TY - JOUR
T1 - 18F-2-fluoro-2-deoxy-D-glucose positron emission tomography in staging of locally advanced breast cancer
AU - Van Der Hoeven, Jacobus J.M.
AU - Krak, Nanda C.
AU - Hoekstra, Otto S.
AU - Comans, Emile F.I.
AU - Boom, Robert P.A.
AU - Van Geldere, Dick
AU - Meijer, Sybren
AU - Van Der Wall, Elsken
AU - Buter, Jan
AU - Pinedo, Herbert M.
AU - Teule, Gerrit J.J.
AU - Lammertsma, Adriaan A.
PY - 2004
Y1 - 2004
N2 - Purpose: To prospectively evaluate the effect of adding whole-body 18F-2-fluoro-2-deoxy-o-glucose (FDG) positron emission tomography (PET) to conventional screening for distant metastases in patients with locally advanced breast cancer (LABC). Patients and Methods: All women with LABC referred for participation in the LABC Spinoza trial were considered eligible for this study. Patients were included if chest x-ray, bone scan, liver ultrasound, or computed tomography scan performed by the referring physician failed to reveal distant metastases. They underwent whole-body FDG PET scanning before therapy. Patients with subsequently proven distant metastases were switched to alternative forms of chemotherapy, hormonal therapy, or both. Results: Among the 48 patients evaluated with PET, 14 had abnormal FDG uptake, and metastases were suspected in 12. After simple clinical evaluation (plain x-ray, history), 10 sites that were suggestive of abnormality remained. Further work-up revealed that four sites were metastases. Proven false positivity occurred in one patient with sarcoidosis. In the other five patients, the reason for abnormal FDG uptake (liver, lung, bone) remained unclear, and patients were treated as planned. Eleven months later, distant metastases were found in one patient at sites unrelated to the previous FDG uptake. Conclusion: The addition of FDG PET to the standard work-up of patients with LABC may lead to the detection of unexpected distant metastases. This may contribute to a more realistic stratification between patients with true stage III breast cancer and those who are in fact suffering from stage IV disease. Abnormal PET findings should be confirmed to prevent patients from being denied appropriate treatment.
AB - Purpose: To prospectively evaluate the effect of adding whole-body 18F-2-fluoro-2-deoxy-o-glucose (FDG) positron emission tomography (PET) to conventional screening for distant metastases in patients with locally advanced breast cancer (LABC). Patients and Methods: All women with LABC referred for participation in the LABC Spinoza trial were considered eligible for this study. Patients were included if chest x-ray, bone scan, liver ultrasound, or computed tomography scan performed by the referring physician failed to reveal distant metastases. They underwent whole-body FDG PET scanning before therapy. Patients with subsequently proven distant metastases were switched to alternative forms of chemotherapy, hormonal therapy, or both. Results: Among the 48 patients evaluated with PET, 14 had abnormal FDG uptake, and metastases were suspected in 12. After simple clinical evaluation (plain x-ray, history), 10 sites that were suggestive of abnormality remained. Further work-up revealed that four sites were metastases. Proven false positivity occurred in one patient with sarcoidosis. In the other five patients, the reason for abnormal FDG uptake (liver, lung, bone) remained unclear, and patients were treated as planned. Eleven months later, distant metastases were found in one patient at sites unrelated to the previous FDG uptake. Conclusion: The addition of FDG PET to the standard work-up of patients with LABC may lead to the detection of unexpected distant metastases. This may contribute to a more realistic stratification between patients with true stage III breast cancer and those who are in fact suffering from stage IV disease. Abnormal PET findings should be confirmed to prevent patients from being denied appropriate treatment.
UR - http://www.scopus.com/inward/record.url?scp=2142762454&partnerID=8YFLogxK
U2 - https://doi.org/10.1200/JCO.2004.07.058
DO - https://doi.org/10.1200/JCO.2004.07.058
M3 - Article
C2 - 15051773
SN - 0732-183X
VL - 22
SP - 1253
EP - 1259
JO - Journal of clinical oncology
JF - Journal of clinical oncology
IS - 7
ER -