Infections

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Rare Diseases

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Emergencies

Hyperthermia

Neutropenia

Fever

Sepsis

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Febrile Neutropenia

Body Temperature Changes

Agranulocytosis

Leukopenia

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Hematologic Diseases

Leukocyte Disorders

Granulocytopenia

Anti-Infective Agents

All Drugs and Chemicals

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Anti-Bacterial Agents

Amoxicillin

Meropenem

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Amoxicillin-Potassium Clavulanate Combination

Levofloxacin

Ofloxacin

Penicillins

Lactams

beta-Lactams

Antibiotics, Antitubercular

Clavulanic Acids

Enzyme Inhibitors

Cytochrome P-450 Enzyme Inhibitors

beta-Lactamase Inhibitors

Patient's blood sample will be expedited for complete blood count with differentials. Intravenous antibiotic is given depending on absolute neutrophil count. If neutropenia is present, broad-spectrum antibiotic (meropenem 1 g or levofloxacin 500 mg) will be given after septic workup within 1 hour of registration in emergency department before transfer to wards. If absent, antibiotic according to "Hospital Authority Interhospital Multi-disciplinary Programme on Antimicrobial ChemoTherapy (IMPACT)" with reference to previous bacterial sensitivity pattern, or amoxiclav 1.2 g if not specified, will be given. Other interventions are given according to clinical needs. The regimen is continued until clinicians recommend an alternative antimicrobial based on clinical grounds, or detection of other pathogens which indicate another antimicrobial.

The control group refers to the existing clinical pathway which guides management of adult patients with suspected NF in ED. Without information of absolute neutrophil count, Meropenem 1 g IV bolus (or Levofloxacin 500 mg IV infusion over 1 hour if Penicillin-allergic) will be given within 1 hour of ED registration after septic workup. Other interventions are given according to clinical needs.

Subsequent treatment in wards will be determined by doctor's clinical judgement, on a personalised basis. Each patient will be assessed by a parent team member. There is no standardised antibiotic de-escalation protocol in place, but it is a usual practice to continue Meropenem or Levofloxacin injections until clinical improvement, rising ANC, and negative culture results. After that it will be replaced with an antibiotic with a narrower spectrum, such as oral Amoxiclav, before discharge.

Given if patient has no known allergies at 1 g IV bolus within 1 hour of ED registration, then every 8 hours

Meropenem Injection

Given if patient is allergic to beta lactam at 500 g IV in 100 mL 0.9% sodium chloride solution, infused over 1 hour started within 1 hour of ED registration, then every 24 hours. If the patient can tolerate oral drugs, 500 mg daily after the first IV dose.

Given if patient has no known allergies at 1.2 g IV bolus within 1 hour of ED registration, then every 8 hours. If the patient can tolerate oral drugs, 1 g twice daily after the first IV bolus.

Amoxicillin Clavulanate

Any antibiotic for empirical therapy of common infections as recommended by the fifth version of "Hospital Authority Interhospital Multi-disciplinary Programme on Antimicrobial ChemoTherapy (IMPACT)" guideline, with reference to previous bacterial sensitivity pattern

Antibiotic

Timothy Hudson Rainer, MBBCh; MRCP

Timothy Hudson Rainer, MBBCh, MRCP

This is a comparative study for adult participants with cancer who are suspected to have neutropenic fever (or fever with low neutrophil count) in emergency department. Neutrophil is a kind of defensive white blood cell combating against infection, especially by bacteria and fungi. Low neutrophil can be part of the disease progress or secondary to some cancer treatment. These participants are at high risk of developing infection-related complications including death.

Currently a dedicated clinical pathway has been in place in emergency department for suspected neutropenic fever, which offers fast-track medical consultation, blood tests and a very strong antibiotic (meropenem) as the first choice within 1 hour of registration. However, majority of such participants' neutrophil counts are not low. Most of them have no bacterial infection in the body, and have unremarkable short hospital stays. Early administration of meropenem in the majority of cases may be unnecessary and imposes risk of developing antibiotic resistance.

This study attempts to answer the question, "In adult participants with cancer presenting to emergency department with suspected neutropenic fever, when compared with conventional treatment, can a new protocol guided by fast-track neutrophil count reduces prescription of meropenem?" Agreed participants will be randomly assigned to the conventional treatment group, or the new treatment group. For those who are assigned to the new treatment group, blood will be taken and sent to the hospital laboratory for urgent analysis of neutrophil count. Participants with proven low neutrophil counts will still receive meropenem, while those without low neutrophil counts will receive less strong antibiotic according to their clinical diagnoses, such as Augmentin. They will be followed up on the first 7 days, and then on the 14th, 30th, 90th, and 180th days after recruitment. Comparisons will be made to see how much less meropenem will be prescribed, and whether more serious adverse events will happen. The study is expected to take 37 months to complete. Duration of data collection, including the day of last follow up, is estimated to be 33 months.

1. Background

1.a. Burden of neutropenic fever Neutropenic fever (NF), or febrile neutropenia, is characterised by high body temperature and low absolute neutrophil count (ANC) following myelosuppressive cancer treatment.\[1\] It occurs in 5 - 10 percent of patients with early-stage solid tumours, 20 - 25 percent with non-leukaemic haematological cancers, 85 - 95 percent with acute leukaemia,\[2\] and 13 - 21 percent with metastatic solid tumours.\[1\] It is more common after the first cycle of chemotherapy. 7.83 per 1,000 cancer patients were hospitalised for NF annually in the United States (US).\[3\] With earlier cancer recognition, and more prescriptions of chemotherapeutic agents and targeted therapies, the figures are expected to rise.

NF is associated with unplanned chemotherapy interruptions and relative dose intensity (RDI) reductions more than 15 percent, which undermine treatment success rates and overall survival.\[2\] When complicated by neutropenic sepsis, a dysregulated host response against infection, NF becomes an oncological emergency. The mortality rate is 3 - 18 percent following complications e.g. hypotension, respiratory failure, encephalopathy, cardiac failure and arrhythmia, renal failure, haemorrhage, and admission to intensive care unit (ICU).\[4\] Risk factors of life-threatening infections are severe neutropenia, protracted neutropenia, and splenectomy.\[5\] Mortality risk increases with advanced age, comorbidities, clinically documented infection, bacteraemia, leukaemia and lung cancer as underlying malignancies.\[4,6\]

The cost of managing NF remains substantial for healthcare systems worldwide. The mean direct hospitalisation costs in the US, Germany, and Singapore were US$19,110 (1995-2000), €3,950 (2005-2006), and US$4,913 (2009-2012) respectively.\[6-8\] Higher costs are associated with inpatient treatment, comorbidities, discharge, deaths, male sex, and infection.\[9\]

1.b. Diagnostic criteria NF is defined by 1) single oral temperature ≥ 38.3 degree Celsius (101ºF), or ≥ 38.0 degree Celsius (100.4ºF) sustained over 1 hour; and 2) ANC \< 1.0 x 109/L ("moderate" neutropenia). Neutropenia becomes "severe", "profound" and "protracted" if ANC \< 0.5 x 109/L, \< 0.1 x 109/L, and lasts for more than one week, respectively.\[10\] This definition applies to oncological and haematological participants only.

1. c. Aetiology Neutrophils are recruited early during the acute phase of bacterial and fungal infections.\[11\] Fever may be the only manifestation of infection during neutropenia because the typical signs of inflammation are obscured. Neutropenia is usually acquired by myelosuppressive cancer treatments, and pre-engraftment phases of haematopoietic stem cell transplantation (HSCT). Bone marrow failure and defective neutrophil maturation are other possible mechanisms.\[12\]

   NF can have infectious and non-infectious causes. Fever of unknown origin, chemotherapy-related oral mucositis, tumour-related cytokine release, transfusion-related reaction, drug reaction, graft-versus-host disease, and thromboembolism are common non-infective causes.\[13\] 30 - 50 percent are infections by clinical presentation or microbiology,\[14\] whilst only 20 - 30 percent are microbiologically documented infections.\[15\] Bloodstream infections, bacterial translocation from respiratory tract and perianal region, and central venous catheter are major sources.

1.d. Situation in Hong Kong Local public emergency departments (EDs) have implemented clinical pathways for suspected NF, which expedite medical consultation, septic workup, and broad-spectrum antibiotics such as Meropenem or Piperacillin/Tazobactam. The target time from ED registration to antibiotic administration, or Door-To-Antibiotic (DTA) time, is within 1 hour disregarding ANC, in line with international guidelines.\[16-18\] DTA times are shortened after implementing clinical pathways in local ED.\[19\] Local epidemiology, antibiotic sensitivity patterns, and healthcare cost in managing NF are understudied. It has been shown that inadequate antibiotic regimen was more significantly associated with ICU admissions and mortality than longer DTA times. Presence of sepsis or septic shock, prior colonisation with drug resistant strains, and risk stratifying indices, are criteria to judge antibiotic adequacy.\[20\]

1. e. Antibiotic stewardship for cancer participants Participants with cancer are frequently exposed to antibiotics for treatment and prophylaxis, therefore they are more vulnerable to multi-drug resistance, and are in special need for antibiotic stewardship.\[21\] Broad-spectrum antibiotics are often started empirically in ED for suspected NF, assuming infection by drug-resistant bacteria. However, clinicians may not proactively de-escalate subsequent antibiotics. Prolonged exposures to parenteral broad-spectrum antibiotic impose risks of nosocomial infection and injection site complications.

   Gram-negative bacilli are more frequent in neutropenia. Staphylococcus aureus, Acinetobacter and Enterobacter species are more frequent in non-neutropenic bloodstream infections.\[22\] More drug resistant (MDR) strains, such as Extended-spectrum Beta-lactamase (ESBL)-producing Enterobacteriaceae, MDR Pseudomonas aeruginosa, and MDR Acinetobacter were isolated from neutropenic patients in a survey in China.\[23\]
2. Research (PICO) question In adult participants with cancer presenting to the ED with suspected NF, can an ED protocol guided by Fast-tRack Absolute Neutrophil Count (FRANC protocol) compared with conventional care guided by clinical suspicion alone improve safe antibiotic stewardship?
3. Objective and purpose

3.a. Objectives

In adult participants presenting to the ED with suspected NF:

* To investigate the effectiveness of the FRANC protocol to improve antibiotic stewardship by restricting meropenem use except for confirmed neutropenic or clinically unstable participants; and
* To investigate the safety of the FRANC protocol. 3.b. Primary hypothesis In participants presenting to ED with suspected NF, the FRANC protocol significantly reduces unnecessary use of Meropenem compared with normal Standard of Care (SoC).

  3.c. Secondary hypothesis In participants presenting to ED with suspected NF, there is no significant difference between those receiving the FRANC protocol and those receiving SoC for serious adverse events including death.

  4. Methods

  4.a. Participants 4.a.1. Target population This trial targets to adult participants attending ED because of fever, who are at risk of neutropenia related to cancer therapies and underlying conditions.

  4.a.2. Study location The trial will be conducted in the ED of Queen Mary Hospital with an average annual attendance of 125,000. The hospital is a tertiary referral centre for HSCT and oncological services which received more than 500 adults with suspected NF via the ED in 2019.

  4.a.3. Recruitment and screening Alert cards are routinely issued to participants at risk of neutropenia during follow-ups in Clinical Oncology and Haematology centres. They are reminded to visit EDs as soon as possible when fever occurs. A neutropenic risk alert is set to pop up in the Clinical Management System (CMS) that is shared among all public medical facilities. It is valid for 6 weeks from the last chemotherapy against solid tumours, or lifelong for haematological malignancies, and HSCT.

When febrile participants with valid alerts attend, the triage nurse will declare "1 - Critical" or "2 - Emergency" categories according to clinical state. Consultations by emergency physician will start within 15 minutes. Participants who receive cancer treatment in other medical facilities will also be included if they meet the same criteria.

Participants will then be screened for eligibility by trained research staff for inclusion and exclusion criteria in the ED. Potential participants will be invited to provide informed consent in written, signed, and dated forms. They can decline at any time.

4.a.4. Sample size For antibiotic stewardship A sample size of 344 participants (172 per group) will achieve 80 percent power to detect a superiority difference between two group rates of meropenem prescription. We set the superiority margin at 10 percent and assume that the control group has Meropenem usage rate of 91.8 percent (based on preliminary data) and 71.8 percent for intervention group. The calculation is based on a one-sided Z test at the significance level of 0.05.

4.a.5. Randomisation \& allocation concealment We aim to achieve balanced treatment assignments in 1:1 ratio with simple randomisation by a computer-generated code list. The code is not broken until the last participant is enrolled and has completed 180 days of follow-up. It will be implemented using independent electronic case data files to ensure allocation concealment.

4.b. Data processing and analysis 4.b.1. Data processing All data will be entered electronically by research staff to password-protected, secured, web-based system with tailor-made recording forms using tablet computers. 5 percent of all data will be checked for accuracy. All hard copies will be restricted and locked in unit cabinets. All prevailing regulations by The University of Hong Kong and the Hospital Authority will be strictly followed. An audit trail will be made to include the number of participants screened, approached, recruited, and excluded (with reasons). Participant and clinical staff responses, and data completeness will be evaluated.

4.b.2. Data analysis 4.b.2.a. Primary analysis Baseline characteristics between two groups will be assessed for potential imbalances, which will be adjusted for when comparing outcomes. Intention-to-treat (ITT) analysis will be used by imputing all non-responses at follow-up with baseline values, which yields more conservative estimates of effect sizes. The missing data for the primary outcome is expected to be \< 1 percent because most data is retrievable from electronic participant records with electronic time stamps. Statistical analysis will be done using Statistical Package of Social Sciences (SPSS) version 26 (IBM SPSS Statistics, New York, US) with biostatistician support.

Main effect: Intervention vs. Control on proportion of participants receiving Meropenem in 7 days using Chi-squared test.

4.b.2.b. Secondary analyses

* All secondary outcomes at different time points using generalised mixed effect model for multiple intra-participant and inter-participant observations. Main and interaction effects will be assessed.
* Subgroup analysis to primary outcome based on age, gender, type of cancer/ conditions, disease status, therapy received, time interval from last chemotherapy or HSCT to ED registration, at 30, 60, 90 days (4) Sensitivity of ITT and per-protocol analyses for pre-defined co-variates, missing data (including participants lost to follow-up), will be done. Imputation method will depend on actual pattern of missing data.
* If the attrition rate is more than 5 percent, risks of attribution bias and influence to statistical power will be assessed.
* Complication rates over time will be compared with Poisson mixed effects models. Uses of inotrope, mechanical ventilation, renal replacement therapy, and ICU are analysed against mortality using appropriate survival analyses with time to event data.

This is a single-center, pragmatic, open-labelled, randomized, controlled trial with 1:1 parallel-group assignment, which aims to establish superiority in antibiotic stewardship.

Fast-track Blood Test for Suspected Fever by Deficiency of a Kind of White Blood Cells As Main Defense Against Infection

Fast-track Absolute Neutrophil Count in Suspected Neutropenic Fever (The FRANCiS-NF Trial): A Single-centre, Pragmatic, Open-label, Randomised, Controlled Trial

Proportion of participants in each group receiving Meropenem

Rate and type of documented infective focus

* Days to defervescence (body temperature less than 38 degree Celsius)
* Days to resolution of symptoms and signs of infection

* Hypotension (systolic blood pressure \< 90 mmHg)
* Respiratory failure (partial pressure of oxygen in arterial blood \< 60 mmHg, or 8 kilopascal, adjusted for hyperventilation)
* Altered mental state (Glasgow Coma Scale \< 15)
* Congestive heart failure documented radiologically
* Acute kidney injury (serum creatinine \> 2x baseline, or estimated glomerular filtration rate (eGFR) \> 50 percent increase from baseline, or urine output \< 0.5 mL/kg/h x 12 h)
* Acute liver failure (International Normalised Ratio (INR) \> 1.5 in non-warfarin user, hepatic encephalopathy, total bilirubin \> 85.5 µmol/L or 5 mg/dL)
* Rate of therapeutic failure (recurrence of fever after defervescence)

* Rate of inotrope/ vasopressor use
* Rate of assisted / mechanical ventilation
* Rate of renal replacement therapy
* Rate of 3 or more units of blood transfusion for haemorrhage
* Rate of additional antimicrobial treatment
* Rate of Intensive Care Unit (ICU) admission

Total in-hospital days from the time of index ED admission

Changes in chemotherapy schedule following index admission (postponement, dose reductions, participant defaults)

Rates of any readmission except for planned chemotherapy

Time from the day of randomisation to the date of death, all-cause or infection-related

Type and route of antibiotics administered, from the time of randomisation to hospital discharge, or from the time of randomisation to the expected date of completion of prescribed antibiotic courses after discharge, whichever the later

Mean total dose of antibiotics used, in milligrams, from the time of randomisation to hospital discharge, or from the time of randomisation to the expected date of completion of prescribed antibiotic courses after discharge, whichever the later

Total days of therapy (DOT) per admission - the unit measure is defined as one day in which a patient is given a drug, regardless of dose per admission.

Defined daily dose (DDD) per admission is the assumed average maintenance dose, in milligrams, per day for a drug used for its main indication.

Development of resistance, defined as clinical isolates resistant to antibiotics previously used in the febrile episode. Surveillance sampling will not be conducted.

Physical, social, emotional and function well being of participants will be evaluated using the standardised 27-item questionnaire, "Functional Assessment of Cancer Therapy - General" (FACT-G).

Physical, social, emotional and function well being of participants will be evaluated using the Functional Assessment of Cancer Therapy - Neutropenia (FACT-N). It is a modified version of the Functional Assessment of Cancer Therapy - General (FACT-G) with the Neutropenia subscale, which is targeted for adult cancer patients with neutropenia.

Financial toxicity is evaluated using the Functional Assessment of Chronic Illness Therapy - COprehensive Score for financial Toxicity (FACIT-COST). The COST is a patient-reported outcome measure that describes the financial distress experienced by cancer patients. The FACIT System screens for financial toxicity and to provide a global summary item for financial toxicity.

Queen Mary Hospital, Hong Kong

The University of Hong Kong

Neoplasms

Behaviors and Mental Disorders

Hematologic Neoplasms

Fever of Unknown Origin

Stress Disorders, Traumatic

Heat Stress Disorders

Imipenem

Cilastatin, Imipenem Drug Combination

Cilastatin

HIV Protease Inhibitors

Protease Inhibitors

Discontinuation of imipenem-cilastatin or meropenem after 3x24 hours irrespective of presence of fever.

Extended treatment with imipenem-cilastatin or meropenem for at least 6 more days. The treatment with a carbapenem will be continued until patients have been treated for at least 9x24 hours and have been afebrile (tympanic membrane temperature \<38.0°C) for at least five consecutive days or until resolution of neutropenia (ANC \> 0,5 x10\^9/L), whichever comes first.

Discontinuation of imipenem-cilastatin or meropenem

Jeroen JWM Janssen, MD, PhD

Michiel A van Agtmael, MD, PhD

Mark MH Kramer, Prof., MD

Sonja Zweegman, Prof.,MD

A multicenter open-label non-inferiority randomized clinical trial comparing the safety (non-inferiority) of short antibiotic treatment (72 hours) with an anti-pseudomonal carbapenem with regard to treatment failure in comparison with extended treatment (at least 9 days) of high-risk febrile neutropenia in hematology patients receiving standard antimicrobial prophylaxis.

Episodes of fever are very common in patients undergoing intensive chemotherapy treatment for malignant hematological disease. More than 80% of patients experience one or more episodes of fever after their first cycle of chemotherapy. Only 20-30% of these patients have a clinically documented focus and mostly include infections of skin, intestinal tract and lung, while at most 10-25% of these patients have microbiologically proven bacteremia during these episodes. Patients with malignant hematological diseases and intensive chemotherapy induced neutropenia are extremely prone to overwhelming bacterial infections. Therefore, empirical antibiotic treatment is initiated at the first occurrence of fever, even if no apparent cause for the fever is evident. Most protocols advice treatment with very broad-spectrum antibiotics, mostly anti-pseudomonal carbapenems or fourth generation anti-pseudomonal cephalosporins.

Prolonged continuation of treatment may induce bacterial resistance. In view of the possible emergence of bacterial resistance due to prolonged antibiotic administration, continuation until recovery of neutropenia is suboptimal because it is costly because of longer hospital admissions, higher antibiotics costs and more possible adverse reactions.

Recent observational data (Slobbe et al) has showed that in adult hematological patients with febrile neutropenia, discontinuation of empiric antibacterial therapy after three days can be safe if no infectious etiology can be found, even in cases with persistent fever. However no RCT has hitherto been performed to support this observational data.

This study compares the safety (non-inferiority) of short treatment (72 hours) versus extended treatment (at least 9 days) with an anti-pseudomonal carbapenem for hematology patients with unexplained high risk febrile neutropenia. We hypothesize that a more restrictive use of broad-spectrum antibiotic use of three days in unexplained fever in neutropenic hematology patients is non-inferior to the present extended use during at least 9 days which would lead to a more restrictive use of antibiotics and less multiresistant strains of bacteria, costs and hospitalization length in the future.

Short Versus Extended Antibiotic Treatment With a Carbapenem for High-risk Febrile Neutropenia in Hematology Patients With FUO

Short Versus Extended Antibiotic Treatment With a Carbapenem for High-risk Febrile Neutropenia in Hematology Patients With Fever of Unknown Origin: a Randomized Multicenter Non-inferiority Trial.

Treatment failure is defined as the occurrence of one of the following events after 3x24 hours and before 9x24hours after treatment initiation with a carbapenem:

-A clinically or microbiologically documented carbapenem-sensitive infection; treatment.

Recurrence of fever after previous defervescence (tympanic temperature \<38.0 °C during 24 hours) which is not attributable to administration of a blood product or to a drug reaction.

o In case of clinical doubt whether the fever is of infectious etiology, the recurrence of fever will be considered as failure.

The occurrence of death, ARDS/respiratory insufficiency, septic shock (systolic blood pressure \<90 mmHg and oliguria \<500 mL/day) due to any cause.

Treatment strategy failure is defined as occurrence of any of the following events after 3x24hours of treatment with a carbapenem and until the end of the neutropenic episode:

1. Any clinically or microbiologically documented infection.
2. The recurrence of fever after previous defervescence during neutropenia.
3. Death, septic shock or ARDS/respiratory failure due to any cause
4. Adverse drug-related events due to a carbapenem requiring (temporary) interruption of treatment, including but not exclusively: liver and kidney dysfunction, convulsion and allergic reactions.
5. Unexpected re-admission within 30 days after discharge other than for planned chemotherapy or other elective treatment.
6. Antibiotic or antifungal treatment within 30days after discharge other than standard antibiotic prophylaxis.

Fever is defined as one single measured tympanic membrane temperature of \>38.5°C or a temperature of \>38.0°C during 2 subsequent measurements separated by at least 2 hours.

Defervescence is defined as three times a tympanic membrane temperature \<37.5 °C with a minimal measurement interval of at least 8 hours

Study title	NCT ID	Conditions	Interventions	Eligibility	Organization
Fast-track Blood Test for Suspected Fever by Deficiency of a Kind of White Blood Cells As Main Defense Against Infection	NCT05393505	Neutropenic Fev...	Meropenem Injec... Levofloxacin Amoxicillin Cla... Antibiotic	18 Years -	The University of Hong Kong
Short Versus Extended Antibiotic Treatment With a Carbapenem for High-risk Febrile Neutropenia in Hematology Patients With FUO	NCT02149329	Febrile Neutrop... Hematological M...	Discontinuation...	18 Years -	Amsterdam UMC, location VUmc
Short Versus Extended Antibiotic Treatment With a Carbapenem for High-risk Febrile Neutropenia in Hematology Patients With FUO	NCT02149329	Febrile Neutrop... Hematological M...	Discontinuation...	18 Years -	Amsterdam UMC, location VUmc
Short Versus Extended Antibiotic Treatment With a Carbapenem for High-risk Febrile Neutropenia in Hematology Patients With FUO	NCT02149329	Febrile Neutrop... Hematological M...	Discontinuation...	18 Years -	Amsterdam UMC, location VUmc

Spots Global Cancer Trial Database for antibiotic stewardship