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...
Gespeichert in:
Veröffentlicht in: | Experimental hematology 1999-12, Vol.27 (12), p.1822-1830 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>pubmed_elsev</sourceid><recordid>TN_cdi_pubmed_primary_10641600</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0301472X99001216</els_id><sourcerecordid>10641600</sourcerecordid><originalsourceid>FETCH-LOGICAL-e263t-92c806c38b7e6a00c65c2813bc4c52dbc03506891f594d8fbb0eef31afdd14ae3</originalsourceid><addsrcrecordid>eNo9UcFu1TAQtBCIvhY-AeQjHALrOPGLuSBUUahUxAGQuFmOvX4YkjiyN634Ib4Tv7ZwWu3uaGdnhrFnAl4JEOr1F5Agmm7ffn-h9UsA0YpGPWA7Mexl00qtH7Ldf8gJOy3lJwD0vYbH7ESA6oQC2LE_l_OaMtnFIU-BzzbndMN9KrVd-JoKUbZLWSe7EE8buTQjjwu3biPkE26_cI72Df-UPE6Fe8zxGj0POc18tRRxocLtRumQbaC6uYn0o9KEVIKdo8dm3fKhzu-ZLXHLS1wO05GmUKSNYlqesEfBTgWf3tcz9u3i_dfzj83V5w-X5--uGmyVpEa3bgDl5DDuUVkAp3rXDkKOrnN960cHsgc1aBF63fkhjCMgBils8F50FuUZe353d93GGb1Zc6yP_Tb_DKuAt3eAqhavI2ZTXBXp0MeMjoxPsYLNMSJzG5E5-m-0NrcRGSX_AtU-iCI</addsrcrecordid><sourcetype>Index Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Importance of marrow dose on posttransplant outcome in acute leukemia: Models derived from patients autografted with mafosfamide-purged marrow at a single institution</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><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</creator><creatorcontrib>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</creatorcontrib><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 <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 >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.</description><identifier>ISSN: 0301-472X</identifier><identifier>EISSN: 1873-2399</identifier><identifier>DOI: 10.1016/S0301-472X(99)00121-6</identifier><identifier>PMID: 10641600</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>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</subject><ispartof>Experimental hematology, 1999-12, Vol.27 (12), p.1822-1830</ispartof><rights>1999 International Society for Experimental Hematology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0301472X99001216$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10641600$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Importance of marrow dose on posttransplant outcome in acute leukemia: Models derived from patients autografted with mafosfamide-purged marrow at a single institution</title><title>Experimental hematology</title><addtitle>Exp Hematol</addtitle><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 <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 >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.</description><subject>Acute leukemia</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Autologous bone marrow transplantation</subject><subject>Bone Marrow Purging</subject><subject>Bone Marrow Transplantation</subject><subject>Cell Count</subject><subject>Child</subject><subject>Cyclophosphamide - analogs & derivatives</subject><subject>Cyclophosphamide - pharmacology</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Dose of stem cells</subject><subject>Female</subject><subject>Graft Survival</subject><subject>Humans</subject><subject>Leukemia, Myeloid, Acute - physiopathology</subject><subject>Leukemia, Myeloid, Acute - therapy</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Purging in vivo with mafosfamide</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Retrospective Studies</subject><subject>Transplantation, Homologous</subject><subject>Treatment Outcome</subject><issn>0301-472X</issn><issn>1873-2399</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UcFu1TAQtBCIvhY-AeQjHALrOPGLuSBUUahUxAGQuFmOvX4YkjiyN634Ib4Tv7ZwWu3uaGdnhrFnAl4JEOr1F5Agmm7ffn-h9UsA0YpGPWA7Mexl00qtH7Ldf8gJOy3lJwD0vYbH7ESA6oQC2LE_l_OaMtnFIU-BzzbndMN9KrVd-JoKUbZLWSe7EE8buTQjjwu3biPkE26_cI72Df-UPE6Fe8zxGj0POc18tRRxocLtRumQbaC6uYn0o9KEVIKdo8dm3fKhzu-ZLXHLS1wO05GmUKSNYlqesEfBTgWf3tcz9u3i_dfzj83V5w-X5--uGmyVpEa3bgDl5DDuUVkAp3rXDkKOrnN960cHsgc1aBF63fkhjCMgBils8F50FuUZe353d93GGb1Zc6yP_Tb_DKuAt3eAqhavI2ZTXBXp0MeMjoxPsYLNMSJzG5E5-m-0NrcRGSX_AtU-iCI</recordid><startdate>19991201</startdate><enddate>19991201</enddate><creator>Gorin, Norbert-Claude</creator><creator>Labopin, Myriam</creator><creator>Laporte, Jean-Philippe</creator><creator>Douay, Luc</creator><creator>Lopez, Manuel</creator><creator>Lesage, Sylvie</creator><creator>Fouillard, Loı̈c</creator><creator>Isnard, Françoise</creator><creator>Jouet, Jean-Pierre</creator><creator>Bellal, Nassima</creator><creator>Perot, Christine</creator><creator>Van Den Akker, Jacqueline</creator><creator>Bauters, Francis</creator><creator>Najman, Albert</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>19991201</creationdate><title>Importance of marrow dose on posttransplant outcome in acute leukemia: Models derived from patients autografted with mafosfamide-purged marrow at a single institution</title><author>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</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 & 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 (>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 <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 >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> |
fulltext | fulltext |
identifier | ISSN: 0301-472X |
ispartof | Experimental hematology, 1999-12, Vol.27 (12), p.1822-1830 |
issn | 0301-472X 1873-2399 |
language | eng |
recordid | cdi_pubmed_primary_10641600 |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T22%3A22%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-pubmed_elsev&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Importance%20of%20marrow%20dose%20on%20posttransplant%20outcome%20in%20acute%20leukemia:%20Models%20derived%20from%20patients%20autografted%20with%20mafosfamide-purged%20marrow%20at%20a%20single%20institution&rft.jtitle=Experimental%20hematology&rft.au=Gorin,%20Norbert-Claude&rft.date=1999-12-01&rft.volume=27&rft.issue=12&rft.spage=1822&rft.epage=1830&rft.pages=1822-1830&rft.issn=0301-472X&rft.eissn=1873-2399&rft_id=info:doi/10.1016/S0301-472X(99)00121-6&rft_dat=%3Cpubmed_elsev%3E10641600%3C/pubmed_elsev%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/10641600&rft_els_id=S0301472X99001216&rfr_iscdi=true |