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Guideline for the Management of Fever and Neutropenia in Children With Cancer and Hematopoietic Stem-Cell
Thomas Lehrnbecher1, Paula Robinson1, Brian Fisher1
1Thomas Lehrnbecher, Hospital for Children and Adolescents, Johann Wolfgang Goethe University, Frankfurt; Andreas H. Groll, University Children's Hospital, Muenster, Germany; Paula Robinson, Pediatric Oncology Group of Ontario; Sarah Alexander, L. Lee Dupuis, and Lillian Sung, The Hospital for Sick Children, Toronto, Ontario, Canada; Brian Fisher and Theo Zaoutis, Children's Hospital of Philadelphia, Philadelphia, PA; Roland A. Ammann, Bern University Hospital, University of Bern, Switzerland; Melissa Beauchemin, Columbia University/Herbert Irving Cancer Center, New York, NY; Fabianne Carlesse, Pediatric Oncology Institute, GRAACC/Federal University of Sao Paulo, Sao Paulo, Brazil; Gabrielle M. Haeusler, Peter MacCallum Cancer Centre, Melbourne; Monash Children's Hospital, Clayton, Victoria, Australia; Maria Santolaya, Hospital Luis Calvo Mackenna, Universidad de Chile, Santiago, Chile; William J. Steinbach, Duke University Medical Center, Durham, NC; Elio Castagnola, Istituto Giannina Gaslini, Genova, Italy; Bonnie L. Davis, High Tor Limited, Nassau, Bahamas; Aditya H. Gaur, St Jude Children's Research Hospital, Memphis, TN; Wim J.E. Tissing, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands; and Robert Phillips, Leeds Teaching Hospital, NHS Trust, Leeds; University of York, York, United Kingdom.
Insights
Updated guidelines for pediatric fever and neutropenia (FN) management now include a fourth-generation cephalosporin for high-risk FN and refined risk stratification for invasive fungal disease (IFD). These changes impact care for children with cancer and stem cell transplant recipients.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Clinical Practice Guidelines
Background:
- Fever and neutropenia (FN) is a common and serious complication in pediatric cancer patients and stem cell transplant recipients.
- Existing clinical practice guidelines (CPGs) require updates to reflect current evidence and improve patient outcomes.
Purpose of the Study:
- To update the clinical practice guideline (CPG) for the empirical management of fever and neutropenia (FN) in pediatric oncology and hematopoietic stem-cell transplantation (HSCT) recipients.
- To incorporate the latest evidence on risk stratification, evaluation, and empirical therapy for pediatric FN.
Main Methods:
- Systematic reviews of observational studies for risk stratification and evaluation.
- Systematic reviews of randomized trials for therapeutic interventions.
- Application of the Grading of Recommendation Assessment, Development and Evaluation (GRADE) approach to formulate recommendations and classify evidence levels.
Main Results:
- Substantial changes focus on empirical antifungal therapy for invasive fungal disease (IFD).
- Key updates include a fourth-generation cephalosporin for high-risk FN, refined risk stratification for high-risk IFD, and updated recommendations for IFD evaluation in prolonged FN.
- A weak recommendation suggests withholding empirical antifungal therapy in low-risk IFD patients with prolonged FN.
Conclusions:
- The updated FN CPG recommendations are expected to significantly influence the care of pediatric cancer patients and HSCT recipients.
- Future research should address identified gaps and facilitate the implementation and adaptation of these guidelines.
Abstract:
Purpose To update a clinical practice guideline (CPG) for the empirical management of fever and neutropenia (FN) in children with cancer and hematopoietic stem-cell transplantation recipients. Methods The International Pediatric Fever and Neutropenia Guideline Panel is a multidisciplinary and multinational group of experts in pediatric oncology and infectious diseases that includes a patient advocate. For questions of risk stratification and evaluation, we updated systematic reviews of observational studies. For questions of therapy, we conducted a systematic review of randomized trials of any intervention applied for the empirical management of pediatric FN. The Grading of Recommendation Assessment, Development and Evaluation approach was used to make strong or weak recommendations and to classify levels of evidence as high, moderate, low, or very low. Results Recommendations related to initial presentation, ongoing management, and empirical antifungal therapy of pediatric FN were reviewed; the most substantial changes were related to empirical antifungal therapy. Key differences from our 2012 FN CPG included the listing of a fourth-generation cephalosporin for empirical therapy in high-risk FN, refinement of risk stratification to define patients with high-risk invasive fungal disease (IFD), changes in recommended biomarkers and radiologic investigations for the evaluation of IFD in prolonged FN, and a weak recommendation to withhold empirical antifungal therapy in IFD low-risk patients with prolonged FN. Conclusion Changes to the updated FN CPG recommendations will likely influence the care of pediatric patients with cancer and those undergoing hematopoietic stem-cell transplantation. Future work should focus on closing research gaps and on identifying ways to facilitate implementation and adaptation.
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