The purpose of this study is to determine the incidence of pegfilgrastim-induced back and leg pain and to determine whether the antihistamine loratadine can prevent pegfilgrastim-induced back and leg pain.
Pegfilgrastim is a myeloid growth factor that stimulates neutrophil precursors and can be used to decrease infection risk associated with neutropenia. However pegfilgrastim may induce back and leg pain in 20-50% of patients. No intervention has been consistently successful in treating or preventing this pain. The exact mechanism of pegfilgrastim-induced pain is unknown but may be related to histamine-mediated inflammation. Several case reports and anecdotal reports have suggested efficacy of antihistamines for this indication. This study will have two parts. In the first part (Observational Phase), patients receiving pegfilgrastim will be surveyed to document the incidence of significant pegfilgrastim-induced back and leg pain. In the second part (Treatment Phase), patients who previously experienced such pain will be randomized to receive a 7-day course of either the antihistamine loratadine or placebo to determine whether pegfilgrastim-induced back and leg pain can be prevented with this intervention.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Enrollment
55
loratadine 10 mg capsule orally once daily for 7 days beginning the day of administration of pegfilgrastim
placebo capsule orally once daily for 7 days beginning the day of administration of pegfilgrastim
Cancer Care of Maine
Brewer, Maine, United States
RECRUITINGMaine Center for Cancer Medicine
Scarborough, Maine, United States
RECRUITINGYork Hospital
York Village, Maine, United States
Prevention of pegfilgrastim-induced back and leg pain by administration of the antihistamine loratadine
Patients who experience significant pegfilgrastim-induced back and leg pain during the first cycle of pegfilgrastim therapy are randomized to receive loratadine or placebo during the second cycle of pegfilgrastim therapy
Time frame: one week after pegfilgrastim
Identification of adverse events when loratadine is given to prevent pegfilgrastim-induced back and leg pain
Adverse events will be recorded for patients receiving loratadine or placebo to prevent pegfilgrastim-induced back and leg pain
Time frame: one week after pegfilgrastim
Incidence of pegfilgrastim-induced back and leg pain
Patients receiving pegfilgrastim for the first time will be surveyed to document the incidence of significant pegfilgrastim-induced back and leg pain
Time frame: One week after pegfilgrastim
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CR Wood Cancer Center
Glens Falls, New York, United States
RECRUITINGMountainview Medical Center
Berlin Corners, Vermont, United States
RECRUITINGVermont Cancer Center
Burlington, Vermont, United States
RECRUITINGVermont Center for Cancer Medicine
Colchester, Vermont, United States
RECRUITING