P. Percivale et al., RADIOIMMUNOGUIDED SURGERY AFTER PRIMARY-TREATMENT OF LOCALLY ADVANCEDBREAST-CANCER, Journal of clinical oncology, 14(5), 1996, pp. 1599-1603
Purpose: To assess the role of radioimmunoguided surgery (RIGS) using
a handheld intraoperative gamma-detecting probe (GDP) to identify neop
lastic disease after primary chemotherapy in locally advanced breast c
ancer (LABC) patients injected with iodine 125-labeled monoclonal anti
bodies (MAbs). Patients and Methods: Twenty-one patients with histolog
ically; were treated with a combined modality approach. After three co
urses of primary chemotherapy and before modified radical mastectomy,
the I-125-radiolabeled MAbs B72.3 (anti-TAG72) and FO23C5 (anticarcino
embryonic antigen [CEA]) were administered to 11 patients (group A) an
d 10 patients (group B), respectively. At surgery, a GDP was used to l
ocate the primary tumor and to assess possible tumor multicentricity a
nd the presence of ipsilateral axillary metastases. Routine pathologic
examination was performed in neoplastic and normal tissue specimens o
f all 21 patients, In addition, immunohistochemical assay for TAG72 an
d CEA expression wets performed. Results: In group A patients, RIGS id
entified primary tumor in seven of 11 patients (63.3%) and unpalpable
multicentric tumor lesions were located in two of four (50%). Positive
axillary lymph nodes were histologically documented in eight of 11 pa
tients (72.7%) and RIGS identified three of eight (37.5%). In group B,
RIGS located the primary tumor lesion in four of 10 patients (40%); i
n two cases, the tumor was not clinically evident, Multicentricity was
observed in one of two patients and lymph node involvement in three o
f nine (33.3%), No false-positive results were observed in either grou
p A or B. Conclusion: RIGS appears to be a safe and reliable technique
. However, the MAbs used in this study are not sufficiently specific.
RIGS represents a technique for which the full potential for intraoper
ative assessment of breast cancer lesions can be reached when more spe
cific antibodies become readily available. (C) 1996 by American Societ
y of Clinical Oncology.