Volume 11, Issue 3 pp. 279-285

Clinical outcomes and graft characteristics in pediatric matched sibling donor transplants using granulocyte colony-stimulating factor-primed bone marrow and steady-state bone marrow

Kuang-Yueh Chiang

Kuang-Yueh Chiang

Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta

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Ann Haight

Ann Haight

Emory University, Atlanta, GA, USA

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John Horan

John Horan

Emory University, Atlanta, GA, USA

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Ellen Olson

Ellen Olson

Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta

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Amy Gartner

Amy Gartner

Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta

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Deborah Hartman

Deborah Hartman

Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta

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Susanne Youssef

Susanne Youssef

Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta

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Diana Worthington-White

Diana Worthington-White

Aflac Cancer Center and Blood Disorders Service, Children's Healthcare of Atlanta

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First published: 06 April 2007
Citations: 15
Kuang-Yueh Chiang, 2015 Uppergate Drive, NE, 4th Floor, Atlanta, GA 30322, USA
Tel.: +1 404 785 1272
Fax: +1 404 785 1421
E-mail: [email protected]

Abstract

Abstract: Matched sibling donor (MSD) transplant is a life-saving procedure for children with various hematological malignancies and non-malignancies. Traditionally, steady-state bone marrow (S-BM) has been used as the source of stem cells. More recently, peripheral blood stem cell (PBSC) after granulocyte-colony stimulating factor (G-CSF) mobilization has gained popularity. Adult studies of G-CSF-primed BM (G-BM) have shown that it produces rapid white blood cell engraftment like PBSC, but with less chronic graft-vs.-host disease. No such study has been published in pediatric patients. We conducted a pilot clinical trial of G-BM for pediatric patients. Ten patients were enrolled and were compared to a contemporaneous group of 12 patients who received S-BM. Patients in the G-BM group received a higher dose of total nucleated cells/kg (7.01 vs. 3.76 × 108, p = 0.0009), higher granulocyte–macrophage colony-forming units (CFU-GM)/kg (7.19 vs. 3.53 × 105, p = 0.01) and had shorter inpatient length of stay (28 vs. 40 days, p = 0.04). The engraftment, transfusion requirement and disease-free survival between the two groups were similar. We concluded that G-BM should be considered as an alternative graft source to S-BM, with the benefits of larger graft cell dose, higher CFU-GM dose and shorter length of stay.

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