TY - JOUR
T1 - Preliminary Results of Treatment with Filgrastim for Relapse of Leukemia and Myelodysplasia after Allogeneic Bone Marrow Transplantation
AU - Giralt, Sergio
AU - Escudier, Susan
AU - Kantarjian, Hagop
AU - Deisseroth, Albert
AU - Freireich, Emil J.
AU - Andersson, Borje S.
AU - O'brien, Susan
AU - Andreeff, Michael
AU - Fisher, Harold
AU - Cork, Ann
AU - Hirsch-Ginsberg, Cheryl
AU - Trujillo, Jose
AU - Stass, Sanford
AU - Champlin, Richard E.
PY - 1993/9/9
Y1 - 1993/9/9
N2 - Patients whose leukemia relapses after allogeneic bone marrow transplantation have a poor prognosis; few respond to further chemotherapy, and almost none survive over the long term. We present preliminary observations on the use of filgrastim (granulocyte colony-stimulating factor) for relapse after transplantation. Seven female patients with leukemia (one with chronic myelogenous leukemia, five with acute myelogenous leukemia, and one with a myelodysplastic syndrome that transformed into acute myelogenous leukemia) whose disease relapsed within 360 days after allogeneic bone marrow transplantation received filgrastim (5 μg per kilogram of body weight per day by subcutaneous injection) to reinduce remission by stimulating residual donor marrow cells. Cytogenetic analysis of bone marrow, fluorescence in situ hybridization, and determination of restriction-fragment-length polymorphisms were used to assess response and chimerism. Three of the seven patients had a complete hematologic and cytogenetic remission, with reestablishment of hematopoiesis of donor origin. Mild chronic graft-versus-host disease developed in one patient, and acute graft-versus-host disease in none. One patient had a relapse 12 months after treatment, and two others remained in remission after 10 and 11 months. In two of the patients with a response, fluorescence in situ hybridization demonstrated stimulation of donor cells without differentiation of the leukemic clone. Filgrastim may be effective in selected cases of leukemic relapse after allogeneic bone marrow transplantation., In many patients with leukemia or myelodysplastic syndromes, the underlying disease recurs after allogeneic bone marrow transplantation1. Attempts to reinduce durable remissions with chemotherapeutic agents or a second bone marrow transplant are usually unsuccessful2–5. The chimeric state that follows transplantation provides an opportunity for novel therapeutic approaches, such as selective stimulation of hematopoiesis of donor origin or augmentation of the graft-versus-leukemia (GVL) reaction6–9. We observed one patient in whom pancytopenia associated with relapse of Philadelphia chromosome-negative chronic myelogenous leukemia developed after allogeneic bone marrow transplantation. Complete hematologic recovery and cytogenetic remission occurred on treatment with…
AB - Patients whose leukemia relapses after allogeneic bone marrow transplantation have a poor prognosis; few respond to further chemotherapy, and almost none survive over the long term. We present preliminary observations on the use of filgrastim (granulocyte colony-stimulating factor) for relapse after transplantation. Seven female patients with leukemia (one with chronic myelogenous leukemia, five with acute myelogenous leukemia, and one with a myelodysplastic syndrome that transformed into acute myelogenous leukemia) whose disease relapsed within 360 days after allogeneic bone marrow transplantation received filgrastim (5 μg per kilogram of body weight per day by subcutaneous injection) to reinduce remission by stimulating residual donor marrow cells. Cytogenetic analysis of bone marrow, fluorescence in situ hybridization, and determination of restriction-fragment-length polymorphisms were used to assess response and chimerism. Three of the seven patients had a complete hematologic and cytogenetic remission, with reestablishment of hematopoiesis of donor origin. Mild chronic graft-versus-host disease developed in one patient, and acute graft-versus-host disease in none. One patient had a relapse 12 months after treatment, and two others remained in remission after 10 and 11 months. In two of the patients with a response, fluorescence in situ hybridization demonstrated stimulation of donor cells without differentiation of the leukemic clone. Filgrastim may be effective in selected cases of leukemic relapse after allogeneic bone marrow transplantation., In many patients with leukemia or myelodysplastic syndromes, the underlying disease recurs after allogeneic bone marrow transplantation1. Attempts to reinduce durable remissions with chemotherapeutic agents or a second bone marrow transplant are usually unsuccessful2–5. The chimeric state that follows transplantation provides an opportunity for novel therapeutic approaches, such as selective stimulation of hematopoiesis of donor origin or augmentation of the graft-versus-leukemia (GVL) reaction6–9. We observed one patient in whom pancytopenia associated with relapse of Philadelphia chromosome-negative chronic myelogenous leukemia developed after allogeneic bone marrow transplantation. Complete hematologic recovery and cytogenetic remission occurred on treatment with…
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U2 - 10.1056/NEJM199309093291103
DO - 10.1056/NEJM199309093291103
M3 - Article
C2 - 7688862
AN - SCOPUS:0027283016
SN - 0028-4793
VL - 329
SP - 757
EP - 761
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 11
ER -