Autologous bone marrow transplantation for patients with relapsed hodgkin's disease

purpose: High-dose therapy and autologous bone marrow transplantation (ABMT) are being increasingly utilized for the management of patients with relapsed Hodgkin's disease. Because patients with relapsed Hodgkin's disease often initially respond to salvage chemotherapy regimens, ABMT is fr...

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Veröffentlicht in:The American journal of medicine 1991-12, Vol.91 (6), p.605-611
Hauptverfasser: Armitage, James O., Bierman, Philip J., Vose, Julie M., Anderson, James R., Weisenburger, Dennis D., Kessinger, Anne, Reed, Elizabeth C., Vaughan, William P., Coccia, Peter F., Purtilo, David T.
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container_end_page 611
container_issue 6
container_start_page 605
container_title The American journal of medicine
container_volume 91
creator Armitage, James O.
Bierman, Philip J.
Vose, Julie M.
Anderson, James R.
Weisenburger, Dennis D.
Kessinger, Anne
Reed, Elizabeth C.
Vaughan, William P.
Coccia, Peter F.
Purtilo, David T.
description purpose: High-dose therapy and autologous bone marrow transplantation (ABMT) are being increasingly utilized for the management of patients with relapsed Hodgkin's disease. Because patients with relapsed Hodgkin's disease often initially respond to salvage chemotherapy regimens, ABMT is frequently delayed until late in the course of the disease. The optimal timing for ABMT has not been identified. The purpose of this study was to determine the value of ABMT earlier in the course of Hodgkin's disease. patients and methods: We treated 70 patients between October 1984 and October 1988 with high-dose cyclophosphamide, carmustine, and etoposide, followed by infusion of previously cryopreserved autologous bone marrow, and analyzed the results to determine the impact of timing of ABMT on treatment outcome. One (17 patients), two (24 patients), or three or more (29 patients) chemotherapy regimens had failed in patients before ABMT. results: The results for all 70 patients included a complete remission rate of 59%, an early death rate of 11%, a 4-year survival of 47%, and 27% of all treated patients alive and in complete remission at 4 years. The median follow-up for patients remaining in complete remission is 56 months (range 26 to 73 months). The frequency of achieving a complete remission was higher in patients in whom fewer regimens had failed before ABMT (i.e., 82% versus 58% versus 45%, p = 0.02), as was the 4-year disease-free survival (i.e., 44% versus 33% versus 21%, p = 0.04). conclusion: ABMT is a more effective therapy when used early for patients with relapsed Hodgkin's disease.
doi_str_mv 10.1016/0002-9343(91)90213-H
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Because patients with relapsed Hodgkin's disease often initially respond to salvage chemotherapy regimens, ABMT is frequently delayed until late in the course of the disease. The optimal timing for ABMT has not been identified. The purpose of this study was to determine the value of ABMT earlier in the course of Hodgkin's disease. patients and methods: We treated 70 patients between October 1984 and October 1988 with high-dose cyclophosphamide, carmustine, and etoposide, followed by infusion of previously cryopreserved autologous bone marrow, and analyzed the results to determine the impact of timing of ABMT on treatment outcome. One (17 patients), two (24 patients), or three or more (29 patients) chemotherapy regimens had failed in patients before ABMT. results: The results for all 70 patients included a complete remission rate of 59%, an early death rate of 11%, a 4-year survival of 47%, and 27% of all treated patients alive and in complete remission at 4 years. The median follow-up for patients remaining in complete remission is 56 months (range 26 to 73 months). The frequency of achieving a complete remission was higher in patients in whom fewer regimens had failed before ABMT (i.e., 82% versus 58% versus 45%, p = 0.02), as was the 4-year disease-free survival (i.e., 44% versus 33% versus 21%, p = 0.04). conclusion: ABMT is a more effective therapy when used early for patients with relapsed Hodgkin's disease.</description><identifier>ISSN: 0002-9343</identifier><identifier>EISSN: 1555-7162</identifier><identifier>DOI: 10.1016/0002-9343(91)90213-H</identifier><identifier>PMID: 1750430</identifier><identifier>CODEN: AJMEAZ</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Anesthesia. Intensive care medicine. Transfusions. 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Because patients with relapsed Hodgkin's disease often initially respond to salvage chemotherapy regimens, ABMT is frequently delayed until late in the course of the disease. The optimal timing for ABMT has not been identified. The purpose of this study was to determine the value of ABMT earlier in the course of Hodgkin's disease. patients and methods: We treated 70 patients between October 1984 and October 1988 with high-dose cyclophosphamide, carmustine, and etoposide, followed by infusion of previously cryopreserved autologous bone marrow, and analyzed the results to determine the impact of timing of ABMT on treatment outcome. One (17 patients), two (24 patients), or three or more (29 patients) chemotherapy regimens had failed in patients before ABMT. results: The results for all 70 patients included a complete remission rate of 59%, an early death rate of 11%, a 4-year survival of 47%, and 27% of all treated patients alive and in complete remission at 4 years. The median follow-up for patients remaining in complete remission is 56 months (range 26 to 73 months). The frequency of achieving a complete remission was higher in patients in whom fewer regimens had failed before ABMT (i.e., 82% versus 58% versus 45%, p = 0.02), as was the 4-year disease-free survival (i.e., 44% versus 33% versus 21%, p = 0.04). conclusion: ABMT is a more effective therapy when used early for patients with relapsed Hodgkin's disease.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation</subject><subject>Bone marrow, stem cells transplantation. Graft versus host reaction</subject><subject>Child</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Hodgkin Disease - drug therapy</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - surgery</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Recurrence</subject><subject>Survival Rate</subject><subject>Transfusions. Complications. Transfusion reactions. 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Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Bone Marrow Transplantation</topic><topic>Bone marrow, stem cells transplantation. Graft versus host reaction</topic><topic>Child</topic><topic>Combined Modality Therapy</topic><topic>Female</topic><topic>Hodgkin Disease - drug therapy</topic><topic>Hodgkin Disease - mortality</topic><topic>Hodgkin Disease - surgery</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Recurrence</topic><topic>Survival Rate</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><topic>Transplantation, Autologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Armitage, James O.</creatorcontrib><creatorcontrib>Bierman, Philip J.</creatorcontrib><creatorcontrib>Vose, Julie M.</creatorcontrib><creatorcontrib>Anderson, James R.</creatorcontrib><creatorcontrib>Weisenburger, Dennis D.</creatorcontrib><creatorcontrib>Kessinger, Anne</creatorcontrib><creatorcontrib>Reed, Elizabeth C.</creatorcontrib><creatorcontrib>Vaughan, William P.</creatorcontrib><creatorcontrib>Coccia, Peter F.</creatorcontrib><creatorcontrib>Purtilo, David T.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Armitage, James O.</au><au>Bierman, Philip J.</au><au>Vose, Julie M.</au><au>Anderson, James R.</au><au>Weisenburger, Dennis D.</au><au>Kessinger, Anne</au><au>Reed, Elizabeth C.</au><au>Vaughan, William P.</au><au>Coccia, Peter F.</au><au>Purtilo, David T.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Autologous bone marrow transplantation for patients with relapsed hodgkin's disease</atitle><jtitle>The American journal of medicine</jtitle><addtitle>Am J Med</addtitle><date>1991-12-01</date><risdate>1991</risdate><volume>91</volume><issue>6</issue><spage>605</spage><epage>611</epage><pages>605-611</pages><issn>0002-9343</issn><eissn>1555-7162</eissn><coden>AJMEAZ</coden><abstract>purpose: High-dose therapy and autologous bone marrow transplantation (ABMT) are being increasingly utilized for the management of patients with relapsed Hodgkin's disease. Because patients with relapsed Hodgkin's disease often initially respond to salvage chemotherapy regimens, ABMT is frequently delayed until late in the course of the disease. The optimal timing for ABMT has not been identified. The purpose of this study was to determine the value of ABMT earlier in the course of Hodgkin's disease. patients and methods: We treated 70 patients between October 1984 and October 1988 with high-dose cyclophosphamide, carmustine, and etoposide, followed by infusion of previously cryopreserved autologous bone marrow, and analyzed the results to determine the impact of timing of ABMT on treatment outcome. One (17 patients), two (24 patients), or three or more (29 patients) chemotherapy regimens had failed in patients before ABMT. results: The results for all 70 patients included a complete remission rate of 59%, an early death rate of 11%, a 4-year survival of 47%, and 27% of all treated patients alive and in complete remission at 4 years. The median follow-up for patients remaining in complete remission is 56 months (range 26 to 73 months). The frequency of achieving a complete remission was higher in patients in whom fewer regimens had failed before ABMT (i.e., 82% versus 58% versus 45%, p = 0.02), as was the 4-year disease-free survival (i.e., 44% versus 33% versus 21%, p = 0.04). conclusion: ABMT is a more effective therapy when used early for patients with relapsed Hodgkin's disease.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>1750430</pmid><doi>10.1016/0002-9343(91)90213-H</doi><tpages>7</tpages></addata></record>
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subjects Adolescent
Adult
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Bone Marrow Transplantation
Bone marrow, stem cells transplantation. Graft versus host reaction
Child
Combined Modality Therapy
Female
Hodgkin Disease - drug therapy
Hodgkin Disease - mortality
Hodgkin Disease - surgery
Humans
Male
Medical sciences
Middle Aged
Recurrence
Survival Rate
Transfusions. Complications. Transfusion reactions. Cell and gene therapy
Transplantation, Autologous
title Autologous bone marrow transplantation for patients with relapsed hodgkin's disease
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