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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
1999-1-5
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pubmed:abstractText |
In a single institution, we have used recombinant interferon- (IFN-) to treat 116 newly diagnosed Philadelphia-positive (Ph+) chronic myeloid leukemia (CML) patients and analyzed the predictive factors for response and survival. The patients whose median age was 50.3 years (range, 9 to 70) were administered IFN- (5 million units/m2/d) subcutaneously. The IFN- dose was subsequently adjusted to maintain the white blood cell and platelet counts between 1.5 and 5 x 10(9)/L, 50 and 100 x 10(9)/L, respectively. At diagnosis, the Sokal score was used to classify the patients into three groups: low (n = 57), intermediate (n = 42), and high risk (n = 16). A complete hematological response (CHR) was achieved in 93 cases (80.2%). Of the 116 patients, 113 were available for cytogenetic evaluation. Fifty patients (43%) achieved a major cytogenetic response (MCR) (=65% marrow Ph- cells), 37 of them having a complete cytogenetic response (CCR). The estimated 5-year survival of the 116 patients was 68% +/- 11% (95% confidence interval [CI]) with a median follow-up of 42 months (range, 3 to 114) and 85% +/- 11% (95% CI) with a median follow-up of 30.9 (range, 3 to 111) when patients were censored at the time of transplantation. Event-free survival at 5 years (adding death and transplant as event) was 46% +/- 11% (95% CI). Using proportional hazards regression to study time-dependent variables, we confirmed that the most significant factor associated with survival was the cytogenetic response (MCR or CCR) (P <.0001). This factor was independent compared with the Sokal score and baseline variables used to calculate the Sokal score. Moreover, using either univariate or multivariate analysis, the achievement of CHR within 3 months was strongly correlated with MCR (P <.0001). Minimum cytogenetic response (mCR, ie, at least 5% of Ph- metaphases) at 3 months was also a significant predictive factor for MCR (P <.0001). These results show that IFN- can induce a high rate of hematological and cytogenetic response when administered in doses leading to myelosuppression. Factors such as the achievement of CHR and mCR within 3 months could be useful to identify early those patients who will not respond to IFN- and who need alternative treatments such as stem cell transplantation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
|
pubmed:issn |
0006-4971
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pubmed:author |
pubmed-author:BernardPP,
pubmed-author:Bilhou-NaberaCC,
pubmed-author:BoironJ MJM,
pubmed-author:CarrèreAA,
pubmed-author:Cony-MakhoulPP,
pubmed-author:FabèresCC,
pubmed-author:MahonF XFX,
pubmed-author:MarisFF,
pubmed-author:MontastrucMM,
pubmed-author:PigneuxAA,
pubmed-author:PueyoSS,
pubmed-author:ReiffersJJ,
pubmed-author:SalmiRR
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pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
92
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
4059-65
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:9834210-Administration, Cutaneous,
pubmed-meshheading:9834210-Adolescent,
pubmed-meshheading:9834210-Adult,
pubmed-meshheading:9834210-Aged,
pubmed-meshheading:9834210-Child,
pubmed-meshheading:9834210-Female,
pubmed-meshheading:9834210-Humans,
pubmed-meshheading:9834210-Interferon Type I,
pubmed-meshheading:9834210-Leukemia, Myelogenous, Chronic, BCR-ABL Positive,
pubmed-meshheading:9834210-Male,
pubmed-meshheading:9834210-Middle Aged,
pubmed-meshheading:9834210-Predictive Value of Tests,
pubmed-meshheading:9834210-Prognosis,
pubmed-meshheading:9834210-Recombinant Proteins,
pubmed-meshheading:9834210-Survival Analysis,
pubmed-meshheading:9834210-Time Factors
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pubmed:year |
1998
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pubmed:articleTitle |
Response at three months is a good predictive factor for newly diagnosed chronic myeloid leukemia patients treated by recombinant interferon-alpha.
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pubmed:affiliation |
Service des Maladies du Sang, Centre Hospitalier Universitaire de Bordeaux, Hôpital Haut-Levêque, Pessac, France.
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pubmed:publicationType |
Journal Article,
Clinical Trial
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