Stenotrophomonas maltophilia: changing spectrum of a serious bacterial pathogen in patients with cancer
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Amar Safdar1, Kenneth V Rolston
1Dept. of Infectious Diseases, Infection Control, and Employee Health, 402, The M. D. Anderson Cancer Center, University of Texas, 1515 Holcombe Blvd., Houston, TX 77030, USA. asafdar@mdanderson.org
Abstract:
Stenotrophomonas maltophilia colonization/infection in patients with cancer has significantly increased over the past 2 decades. Patients with prolonged neutropenia, exposure to broad-spectrum antibiotics, and those requiring mechanical ventilation have higher risk of infection. These micro-organisms are intrinsically resistant to carbapenems, and exposure to these agents has been linked to selection of S. maltophilia. Recently, these infections are being documented in patients without traditional risk factors. The spectrum of infection includes bacteremia, catheter-related infection, pneumonia, complicated biliary and urinary tract infection, and skin and skin-structure infection. Trimethoprim-sulfamethoxazole is the therapeutic agent of choice, but resistance is increasingly being reported. Susceptibility to alternative agents is unpredictable. Combination therapy and alternative routes of drug administration, such as aerosolized aminoglycoside, might be necessary. New insights into the mechanisms of drug resistance might lead to identification of new target sites. Agents that improve outer-membrane permeability and broad-spectrum beta-lactamase inhibitors may favorably impact difficult-to-treat (i.e., multidrug resistant) S. maltophilia infections.
Insights
Stenotrophomonas maltophilia infections are rising in cancer patients, even those without typical risk factors. Treatment challenges include rising resistance to trimethoprim-sulfamethoxazole and unpredictable susceptibility to other drugs.
Area of Science:
- Infectious Diseases
- Oncology
- Microbiology
Background:
- Stenotrophomonas maltophilia infections and colonization have markedly increased in cancer patients over the last two decades.
- Risk factors include prolonged neutropenia, broad-spectrum antibiotic exposure, and mechanical ventilation, with carbapenem use linked to S. maltophilia selection due to intrinsic resistance.
- Emerging infections are noted in patients lacking traditional risk factors.
Purpose of the Study:
- To review the increasing incidence, clinical spectrum, and therapeutic challenges of Stenotrophomonas maltophilia infections in cancer patients.
- To highlight the growing resistance patterns and explore potential alternative treatment strategies.
Main Methods:
- Literature review focusing on recent trends in S. maltophilia epidemiology and clinical management in oncology.
- Analysis of antimicrobial resistance patterns, particularly to trimethoprim-sulfamethoxazole and other agents.
- Discussion of current and potential future therapeutic interventions.
Main Results:
- S. maltophilia infections present with a wide spectrum, including bacteremia, pneumonia, and various localized infections.
- Intrinsic resistance to carbapenems is a key feature, and resistance to trimethoprim-sulfamethoxazole is increasing.
- Susceptibility to alternative antimicrobial agents is often unpredictable, complicating treatment decisions.
Conclusions:
- Effective management of S. maltophilia in cancer patients is challenging due to rising resistance and unpredictable drug susceptibility.
- Combination therapies, alternative drug administration routes (e.g., aerosolized aminoglycosides), and novel therapeutic targets are crucial for addressing multidrug-resistant strains.
- Further research into resistance mechanisms and novel agents is needed to improve outcomes for these difficult-to-treat infections.
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