Literature DB >> 28120115

Impact of recommended weight-based dosing of granulocyte-colony stimulating factors in acute leukemia and stem cell transplant patients.

Jennifer K Hockings1, Diwura K Owolabi1, Joyce E Broyles1, Susan C Wheelis2.   

Abstract

PURPOSE: Febrile neutropenia (FN) is a major risk factor for infection-related morbidity and mortality. The National Comprehensive Cancer Network recommends the prophylactic use of granulocyte-colony stimulating factors (G-CSF), dosed at 5 mcg/kg and rounded to the nearest vial size. A previous medication use evaluation conducted within a multi-hospital healthcare system demonstrated that only 67% of patients were started on appropriate weight-based dosing. The purpose of this study was to evaluate the effect of appropriate weight-based G-CSF dosing in patients on clinical outcomes.
METHODS: A retrospective chart review of patients with acute leukemia or stem cell transplant recipients who received G-CSF from May 2009 to September 2015 was conducted. Patient admissions were reviewed in regards to neutropenia length, incidence of FN, length of stay, and final disposition (alive or deceased). Admissions were divided into one of three weight-based dosing groups of under 5 mcg/kg, recommended 5 mcg/kg within a 10% range, and over 5 mcg/kg which were named under, recommended, and over, respectively.
RESULTS: Ninety-four admissions were included. Average age of this patient population was 58 years old, and the majority of patients were male (53%) and Caucasian (55%). Majority of patients had been diagnosed with acute myeloid leukemia (91%). Data showed average duration of neutropenia was around 10 days regardless if the patient received under 5 mcg/kg, the recommended 5 mcg/kg or over 5 mcg/kg G-CSF (10.1 ± 6.7 days, 8.9 ± 9.2 days, 10.1 ± 9.1 days, respectively). Length of stay was similar for patients regardless of initial G-CSF dose (29.6 ± 16.0 days, 29.1 ± 18.4 days, and 24.5 ± 17.0, respectively). However, the incidence of FN was significantly greater for those who received under 5 mcg/kg of G-CSF (87% for under, 68% for recommended, and 54% for over).
CONCLUSIONS: In this retrospective analysis, variations from the recommended 5 mcg/kg G-CSF dose did not significantly impact length of neutropenia, length of stay, nor mortality. However, patients who received under the 5 mcg/kg of G-CSF dose may be at a greater risk of FN.

Entities:  

Keywords:  Febrile neutropenia; Granulocyte-colony stimulating factors; Leukemia; Stem cell transplant

Mesh:

Substances:

Year:  2017        PMID: 28120115     DOI: 10.1007/s00520-017-3570-6

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  11 in total

1.  Prophylaxis of chemotherapy-induced febrile neutropenia with granulocyte colony-stimulating factors: where are we now?

Authors:  Matti Aapro; Jeffrey Crawford; Didier Kamioner
Journal:  Support Care Cancer       Date:  2010-02-27       Impact factor: 3.603

2.  Use of colony-stimulating factors with chemotherapy: opportunities for cost savings and improved outcomes.

Authors:  Arnold L Potosky; Jennifer L Malin; Benjamin Kim; Elizabeth A Chrischilles; Solomon B Makgoeng; Nadia Howlader; Jane C Weeks
Journal:  J Natl Cancer Inst       Date:  2011-06-13       Impact factor: 13.506

3.  Treatment of chemotherapy-induced neutropenia by subcutaneously administered granulocyte colony-stimulating factor with optimization of dose and duration of therapy.

Authors:  G Morstyn; L Campbell; G Lieschke; J E Layton; D Maher; M O'Connor; M Green; W Sheridan; M Vincent; K Alton
Journal:  J Clin Oncol       Date:  1989-10       Impact factor: 44.544

4.  Mortality, morbidity, and cost associated with febrile neutropenia in adult cancer patients.

Authors:  Nicole M Kuderer; David C Dale; Jeffrey Crawford; Leon E Cosler; Gary H Lyman
Journal:  Cancer       Date:  2006-05-15       Impact factor: 6.860

5.  A randomized, double-blind, placebo-controlled, phase III study of filgrastim in remission induction and consolidation therapy for adults with de novo acute myeloid leukemia. The International Acute Myeloid Leukemia Study Group.

Authors:  G Heil; D Hoelzer; M A Sanz; K Lechner; J A Liu Yin; G Papa; L Noens; J Szer; A Ganser; C O'Brien; J Matcham; A Barge
Journal:  Blood       Date:  1997-12-15       Impact factor: 22.113

6.  Recombinant human granulocyte-macrophage colony-stimulating factor in the treatment of febrile neutropenia: a double blind placebo-controlled study in children.

Authors:  P Riikonen; U M Saarinen; A Mäkipernaa; L Hovi; A Komulainen; J Pihkala; H Jalanko
Journal:  Pediatr Infect Dis J       Date:  1994-03       Impact factor: 2.129

7.  Low-dose filgrastim in patients with breast cancer treated with docetaxel, doxorubicin, and cyclophosphamide.

Authors:  Eric J Ip; Annette Lee-Ma; Lawrence S Troxell; James Chan
Journal:  Am J Health Syst Pharm       Date:  2008-08-15       Impact factor: 2.637

8.  Impact of obesity in favorable-risk AML patients receiving intensive chemotherapy.

Authors:  Suzanne Tavitian; Amélia Denis; François Vergez; Emilie Berard; Audrey Sarry; Anne Huynh; Eric Delabesse; Isabelle Luquet; Françoise Huguet; Christian Récher; Sarah Bertoli
Journal:  Am J Hematol       Date:  2015-11-26       Impact factor: 10.047

Review 9.  Impact of primary prophylaxis with granulocyte colony-stimulating factor on febrile neutropenia and mortality in adult cancer patients receiving chemotherapy: a systematic review.

Authors:  Nicole M Kuderer; David C Dale; Jeffrey Crawford; Gary H Lyman
Journal:  J Clin Oncol       Date:  2007-07-20       Impact factor: 44.544

10.  Filgrastim in patients with chemotherapy-induced febrile neutropenia. A double-blind, placebo-controlled trial.

Authors:  D W Maher; G J Lieschke; M Green; J Bishop; R Stuart-Harris; M Wolf; W P Sheridan; R F Kefford; J Cebon; I Olver; J McKendrick; G Toner; K Bradstock; M Lieschke; S Cruickshank; D K Tomita; E W Hoffman; R M Fox; G Morstyn
Journal:  Ann Intern Med       Date:  1994-10-01       Impact factor: 25.391

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