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Prospective study of empiric monotherapy with ceftazidime for low-risk grade IV febrile neutropenia after cytotoxic chemotherapy in cancer patients.

AbstractPURPOSE:
It was the aim of this study to evaluate the results of a prospective study in a single medical center using ceftazidime monotherapy in cancer patients with chemotherapy-induced grade IV febrile neutropenia and a low risk for gram-negative bacteremia.
SUBJECTS AND METHODS:
Thirty-eight patients were admitted with low-risk grade IV febrile neutropenia after chemotherapy for solid tumors. The median patient age was 57 years (range 18-74). Sixteen patients (42%) developed febrile neutropenia after the first cycle of current chemotherapy line, 9 patients (24%) received 2-3 cycles and 13 patients (34%) received more than 3 chemotherapy cycles before manifesting febrile neutropenia. Five patients were treated with prophylactic granulocyte colony-stimulating factor commenced 24 h after completion of the chemotherapy cycle. Empiric monotherapy with intravenous ceftazidime was started on admission and administered 2 g every 8 h.
RESULTS:
The mean polymorphic nuclear cell count on admission was 231 cells/mm(3). Ceftazidime therapy was well tolerated. Twenty-five (66%) patients responded with clinical improvement and complete resolution of fever within 48 h after initiation of ceftazidime therapy. Thirty-two (84%) patients were afebrile after 72 h of therapy. Thirty-three patients (87%) remained on unmodified ceftazidime therapy throughout their hospitalization. Five patients (13%) subsequently required modification of the treatment regimen for various reasons. Mean duration of fever and neutropenia were 2 (1-10) days and 4 (1-11) days, respectively. None of the patients discontinued therapy because of adverse effects. No positive blood cultures were obtained. No events of septic shock were observed. Mean duration of hospitalization was 6 days (range 3-12).
CONCLUSION:
In our series, monotherapy with intravenous ceftazidime appears safe and effective in cancer patients with low-risk grade IV febrile neutropenia after cytotoxic chemotherapy and may appreciably reduce antibiotics costs.
AuthorsPnina Chernobelski, Konstantin Lavrenkov, Doron Rimar, Klaris Riesenberg, Francisc Schlaeffer, Samuel Ariad, Wilmosh Mermershtain
JournalChemotherapy (Chemotherapy) Vol. 52 Issue 4 Pg. 185-9 ( 2006) ISSN: 0009-3157 [Print] Switzerland
PMID16675902 (Publication Type: Comparative Study, Journal Article)
Chemical References
  • Anti-Bacterial Agents
  • Ceftazidime
Topics
  • Adult
  • Aged
  • Anti-Bacterial Agents (therapeutic use)
  • Antineoplastic Combined Chemotherapy Protocols (adverse effects)
  • Ceftazidime (therapeutic use)
  • Female
  • Humans
  • Male
  • Middle Aged
  • Neoplasms (drug therapy)
  • Neutropenia (chemically induced, drug therapy)
  • Prospective Studies
  • Survival Rate
  • Time Factors
  • Treatment Outcome

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