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Trial for the Treatment of Extensively Drug-Resistant Gram-negative Bacilli (OVERCOME)

Phase 3
Completed
Conditions
Pneumonia
Blood Stream Infection
Interventions
Registration Number
NCT01597973
Lead Sponsor
University of Michigan
Brief Summary

Approximately 444 subjects who are greater than or equal to 18 to 95 years of age, are non-pregnant, and are in the inpatient setting of one of the study sites will be evaluated to treatment efficacy. Analysis will include subjects with bloodstream infection (BSI) or pneumonia due to at least one of the following gram-negative bacilli organisms: Acinetobacter baumannii, Klebsiella spp, Escherichia coli, Enterobacter spp. and/or Pseudomonas aeruginosa that demonstrates in vitro non-susceptibility defined as extensively drug-resistant Gram-negative bacilli (XDR-GNB) which includes XDR-AB, XDR-PA and CRE. If a subject has both BSI and pneumonia at the time of study enrollment, they will be included as a subject with pneumonia.

Objectives:

Primary:

•Determine whether the treatment regimen of Colistimethate sodium (colistin) combined with a carbapenem (imipenem or meropenem) is associated with a decreased risk for mortality compared to colistin alone for subjects with bloodstream infection (BSI) and/or pneumonia due to XDR-GNB.

Secondary:

•Determine what treatment regimen (colistin monotherapy or colistin combined with a carbapenem (imipenem or meropenem) is more likely to reduce the emergence of colistin resistance among XDR-GNB isolates during therapy.

Detailed Description

The Gram-negative bacilli organisms Acinetobacter baumannii, Klebsiella spp., Escherichia coli, Enterobacter spp. and Pseudomonas aeruginosa have become a frequent cause of bloodstream infection and pneumonia in the hospital and other healthcare settings. Among these pathogens, antimicrobial resistance has emerged to many classes of antimicrobial agents. Most concerning, has been the emergence of resistance to group 2 carbapenems (such as imipenem). In several regions of the world, including Southeastern Michigan, strains of extensively-drug resistant Gram-negative bacilli (XDR-GNB) that exhibit resistance to most, and in some cases all types of available antimicrobial agents, including group 2 carbapenems, have emerged and disseminated. Treatment options for XDR-GNB typically include Colistimethate sodium (referred to as colistin in this study), used alone (monotherapy) or in combination with other agents. Unfortunately, resistance to colistin has begun to emerge in some strains of XDR-GNB, which is a truly concerning development, since colistin is one of the last remaining treatment options for XDR-GNB. No prospective, randomized controlled trials have been conducted to evaluate the clinical efficacy of colistin monotherapy versus colistin-containing combination therapy or the impact of these therapeutic modalities on the emergence of colistin resistance among XDR-GNB. We plan to conduct a double-blind randomized controlled trial including patients with pneumonia and bloodstream infection due to XDR-GNB. After enrollment, subjects will be randomized to receive 14 days of either colistin monotherapy or colistin plus meropenem.

In the Detroit metro area, infections due to XDR-GNB have developed into a regional challenge and common problem. We have assembled a multi-disciplinary team that includes Infectious Diseases researchers, clinicians, infectious diseases pharmacists, microbiologists, epidemiologists and statistical experts to address critically important questions and challenges regarding the management of bloodstream infection and pneumonia due to XDR-GNB. Specifically, we hypothesize that the combination of colistin and imipenem will provide superior efficacy in the treatment of XDR-GNB pneumonia and bloodstream infection and will prevent the emergence of decreased susceptibility to colistin among XDR-GNB strains. We also aim to analyze tools that could be used in "real time" to aid clinicians treating patients with infection due to XDR-GNB. For example, we aim to analyze the association between the presence of in vitro synergy of the colistin and carbapenem (imipenem or meropenem) combination (as determined by E-test) and clinical outcomes; and the association between colistin plasma levels and clinical outcomes and the development of nephrotoxicity.

Due to the growing threat of XDR-GNB around the world, several international sites were subsequently added including sites in Asia, Israel, and Europe.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
467
Inclusion Criteria
  • Hospitalized Adults (> 18 years to 95 years of age), at one of the study sites.

  • Diagnosis of BSI and/or pneumonia due to a preliminary result of gram-negative non-lactose fermenter that is oxidase negative; or a final results of XDR-A. baumannii; carbapenem-resistant Enterobacteriaceae; or XDR- P. aeruginosa and/or patients with suspected BSI and/or HAP (hospital acquired pneumonia) and who have had a prior history (within last 6 months) of XDR-GNB that was susceptible to colistin.

    o If final results do not indicate that the pathogen is an XDR-GNB, and identifies alternative treatment options, the patient would be eligible for the study if the subject is allergic to all the alternative treatment options.

  • Patients with polymicrobial respiratory or blood infections, including XDR-GNB and one or more pathogens, will be included in the study, as long as the XDR-GNB is determined to be a true pathogen (AB, CRE or PA). Other pathogens will be treated with antimicrobial agents as determined by the treating physician.

  • If more than one XDR-GNB study pathogens is identified as a study pathogen causing BSI and/or pneumonia, then the first study pathogen recovered will be considered as the primary study pathogen. If more than one study pathogen is recovered from the same culture, then the infection will be categorized as being caused by multiple study pathogens.

  • Patients with a life expectancy of > 24 hours

  • Signed written informed consent and HIPAA Authorization form (US sites)

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Exclusion Criteria
  • Female patients who are pregnant
  • Female patients who are nursing
  • Patients who are prisoners
  • Patients who are less than 18 years of age or greater than or equal to 96 years of age
  • Patients with neutropenia (WBC < 500 cells/mm3)
  • The presence of any of the following known clinical syndromes involving XDR-GNB as a pathogen which necessitate durations of antimicrobial therapies greater than 14 days: endocarditis, osteomyelitis, prosthetic joint infections, meningitis and/or other central nervous system infections.
  • Patients receiving valproic acid (with or without a known seizure disorder).
  • Patients who received 72 hours or more of polymyxin treatment (intravenous or inhaled [pneumonia]) within 96 hours of enrollment.
  • Patients who have end-stage renal disease requiring hemodialysis, will be excluded from evaluation pertaining to nephrotoxicity in the per protocol population.
  • Patients with known Type 1 or other severe drug allergy to either of the study drugs or to β-lactams.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
colistin and meropenemcolistin and meropenem-
colistin and placebocolistin and placebo-
Primary Outcome Measures
NameTimeMethod
Mortalityparticipants will be followed daily for the duration of hospital stay, an expected average of 4 weeks

Determine whether the treatment regimen of colistin combined with a carbapenem (imipenem or meropenem) is associated with a decreased risk for all-cause mortality during the 30 day post-enrollment period compared to colistin combined with a placebo for subjects with bloodstream infection (BSI) and/or pneumonia due to extensively drug-resistant Gram-negative bacilli (XDR-GNB).

Secondary Outcome Measures
NameTimeMethod
Number of Participants Who Develop Colistin Resistancepatients' resistance data will be collected up to 30 days

Determine what treatment regimen (colistin monotherapy (combined with placebo)) or colistin combined a carbapenem (imipenem or meropenem) is more likely to reduce the frequency of emergence of colistin resistance among XDR-GNB isolates during therapy. Measurements of Minimum Inhibitory Concentration of colistin to XDR-GNB. This is shown below as numbers of those subjects who develop colistin resistance and their percentages of the total completed population.

Clinical Failure at the End of Therapy48 hours after end of treatment, that is up to 16 days

Clinical failure as defined by either Blood Stream Infection (BSI) or Pneumonia; based on death between 48 hours and end of treatment, medication change from protocol, a positive blood culture after 5 days of blood stream infection treatment, or no improvements in PaO2/FiO2 at end of treatment.

Microbiologic Cure at the End of TherapyFrom 5 days after enrollment up to 14 days following enrollment (i.e. end of treatment)

Microbiologic cure at the end of therapy as defined by the number of participants who no longer have the causative XDR-GNB pathogens for their BSI or pneumonia identified based on microbiologic testing

Number of Participants With Toxicities Related to Treatment MedicationsUp to 16 days

Frequency is shown for each of the following: Nephrotoxicity, Hepatotoxicity, Seizures, Neurotoxicity, Hypersensitivity reaction

Trial Locations

Locations (19)

The Ohio State University Wexner Medical Center

🇺🇸

Columbus, Ohio, United States

Jackson Memorial Hospital-Jackson Health System

🇺🇸

Miami, Florida, United States

Beaumont Health System

🇺🇸

Royal Oak, Michigan, United States

Universita della Campania 'Luigi Vanvitelli'

🇮🇹

Naples, Italy

University Hospital of Heraklion

🇬🇷

Crete, Greece

Rambam Health Care Campus

🇮🇱

Haifa, Israel

University Multiprofile Hospital for Active Treatment and Emergency Medicine "N.I. Pirogov"

🇧🇬

Sofia, Bulgaria

Chang Gung Memorial Hospital

🇨🇳

Tao-Yuan, Kwei-San, Taiwan

Evangelismos General Hospital of Athens

🇬🇷

Athens, Greece

Attikon University General Hospital of Athens

🇬🇷

Athens, Greece

General Hospital of Athens "Laiko" 1st Department of Medicine

🇬🇷

Athens, Greece

Tel-Aviv Sourasky Medical Center

🇮🇱

Tel Aviv, Israel

Siriraj Hospital

🇹🇭

Bangkoknoi, Bangkok, Thailand

Rabin Medical Centre, Beilinson Campus

🇮🇱

Petach Tikva, Central District, Israel

Hippokration General Hospital of Thessaloniki

🇬🇷

Thessaloníki, Greece

Wayne State University

🇺🇸

Detroit, Michigan, United States

Mount Sinai Hospital

🇺🇸

New York, New York, United States

Henry Ford Health System

🇺🇸

Detroit, Michigan, United States

Assaf Harofeh Medical Center

🇮🇱

Zerifin, Beer Yaakov, Israel

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