Phase I trial of m-BACOD and granulocyte macrophage colony stimulating factor in HIV-associated non-Hodgkin's lymphoma

The use of full-dose intensive regimens of chemotherapy in patients with HIV-associated lymphoma has often resulted in severe toxicity, treatment delay, and reduced subsequent dosing. We conducted a Phase I trial to evaluate the toxicity of the combination of m-BACOD (methotrexate, Bleomycin, doxoru...

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Veröffentlicht in:Journal of acquired immune deficiency syndromes (1988) 1993-03, Vol.6 (3), p.265-271
Hauptverfasser: WALSH, C, WERNZ, J. C, LEVINE, A, RARICK, M, WILLSON, E, MELENDEZ, D, BONNEM, E, THOMPSON, J, SHELTON, B
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container_issue 3
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container_title Journal of acquired immune deficiency syndromes (1988)
container_volume 6
creator WALSH, C
WERNZ, J. C
LEVINE, A
RARICK, M
WILLSON, E
MELENDEZ, D
BONNEM, E
THOMPSON, J
SHELTON, B
description The use of full-dose intensive regimens of chemotherapy in patients with HIV-associated lymphoma has often resulted in severe toxicity, treatment delay, and reduced subsequent dosing. We conducted a Phase I trial to evaluate the toxicity of the combination of m-BACOD (methotrexate, Bleomycin, doxorubicin, cyclophosphamide, vincristine, dexamethasone) with granulocyte-macrophage colony stimulating factor (GMCSF) in these patients. A total of 17 patients were entered and treated at three dose levels of m-BACOD in combination with a fixed dose of GMCSF. Eight patients received standard dose m-BACOD plus GMCSF without experiencing dose-limiting hematologic toxicity, although significant nonhematologic toxicity was seen. We conclude that it is feasible to treat patients with HIV-associated lymphoma using standard dose m-BACOD plus GMCSF, but further study is needed to determine whether full-dose regimens improve survival when compared with reduced dose regimens in these individuals.
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We conclude that it is feasible to treat patients with HIV-associated lymphoma using standard dose m-BACOD plus GMCSF, but further study is needed to determine whether full-dose regimens improve survival when compared with reduced dose regimens in these individuals.</description><identifier>ISSN: 0894-9255</identifier><identifier>ISSN: 1525-4135</identifier><identifier>EISSN: 2331-2289</identifier><identifier>EISSN: 1944-7884</identifier><identifier>PMID: 7680712</identifier><identifier>CODEN: JAISET</identifier><language>eng</language><publisher>New York, NY: Raven Press</publisher><subject><![CDATA[Adult ; AIDS-Related Opportunistic Infections - complications ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Biological and medical sciences ; Bleomycin - administration & dosage ; Bleomycin - adverse effects ; Cancer ; Chemotherapy ; Cyclophosphamide - administration & dosage ; Cyclophosphamide - adverse effects ; Dexamethasone - administration & dosage ; Dexamethasone - adverse effects ; Doxorubicin - administration & dosage ; Doxorubicin - adverse effects ; Drug therapy ; Granulocyte-Macrophage Colony-Stimulating Factor - adverse effects ; Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use ; HIV ; HIV Core Protein p24 - blood ; Human immunodeficiency virus ; Humans ; Kidney - drug effects ; Leucovorin - administration & dosage ; Leucovorin - adverse effects ; Leukocyte Count - drug effects ; Lung - drug effects ; Lymphoma, AIDS-Related - blood ; Lymphoma, AIDS-Related - drug therapy ; Lymphoma, Non-Hodgkin - blood ; Lymphoma, Non-Hodgkin - drug therapy ; Male ; Medical research ; Medical sciences ; Methotrexate - administration & dosage ; Methotrexate - adverse effects ; Neutropenia - chemically induced ; Pharmacology. Drug treatments ; Remission Induction ; Vincristine - administration & dosage ; Vincristine - adverse effects]]></subject><ispartof>Journal of acquired immune deficiency syndromes (1988), 1993-03, Vol.6 (3), p.265-271</ispartof><rights>1993 INIST-CNRS</rights><rights>Copyright Lippincott Williams &amp; Wilkins Mar 1993</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=4626119$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7680712$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WALSH, C</creatorcontrib><creatorcontrib>WERNZ, J. C</creatorcontrib><creatorcontrib>LEVINE, A</creatorcontrib><creatorcontrib>RARICK, M</creatorcontrib><creatorcontrib>WILLSON, E</creatorcontrib><creatorcontrib>MELENDEZ, D</creatorcontrib><creatorcontrib>BONNEM, E</creatorcontrib><creatorcontrib>THOMPSON, J</creatorcontrib><creatorcontrib>SHELTON, B</creatorcontrib><title>Phase I trial of m-BACOD and granulocyte macrophage colony stimulating factor in HIV-associated non-Hodgkin's lymphoma</title><title>Journal of acquired immune deficiency syndromes (1988)</title><addtitle>J Acquir Immune Defic Syndr (1988)</addtitle><description>The use of full-dose intensive regimens of chemotherapy in patients with HIV-associated lymphoma has often resulted in severe toxicity, treatment delay, and reduced subsequent dosing. 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Drug treatments</subject><subject>Remission Induction</subject><subject>Vincristine - administration &amp; dosage</subject><subject>Vincristine - adverse effects</subject><issn>0894-9255</issn><issn>1525-4135</issn><issn>2331-2289</issn><issn>1944-7884</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkE1LxDAYhIsoun78BCGI6KnQfDRpjuv6sQuCHtRreZu-3c2aJrVphf33Flw8eJrDPAwzc5DMGOc0ZazQh8ksK7RINcvzk-Q0xm2W5YVW_Dg5VrLIFGWz5Pt1AxHJigy9BUdCQ9r0br54uSfga7LuwY8umN2ApAXTh24DayQmuOB3JA62HR0M1q9JA2YIPbGeLFcfKcQYjIUBa-KDT5ehXn9afxuJ27XdJrRwnhw14CJe7PUseX98eFss0-eXp9Vi_px2TPMh1QIBBGUSeDVtqbIGdaWg0ah4hWCooihqgyrjZtpd50VNaV2w3CDmQlX8LLn5ze368DViHMrWRoPOgccwxpJKUQgp1QRe_QO3Yez91K2cgqXkXNAJutxDY9ViXXa9baHflfs3J_9670M04JrpPWPjHyYkk5Rq_gNanH7S</recordid><startdate>19930301</startdate><enddate>19930301</enddate><creator>WALSH, C</creator><creator>WERNZ, J. 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C</au><au>LEVINE, A</au><au>RARICK, M</au><au>WILLSON, E</au><au>MELENDEZ, D</au><au>BONNEM, E</au><au>THOMPSON, J</au><au>SHELTON, B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phase I trial of m-BACOD and granulocyte macrophage colony stimulating factor in HIV-associated non-Hodgkin's lymphoma</atitle><jtitle>Journal of acquired immune deficiency syndromes (1988)</jtitle><addtitle>J Acquir Immune Defic Syndr (1988)</addtitle><date>1993-03-01</date><risdate>1993</risdate><volume>6</volume><issue>3</issue><spage>265</spage><epage>271</epage><pages>265-271</pages><issn>0894-9255</issn><issn>1525-4135</issn><eissn>2331-2289</eissn><eissn>1944-7884</eissn><coden>JAISET</coden><abstract>The use of full-dose intensive regimens of chemotherapy in patients with HIV-associated lymphoma has often resulted in severe toxicity, treatment delay, and reduced subsequent dosing. We conducted a Phase I trial to evaluate the toxicity of the combination of m-BACOD (methotrexate, Bleomycin, doxorubicin, cyclophosphamide, vincristine, dexamethasone) with granulocyte-macrophage colony stimulating factor (GMCSF) in these patients. A total of 17 patients were entered and treated at three dose levels of m-BACOD in combination with a fixed dose of GMCSF. Eight patients received standard dose m-BACOD plus GMCSF without experiencing dose-limiting hematologic toxicity, although significant nonhematologic toxicity was seen. We conclude that it is feasible to treat patients with HIV-associated lymphoma using standard dose m-BACOD plus GMCSF, but further study is needed to determine whether full-dose regimens improve survival when compared with reduced dose regimens in these individuals.</abstract><cop>New York, NY</cop><pub>Raven Press</pub><pmid>7680712</pmid><tpages>7</tpages></addata></record>
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identifier ISSN: 0894-9255
ispartof Journal of acquired immune deficiency syndromes (1988), 1993-03, Vol.6 (3), p.265-271
issn 0894-9255
1525-4135
2331-2289
1944-7884
language eng
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source Freely Accessible Journals; MEDLINE; Journals@Ovid LWW Legacy Archive; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Journals@Ovid Complete
subjects Adult
AIDS-Related Opportunistic Infections - complications
Antineoplastic agents
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Bleomycin - administration & dosage
Bleomycin - adverse effects
Cancer
Chemotherapy
Cyclophosphamide - administration & dosage
Cyclophosphamide - adverse effects
Dexamethasone - administration & dosage
Dexamethasone - adverse effects
Doxorubicin - administration & dosage
Doxorubicin - adverse effects
Drug therapy
Granulocyte-Macrophage Colony-Stimulating Factor - adverse effects
Granulocyte-Macrophage Colony-Stimulating Factor - therapeutic use
HIV
HIV Core Protein p24 - blood
Human immunodeficiency virus
Humans
Kidney - drug effects
Leucovorin - administration & dosage
Leucovorin - adverse effects
Leukocyte Count - drug effects
Lung - drug effects
Lymphoma, AIDS-Related - blood
Lymphoma, AIDS-Related - drug therapy
Lymphoma, Non-Hodgkin - blood
Lymphoma, Non-Hodgkin - drug therapy
Male
Medical research
Medical sciences
Methotrexate - administration & dosage
Methotrexate - adverse effects
Neutropenia - chemically induced
Pharmacology. Drug treatments
Remission Induction
Vincristine - administration & dosage
Vincristine - adverse effects
title Phase I trial of m-BACOD and granulocyte macrophage colony stimulating factor in HIV-associated non-Hodgkin's lymphoma
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