Autologous stem cell transplantation followed by a dose-reduced allograft induces high complete remission rate in multiple myeloma.
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Autologous stem cell transplantation followed by a dose-reduced allograft induces high complete remission rate in multiple myeloma. / Kröger, Nicolaus-Martin; Schwerdtfeger, Rainer; Kiehl, Michael; Sayer, Herbert Gottfried; Renges, Helmut-Hans; Zabelina, Tatjana; Fehse, Boris; Tögel, Florian; Wittkowsky, Georg; Kuse, Rolf; Zander, Axel.
In: BLOOD, Vol. 100, No. 3, 3, 2002, p. 755-760.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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T1 - Autologous stem cell transplantation followed by a dose-reduced allograft induces high complete remission rate in multiple myeloma.
AU - Kröger, Nicolaus-Martin
AU - Schwerdtfeger, Rainer
AU - Kiehl, Michael
AU - Sayer, Herbert Gottfried
AU - Renges, Helmut-Hans
AU - Zabelina, Tatjana
AU - Fehse, Boris
AU - Tögel, Florian
AU - Wittkowsky, Georg
AU - Kuse, Rolf
AU - Zander, Axel
PY - 2002
Y1 - 2002
N2 - We evaluated toxicity, engraftment, chimerism, graft-versus-host disease (GVHD), and response to a dose-reduced allograft after cytoreductive autografting in 17 patients with advanced stage II/III multiple myeloma (MM). After autografting with melphalan (200 mg/m2) the patients received after a median interval of 119 days (range 60-210) a dose-reduced regimen consisting of fludarabine (180 mg/m2), melphalan (100 mg/m2), and antithymocyte globulin (3 x 10 mg/kg) followed by allografting from related (n = 7), mismatched related (n = 2), or unrelated (n = 8) donors to induce a graft-versus-myeloma effect. After dose-reduced allografting all patients became neutropenic (<0.2 x 10(9)/L) for at least 8 days. All patients engrafted with a median time for leukocyte (> 1 x 10(9)/L) and platelet (> 20 x 10(9)/L) counts of 16 (range, 11-24) and 23 days (range, 12-43), respectively. Complete donor chimerism was detected after a median of 30 days (range, 19-38). Acute GVHD stage II occurred in 4 patients (25%) and grade III GVHD in 2 patients (13%). Chronic GVHD developed in 40% of the patients, but only 1 patient experienced extensive chronic GVHD requiring further immunosuppressive therapy. Two patients died of alveolar hemorrhage and pneumonia, resulting in a day 100 mortality rate of 11%. The rate of complete remission with negative immunofixation increased from 18% after autografting to 73% after allografting. After a median follow-up of 17 months after autologous and 13 months after allogeneic transplantation 13 patients are alive and 12 of them free of relapse or progression. The tandem auto-allotransplant protocol is highly active and provides rapid engraftment with complete donor chimerism and tolerable toxicity.
AB - We evaluated toxicity, engraftment, chimerism, graft-versus-host disease (GVHD), and response to a dose-reduced allograft after cytoreductive autografting in 17 patients with advanced stage II/III multiple myeloma (MM). After autografting with melphalan (200 mg/m2) the patients received after a median interval of 119 days (range 60-210) a dose-reduced regimen consisting of fludarabine (180 mg/m2), melphalan (100 mg/m2), and antithymocyte globulin (3 x 10 mg/kg) followed by allografting from related (n = 7), mismatched related (n = 2), or unrelated (n = 8) donors to induce a graft-versus-myeloma effect. After dose-reduced allografting all patients became neutropenic (<0.2 x 10(9)/L) for at least 8 days. All patients engrafted with a median time for leukocyte (> 1 x 10(9)/L) and platelet (> 20 x 10(9)/L) counts of 16 (range, 11-24) and 23 days (range, 12-43), respectively. Complete donor chimerism was detected after a median of 30 days (range, 19-38). Acute GVHD stage II occurred in 4 patients (25%) and grade III GVHD in 2 patients (13%). Chronic GVHD developed in 40% of the patients, but only 1 patient experienced extensive chronic GVHD requiring further immunosuppressive therapy. Two patients died of alveolar hemorrhage and pneumonia, resulting in a day 100 mortality rate of 11%. The rate of complete remission with negative immunofixation increased from 18% after autografting to 73% after allografting. After a median follow-up of 17 months after autologous and 13 months after allogeneic transplantation 13 patients are alive and 12 of them free of relapse or progression. The tandem auto-allotransplant protocol is highly active and provides rapid engraftment with complete donor chimerism and tolerable toxicity.
M3 - SCORING: Zeitschriftenaufsatz
VL - 100
SP - 755
EP - 760
JO - BLOOD
JF - BLOOD
SN - 0006-4971
IS - 3
M1 - 3
ER -