Source:http://linkedlifedata.com/resource/pubmed/id/18089850
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2008-2-26
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pubmed:databankReference | |
pubmed:abstractText |
Multisystem Langerhans cell histiocytosis (MS-LCH) is associated with high mortality when patients have risk organ involvement (RO(+)) or are younger than 2 years. In an international randomized trial, LCH-II, we intensified their treatment: arm A consisted of 6 weeks of daily prednisone and weekly vinblastine followed by 18 weeks of daily 6-mercaptopurine with vinblastine/prednisone pulses; etoposide was added in arm B. Considering all 193 randomized risk patients, there were similar outcomes: rapid (6 weeks) response (arm A vs arm B: 63%/71%), 5-year survival probability (74%/79%), disease reactivation frequency (46%/46%), and permanent consequences (43%/37%). However, (1) patients younger than 2 years without RO involvement (RO(-)) had 100% survival and uniformly high (> 80%) rapid response, (2) RO(+) patients not responding within 6 weeks had highest mortality, and (3) importantly, the more intensive arm B reduced mortality in RO(+) patients (relative hazard rate, accounting for differences in risk organ involvement, of 0.54; 95% CI = 0.29-1.00). Finally, comparison of RO(+) patients in LCH-I and LCH-II confirmed that increasing treatment intensity increased rapid responses (from 43% in arm A LCH-I to 68% in arm B LCH-II; P = .027) and reduced mortality (from 44% in arm A LCH-I to 27% in arm B LCH-II; P = .042). We conclude that intensified treatment significantly increases rapid response and reduces mortality in risk MS-LCH. This trial was registered at http://www.controlled-trials.com as no. ISRCTN57679341.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:AricòMaurizioM,
pubmed-author:BraierJorgeJ,
pubmed-author:BroadbentValerieV,
pubmed-author:DonadieuJeanJ,
pubmed-author:GadnerHelmutH,
pubmed-author:GroisNicoleN,
pubmed-author:HenterJan-IngeJI,
pubmed-author:Histiocyte Society,
pubmed-author:LadischStephanS,
pubmed-author:McCarterRobertR,
pubmed-author:MinkovMilenM,
pubmed-author:PötschgerUlrikeU
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pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
111
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2556-62
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pubmed:dateRevised |
2008-10-16
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pubmed:meshHeading |
pubmed-meshheading:18089850-Child, Preschool,
pubmed-meshheading:18089850-Demography,
pubmed-meshheading:18089850-Female,
pubmed-meshheading:18089850-Histiocytosis, Langerhans-Cell,
pubmed-meshheading:18089850-Humans,
pubmed-meshheading:18089850-Infant,
pubmed-meshheading:18089850-Male,
pubmed-meshheading:18089850-Risk Factors,
pubmed-meshheading:18089850-Survival Rate,
pubmed-meshheading:18089850-Treatment Outcome
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pubmed:year |
2008
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pubmed:articleTitle |
Improved outcome in multisystem Langerhans cell histiocytosis is associated with therapy intensification.
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pubmed:affiliation |
Children's Cancer Research Institute, St Anna Children's Hospital, Vienna, Austria. h.gadner@stanna.at
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pubmed:publicationType |
Journal Article,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't,
Multicenter Study
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