TABLE 3

Clinical Outcomes After Intraperitoneal Treatment with 211At-MX35 F(ab′)2

Time to progression after 211At (mo)Survival (y)Time on chemo after 211At (mo)Number of lines§ after 211AtAdmin. total activity (MBq)Activity concentration MBq/LApprox. specific activity (no. 211At/mAb)Effective dose (Sv)
14.11.76.5234221/2,4000.3
4.0*4.143648241/1,4000.3
5412.328640201/1,8000.3
5.15.7461042211/7000.3
NA12.192461/2,1000.6
3.3*2.6224103471/1,8000.6
4.02.32661191011/1,5001.3
3.02.721583731/2,3000.9
41.39.622565531/2,9000.7
5.0*2.91422971801/5002.3
3.7*1.61433332031/2002.6
9.64.83663552151/2002.8
  • * Patients with signs of disease activity at time of therapy.

  • Patients with longer time to progression after 211At than after chemotherapy regimen given before 211At.

  • Three patients are alive; one (+12 y) with no evidence of ovarian cancer recurrence.

  • § Total number of chemotherapy regimens given to patients with progressive disease; number is based on individual assessment, resulting in variety of periods on chemotherapy after 211At.

  • NA = not applicable.