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1.
Journal of Chinese Physician ; (12): 701-704, 2017.
Article in Chinese | WPRIM | ID: wpr-610059

ABSTRACT

Objective To explore the value of minimal residual disease with acute myeloid leukemia in prognostic evaluation and its correlation with cell morphology and genetics.Methods A total of 105 patients with acute myeloid leukemia (AML) (non M3) was used as the research subjects to evaluate the correlation between the level of minimal residual disease (MRD) and the degree of cellular morphological remission,and cytogenetics.According to the different levels of MRD,78 patients of cell morphology complete remission (CR) were grouped to evaluate the one-year recurrence rate after the first chemotherapy treatment.Results The correlation was evaluated between MRD level and morphological remission in 105 patients with AML after initial chemotherapy.In the degree of cellular morphological remission cell evaluation showed 78 (74.29%) cases of CR,27 (25.71%) cases of partial remission (PR) or non remission (NR).Among 78 cases of CR,MRD negative rate was 66.67% (52/78),MRD was 33.33% (26/78);and 27 cases of NR or PR,MRD was 100% (27/27).The correlation between MRD level and cytogenetic evaluation,cytogenetic prognosis group and prognosis of middle group and poor prognosis group,and the negative rate of MRD were 66.67%,45.90%,and 35.29%,without significant difference (P > 0.05).Seventy eight patients with CR were divided into two groups according to the level of MRD to evaluate the recurrence rate of the 1 year,the recurrence rate of the positive group was significantly higher than that of the negative group (P < 0.05).Conclusions With the development of hematology,the meaning of CR deeply,using flow cytometry method to detect the MRD,MRD positive cells relapse earlier than the traditional morphology,it has important clinical significance for guiding treatment and early prediction of recurrence of CR AML.

2.
Journal of Zhejiang University. Medical sciences ; (6): 59-65, 2017.
Article in Chinese | WPRIM | ID: wpr-300823

ABSTRACT

To establish a fetal biparietal diameter (BPD)-gestational age formula based on the data of pregnant women from Xiaoshan District of Hangzhou, and to evaluate its application in prenatal screening.Data of 3500 pregnant women with gestational age between 15 weeks and 19 weeks+6 receiving prenatal screening in Xiaoshan Hospital during May 2014 and May 2015 were collected. BPDs were used to establish a localized BPD-gestational age formula. The localized formula was used to evaluate the prenatal screening risks in 1759 pregnant women with irregular menstrual cycles or uncertain last menstrual period (LMP) in Xiaoshan District, and the results were compared with those calculated using formula in LifeCycle 4.0.With localized formula, the total positive rate of Down syndrome, trisomy 18 syndrome and deformity of neural tube was decreased from 6.96% to 5.85% (<0.05), in which the positive rate of Down syndrome decreased (<0.05), that of deformity of neural tube increased (<0.05), and that of trisomy 18 syndrome remained the same (>0.05). The median MoMs of free-hCG β and α-fetoprotein calculated using localized formula were significantly different from those calculated using the formula in LifeCycle 4.0 (all<0.05), and the former ones were more closer to 1. For women of fetus diagnosed with the above diseases, the positive rate calculated using localized formula was almost the same as that calculated using the formula in LifeCycle 4.0.BPD-gestational age formula should be localized based on the statistical analysis of the local population, which will help to reduce the false positive rate, and make the results more accurate and reliable in prenatal screening.


Subject(s)
Adult , Female , Humans , Pregnancy , Body Weights and Measures , Reference Standards , Cephalometry , Reference Standards , Chorionic Gonadotropin, beta Subunit, Human , Blood , Reference Standards , Chromosomes, Human, Pair 18 , Down Syndrome , Diagnosis , Embryology , Epidemiologic Measurements , Fetal Development , Gestational Age , Head , Embryology , Mass Screening , Methods , Reference Standards , Menstrual Cycle , Neural Tube Defects , Diagnosis , Embryology , Prenatal Diagnosis , Methods , Reference Standards , Reference Values , Trisomy , Diagnosis , Trisomy 18 Syndrome , alpha-Fetoproteins , Reference Standards
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