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From the Department of Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, DC.
| Abstract |
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METHODS. This was an observational series of 100 samples of uveal melanoma in which histologic sections were studied. The cases were selected so that approximately half (n = 49) of the tumors were from patients who had died of metastatic malignant melanoma. The 51 remaining tumors were from patients who had survived at least 9 years without development of metastasis. Central sections from the uveal melanomas were stained using the colloidal silver nitrate stain for nucleolar organizing regions (AgNOR). These were compared with an adjacent hematoxylin and eosin (H&E)stained section. A light microscope with a micrometer inset into the eyepiece (x10) was used at a final magnification of x1000 under oil immersion to measure the length of the nucleolus along the longest axis and the width perpendicular to that axis. From at least twenty cells selected from random fields throughout the tumor, the mean of the 10 longest and widest nucleoli (MLN) was calculated. Seven samples had to be discarded because the nucleoli were unmeasurable.
RESULTS. T-tests and Cox proportional hazard regression analysis indicated that the MLN of nucleolar length as measured on AgNOR-stained slides was as significant as cell type but was more significant than other histopathologic prognosticating variables measured and evaluated in this study. These prognosticators included tumor size, calculated as the largest tumor dimension; MLN width; and MLN length, as measured on H&E-stained sections.
CONCLUSIONS. It has previously been demonstrated that AgNOR-stained nucleoli, unlike H&E-stained nucleoli, can be captured and measured by an automated image analyzer with prognostically significant results. This new method of simple oil-immersion measurements of the longest AgNOR-stained nucleoli length in microscopic sections of uveal melanoma provides an inexpensive and highly significant method for predicting outcome in patients with uveal melanoma. Because of the high contrast with the background, the silver-stained nucleoli clearly define the nucleolar boundaries, rendering them readily discernible and allowing greater ease and speed of measurement when compared with H&E-stained nucleoli. The method of random sampling that was used was comparable with linear sampling in predicting outcome. Highly necrotic tumors, however, had to be excluded from the study because of loss of nucleolar morphology.
| Introduction |
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Gamel and McLean4 and McLean et al.5 focused attention on the large size of the nucleolus as the feature of Callenders epithelioid cells that has the greatest prognostic significance. Thereafter, numerous techniques (Table 1) were developed and refined to objectively measure the mean of the 10 largest nucleoli (MLN).6 7 8 9 10 Predictive results of high correlation between nucleolar diameter and malignant potential were delivered with the studies of both Huntington et al.6 and McCurdy et al.7 However, Coleman et al.8 and Peer et al.9 found no association between their measurements of MLN, made by using computer-assisted automated image capture and analysis (AICA), and patients outcomes.
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McLean et al.10 argued that the size of the nucleolus measured in sections that were stained with silver nitrate for nucleolar organizing regions (AgNOR stain) should correlate with the size of the eosin-stained nucleolus in H&E-stained sections. They found that nucleoli on AgNOR-stained sections were measurable with AICA of monochromatic images, and several of the measurements were superior predictors of the patients outcome when compared with MLN measured by the method of McCurdy et al.7
McLean et al.10 indicated that computer-assisted AICA could be used to measure MLN on silver-stained sections, but their study also left a number of unanswered questions. These included: Was the better prediction of outcome observed with AICA of silver-stained sections than with the method of McCurdy et al.7 a valid finding? If valid, what was the reason for its success? In this study we demonstrated that light micrometer random-field measurements of nucleolar area on silver-stained sections provide more prognostic information on uveal melanomas than these measurements made on H&E-stained sections.
| Materials and Methods |
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The unstained slides were heated in a 60°C oven for 20 minutes to promote adhesion. The sections were deparaffinized and bleached. One-step AgNOR4 staining was performed using two solutions. The first solution was 40 ml of 2% gelatin (Bloom type A; Fisher Scientific, Fair Lawn, NJ) and 0.88% formic acid. The second solution was 80 ml of distilled water in which 40 g of silver nitrate was dissolved. In the dark, the two solutions were mixed, poured into the slide dish to cover the sections, and used to stain them for 30 minutes. The sections were then washed in distilled water, dehydrated, and coverslipped.
Image Analysis
A standard light microscope with a reticle inset into the
eyepiece (x10) and a x100 oil-immersion objective at a final
magnification of x1000 was used to measure the nucleoli. Measurements
were made first on the 100 silver-stained sections and then on the 100
H&E-stained sections. The length of the nucleolus was measured by
turning the eyepiece micrometer to measure along the longest nucleolar
axis. The width was measured perpendicular to the longest axis. The
whole tumor section was scanned, and the observer (AM) selected for
measurement only those nucleoli judged to be the largest in each field.
Measurements on 20 of these nucleoli were retained per tumor, but only
the longest and widest 10 were used for final computation of MLN. The
observer had no knowledge of the patients outcome. Seven samples were
discarded because the nucleoli were unmeasurable, either on the
AgNOR-stained slides (six samples) or on H&E-stained slides (one
additional sample).
Statistical Analysis
Descriptive statistics and t-tests were performed
using standard algorithms. Univariate Cox regression analysis was used
to determine the relative prognostic value of the different
measurements of MLN, cell type, and tumor size (LTD). Cox regression
was chosen for two reasons. First, it is the most frequently used
method of analyzing follow-up data with varying lengths of follow-up
times, and, second, in all previous studies of MLN,6
7
8
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except in the study by McLean et al.,10
Cox regression
Pearson correlation was used to examine the amount of association
between the variables.
After performing Cox regression, we converted each of the variables to a two-group categorical variable by using the cut point closest to the median, so that for each variable, standard measures of the reliability (sensitivity, specificity, and correct prediction) could be calculated. The proportion correctly predicted for two groups is the equivalent of the receiver operating characteristic area reported by McLean et al.10 All analyses were performed by computer (Prodas Statistical Software; Conceptual Software, Houston, TX), with P < 0.05 regarded as significant.
| Results |
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| Discussion |
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It is likely that the eosin and AgNOR stains do not stain the entire nucleolus. Neither of these should stain the granular component that is present in the outermost coating of the nucleolus.12 This coating of granular material and any condensed nuclear chromatin around the nucleolus should stain with hematoxylin on H&E-stained sections. Segmentation of the nucleolus using AICA on monochromatic images would not distinguish hematoxylin from eosin staining. If the amount of this staining were not important in predicting the outcome of patients, then this could be an explanation for the failures of Coleman et al.8 and Peer et al.9 to find a significant association between their measurements of MLN and patient outcome.
| Footnotes |
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The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Department of the Air Force, Department of the Army, Department of the Navy, or Department of Defense.
Submitted for publication June 5, 2000; revised August 30 and December 7, 2000; accepted January 8, 2001.
Commercial relationships policy: N.
Corresponding author: Anouche Moshari, Division of Ophthalmic Pathology, Armed Forces Institute of Pathology, Washington, DC 20306-6000. anouche{at}hotmail.com
| References |
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