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자료유형
학술저널
저자정보
Adam M. Greenbaum (Fred Hutchinson Cancer Research Center) Damian J. Green (Fred Hutchinson Cancer Research Center) Leona A. Holmberg (Fred Hutchinson Cancer Research Center) Ted Gooley (Fred Hutchinson Cancer Research Center) Brian G. Till (Fred Hutchinson Cancer Research Center) Lihua E. Budde (City of Hope National Medical Center) Heather Rasmussen (Fred Hutchinson Cancer Research Center) Oliver W. Press (Fred Hutchinson Cancer Research Center) Ajay K. Gopal (Fred Hutchinson Cancer Research Center)
저널정보
대한혈액학회 Blood Research Blood Research Vol.53 No.3
발행연도
2018.1
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223 - 226 (4page)

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Background Bendamustine is a chemotherapeutic agent that has shown broad activity in patients with lymphoid malignancies. It contains both alkylating and nucleoside analog moieties, and thus, is not commonly used for stem cell mobilization due to concerns that it may ad-versely affect stem cell collection. Here we describe the lymphoma subset of a pro-spective, non-randomized phase II study of bendamustine, etoposide, and dex-amethasone (BED) as a mobilization agent for lymphoid malignancies. Methods This subset analysis includes diffuse large B-cell lymphoma (N=3), follicular lymphoma (N=1), primary mediastinal B-cell lymphoma (N=1), and NK/T-cell lymphoma (N=1). Patients received bendamustine (120 mg/m2 IV d 1, 2), etoposide (200 mg/m2 IV d 1‒3), and dexamethasone (40 mg PO d 1‒4) followed by filgrastim (10 mcg/kg/d sc. through collection). Results We successfully collected stem cells from all patients, with a median of 7.9×106/kg of body weight (range, 4.4 to 17.3×106/kg) over a median of 1.5 days (range, 1 to 3) of apheresis. All patients who received transplants were engrafted using kinetics that were comparable to those of other mobilization regimens. Three non-hematologic significant adverse events were observed in one patient, and included bacterial sepsis (grade 3), tumor lysis syndrome (grade 3), and disease progression (grade 5). Conclusion For non-Hodgkin lymphoma, mobilization with bendamustine is safe and effective.

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