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Alkylating cytostatic treatment in renal amyloidosis secondary to rheumatic disease
Fourteen consecutive patients with chronic inflammatory rheumatic disease and reactive renal amyloidosis were treated with alkylating cytostatics in 22 separate periods varying in duration between six and 30 months. Chlorambucil alone was given in 14 treatment periods, cyclophosphamide alone in six,...
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Published in: | Annals of the rheumatic diseases 1987-10, Vol.46 (10), p.757-762 |
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container_title | Annals of the rheumatic diseases |
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creator | Berglund, K Keller, C Thysell, H |
description | Fourteen consecutive patients with chronic inflammatory rheumatic disease and reactive renal amyloidosis were treated with alkylating cytostatics in 22 separate periods varying in duration between six and 30 months. Chlorambucil alone was given in 14 treatment periods, cyclophosphamide alone in six, and both alternately in two. The dosage was adjusted to attain a major suppression of the rheumatic inflammation and a blood lymphocyte level below 1.0 X 10(9)/l. Renal function improved in 12 treatment periods, renal deterioration was arrested in three periods, and in another four periods the rate of functional decline slowed down. In the remaining three treatment periods, associated with further deterioration in renal function, treatment was inadequate owing to blood dyscrasia and failure to control hypertension. Glomerular filtration rate (GFR) was followed more closely in 10 treatment periods, in all of which the falling trend was arrested or reduced. The survival rate at five years was 93%. Three patients who dropped out of the treatment programme are so far the only ones not still alive. Nine are still being followed up after 6-17 years, and the other two remaining live patients have had renal transplants for five years. |
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Chlorambucil alone was given in 14 treatment periods, cyclophosphamide alone in six, and both alternately in two. The dosage was adjusted to attain a major suppression of the rheumatic inflammation and a blood lymphocyte level below 1.0 X 10(9)/l. Renal function improved in 12 treatment periods, renal deterioration was arrested in three periods, and in another four periods the rate of functional decline slowed down. In the remaining three treatment periods, associated with further deterioration in renal function, treatment was inadequate owing to blood dyscrasia and failure to control hypertension. Glomerular filtration rate (GFR) was followed more closely in 10 treatment periods, in all of which the falling trend was arrested or reduced. The survival rate at five years was 93%. Three patients who dropped out of the treatment programme are so far the only ones not still alive. Nine are still being followed up after 6-17 years, and the other two remaining live patients have had renal transplants for five years.</description><identifier>ISSN: 0003-4967</identifier><identifier>EISSN: 1468-2060</identifier><identifier>DOI: 10.1136/ard.46.10.757</identifier><identifier>PMID: 3500678</identifier><identifier>CODEN: ARDIAO</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and European League Against Rheumatism</publisher><subject>Adult ; Amyloidosis - drug therapy ; Amyloidosis - etiology ; Amyloidosis - physiopathology ; Antineoplastic agents ; Biological and medical sciences ; Chlorambucil - therapeutic use ; Cyclophosphamide - therapeutic use ; Female ; General aspects ; Humans ; Kidney - physiopathology ; Kidney Diseases - drug therapy ; Kidney Diseases - etiology ; Kidney Diseases - physiopathology ; Male ; Medical sciences ; Pharmacology. Drug treatments ; Rheumatic Diseases - complications ; Rheumatic Diseases - drug therapy</subject><ispartof>Annals of the rheumatic diseases, 1987-10, Vol.46 (10), p.757-762</ispartof><rights>1988 INIST-CNRS</rights><rights>Copyright BMJ Publishing Group LTD Oct 1987</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b510t-6097fb20cdbb4a343f2b2959bc82eb7fc88379cfa3dcb9b81999baa2a68397f03</citedby><cites>FETCH-LOGICAL-b510t-6097fb20cdbb4a343f2b2959bc82eb7fc88379cfa3dcb9b81999baa2a68397f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1003383/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC1003383/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7778664$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3500678$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Berglund, K</creatorcontrib><creatorcontrib>Keller, C</creatorcontrib><creatorcontrib>Thysell, H</creatorcontrib><title>Alkylating cytostatic treatment in renal amyloidosis secondary to rheumatic disease</title><title>Annals of the rheumatic diseases</title><addtitle>Ann Rheum Dis</addtitle><description>Fourteen consecutive patients with chronic inflammatory rheumatic disease and reactive renal amyloidosis were treated with alkylating cytostatics in 22 separate periods varying in duration between six and 30 months. Chlorambucil alone was given in 14 treatment periods, cyclophosphamide alone in six, and both alternately in two. The dosage was adjusted to attain a major suppression of the rheumatic inflammation and a blood lymphocyte level below 1.0 X 10(9)/l. Renal function improved in 12 treatment periods, renal deterioration was arrested in three periods, and in another four periods the rate of functional decline slowed down. In the remaining three treatment periods, associated with further deterioration in renal function, treatment was inadequate owing to blood dyscrasia and failure to control hypertension. Glomerular filtration rate (GFR) was followed more closely in 10 treatment periods, in all of which the falling trend was arrested or reduced. The survival rate at five years was 93%. Three patients who dropped out of the treatment programme are so far the only ones not still alive. Nine are still being followed up after 6-17 years, and the other two remaining live patients have had renal transplants for five years.</description><subject>Adult</subject><subject>Amyloidosis - drug therapy</subject><subject>Amyloidosis - etiology</subject><subject>Amyloidosis - physiopathology</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Chlorambucil - therapeutic use</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Female</subject><subject>General aspects</subject><subject>Humans</subject><subject>Kidney - physiopathology</subject><subject>Kidney Diseases - drug therapy</subject><subject>Kidney Diseases - etiology</subject><subject>Kidney Diseases - physiopathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Rheumatic Diseases - complications</subject><subject>Rheumatic Diseases - drug therapy</subject><issn>0003-4967</issn><issn>1468-2060</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNqFkU1PGzEQhi1URNOUI0ekldpDL5va611_XCqhCCgSgkP4OFpjrxccdtfUdhD595gmiuipkiV79D4z83oGoSOCZ4RQ9hNCO6vZLIe84XtoQmomygoz_AlNMMa0rCXjn9GXGJc5xIKIA3RAG4wZFxO0OOmf1j0kNz4UZp18TPltihQspMGOqXBjEewIfQHDuveu9dHFIlrjxxbCuki-CI92NfzNal20EO1XtN9BH-3h9p6i27PTm_nv8vL6_GJ-clnqhuBUMix5pytsWq1roDXtKl3JRmojKqt5Z4SgXJoOaGu01IJIKTVABUzQnInpFP3a1H1e6cG2JtsN0Kvn4IZsTXlw6l9ldI_qwb8oksdCBc0Fvm0LBP9nZWNSS78K-bNREc4kr_KpM1VuKBN8jMF2uw4Eq_cVqLwCVbP3MK8g88cfbe3o7cyz_n2rQzTQdwFG4-IO45wLxj60dTHZ150M4UkxTnmjru7mSt5RKRY392qe-R8bXg_L_zh8A1NirUg</recordid><startdate>19871001</startdate><enddate>19871001</enddate><creator>Berglund, K</creator><creator>Keller, C</creator><creator>Thysell, H</creator><general>BMJ Publishing Group Ltd and European League Against Rheumatism</general><general>BMJ</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>19871001</creationdate><title>Alkylating cytostatic treatment in renal amyloidosis secondary to rheumatic disease</title><author>Berglund, K ; Keller, C ; Thysell, H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b510t-6097fb20cdbb4a343f2b2959bc82eb7fc88379cfa3dcb9b81999baa2a68397f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Adult</topic><topic>Amyloidosis - drug therapy</topic><topic>Amyloidosis - etiology</topic><topic>Amyloidosis - physiopathology</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Chlorambucil - therapeutic use</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Female</topic><topic>General aspects</topic><topic>Humans</topic><topic>Kidney - physiopathology</topic><topic>Kidney Diseases - drug therapy</topic><topic>Kidney Diseases - etiology</topic><topic>Kidney Diseases - physiopathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Rheumatic Diseases - complications</topic><topic>Rheumatic Diseases - drug therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Berglund, K</creatorcontrib><creatorcontrib>Keller, C</creatorcontrib><creatorcontrib>Thysell, H</creatorcontrib><collection>Istex</collection><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>ProQuest Central (Corporate)</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>ProQuest Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Science Journals (ProQuest Database)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Annals of the rheumatic diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Berglund, K</au><au>Keller, C</au><au>Thysell, H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alkylating cytostatic treatment in renal amyloidosis secondary to rheumatic disease</atitle><jtitle>Annals of the rheumatic diseases</jtitle><addtitle>Ann Rheum Dis</addtitle><date>1987-10-01</date><risdate>1987</risdate><volume>46</volume><issue>10</issue><spage>757</spage><epage>762</epage><pages>757-762</pages><issn>0003-4967</issn><eissn>1468-2060</eissn><coden>ARDIAO</coden><abstract>Fourteen consecutive patients with chronic inflammatory rheumatic disease and reactive renal amyloidosis were treated with alkylating cytostatics in 22 separate periods varying in duration between six and 30 months. Chlorambucil alone was given in 14 treatment periods, cyclophosphamide alone in six, and both alternately in two. The dosage was adjusted to attain a major suppression of the rheumatic inflammation and a blood lymphocyte level below 1.0 X 10(9)/l. Renal function improved in 12 treatment periods, renal deterioration was arrested in three periods, and in another four periods the rate of functional decline slowed down. In the remaining three treatment periods, associated with further deterioration in renal function, treatment was inadequate owing to blood dyscrasia and failure to control hypertension. Glomerular filtration rate (GFR) was followed more closely in 10 treatment periods, in all of which the falling trend was arrested or reduced. The survival rate at five years was 93%. Three patients who dropped out of the treatment programme are so far the only ones not still alive. Nine are still being followed up after 6-17 years, and the other two remaining live patients have had renal transplants for five years.</abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and European League Against Rheumatism</pub><pmid>3500678</pmid><doi>10.1136/ard.46.10.757</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Amyloidosis - drug therapy Amyloidosis - etiology Amyloidosis - physiopathology Antineoplastic agents Biological and medical sciences Chlorambucil - therapeutic use Cyclophosphamide - therapeutic use Female General aspects Humans Kidney - physiopathology Kidney Diseases - drug therapy Kidney Diseases - etiology Kidney Diseases - physiopathology Male Medical sciences Pharmacology. Drug treatments Rheumatic Diseases - complications Rheumatic Diseases - drug therapy |
title | Alkylating cytostatic treatment in renal amyloidosis secondary to rheumatic disease |
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