ORAL ENOXACIN FOR INFECTION PREVENTION IN ADULTS WITH ACUTE NONLYMPHOCYTIC LEUKEMIA

被引:42
作者
TALBOT, GH
CASSILETH, PA
PARADISO, L
CORREACORONAS, R
BOND, L
RAZA, A
PREISLER, H
VOGLER, WR
GOLDBERG, J
WIERNIK, P
GULCALP, R
MAZZA, J
KAHN, SB
HINES, J
机构
[1] UNIV PENN,MED CTR,DEPT MED,INFECT DIS SECT,PHILADELPHIA,PA 19104
[2] UNIV PENN,MED CTR,DEPT MED,HEMATOL ONCOL SECT,PHILADELPHIA,PA 19104
[3] PARKE DAVIS PHARMACEUT RES INC,ANN ARBOR,MI
[4] NEW YORK STATE DEPT HLTH,ROSWELL PK MEM INST,BUFFALO,NY 14263
[5] EMORY UNIV,SCH MED,ATLANTA,GA 30322
[6] SUNY SYRACUSE,CTR REG ONCOL,SYRACUSE,NY
[7] VAN ETTEN HOSP,BRONX,NY
[8] MARSHFIELD CLIN FDN MED RES & EDUC,MARSHFIELD,WI 54449
[9] HAHNEMANN UNIV,PHILADELPHIA,PA 19102
[10] MAHNEMAN HOSP,PHILADELPHIA,PA
[11] CLEVELAND METROPOLITAN GEN HOSP,CLEVELAND,OH 44109
关键词
D O I
10.1128/AAC.37.3.474
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A randomized, double-blind, placebo-controlled trial was conducted in eight hematologic units to determine the efficacy and safety of oral enoxacin for infection prevention in adult patients with acute nonlymphocytic leukemia. One hundred nineteen patients undergoing remission induction or consolidation chemotherapy were enrolled; 62 of them received enoxacin (400 mg orally every 12 h). Patients received antifungal prophylaxis with oral mycostatin (1,000,000 U four times daily) or clotrimazole (1 troche five times daily). Analysis was performed on an intent-to-treat basis. There was no significant difference between groups in race, age, or type and stage of leukemia, but there were more males in the placebo group (P = 0.073 [Fisher's exact test]). Fewer enoxacin patients had gram-negative bacteremia (I versus 14 [P < 0.001]), gram-negative infection at any site (2 versus 19 [P < 0.001]), or bacterial and/or fungal infection (17 versus 26 [P = 0.0561). There was no significant difference in the number of patients with gram-positive infection at any site (12 versus 16), gram-positive bacteremia (9 versus 10), deep fungal infection (6 versus 2), death (2 versus 3), other antimicrobial therapy required (48 versus 48), therapy with amphotericin B (15 versus 7 [P = 0.1051), any adverse event (45 versus 36), or any study drug-associated adverse events (13 versus 6). Logistic regression confirmed (odds ratios and 95% confidence intervals are given in parentheses) that enoxacin reduced the risk of gram-negative infection (0.07; 0.01 to 0.30), especially gram-negative bacillary bacteremia (0.05; 0.01 to 0.37), without altering the risk of gram-positive bacterial (0.63; 0.26 to 1.5), deep fungal (2.57; 0.47 to 13.9), or Clostridium difficile (1.16; 0.3 to 4.56) infection. The median time to the onset of fever of greater-than-or-equal-to 102.8-degrees-F (39.3-degrees-C) was 32 days for the enoxacin group versus 15 days for patients receiving placebo (P = 0.0007 [Wilcoxon test]). In patients with acute nonlymphocytic leukemia, oral enoxacin prevents gram-negative infections, delays the onset of fever, does not alter the incidence of gram-positive or proven deep fungal infections, and is well tolerated.
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收藏
页码:474 / 482
页数:9
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