Vj. Lowe et al., EVALUATION OF CHEMOTHERAPY RESPONSE IN PATIENTS WITH ADVANCED HEAD AND NECK-CANCER USING [F-18] FLUORODEOXYGLUCOSE POSITRON-EMISSION-TOMOGRAPHY, Head & neck, 19(8), 1997, pp. 666-674
Background. [F-18]Fluorodeoxyglucose (FDG)-positron emission tomograph
y (PET) can measure the metabolic activity of tissues; FDG-PET may be
able to predict response to chemotherapy by identifying changes in tum
or metabolism. Measurement of response to treatment may help improve s
urvival in the management of advanced head and neck cancer. We evaluat
ed this particular use of FDG-PET in patients participating in a neoad
juvant organ-preservation protocol using taxol and carboplatin and com
pared pathologic response after chemotherapy with changes in tumor met
abolism measured by FDG-PET. Methods. Serial FDG-PET studies (n = 56)
were performed in patients (n = 28) with stage III/IV head and neck ca
ncer participating in a neoadjuvant organ-preservation protocol. The F
DG-PET studies were performed before and after chemotherapy. All patie
nts had tissue biopsies before and after chemotherapy. Patients were c
lassified as pathologic complete response (PCR) or residual disease (R
D) based on tissue biopsies. Visual analysis of PET scans was performe
d to identify patients with complete response by PET, and these findin
gs were compared with pathology results. Metabolic changes were also e
valuated using standardized uptake ratios (SUR) of FDG. Results. The s
ensitivity and specificity of PET for residual cancer after therapy wa
s 90% (19/21) and 83% (5/6), respectively. Two patients had initially
negative biopsies and positive PET studies for persistent disease. Pat
hology review and rebiospy led to confirmation of the PET results in t
hese cases, giving a sensitivity of 90% for initial tissue biopsy. Con
clusions. In this preliminary analysis, FDG-PET was accurate in classi
fying response to chemotherapy in most patients. Fluorodeoxyglucose-PE
T may identify residual viable tumor when it is otherwise undetectable
. (C) 1997 John Wiley & Sons, Inc.