Empirical antimicrobial monotherapy in patients after high-dose chemotherapy and autologous stem cell transplantation: a randomised, multicentre trial

Br J Haematol. 2005 Jul;130(2):265-70. doi: 10.1111/j.1365-2141.2005.05608.x.

Abstract

We report on 232 patients undergoing autologous haematopoietic stem cell transplantation (ASCT) entered into a multicentre, randomised trial comparing the efficacy and tolerability of meropenem (MPM) with that of piperacillin/tazobactam (P/T) as empirical antimicrobial first-line therapy for febrile neutropenia. In 27.6% of patients in the MPM group and 22.4% in the P/T group, therapy was initially supplemented with a glycopeptide for venous catheter infection or bacteraemia because of coagulase-negative staphylococci. Complete response rate after 72 h was 63.8% in the MPM group and 49.6% in the P/T group (P = 0.034). Overall complete response rate after treatment modification was 94.0% in the MPM group and 93.1% in the P/T group. Median time to defervescence was 2 d in the MPM group and 3 d in the P/T group. The most frequently isolated pathogens were Gram-positive cocci. Treatment was well tolerated in both groups. One patient (0.4%) died from infection. Empirical first-line therapy with MPM as well as with P/T is safe and effective in febrile episodes emerging after ASCT. Higher response rates to primary treatment can be achieved with MPM.

Publication types

  • Clinical Trial
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antineoplastic Agents / adverse effects
  • Drug Therapy, Combination / therapeutic use
  • Female
  • Fever / drug therapy
  • Fever / etiology
  • Fever / microbiology
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Male
  • Meropenem
  • Middle Aged
  • Neoplasms / therapy*
  • Neutropenia / complications*
  • Neutropenia / etiology
  • Opportunistic Infections / drug therapy*
  • Opportunistic Infections / etiology
  • Opportunistic Infections / microbiology
  • Penicillanic Acid / analogs & derivatives
  • Penicillanic Acid / therapeutic use
  • Piperacillin / therapeutic use
  • Prospective Studies
  • Tazobactam
  • Thienamycins / therapeutic use*

Substances

  • Antineoplastic Agents
  • Thienamycins
  • Penicillanic Acid
  • Meropenem
  • Tazobactam
  • Piperacillin