Dihydroxyanthracenedione: A Promising New Drug in the Treatment of Metastatic Breast Cancer

  1. HWEE-YONG YAP, M.D.;
  2. GEORGE R. BLUMENSCHEIN, M.D.;
  3. FRANK C. SCHELL, M.D.;
  4. AMAN U. BUZDAR, M.D.;
  5. MANUEL VALDIVIESO, M.D.; and
  6. GERALD P. BODEY, M.D.
  1. Houston, Texas

    Abstract

    Thirty-one patients who had metastatic breast cancer extensively pretreated with combination chemotherapy, including doxorubicin, were treated with dihydroxyanthracenedione, 3 to 4 mg/m2 body surface are a daily for 5 consecutive days every 4 weeks. Of 27 evaluable patients, one achieved a complete response and five had partial responses. Furthermore, responses were seen in patients who were refractory to doxorubicin, indicating a lack of cross-resistance between doxorubicin and dihydroxyanthracenedione. Acute drug toxicity was insignificant except for severe granulocytopenia at the dose level of 4 mg/m2 · d. The median duration of remission had not been reached, but was more than 26 weeks, with four of the six responding patients still in remission at last follow-up. We believe that dihydroxyanthracenedione has significant activity against refractory metastatic breast cancer and further evaluation is warranted.

    Article and Author Information

    • ▸From the University of Texas System Cancer Center, M.D. Anderson Hospital and Tumor Institute, Medical Breast Service and Department of Developmental Therapeutics; Houston, Texas.

    • ▸Requests for reprints should be addressed to Hwee-Yong Yap, M.D.; Medical Breast Service; M.D. Anderson Hospital and Tumor Institute; 6723 Bertner Avenue; Houston, TX 77030.

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