Prospective Evaluation of Xerava Prophylaxis in Hematological Malignancy Patients With Prolonged Neutropenia
Study Details
Study Description
Brief Summary
Antibacterial prophylaxis is recommended in patients at high risk of infection, specifically patients undergoing acute leukemia induction therapy or hematopoietic stem cell transplant (HSCT) who are expected to have profound neutropenia (ANC<100 neutrophils/milliliter) for more than seven days. Xerava™ (eravacycline) has a broad spectrum of activity including many multi-drug resistant strains of bacteria. It is not an agent used for treatment of febrile neutropenia, making eravacycline a very attractive alternative to consider in this prophylactic setting. Eravacycline has activity against MRSA, VRE, and Clostridioides difficile, all of which are common problems in this patient population. It also covers the majority of enteric gram-negative pathogens while also producing satisfactory tissue penetration and adequate plasma concentrations, which has classically been a concern with prior agents. Eravacycline has activity against coagulase-negative staphylococcus, which is a common catheter-related infection in leukemia and HSCT patients. The primary objective will be report the incidence of antibiotic prophylaxis failure with eravacycline prophylaxis for hematologic malignancy patients with prolonged neutropenia.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 2 |
Detailed Description
Antibacterial prophylaxis is recommended in patients at high risk of infection, specifically patients undergoing acute leukemia induction therapy or hematopoietic stem cell transplant (HSCT) who are expected to have profound neutropenia (ANC<100 neutrophils/milliliter) for more than seven days.
Xerava™ (eravacycline) is a synthetic halogenated tetracycline class antibiotic, with a broad spectrum of activity including many multi-drug resistant strains of bacteria. It is not an agent used for treatment of febrile neutropenia, making eravacycline a very attractive alternative to consider in this prophylactic setting. Adverse effects with this agent are minimal including infusion site reactions and gastrointestinal disorders. Eravacycline has activity against MRSA, VRE, and Clostridioides difficile, all of which are common problems in this patient population. It also covers the majority of enteric gram-negative pathogens while also producing satisfactory tissue penetration and adequate plasma concentrations, which has classically been a concern with prior agents. Eravacycline has activity against coagulase-negative staphylococcus, which is a common catheter-related infection in leukemia and HSCT patients. The primary objective will be report the incidence of antibiotic prophylaxis failure with eravacycline prophylaxis for hematologic malignancy patients with prolonged neutropenia.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Xerava Eravacycline- 1 mg/kg actual body weight IV Infusion over 60 minutes every 12 hours |
Drug: Eravacycline
Eravacycline will be continued until one of the following criteria is met:
neutrophil recovery (ANC >500, post-nadir)
febrile neutropenia
breakthrough infection
any grade 3-4 toxicity related to eravacycline use
Other Names:
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Outcome Measures
Primary Outcome Measures
- Antibiotic Prophylaxis Failure-Incidence [Up to 114 days]
Incidence of antibiotic failure--Antibiotic prophylaxis failure is defined as development of febrile neutropenia (temperature >38.2 degrees C and ANC is <500 cells/mm3).
- Antibiotic Prophylaxis Failure- Time [Up to 114 days]
Time to failure--Antibiotic prophylaxis failure is defined as development of febrile neutropenia (temperature >38.2 degrees C and ANC is <500 cells/mm3).
Secondary Outcome Measures
- Adverse Events [Daily during Eravacycline]
Incidence of Adverse Events: CTCAE criteria. CTCAE stands for Common Terminology Criteria for Adverse Events; these criteria are also called "common toxicity criteria." In CTCAE, an adverse event (AE) is defined as any abnormal clinical finding temporally associated with the use of a therapy for cancer; causality is not required. These criteria are used for the management of chemotherapy administration and dosing, and in clinical trials to provide standardization and consistency in the definition of treatment-related toxicity.
- Infection-related mortality [Up to 114 days]
Incidence of Infection-related mortality. Infection-related mortality is defined as any death that occurred in the presence of clinical or microbiological documented infection
- All-cause mortality [Up to 114 days]
Incidence of All-cause mortality defined as any death occurring during the clinical trial period.
- Acute GVHD [Up to 114 days]
Incidence of Acute Graft vs Host Disease (GVHD). GVHD is a complication of a bone marrow or stem cell transplant in which cells from a donor attack the tissues of the recipient.
Eligibility Criteria
Criteria
Inclusion Criteria:
-
All patients receiving induction chemotherapy for treatment of acute leukemia or receiving preparative regimen for HSCT
-
Patient must provide informed consent.
-
Bilirubin ≤ 3 x the ULN and AST/ALT ≤ 5 x ULN
Exclusion Criteria:
-
Uncontrolled bacterial, viral or fungal infection at the time of study enrollment.
-
Urinary tract infection receiving active treatment
-
Acute pancreatitis (not necessary to work-up unless symptomatic)
-
History of known hypersensitivity to eravacycline, tetracycline, doxycycline, minocycline, tigecycline, sarecycline, oxytetracycline, or omadacycline
-
Pseudomonas infection within 30 days prior to study enrollment
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Receiving strong inhibitors or inducers of cytochrome P450 3A4 will be excluded from the study (see Appendix B for complete list of medications)
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Pregnant or lactating women
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Aaron Cumpston | Morgantown | West Virginia | United States | 26506 |
Sponsors and Collaborators
- West Virginia University
Investigators
- Principal Investigator: Aaron Cumpston, PharmD, BCOP, West Virginia University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2206591296