Febrile neutropenia (FN) occurrence outside of clinical trials : occurrence and predictive factors in adult patients treated with chemotherapy and an expected moderate FN risk. Rationale and design of a real-world prospective, observational, multinational study

dc.contributor.authorRapoport, Bernardo Leon
dc.contributor.authorAapro, Matti
dc.contributor.authorPaesmans, Marianne
dc.contributor.authorVan Eeden, Ronwyn
dc.contributor.authorSmit, Teresa
dc.contributor.authorKrendyukov, Andriy
dc.contributor.authorKlastersky, Jean
dc.date.accessioned2019-02-28T12:40:25Z
dc.date.available2019-02-28T12:40:25Z
dc.date.issued2018-09-24
dc.description.abstractBACKGROUND : Febrile neutropenia (FN) is a common occurrence during chemotherapy. Granulocyte colony-stimulating factors (G-CSFs) can significantly reduce the risk of FN. International guidelines recommend G-CSF for patients receiving chemotherapy with FN risk of ≥20% or 10% to 20% with defined risk factors. Prophylaxis is not typically recommended for FN risk of < 10%; however, few studies have investigated FN incidence in lower-risk patients in real-world settings and tried to identify higher-risk subgroups. METHODS : This real-world prospective, observational, multinational study aims to estimate the rate of development of FN with a chemotherapy line expected to be associated with a 10% to 20% risk of FN. Eligible patients (> 18 years of age) will have a solid tumour or Hodgkin/non-Hodgkin lymphoma and a planned chemotherapy regimen with expected risk of FN of 10% to 20% (according to published guidelines). Patients will be observed for the duration of the chemotherapy line (first cycle administered without FN prophylaxis). Primary endpoint is incidence of FN after the first chemotherapy cycle. Secondary outcomes include: FN-associated morbidity and mortality; time to first FN occurrence; other FN risk factors and impact of FN on quality of life. A risk model using occurrence of FN as a binary outcome will be developed. Data will be stratified by age, comorbidities and other risk factors. DISCUSSION : This study will provide insight into the real FN risk for common chemotherapy regimens and predictive factors for FN, including patients generally excluded from randomised clinical trials, from which reported FN rates have been variable. This study builds on knowledge of predictive factors from other research and will provide information on patients with 10% to 20% FN risk.en_ZA
dc.description.departmentImmunologyen_ZA
dc.description.librarianam2019en_ZA
dc.description.sponsorshipHexal AGen_ZA
dc.description.urihttps://bmccancer.biomedcentral.comen_ZA
dc.identifier.citationRapoport, B.L., Aapro, M., Paesmans, M. et al. 2018, 'Febrile neutropenia (FN) occurrence outside of clinical trials : occurrence and predictive factors in adult patients treated with chemotherapy and an expected moderate FN risk. Rationale and design of a real-world prospective, observational, multinational study', BMC Cancer, vol. 18, art. 917, pp. 1-8.en_ZA
dc.identifier.issn1471-2407 (online)
dc.identifier.other10.1186/s12885-018-4838-z
dc.identifier.urihttp://hdl.handle.net/2263/68525
dc.language.isoenen_ZA
dc.publisherBioMed Centralen_ZA
dc.rights© The Author(s). 2018. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).en_ZA
dc.subjectChemotherapy-induced neutropeniaen_ZA
dc.subjectNeutropeniaen_ZA
dc.subjectChemotherapyen_ZA
dc.subjectCytotoxic chemotherapyen_ZA
dc.subjectMyelosuppressive chemotherapyen_ZA
dc.subjectFebrile neutropenia (FN)en_ZA
dc.subjectGranulocyte colony-stimulating factors (G-CSFs)en_ZA
dc.titleFebrile neutropenia (FN) occurrence outside of clinical trials : occurrence and predictive factors in adult patients treated with chemotherapy and an expected moderate FN risk. Rationale and design of a real-world prospective, observational, multinational studyen_ZA
dc.typeArticleen_ZA

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