2002 CTOS
Annual Meeting Oral Presentations — Medical Oncology
FLUORODEOXYGLUCOSE
UPTAKE IN ADULT SOFT TISSUE SARCOMA PREDICTS RISK OF RECURRENCE
AFTER CHEMOTHERAPY
[Abstract
ID: 31]
Category:
Medical Oncology
Presentation:
Oral
Authors:
Scott M Schuetze1, Brian P Rubin1, Cheryl
Vernon1, James D Bruckner1, Ernest U Conrad
III1, Janet F Eary1
Author Institutions:
1University of Washington, Seattle, Washington, United
States
Presenter:
Scott M Schuetze
sschuetz@fhcrc.org
Correspondent:
Scott M Schuetze
sschuetz@fhcrc.org
Seattle Washington United States 98109
Ph: 206 288-2052
Fax: 206 288-2042
Objectives: Patients
with localized, high-grade soft tissue sarcomas (STS) are at significant
risk of developing metastasis. Chemotherapy may reduce the risk
of relapse; however, not all patients benefit from treatment. High-grade
STS metabolize fluorodeoxyglucose (FDG) to a greater extent than
normal tissue which can be quantified by positron emission tomography
(PET). We sought to determine whether the change in metabolic activity
of STS in response to chemotherapy could serve as a surrogate measure
for chemosensitivity and correlate with risk of disease recurrence.
Methods: FDG-PET
was performed prior to doxorubicin-based chemotherapy and prior
to surgery. Patients were followed for a minimum of 2 years for
recurrence of disease and death. Patient outcomes were analyzed
by Kaplan-Meier analyses stratified by change in FDG uptake, tumor
grade, tumor size and pathologic response.
Results: Thirty-eight patients with localized, high-grade
STS were retrospectively studied. Seventeen patients remain free
of tumor with a median follow-up of 3 years. Patients with a greater
than 40% decrement in the maximum FDG uptake in STS in response
to chemotherapy had a significantly lower risk of relapse and improved
survival. Risk of relapse did not correlate with tumor grade, size
or pathologic response to therapy.
Conclusions: A change in the metabolism of FDG in response
to chemotherapy may serve as a surrogate measure of chemotherapy
sensitivity in high-grade soft tissue sarcomas. Patients with a
large decrement in FDG uptake in response to doxorubicin-based therapy
have a lower risk of disease recurrence and improved survival.
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