1. Academic Validation
  2. 4,4'-Dihydroxybenzophenone-2,4-dinitrophenylhydrazone (A-007): a topical treatment for cutaneous metastases from malignant cancers

4,4'-Dihydroxybenzophenone-2,4-dinitrophenylhydrazone (A-007): a topical treatment for cutaneous metastases from malignant cancers

  • Cancer Chemother Pharmacol. 2006 Jun;57(6):719-26. doi: 10.1007/s00280-005-0124-2.
David Eilender 1 Patricia LoRusso Leonard Thomas Catherine McCormick Andrew H Rodgers Catherine L Hooper Karl Tornyos Edward T Krementz Steven Parker Lee Roy Morgan
Affiliations

Affiliation

  • 1 Harper Hospital, 5 Hudson, 3990 John R., Detroit, MI 48201, USA.
Abstract

Purpose: This study is to document the activity and acceptability for a new topical agent, A-007, in the treatment of cutaneous metastases from Cancer.

Patients and methods: This is a multicenter study involving 27 patients with inoperable skin lesions from histologically confirmed cancers of the breast and oral cavity, non-Hodgkin's lymphoma, Kaposi's sarcoma, and angiosarcoma that had failed radiotherapy or systemic treatment. A-007, as a 0.25% gel, was applied twice daily to the areas of Cancer to be measured as well as applied to a healthy control area distant from the Cancer areas. An untreated Cancer area was also included and documented as a Cancer control.

Results: The overall objected response rate with A-007 was 26%, with an additional 19% minimum response/stabilization of Cancer. For patients with breast Cancer, hormonal status did not have an impact on response. The median duration of response was 15 weeks (with one patient having a response for 3.5 years). Toxicities observed were itching, burning, and a rash, in 6 of the 27 patients. The skin toxicities were in the cancer-treated fields; none were observed in the A-007 control areas. All irritated areas cleared while continuing treatment, and the tumor lesions in the areas of itching also improved.

Conclusion: A-007, as a 0.25% gel, is confirmed as an effective palliative treatment option for cutaneous metastases from cancers. Skin reactions were minimal, tolerated, and no cessation of treatment was required.

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