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  • 1
    ISSN: 1432-0843
    Keywords: Key words Mitotic index ; Chemotherapy ; Sensitivity ; SRCA ; Morphometry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The subrenal capsule assay (SRCA) is used in clinical oncology to assess the sensitivity of individual malignant tumors to various anticancer agents and their combinations. Mitotic indices reflect cancer cell proliferation and have prognostic value in epithelial neoplasms, including ovarian carcinoma. We combined the two tests (SRCA, mitotic index) by evaluating the numbers of mitotic figures per square millimeter of neoplastic epithelium (M/V) in paraffin-embedded tumor samples after SRCA. The M/V index was compared with the tumor size measurement (dTS), which is used in conventional SRCA to predict the drug response. Histology examination showed insignificant changes in the size of tumor transplants due to host reaction but disclosed a number of potential errors in the use of dTS to evaluate transplant growth and drug effects. In our series of 62 patients with advanced ovarian carcinoma the M/V value was superior to the dTS in explaining the clinical response after 6 months as assessed at second-look laparotomy. Patients showing no response had significantly higher M/V values than did those displaying complete or partial responses (P 〈 0.033). The use of 6 mitotic figures/mm2 as a limit differentiating responders from nonresponders resulted in an overall predictive accuracy of 79% in the logistic regression analysis. In comparison to the FIGO stage, residual tumor size, and the dTS, the M/V value obtained for the cytostatic combination given to the patient was the single most significant factor predicting the 6-month clinical response. The results indicate that the combined use of the M/V index and SRCA is a promising new approach to prediction of the drug response in ovarian adenocarcinoma.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0428
    Keywords: Insulin profiles ; hypoinsulinaemia ; diabetic children ; C-peptide ; glucose profiles ; hypoglycaemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We studied associations of 24-h serum insulin profiles with insulin dose, age, gender, haemoglobin A1c (HbA1c) and C-peptide values, as well as blood glucose profiles in 77 consecutive childrennine aged 2–4, 14 aged 5–8, 26 aged 9–12, and 28 aged 13–17 years—2 years after the onset of insulindependent diabetes mellitus (IDDM). Mean weightbased insulin doses in the four age groups were similar (0.7±0.2 U·kg−1·day−1 in all); body surface-area-based doses differed. Insulin doses correlated significantly with the 24-h mean and area-under-thecurve (AUC) values, and with mean values at 03.00 hours of serum insulin in the children aged 5–8 and 13–17 years. The mean insulin concentrations of the age groups (95% confidence intervals) increased with age [6.1 (3.8, 9.7), 7.6 (5.9, 9.8), 10.4 (8.6, 12.4), and 14.0 (11.6, 16.8) mU/l;p〈0.0002]. The 24-h mean of serum insulin together with HbA1c concentration predicted 32% of the variation of mean blood glucose concentrations. Of children aged less than 9 years, 50% had insulin values less than 5 mU/l (healthy subjects' lower reference limit), and 14% were of less than 2 mU/l (detection limit of the assay) at 03.00 hours. At 07.00 hours, 82% had insulin values of less than 5 mU/l, and 36% were of less than 2 mU/l, respectively. Some young children had night-time hypoglycaemia with simultaneous hypoinsulinaemia. Insulin profiles correlated poorly with the HbA1c and peak C-peptide values. We conclude that in children the mean and AUC values of serum insulin profiles are age-dependent but C-peptide independent 2 years after the diagnosis of IDDM despite similar weight-based mean insulin doses. Nocturnal and morning hypoinsulinaemia was a frequent finding in the younger children, as was biochemical hypoglycaemia. These findings suggest that insulin kinetics and sensitivity differ markedly in children according to age. [Diabetologia (1995) 38:97–105]
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-0428
    Keywords: Key words Insulin profiles ; hypoinsulinaemia ; diabetic children ; C-peptide ; glucose profiles ; hypoglycaemia.
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We studied associations of 24-h serum insulin profiles with insulin dose, age, gender, haemoglobin A1c (HbA1c) and C-peptide values, as well as blood glucose profiles in 77 consecutive children – nine aged 2–4, 14 aged 5–8, 26 aged 9–12, and 28 aged 13–17 years – 2 years after the onset of insulin-dependent diabetes mellitus (IDDM). Mean weight-based insulin doses in the four age groups were similar (0.7 ± 0.2 U · kg−1· day−1 in all); body surface-area-based doses differed. Insulin doses correlated significantly with the 24-h mean and area-under-the-curve (AUC) values, and with mean values at 03.00 hours of serum insulin in the children aged 5–8 and 13–17 years. The mean insulin concentrations of the age groups (95 % confidence intervals) increased with age [6.1 (3.8, 9.7), 7.6 (5.9, 9.8), 10.4 (8.6, 12.4), and 14.0 (11.6, 16.8) mU/l; p 〈 0.0002]. The 24-h mean of serum insulin together with HbA1c concentration predicted 32 % of the variation of mean blood glucose concentrations. Of children aged less than 9 years, 50 % had insulin values less than 5 mU/l (healthy subjects' lower reference limit), and 14 % were of less than 2 mU/l (detection limit of the assay) at 03.00 hours. At 07.00 hours, 82 % had insulin values of less than 5 mU/l, and 36 % were of less than 2 mU/l, respectively. Some young children had night-time hypoglycaemia with simultaneous hypoinsulinaemia. Insulin profiles correlated poorly with the HbA1c and peak C-peptide values. We conclude that in children the mean and AUC values of serum insulin profiles are age-dependent but C-peptide independent 2 years after the diagnosis of IDDM despite similar weight-based mean insulin doses. Nocturnal and morning hypoinsulinaemia was a frequent finding in the younger children, as was biochemical hypoglycaemia. These findings suggest that insulin kinetics and sensitivity differ markedly in children according to age. [Diabetologia (1995) 38: 97–105]
    Type of Medium: Electronic Resource
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