TY - JOUR
T1 - Autologous bone marrow transplantation in poor-prognosis intermediate-grade and high-grade B-cell non-Hodgkin's lymphoma in first remission
T2 - A pilot study
AU - Freedman, Arnold S.
AU - Takvorian, Tak
AU - Neuberg, Donna
AU - Mauch, Peter
AU - Rabinowe, Susan N.
AU - Anderson, Kenneth C.
AU - Soiffer, Robert J.
AU - Spector, Neil
AU - Grossbard, Michael
AU - Robertson, Michael J.
AU - Blake, Kelly
AU - Coral, Felice
AU - Canellos, George P.
AU - Ritz, Jerome
AU - Nadler, Lee M.
PY - 1993
Y1 - 1993
N2 - Purpose: Using high-dose therapy and outologous bone marrow transplantation (ABMT) to overcome cellular resistance and eradicate minimal disease, we initiated a pilot study during first remission in patients with non-Hodgkin's lymphoma (NHL) to examine whether the long-term disease-free survival (DPS) rate can be improved for patients with poor-prognosis intermediate/ high-grade NHL. Patients and Methods: Twenty-six patients with advanced-stage diffuse intermediate/high-grade B-cell NHL (including 16 patients with diffuse small cleaved-cell [DSC]) were selected at presentation by histologic and clinical characteristics to have less than a 25% probability of long-term DFS with conventional treatment. After induction chemotherapy, 16 patients were in complete remission (CR) and 10 were in a minimal disease state. Patients were then treated with high-dose cyclophosphamide, total-body irradiation (TBI), and anti-B-cell monoclonal antibody-purged ABMT. Results: Following ABMT, no acute in-hospital treatment deaths occurred, and engraftment of granulocytes and platelets was significantly faster than for patients undergoing ABMT who were in second or subsequent remission. Of 26 patients, 21 remain in CR maintained without continued therapy, three relapsed in sites of prior nodal disease (4.8, 5.4, and 28 months post-ABMT), and two died in remission. The DPS rate is estimated to be 85% at 28 months and thereafter. The median followup period for the 21 patients who are alive and disease-free is 32 months. Conclusion: This pilot study suggests that consolidation of first remission with ABMT may improve the longterm DFS rate for diffuse intermediate/high-grade NHL patients at high risk for relapse.
AB - Purpose: Using high-dose therapy and outologous bone marrow transplantation (ABMT) to overcome cellular resistance and eradicate minimal disease, we initiated a pilot study during first remission in patients with non-Hodgkin's lymphoma (NHL) to examine whether the long-term disease-free survival (DPS) rate can be improved for patients with poor-prognosis intermediate/ high-grade NHL. Patients and Methods: Twenty-six patients with advanced-stage diffuse intermediate/high-grade B-cell NHL (including 16 patients with diffuse small cleaved-cell [DSC]) were selected at presentation by histologic and clinical characteristics to have less than a 25% probability of long-term DFS with conventional treatment. After induction chemotherapy, 16 patients were in complete remission (CR) and 10 were in a minimal disease state. Patients were then treated with high-dose cyclophosphamide, total-body irradiation (TBI), and anti-B-cell monoclonal antibody-purged ABMT. Results: Following ABMT, no acute in-hospital treatment deaths occurred, and engraftment of granulocytes and platelets was significantly faster than for patients undergoing ABMT who were in second or subsequent remission. Of 26 patients, 21 remain in CR maintained without continued therapy, three relapsed in sites of prior nodal disease (4.8, 5.4, and 28 months post-ABMT), and two died in remission. The DPS rate is estimated to be 85% at 28 months and thereafter. The median followup period for the 21 patients who are alive and disease-free is 32 months. Conclusion: This pilot study suggests that consolidation of first remission with ABMT may improve the longterm DFS rate for diffuse intermediate/high-grade NHL patients at high risk for relapse.
UR - http://www.scopus.com/inward/record.url?scp=0027194946&partnerID=8YFLogxK
U2 - 10.1200/JCO.1993.11.5.931
DO - 10.1200/JCO.1993.11.5.931
M3 - Article
C2 - 8487057
AN - SCOPUS:0027194946
SN - 0732-183X
VL - 11
SP - 931
EP - 936
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 5
ER -