Importance of marrow dose on posttransplant outcome in acute leukemia: Models derived from patients autografted with mafosfamide-purged marrow at a single institution

Several prospective randomized trials in acute myelocytic leukemia (AML) documented a lower relapse rate with autologous bone marrow transplantation (ABMT) than with conventional chemotherapy. However, they also identified some transplant difficulties, such as failure to collect sufficient numbers o...

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Veröffentlicht in:Experimental hematology 1999-12, Vol.27 (12), p.1822-1830
Hauptverfasser: Gorin, Norbert-Claude, Labopin, Myriam, Laporte, Jean-Philippe, Douay, Luc, Lopez, Manuel, Lesage, Sylvie, Fouillard, Loı̈c, Isnard, Françoise, Jouet, Jean-Pierre, Bellal, Nassima, Perot, Christine, Van Den Akker, Jacqueline, Bauters, Francis, Najman, Albert
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container_end_page 1830
container_issue 12
container_start_page 1822
container_title Experimental hematology
container_volume 27
creator Gorin, Norbert-Claude
Labopin, Myriam
Laporte, Jean-Philippe
Douay, Luc
Lopez, Manuel
Lesage, Sylvie
Fouillard, Loı̈c
Isnard, Françoise
Jouet, Jean-Pierre
Bellal, Nassima
Perot, Christine
Van Den Akker, Jacqueline
Bauters, Francis
Najman, Albert
description Several prospective randomized trials in acute myelocytic leukemia (AML) documented a lower relapse rate with autologous bone marrow transplantation (ABMT) than with conventional chemotherapy. However, they also identified some transplant difficulties, such as failure to collect sufficient numbers of stem cells, slow kinetics of engraftment, and a high transplant-related mortality that diminished or negated positive impact on overall survival. Data for ABMT are inconclusive in acute lymphocytic leukemia (ALL) in adults. We retrospectively analyzed patients with acute leukemia autografted with marrow purged with mafosfamide after January 1983 in our institution. The population comprised 229 consecutive patients; 165 with AML [123 in first remission (CR1), 32 in second remission (CR2)]; 61 with ALL (46 in CR1, 4 in CR2); and 3 with undifferentiated acute leukemia. All patients were autografted with marrow purged with mafosfamide. Mafosfamide was given at a constant dose of 50 μg/mL in 103 and adjusted individually to produce a CFU-GM LD 95 (5% residual CFU-GM post purging) in 126. The outcome was analyzed for correlation with patient characteristics, the disease including cytogenetics, and the graft itself. Prognostic factors identified by multivariate analysis were used to derive a prognostic classification. Patients receiving higher doses of marrow submitted to purging (>5.46 × 10 4 CFU-GM/kg) experienced a lower treatment-related mortality ( RR = 0.11, p = 0.005) and a higher leukemia-free ( RR = 0.5, p = 0.005) and overall survival ( RR = 0.4, p = 0.001) . Patients receiving 5.46 × 10 4 CFU-GM/kg and doses actually infused post purging of ≤0.02 × 10 4/kg had a treatment-related mortality of only 2 ± 2%, a leukemia-free survival of 70%, and an overall survival of 77 ± 7% at 10 years. In this study of autotransplantation for acute leukemia using mafosfamide-purged marrow, the stem cell dose used for purging and the intensity of purging were the most important factors predicting outcome.
doi_str_mv 10.1016/S0301-472X(99)00121-6
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However, they also identified some transplant difficulties, such as failure to collect sufficient numbers of stem cells, slow kinetics of engraftment, and a high transplant-related mortality that diminished or negated positive impact on overall survival. Data for ABMT are inconclusive in acute lymphocytic leukemia (ALL) in adults. We retrospectively analyzed patients with acute leukemia autografted with marrow purged with mafosfamide after January 1983 in our institution. The population comprised 229 consecutive patients; 165 with AML [123 in first remission (CR1), 32 in second remission (CR2)]; 61 with ALL (46 in CR1, 4 in CR2); and 3 with undifferentiated acute leukemia. All patients were autografted with marrow purged with mafosfamide. Mafosfamide was given at a constant dose of 50 μg/mL in 103 and adjusted individually to produce a CFU-GM LD 95 (5% residual CFU-GM post purging) in 126. The outcome was analyzed for correlation with patient characteristics, the disease including cytogenetics, and the graft itself. Prognostic factors identified by multivariate analysis were used to derive a prognostic classification. Patients receiving higher doses of marrow submitted to purging (&gt;5.46 × 10 4 CFU-GM/kg) experienced a lower treatment-related mortality ( RR = 0.11, p = 0.005) and a higher leukemia-free ( RR = 0.5, p = 0.005) and overall survival ( RR = 0.4, p = 0.001) . Patients receiving &lt;0.004% CFU-GM of marrow actually infused post purging had a lower relapse rate ( RR = 0.51, p = 0.003) . Modeling of prognostic groups identified good-, intermediate-, and poor-risk categories. Patients receiving a stem cell dose evaluated before purging of &gt;5.46 × 10 4 CFU-GM/kg and doses actually infused post purging of ≤0.02 × 10 4/kg had a treatment-related mortality of only 2 ± 2%, a leukemia-free survival of 70%, and an overall survival of 77 ± 7% at 10 years. 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However, they also identified some transplant difficulties, such as failure to collect sufficient numbers of stem cells, slow kinetics of engraftment, and a high transplant-related mortality that diminished or negated positive impact on overall survival. Data for ABMT are inconclusive in acute lymphocytic leukemia (ALL) in adults. We retrospectively analyzed patients with acute leukemia autografted with marrow purged with mafosfamide after January 1983 in our institution. The population comprised 229 consecutive patients; 165 with AML [123 in first remission (CR1), 32 in second remission (CR2)]; 61 with ALL (46 in CR1, 4 in CR2); and 3 with undifferentiated acute leukemia. All patients were autografted with marrow purged with mafosfamide. Mafosfamide was given at a constant dose of 50 μg/mL in 103 and adjusted individually to produce a CFU-GM LD 95 (5% residual CFU-GM post purging) in 126. The outcome was analyzed for correlation with patient characteristics, the disease including cytogenetics, and the graft itself. Prognostic factors identified by multivariate analysis were used to derive a prognostic classification. Patients receiving higher doses of marrow submitted to purging (&gt;5.46 × 10 4 CFU-GM/kg) experienced a lower treatment-related mortality ( RR = 0.11, p = 0.005) and a higher leukemia-free ( RR = 0.5, p = 0.005) and overall survival ( RR = 0.4, p = 0.001) . Patients receiving &lt;0.004% CFU-GM of marrow actually infused post purging had a lower relapse rate ( RR = 0.51, p = 0.003) . Modeling of prognostic groups identified good-, intermediate-, and poor-risk categories. Patients receiving a stem cell dose evaluated before purging of &gt;5.46 × 10 4 CFU-GM/kg and doses actually infused post purging of ≤0.02 × 10 4/kg had a treatment-related mortality of only 2 ± 2%, a leukemia-free survival of 70%, and an overall survival of 77 ± 7% at 10 years. 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Labopin, Myriam ; Laporte, Jean-Philippe ; Douay, Luc ; Lopez, Manuel ; Lesage, Sylvie ; Fouillard, Loı̈c ; Isnard, Françoise ; Jouet, Jean-Pierre ; Bellal, Nassima ; Perot, Christine ; Van Den Akker, Jacqueline ; Bauters, Francis ; Najman, Albert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e263t-92c806c38b7e6a00c65c2813bc4c52dbc03506891f594d8fbb0eef31afdd14ae3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Acute leukemia</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Autologous bone marrow transplantation</topic><topic>Bone Marrow Purging</topic><topic>Bone Marrow Transplantation</topic><topic>Cell Count</topic><topic>Child</topic><topic>Cyclophosphamide - analogs &amp; derivatives</topic><topic>Cyclophosphamide - pharmacology</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Dose of stem cells</topic><topic>Female</topic><topic>Graft Survival</topic><topic>Humans</topic><topic>Leukemia, Myeloid, Acute - physiopathology</topic><topic>Leukemia, Myeloid, Acute - therapy</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Purging in vivo with mafosfamide</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Retrospective Studies</topic><topic>Transplantation, Homologous</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gorin, Norbert-Claude</creatorcontrib><creatorcontrib>Labopin, Myriam</creatorcontrib><creatorcontrib>Laporte, Jean-Philippe</creatorcontrib><creatorcontrib>Douay, Luc</creatorcontrib><creatorcontrib>Lopez, Manuel</creatorcontrib><creatorcontrib>Lesage, Sylvie</creatorcontrib><creatorcontrib>Fouillard, Loı̈c</creatorcontrib><creatorcontrib>Isnard, Françoise</creatorcontrib><creatorcontrib>Jouet, Jean-Pierre</creatorcontrib><creatorcontrib>Bellal, Nassima</creatorcontrib><creatorcontrib>Perot, Christine</creatorcontrib><creatorcontrib>Van Den Akker, Jacqueline</creatorcontrib><creatorcontrib>Bauters, Francis</creatorcontrib><creatorcontrib>Najman, Albert</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Experimental hematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gorin, Norbert-Claude</au><au>Labopin, Myriam</au><au>Laporte, Jean-Philippe</au><au>Douay, Luc</au><au>Lopez, Manuel</au><au>Lesage, Sylvie</au><au>Fouillard, Loı̈c</au><au>Isnard, Françoise</au><au>Jouet, Jean-Pierre</au><au>Bellal, Nassima</au><au>Perot, Christine</au><au>Van Den Akker, Jacqueline</au><au>Bauters, Francis</au><au>Najman, Albert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Importance of marrow dose on posttransplant outcome in acute leukemia: Models derived from patients autografted with mafosfamide-purged marrow at a single institution</atitle><jtitle>Experimental hematology</jtitle><addtitle>Exp Hematol</addtitle><date>1999-12-01</date><risdate>1999</risdate><volume>27</volume><issue>12</issue><spage>1822</spage><epage>1830</epage><pages>1822-1830</pages><issn>0301-472X</issn><eissn>1873-2399</eissn><abstract>Several prospective randomized trials in acute myelocytic leukemia (AML) documented a lower relapse rate with autologous bone marrow transplantation (ABMT) than with conventional chemotherapy. However, they also identified some transplant difficulties, such as failure to collect sufficient numbers of stem cells, slow kinetics of engraftment, and a high transplant-related mortality that diminished or negated positive impact on overall survival. Data for ABMT are inconclusive in acute lymphocytic leukemia (ALL) in adults. We retrospectively analyzed patients with acute leukemia autografted with marrow purged with mafosfamide after January 1983 in our institution. The population comprised 229 consecutive patients; 165 with AML [123 in first remission (CR1), 32 in second remission (CR2)]; 61 with ALL (46 in CR1, 4 in CR2); and 3 with undifferentiated acute leukemia. All patients were autografted with marrow purged with mafosfamide. Mafosfamide was given at a constant dose of 50 μg/mL in 103 and adjusted individually to produce a CFU-GM LD 95 (5% residual CFU-GM post purging) in 126. The outcome was analyzed for correlation with patient characteristics, the disease including cytogenetics, and the graft itself. Prognostic factors identified by multivariate analysis were used to derive a prognostic classification. Patients receiving higher doses of marrow submitted to purging (&gt;5.46 × 10 4 CFU-GM/kg) experienced a lower treatment-related mortality ( RR = 0.11, p = 0.005) and a higher leukemia-free ( RR = 0.5, p = 0.005) and overall survival ( RR = 0.4, p = 0.001) . Patients receiving &lt;0.004% CFU-GM of marrow actually infused post purging had a lower relapse rate ( RR = 0.51, p = 0.003) . Modeling of prognostic groups identified good-, intermediate-, and poor-risk categories. Patients receiving a stem cell dose evaluated before purging of &gt;5.46 × 10 4 CFU-GM/kg and doses actually infused post purging of ≤0.02 × 10 4/kg had a treatment-related mortality of only 2 ± 2%, a leukemia-free survival of 70%, and an overall survival of 77 ± 7% at 10 years. In this study of autotransplantation for acute leukemia using mafosfamide-purged marrow, the stem cell dose used for purging and the intensity of purging were the most important factors predicting outcome.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>10641600</pmid><doi>10.1016/S0301-472X(99)00121-6</doi><tpages>9</tpages></addata></record>
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ispartof Experimental hematology, 1999-12, Vol.27 (12), p.1822-1830
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source MEDLINE; Elsevier ScienceDirect Journals
subjects Acute leukemia
Adolescent
Adult
Aged
Antineoplastic Agents - pharmacology
Antineoplastic Agents - therapeutic use
Autologous bone marrow transplantation
Bone Marrow Purging
Bone Marrow Transplantation
Cell Count
Child
Cyclophosphamide - analogs & derivatives
Cyclophosphamide - pharmacology
Cyclophosphamide - therapeutic use
Dose of stem cells
Female
Graft Survival
Humans
Leukemia, Myeloid, Acute - physiopathology
Leukemia, Myeloid, Acute - therapy
Male
Middle Aged
Purging in vivo with mafosfamide
Randomized Controlled Trials as Topic
Retrospective Studies
Transplantation, Homologous
Treatment Outcome
title Importance of marrow dose on posttransplant outcome in acute leukemia: Models derived from patients autografted with mafosfamide-purged marrow at a single institution
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