2-STEP IMMUNOSCINTIGRAPHY FOR NON-SMALL-CELL LUNG-CANCER STAGING USING A BISPECIFIC ANTI-CEA ANTI-INDIUM-DTPA ANTIBODY AND AN INDIUM-111-LABELED DTPA DIMER/
Jp. Vuillez et al., 2-STEP IMMUNOSCINTIGRAPHY FOR NON-SMALL-CELL LUNG-CANCER STAGING USING A BISPECIFIC ANTI-CEA ANTI-INDIUM-DTPA ANTIBODY AND AN INDIUM-111-LABELED DTPA DIMER/, The Journal of nuclear medicine, 38(4), 1997, pp. 507-511
Immunoscintigraphy (IS) using anti-CEA F(ab')(2) monoclonal antibody (
MAb) is useful for improving mediastinal staging of nonsmall cell lung
cancer (NSCLC), but the technique was limited because of an insuffici
ent contrast between tumor and normal tissues. The aim of this study w
as to determine if the method could be improved by a two-step method w
hich uses a bispecific anti-CEA/anti-di-DTPA antibody (Bs-MAb) and In-
111-labeled di-DTPA-tyrosyl-lysine bivalent hapten. Methods: Twelve pa
tients were intravenously given a 30 min Bs-MAb infusion (0.1 mg/kg).
Four days later, they were injected intravenously with 0.1 mu g/kg hap
ten labeled with 185 MBq In-111 (5 mCi). Images were recorded immediat
ely and 6 and 24 hr after hapten injection. A pharmacokinetic analysis
was performed. Surgery was performed 3 days after In-111-hapten injec
tion, and samples of tumor and normal tissues were collected for immun
ohistochemical and biodistribution studies. IS results were classified
as true-positive CTP), false-positive (FP), true-negative (TN) or fal
se-negative (FN) according to the surgical data Results: Primary tumor
s were visualized in nine patients. The contrast was excellent, genera
lly higher than that obtained with direct labeling of anti-CEA. In the
mediastinum, IS results were (after surgery) five TN, two TP and one
FP. One case remains undetermined. The FP result was due to a Bs-MAb u
ptake in intrapulmonary lymph nodes. IS was in agreement with preopera
tive staging in six of these nine patients and discordant in three. Co
nclusion: Our study confirmed that the two-step method whith a bispeci
fic antibody could greatly improve the performances of IS for lung can
cer staging.