Autologous and allogeneic bone marrow transplantation for chronic lymphocytic leukemia: preliminary results.
Autologous and allogeneic bone marrow transplantation for chronic lymphocytic leukemia: preliminary results.
复制标题
自体和同种异体骨髓移植治疗慢性淋巴细胞白血病:初步结果。
DOI:
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发表时间:
1994
影响因子:
45.3
通讯作者:
S. Giralt
中科院分区:
文献类型:
--
作者:
I. Khouri;M. Keating;H. Vriesendorp;C. Reading;D. Przepiorka;Y. Huh;B. Andersson;K. V. Besien;R. Mehra;S. Giralt
PURPOSE
This study was undertaken to evaluate the feasibility and therapeutic effect of high-dose chemoradiotherapy with autologous or allogeneic bone marrow transplantation (BMT) in patients with advanced chronic lymphocytic leukemia (CLL) who relapse after fludarabine treatment.
PATIENTS AND METHODS
Twenty-two patients with advanced CLL received high-dose cyclophosphamide, total-body irradiation, and BMT. Eleven patients with relapsed CLL received autologous BMT with marrow collected during a prior fludarabine-induced remission; leukemia cells were depleted from the autologous marrow in seven patients using an anti-CD19 monoclonal antibody and immunomagnetic separation. Eleven patients received allogeneic or syngeneic BMT, seven of whom had refractory Rai stage III or IV disease.
RESULTS
Six autologous transplant recipients achieved a complete remission (CR), four a nodular CR (nCR), and one a partial remission (PR). Two recurred with CLL, and three developed Richter's transformation. Two patients had recurrence of immune cytopenias while in morphologic remission; one of these patients died of cytomegalovirus pneumonia. Six of 11 patients survive in remission 2 to 29 months following BMT. Of the 11 patients who received allogeneic or syngeneic BMT, seven achieved a CR, two a nCR, and one a PR; 10 survive 2 to 36 months following BMT.
CONCLUSION
These data indicate that high-dose chemotherapy with allogeneic BMT is effective at producing CRs in patients with CLL. Autologous transplantation in CLL is feasible and is capable of producing remissions in patients with advanced CLL. Further studies are warranted to assess the role of BMT in the treatment of CLL.
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影响因子:
20.3
作者:
Pedrazzini,A;Freedman,AS;Andersen,J;Heflin,L;Anderson,K;Takvorian,T;Canellos,GP;Whitman,J;Coral,F;Ritz,J
通讯作者:
Ritz,J
影响因子:
20.3
作者:
Perri,RT;Royston,I;LeBien,TW;Kay,NE
通讯作者:
Kay,NE
影响因子:
20.3
作者:
Keating,MJ;Kantarjian,H;Talpaz,M;Redman,J;Koller,C;Barlogie,B;Velasquez,W;Plunkett,W;Freireich,EJ;McCredie,KB
通讯作者:
McCredie,KB
影响因子:
20.3
作者:
T. Kipps;D. Carson
通讯作者:
T. Kipps;D. Carson
影响因子:
20.3
作者:
Freedman,AS;Boyd,AW;Bieber,FR;Daley,J;Rosen,K;Horowitz,JC;Levy,DN;Nadler,LM
通讯作者:
Nadler,LM