A phase II study of the bispecific antibody MDX-H210 (anti-HER2 × CD64) with GM-CSF in HER2+ advanced prostate cancer
2001

Study of MDX-H210 and GM-CSF in Advanced Prostate Cancer

Sample size: 25 publication Evidence: moderate

Author Information

Author(s): James N D, Atherton P J, Jones J, Howie A J, Tchekmedyian S, Curnow R T

Primary Institution: CRC Institute for Cancer Studies, University of Birmingham

Hypothesis

Is the bispecific antibody MDX-H210 effective in treating HER2+ advanced prostate cancer?

Conclusion

The combination of GM-CSF and MDX-H210 shows activity in hormone refractory prostate cancer with manageable toxicity.

Supporting Evidence

  • 35% of evaluable patients had a greater than 50% PSA response.
  • 58% of patients with evaluable pain reported improvements in pain scores.
  • 83% of assessable patients showed a decrease in PSA relative velocity on therapy.

Takeaway

This study tested a new treatment for prostate cancer and found that it helped some patients feel better without causing too many bad side effects.

Methodology

Patients received MDX-H210 and GM-CSF for 4 days weekly for 6 weeks, with follow-up for toxicity and response.

Limitations

Some patients received less than the full treatment, and the follow-up duration varied.

Participant Demographics

Patients with HER2+ advanced prostate cancer.

Digital Object Identifier (DOI)

10.1054/bjoc.2001.1878

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication