U. Cremerius et al., Positron emission tomography with F-18-FDG to detect residual disease after therapy for malignant lymphoma, NUCL MED C, 19(11), 1998, pp. 1055-1063
We retrospectively evaluated the use of F-18-FDG PET for assessment of resi
dual disease in 27 patients after therapy for malignant lymphoma. The image
s were evaluated qualitatively and quantitatively using standardized uptake
values (SUV). All findings were validated either by biopsy or by clinical
follow-up and compared with corresponding CT findings. The impact of blood
glucose concentration, body weight, body surface area, lesion diameter and
the time between injection and imaging on the SUVs were analysed. All 15 pa
tients with biopsy-proven residual disease or relapse during follow-up and
11 of 12 patients who remained relapse-free were correctly identified by qu
alitative interpretation of the PET images. A case of pneumonitis after rad
iotherapy/chemotherapy accounted for the only false-positive finding. Compa
red with CT imaging, PET had a significantly higher specificity (P < 0.01),
accuracy (P < 0.05) and positive predictive value (P < 0.05). The mean and
maximum SUV of the tumour lesions were positively correlated to lesion dia
meter (P < 0.01) and imaging time post-injection (P < 0.01). Standardized u
ptake values corrected for the partial volume effect and normalized to a st
andardized imaging time (SUVBPT) were significantly higher (P < 0.05) in hi
gh-grade than in low-grade non-Hodgkin's lymphoma. In conclusion F-18-FDG P
ET may help in the identification of patients who need additional treatment
after the completion of conventional therapy. Qualitative image interpreta
tion appears sufficient for this purpose. ((C) 1998 Lippincott Williams & W
ilkins).