Abstract
This Phase I trial explores the use of high-dose 90Y conjugated to the antibreast cancer monoclonal antibody BrE-3 and autologous hematologic cell support in the treatment of women with stage four breast cancer. Nine women with heavily pretreated disease were enrolled. All of the patients had BrE-3-positive tumors by immunostaining and were treated with increasing doses of 90Y (15 mCi/m2, 3 patients), 20 mCi/M2 (six patients), and a fixed (50 mg) dose of BrE-3.111 In-labeled BrE-3 (5 mCi) was given simultaneously for scanning purposes. The only toxkity noted was hematological. Grade 4 platelet toxicity requiring transfusion support occurred in four patients. Grade 4 WBC toxicity was seen in two patients that resolved in 3-9 days. All hematological nadirs occurred approximately 25 days after treatment Objective partial responses were noted in 4 of 8 (50%) patients with measurable tumors. Dose escalation is ongoing.
Original language | English (US) |
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Pages (from-to) | 5921S-5924S |
Journal | Cancer Research |
Volume | 55 |
Issue number | 23 SUPPL. |
State | Published - 1995 |
ASJC Scopus subject areas
- Oncology
- Cancer Research