Prophylactic Trimethoprim-Sulfamethoxazole During Consolidation Chemotherapy for Acute Leukemia: A Controlled Trial

  1. BARBARA WEISER, M.D.;
  2. MICHAEL LANGE, M.D.;
  3. MARK A. FIALK, M.D.;
  4. CAROL SINGER, M.D.;
  5. TED H. SZATROWSKI, Ph.D.; and
  6. DONALD ARMSTRONG, M.D.
  1. New York, New York; and New Brunswick, New Jersey

    Abstract

    We conducted a prospective, controlled, randomized trial of oral trimethoprim-sulfamethoxazole treatment in patients with acute leukemia receiving consolidation chemotherapy. We followed 14 treatment patients during 33 episodes and 15 control patients during 34 episodes of granulocytopenia (less than 1000 granulocytes/mm3). We found no significant difference in the incidence of febrile episodes (13 in treatment group versus 14 in control group), hospitalizations to treat fever or infection (10 versus 12), number of documented infections (eight versus 10), number of septicemias (one versus two), or mean duration of hospital stay to treat fever or infection (8.9 versus 9.2 days) in the two groups. There was little colonization with organisms resistant to trimethoprim-sulfamethoxazole, including Candida, in either group. Prophylactic trimethoprim-sulfamethoxazole did not significantly reduce the incidence of fever, hospitalization, or infection in granulocytopenic patients during consolidation chemotherapy.

    Article and Author Information

    • ▸From the Infectious Disease Service, Memorial Sloan-Kettering Cancer Center; New York, New York; and the Department of Statistics, Rutgers University; New Brunswick, New Jersey.

    • Grant support: Dr. Barbara Weiser was supported by the Cancer Chemotherapy Training Grant T-32CA09207 02 of the National Institutes of Health. This study was partially supported by Hoffmann-LaRoche Inc., Nutley, New Jersey.

    • ▸Requests for reprints should be addressed to Dr. Donald Armstrong; Chief, Infectious Disease Service, Memorial Sloan-Kettering Cancer Center; 1275 York Avenue; New York, NY 10021.

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