EF5 binding and clinical outcome in human soft tissue sarcomas

Journal Article · Wed Mar 01 04:00:00 EST 2006 · International Journal of Radiation Oncology, Biology and Physics

DOI:https://doi.org/10.1016/J.IJROBP.2005.0· OSTI ID:20793365

Evans, Sydney M. V. . ^[1]; Fraker, Douglas ^[1]; Hahn, Stephen M ^[1]; Gleason, Kristen ^[1]; Jenkins, W Timothy ^[1]; Jenkins, Kevin ^[1]

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1. Department of Radiation Oncology, University of Pennsylvania, Philadelphia, PA (United States)

Purpose: To study the 2-nitroimidazole agent EF5 as a surrogate for measuring hypoxia in a series of patients with soft tissue sarcomas, and to determine whether hypoxia measured with this technique was associated with patient outcome. Methods and Materials: Patients with soft tissue sarcomas of the head and neck, extremity, trunk, or retroperitoneum for whom surgical excision was the initial treatment of choice, were given 21 mg/kg EF5 24-48 hours before surgery. Biopsy specimens were stained for EF5 binding with fluorescence-labeled monoclonal antibodies, and the images were analyzed quantitatively. Endpoints included the relationship between EF5 binding, clinically important prognostic factors, and patient outcome. Results: Two patients with recurrent and 14 patients with de novo sarcomas were studied. There were seven low-grade, one intermediate-grade, and eight high-grade tumors. No relationship was found between EF5 binding and patient age, sex, hemoglobin level, or tumor size. In de novo tumors, the presence of mitoses and histologic grade were positively correlated with hypoxia. High-grade and -stage de novo tumors had higher levels of EF5 binding compared with low-grade and -stage tumors. Patients with de novo tumors containing moderate to severe hypoxia ({>=}20% EF5 binding), high grade, or {>=}7% mitoses were more likely to develop metastases. Conclusions: Further studies in a larger cohort of patients are necessary to determine whether hypoxia, as measured by EF5 binding, is an independent prognostic factor for outcome in high-grade sarcomas. Such data should be useful to identify high-risk patients for clinical trials to determine whether early chemotherapy will influence the occurrence of metastasis.

• OSTI ID: 20793365
• Journal Information: International Journal of Radiation Oncology, Biology and Physics, Journal Name: International Journal of Radiation Oncology, Biology and Physics Journal Issue: 3 Vol. 64; ISSN IOBPD3; ISSN 0360-3016
• Country of Publication: United States
• Language: English

Related Subjects

62 RADIOLOGY AND NUCLEAR MEDICINE
ANOXIA
BIOPSY
CHEMOTHERAPY
CLINICAL TRIALS
FLUORESCENCE
HEAD
HEMOGLOBIN
IMAGES
METASTASES
MONOCLONAL ANTIBODIES
NECK
PATIENTS
SARCOMAS
SURGERY