Favorable outcome of patients with relapsed or refractory Hodgkin's disease treated with high-dose chemotherapy and stem cell rescue at the time of maximal response to conventional salvage therapy (Dexa-BEAM)

Background: Disease status before high-dose chemotherapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell transplantation (PBSCT) is an important predictor of transplantation-related toxicity and event-free survival (EFS) for patients with relapsed or refractory Hodgk...

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Veröffentlicht in:Annals of oncology 1998-03, Vol.9 (3), p.289-295
Hauptverfasser: Josting, A., Kátay, I., Rueffer, U., Winter, S., Tesch, H., Engert, A., Diehl, V., Wickramanayake, P. D.
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container_end_page 295
container_issue 3
container_start_page 289
container_title Annals of oncology
container_volume 9
creator Josting, A.
Kátay, I.
Rueffer, U.
Winter, S.
Tesch, H.
Engert, A.
Diehl, V.
Wickramanayake, P. D.
description Background: Disease status before high-dose chemotherapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell transplantation (PBSCT) is an important predictor of transplantation-related toxicity and event-free survival (EFS) for patients with relapsed or refractory Hodgkin's disease (HD). We performed a phase II study in patients with relapsed or refractory HD to evaluate the feasibility of four cycles of Dexa-BEAM followed by high-dose chemotherapy with ABMT or PBSCT. Patients and methods:Twenty-six patients (median age 30, range 20–40 years) were treated with 2–4 courses of dexa-methasone, carmustine, etoposide, cytarabine and melphalan (Dexa-BEAM) as salvage chemotherapy in order to attain maximal response. Patients achieving complete response (CR) or partial response (PR) high-dose chemotherapy with ABMT or PBSCT. The conditioning regimen used was CVB (cyclophosphamide, carmustine, etoposide). Results: Eighteen patients responded to Dexa-BEAM, resulting in a response rate of 69%. At the time of transplant 16 patients were in CR two patients in PR. At present 14 patients transplanted are in continous CR (median follow-up 40 months, range 14–60 months). Two patients with PR after four courses of Dexa-BEAM relapsed and died three months posttransplantation. Two patients with CR at the time of transplant relapsed after nine and 13 months respectively. Eight patients had rapid progressive disease after 2–4 cycles of Dexa-BEAM. One patient with progressive disease died in gram-negative sepsis after four cycles of Dexa-BEAM. There was no transplantation-related death. Conclusion: These data suggests the use of high-dose chemotherapy followed by stem cell transplantation at the time of maximal response.
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D.</creator><creatorcontrib>Josting, A. ; Kátay, I. ; Rueffer, U. ; Winter, S. ; Tesch, H. ; Engert, A. ; Diehl, V. ; Wickramanayake, P. D.</creatorcontrib><description>Background: Disease status before high-dose chemotherapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell transplantation (PBSCT) is an important predictor of transplantation-related toxicity and event-free survival (EFS) for patients with relapsed or refractory Hodgkin's disease (HD). We performed a phase II study in patients with relapsed or refractory HD to evaluate the feasibility of four cycles of Dexa-BEAM followed by high-dose chemotherapy with ABMT or PBSCT. Patients and methods:Twenty-six patients (median age 30, range 20–40 years) were treated with 2–4 courses of dexa-methasone, carmustine, etoposide, cytarabine and melphalan (Dexa-BEAM) as salvage chemotherapy in order to attain maximal response. Patients achieving complete response (CR) or partial response (PR) high-dose chemotherapy with ABMT or PBSCT. The conditioning regimen used was CVB (cyclophosphamide, carmustine, etoposide). Results: Eighteen patients responded to Dexa-BEAM, resulting in a response rate of 69%. At the time of transplant 16 patients were in CR two patients in PR. At present 14 patients transplanted are in continous CR (median follow-up 40 months, range 14–60 months). Two patients with PR after four courses of Dexa-BEAM relapsed and died three months posttransplantation. Two patients with CR at the time of transplant relapsed after nine and 13 months respectively. Eight patients had rapid progressive disease after 2–4 cycles of Dexa-BEAM. One patient with progressive disease died in gram-negative sepsis after four cycles of Dexa-BEAM. There was no transplantation-related death. Conclusion: These data suggests the use of high-dose chemotherapy followed by stem cell transplantation at the time of maximal response.</description><identifier>ISSN: 0923-7534</identifier><identifier>EISSN: 1569-8041</identifier><identifier>DOI: 10.1023/A:1008283909959</identifier><identifier>PMID: 9602263</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject><![CDATA[ABMT ; Adult ; Antineoplastic Combined Chemotherapy Protocols - administration & dosage ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Bone Marrow Transplantation ; Carmustine - administration & dosage ; Combined Modality Therapy ; Cyclophosphamide - administration & dosage ; Cytarabine - administration & dosage ; Dexa-BEAM regimen ; Dexamethasone - administration & dosage ; Disease-Free Survival ; Dose-Response Relationship, Drug ; Etoposide - administration & dosage ; Female ; Hematologic and hematopoietic diseases ; Hematopoietic Stem Cell Transplantation ; high-dose chemotherapy ; Hodgkin Disease - mortality ; Hodgkin Disease - pathology ; Hodgkin Disease - therapy ; Hodgkin's disease ; Humans ; Leukemias. 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Myelofibrosis ; Male ; Medical sciences ; Melphalan - administration & dosage ; Middle Aged ; Neoplasm Recurrence, Local - therapy ; PBSCT ; Salvage Therapy ; Survival Rate ; Treatment Outcome]]></subject><ispartof>Annals of oncology, 1998-03, Vol.9 (3), p.289-295</ispartof><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-2cbc040466b8263e2f616856027201faa81d4e1f4aacadc5b0cd5842f531b0e23</citedby><cites>FETCH-LOGICAL-c446t-2cbc040466b8263e2f616856027201faa81d4e1f4aacadc5b0cd5842f531b0e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2227743$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9602263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Josting, A.</creatorcontrib><creatorcontrib>Kátay, I.</creatorcontrib><creatorcontrib>Rueffer, U.</creatorcontrib><creatorcontrib>Winter, S.</creatorcontrib><creatorcontrib>Tesch, H.</creatorcontrib><creatorcontrib>Engert, A.</creatorcontrib><creatorcontrib>Diehl, V.</creatorcontrib><creatorcontrib>Wickramanayake, P. D.</creatorcontrib><title>Favorable outcome of patients with relapsed or refractory Hodgkin's disease treated with high-dose chemotherapy and stem cell rescue at the time of maximal response to conventional salvage therapy (Dexa-BEAM)</title><title>Annals of oncology</title><addtitle>Ann Oncol</addtitle><description>Background: Disease status before high-dose chemotherapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell transplantation (PBSCT) is an important predictor of transplantation-related toxicity and event-free survival (EFS) for patients with relapsed or refractory Hodgkin's disease (HD). We performed a phase II study in patients with relapsed or refractory HD to evaluate the feasibility of four cycles of Dexa-BEAM followed by high-dose chemotherapy with ABMT or PBSCT. Patients and methods:Twenty-six patients (median age 30, range 20–40 years) were treated with 2–4 courses of dexa-methasone, carmustine, etoposide, cytarabine and melphalan (Dexa-BEAM) as salvage chemotherapy in order to attain maximal response. Patients achieving complete response (CR) or partial response (PR) high-dose chemotherapy with ABMT or PBSCT. The conditioning regimen used was CVB (cyclophosphamide, carmustine, etoposide). Results: Eighteen patients responded to Dexa-BEAM, resulting in a response rate of 69%. At the time of transplant 16 patients were in CR two patients in PR. At present 14 patients transplanted are in continous CR (median follow-up 40 months, range 14–60 months). Two patients with PR after four courses of Dexa-BEAM relapsed and died three months posttransplantation. Two patients with CR at the time of transplant relapsed after nine and 13 months respectively. Eight patients had rapid progressive disease after 2–4 cycles of Dexa-BEAM. One patient with progressive disease died in gram-negative sepsis after four cycles of Dexa-BEAM. There was no transplantation-related death. Conclusion: These data suggests the use of high-dose chemotherapy followed by stem cell transplantation at the time of maximal response.</description><subject>ABMT</subject><subject>Adult</subject><subject>Antineoplastic Combined Chemotherapy Protocols - administration &amp; dosage</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Bone Marrow Transplantation</subject><subject>Carmustine - administration &amp; dosage</subject><subject>Combined Modality Therapy</subject><subject>Cyclophosphamide - administration &amp; dosage</subject><subject>Cytarabine - administration &amp; dosage</subject><subject>Dexa-BEAM regimen</subject><subject>Dexamethasone - administration &amp; dosage</subject><subject>Disease-Free Survival</subject><subject>Dose-Response Relationship, Drug</subject><subject>Etoposide - administration &amp; dosage</subject><subject>Female</subject><subject>Hematologic and hematopoietic diseases</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>high-dose chemotherapy</subject><subject>Hodgkin Disease - mortality</subject><subject>Hodgkin Disease - pathology</subject><subject>Hodgkin Disease - therapy</subject><subject>Hodgkin's disease</subject><subject>Humans</subject><subject>Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Melphalan - administration &amp; dosage</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - therapy</subject><subject>PBSCT</subject><subject>Salvage Therapy</subject><subject>Survival Rate</subject><subject>Treatment Outcome</subject><issn>0923-7534</issn><issn>1569-8041</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVUcuO0zAUtRBoKANrVkheIAGLMH7Fidm1wwxFGsSmSGg20Y3jNGaSOLLd0v4ln4Q7LZVYXcvnca_OQeg1JR8pYfxq_okSUrKSK6JUrp6gGc2lykoi6FM0I4rxrMi5eI5ehPCLECIVUxfoQknCmOQz9OcWts5D3RvsNlG7Ic0WTxCtGWPAv23ssDc9TME02Pn0bj3o6PweL12zfrDju4AbGwwEg6M3EBPvUdXZdZc1Ln3rzgwudsbDtMcwNjhEM2Bt-j7ZBb0xGCJOOI72uH6AnR3gEZ3ceDB2WLtxm06ybkxAgH4La4P_mb7_bHaQLW7m3z68RM9a6IN5dZqX6Mftzep6md19__L1en6XaSFkzJiuNRFESFmXKQjDWkllmadYCkZoC1DSRhjaCgANjc5ropu8FKzNOa2JYfwSXR19tXchpFiqyaej_b6ipDpUU82r_6pJijdHxbSpB9Oc-acuEv72hEPQ0KecR23DmcYYKwpxoGVHmk0x7s4w-IdKFrzIq-XP-2qxuleSLYpqxf8CslKpdw</recordid><startdate>19980301</startdate><enddate>19980301</enddate><creator>Josting, A.</creator><creator>Kátay, I.</creator><creator>Rueffer, U.</creator><creator>Winter, S.</creator><creator>Tesch, H.</creator><creator>Engert, A.</creator><creator>Diehl, V.</creator><creator>Wickramanayake, P. 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Malignant lymphomas. Malignant reticulosis. Myelofibrosis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Melphalan - administration &amp; dosage</topic><topic>Middle Aged</topic><topic>Neoplasm Recurrence, Local - therapy</topic><topic>PBSCT</topic><topic>Salvage Therapy</topic><topic>Survival Rate</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Josting, A.</creatorcontrib><creatorcontrib>Kátay, I.</creatorcontrib><creatorcontrib>Rueffer, U.</creatorcontrib><creatorcontrib>Winter, S.</creatorcontrib><creatorcontrib>Tesch, H.</creatorcontrib><creatorcontrib>Engert, A.</creatorcontrib><creatorcontrib>Diehl, V.</creatorcontrib><creatorcontrib>Wickramanayake, P. 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D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Favorable outcome of patients with relapsed or refractory Hodgkin's disease treated with high-dose chemotherapy and stem cell rescue at the time of maximal response to conventional salvage therapy (Dexa-BEAM)</atitle><jtitle>Annals of oncology</jtitle><addtitle>Ann Oncol</addtitle><date>1998-03-01</date><risdate>1998</risdate><volume>9</volume><issue>3</issue><spage>289</spage><epage>295</epage><pages>289-295</pages><issn>0923-7534</issn><eissn>1569-8041</eissn><abstract>Background: Disease status before high-dose chemotherapy with autologous bone marrow transplantation (ABMT) or peripheral blood stem cell transplantation (PBSCT) is an important predictor of transplantation-related toxicity and event-free survival (EFS) for patients with relapsed or refractory Hodgkin's disease (HD). We performed a phase II study in patients with relapsed or refractory HD to evaluate the feasibility of four cycles of Dexa-BEAM followed by high-dose chemotherapy with ABMT or PBSCT. Patients and methods:Twenty-six patients (median age 30, range 20–40 years) were treated with 2–4 courses of dexa-methasone, carmustine, etoposide, cytarabine and melphalan (Dexa-BEAM) as salvage chemotherapy in order to attain maximal response. Patients achieving complete response (CR) or partial response (PR) high-dose chemotherapy with ABMT or PBSCT. The conditioning regimen used was CVB (cyclophosphamide, carmustine, etoposide). Results: Eighteen patients responded to Dexa-BEAM, resulting in a response rate of 69%. At the time of transplant 16 patients were in CR two patients in PR. At present 14 patients transplanted are in continous CR (median follow-up 40 months, range 14–60 months). Two patients with PR after four courses of Dexa-BEAM relapsed and died three months posttransplantation. Two patients with CR at the time of transplant relapsed after nine and 13 months respectively. Eight patients had rapid progressive disease after 2–4 cycles of Dexa-BEAM. One patient with progressive disease died in gram-negative sepsis after four cycles of Dexa-BEAM. There was no transplantation-related death. Conclusion: These data suggests the use of high-dose chemotherapy followed by stem cell transplantation at the time of maximal response.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>9602263</pmid><doi>10.1023/A:1008283909959</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects ABMT
Adult
Antineoplastic Combined Chemotherapy Protocols - administration & dosage
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Bone Marrow Transplantation
Carmustine - administration & dosage
Combined Modality Therapy
Cyclophosphamide - administration & dosage
Cytarabine - administration & dosage
Dexa-BEAM regimen
Dexamethasone - administration & dosage
Disease-Free Survival
Dose-Response Relationship, Drug
Etoposide - administration & dosage
Female
Hematologic and hematopoietic diseases
Hematopoietic Stem Cell Transplantation
high-dose chemotherapy
Hodgkin Disease - mortality
Hodgkin Disease - pathology
Hodgkin Disease - therapy
Hodgkin's disease
Humans
Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis
Male
Medical sciences
Melphalan - administration & dosage
Middle Aged
Neoplasm Recurrence, Local - therapy
PBSCT
Salvage Therapy
Survival Rate
Treatment Outcome
title Favorable outcome of patients with relapsed or refractory Hodgkin's disease treated with high-dose chemotherapy and stem cell rescue at the time of maximal response to conventional salvage therapy (Dexa-BEAM)
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