Nielsen TG; Product Development Oncology, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Sahin D; Product Development Oncology, F. Hoffmann-La Roche Ltd., Basel, Switzerland.
  • Wenger M; Pharma Development Oncology, Genentech Inc., South San Francisco, California.
  • Kostakoglu L; Department of Radiology and Medical Imaging, University of Virginia, Charlottesville, Virginia.
  • Trotman J; Hematology Department, Concord Repatriation General Hospital, University of Sydney, Concord, New South Wales, Australia; and.
  • Meignan M; LYSA Imaging, Hôpitaux Universitaires Henri Mondor and Université Paris-Est Créteil, Créteil, France.
J Nucl Med ; 63(8): 1149-1154, 2022 08.
Article em En | MEDLINE | ID: mdl-34857656
ABSTRACT
Complete metabolic response (CMR) on PET/CT was the sole independent predictor of overall survival in the PET substudy of the phase III GALLIUM trial (NCT01332968) in first-line treatment of high-tumor-burden follicular lymphoma. The aim of this analysis was to further investigate the outcome of patients not achieving CMR.

Methods:

Two international experts rereviewed PET/CT scans from patients failing to achieve CMR assessed by the Independent Review Committee masked otherwise to committee results. Metabolic response category and Deauville score were assigned. Progression-free survival (PFS) was investigator-assessed with contrast-enhanced CT. Kaplan-Meier methodology was used to estimate landmark PFS and time to next treatment from end of induction by Deauville score. Patients who experienced CT-based progressive disease at the end of induction were excluded.

Results:

Fifty-four patients were reviewed. Six had CMR, 37 had a partial metabolic response, 2 had no metabolic response, and 9 had progressive metabolic disease. Patients were reassigned to CMR because 18F-FDG uptake was considered inflammatory (n = 2), was considered incidental neoplasia (n = 2), or was visually close to liver uptake but quantitatively lower (n = 2). There was a trend for shorter PFS and time to next treatment for patients with a Deauville score of 5 than a score of 4. High-grade mesenteric uptake at the end of induction was common, occurring in 20 patients with non-CMR, 14 of whom achieved CMR at all other sites. Only 3 of 14 (21%) patients with mesenteric uptake as the only site of disease experienced progression or death within 24 mo, whereas 4 of 6 patients (67%) with mesenteric and additional sites of 18F-FDG-avid disease experienced progression or death within 24 mo. All patients with early progression had measurable disease on contrast-enhanced CT at 18F-FDG-avid sites at the end of induction.

Conclusion:

After induction immunochemotherapy, CMR was assigned after reassessment in some patients, in whom increased 18F-FDG uptake was considered due to inflammation or incidental neoplasia rather than to lymphoma. Quantitative assessment to confirm the visual impression of residual uptake in lesions is suggested. Isolated mesenteric 18F-FDG uptake is likely a common false-positive finding at the end of induction and does not warrant changes in clinical management or disease surveillance unless there is measurable disease on contrast-enhanced CT or clinical suspicion of active disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Folicular / Gálio Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Nucl Med Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Folicular / Gálio Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: J Nucl Med Ano de publicação: 2022 Tipo de documento: Article