Combination of baseline metabolic tumour volume and early response on PET/CT improves progression-free survival prediction in DLBCL
Creators
- 1. Guy's and St Thomas' NHS Foundation Trust, Department of Clinical Oncology, London (United Kingdom)
- 2. King's College London, PET Imaging Centre at St Thomas' Hospital, Division of Imaging Sciences and Biomedical Engineering, London (United Kingdom)
- 3. King's College London, Department of Cancer Epidemiology and Population Health, London (United Kingdom)
- 4. Guy's and St Thomas' NHS Foundation Trust, Department of Haematology, London (United Kingdom)
Description
The study objectives were to assess the prognostic value of quantitative PET and to test whether combining baseline metabolic tumour burden with early PET response could improve predictive power in DLBCL. A total of 147 patients with DLBCL underwent FDG-PET/CT scans before and after two cycles of RCHOP. Quantitative parameters including metabolic tumour volume (MTV) and total lesion glycolysis (TLG) were measured, as well as the percentage change in these parameters. Cox regression analysis was used to test the relationship between progression-free survival (PFS) and the study variables. Receiver operator characteristics (ROC) analysis determined the optimal cut-off for quantitative variables, and Kaplan-Meier survival analysis was performed. The median follow-up was 3.8 years. As MTV and TLG measures correlated strongly, only MTV measures were used for multivariate analysis (MVA). Baseline MTV (MTV-0) was the only statistically significant predictor of PFS on MVA. The optimal cut-off for MTV-0 was 396 cm3. A model combing MTV-0 and Deauville score (DS) separated the population into three distinct prognostic groups: good (MTV-0 < 400; 5-year PFS > 90 %), intermediate (MTV-0 ≥ 400+ DS1-3; 5-year PFS 58.5 %) and poor (MTV-0 ≥ 400+ DS4-5; 5-year PFS 29.7 %) MTV-0 is an important prognostic factor in DLBCL. Combining MTV-0 and early PET/CT response improves the predictive power of interim PET and defines a poor-prognosis group in whom most of the events occur. (orig.)
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00259-016-3315-7Additional details
Identifiers
Publishing Information
- Journal Title
- European Journal of Nuclear Medicine and Molecular Imaging
- Journal Volume
- 43
- Journal Issue
- 7
- Journal Page Range
- p. 1209-1219
- ISSN
- 1619-7070
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 47080637
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CHEMOTHERAPY; COMPUTERIZED TOMOGRAPHY; CORRELATIONS; FLUORINE 18; FLUORODEOXYGLUCOSE; GLYCOLYSIS; LYMPHOMAS; MEDICAL SURVEILLANCE; METABOLIC DISEASES; POSITRON COMPUTED TOMOGRAPHY; RADIOPHARMACEUTICALS; REGRESSION ANALYSIS; SENSITIVITY; SPECIFICITY; SURVIVAL CURVES; SURVIVAL TIME; UPTAKE; VOLUME
- Descriptors DEC
- ANTIMETABOLITES; BETA DECAY RADIOISOTOPES; BETA-PLUS DECAY RADIOISOTOPES; CHEMICAL REACTIONS; COMPUTERIZED TOMOGRAPHY; DECOMPOSITION; DIAGNOSTIC TECHNIQUES; DISEASES; DRUGS; EMISSION COMPUTED TOMOGRAPHY; FLUORINE ISOTOPES; HOURS LIVING RADIOISOTOPES; IMMUNE SYSTEM DISEASES; ISOMERIC TRANSITION ISOTOPES; ISOTOPES; LABELLED COMPOUNDS; LIGHT NUCLEI; MATERIALS; MATHEMATICS; MEDICINE; METABOLISM; NANOSECONDS LIVING RADIOISOTOPES; NEOPLASMS; NUCLEI; ODD-ODD NUCLEI; RADIOACTIVE MATERIALS; RADIOISOTOPES; STATISTICS; THERAPY; TOMOGRAPHY